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Pediatric Disease Annotations & Medicines



   c syndrome
  

Disease ID 548
Disease c syndrome
Definition
A rare multiple congenital anomaly/intellectual disability syndrome characterised by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability. The aetiology of C syndrome is still unknown. Although most of the reported patients are sporadic, rare cases of familial occurrence have been described.
Synonym
opitz trigonocephaly syndrome
syndrome c
trigonocephaly c syndrome
trigonocephaly c syndrome (disorder)
trigonocephaly syndrome
Orphanet
OMIM
UMLS
C0796095
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:841)
C0028754  |  obesity  |  377
C0011847  |  diabetes  |  186
C0020538  |  hypertension  |  140
C0042373  |  vascular disease  |  82
C0011860  |  type 2 diabetes  |  80
C0007222  |  cardiovascular disease  |  69
C0023895  |  liver disease  |  62
C0033687  |  proteinuria  |  61
C0036341  |  schizophrenia  |  59
C0011849  |  diabetes mellitus  |  49
C0004153  |  atherosclerosis  |  49
C0022658  |  nephropathy  |  45
C0002871  |  anemia  |  41
C0033860  |  psoriasis  |  38
C0010068  |  coronary artery disease  |  38
C0035078  |  renal failure  |  33
C0242379  |  lung cancer  |  33
C0022658  |  kidney disease  |  33
C0028754  |  adiposity  |  31
C0024299  |  lymphoma  |  31
C0023418  |  leukemia  |  30
C0040053  |  thrombosis  |  29
C0006142  |  breast cancer  |  28
C0018799  |  heart disease  |  28
C0011860  |  type 2 diabetes mellitus  |  27
C0011570  |  depression  |  27
C0022661  |  chronic kidney disease  |  25
C0520679  |  obstructive sleep apnea  |  24
C0032460  |  polycystic ovary syndrome  |  24
C0282193  |  iron overload  |  23
C0740394  |  hyperuricemia  |  23
C0037315  |  sleep apnea  |  23
C0017665  |  membranous nephropathy  |  21
C0018801  |  heart failure  |  21
C0023467  |  acute myeloid leukemia  |  21
C0024141  |  systemic lupus erythematosus  |  20
C0020459  |  hyperinsulinemia  |  20
C0042373  |  vascular diseases  |  20
C0003873  |  rheumatoid arthritis  |  20
C0027051  |  myocardial infarction  |  20
C0027051  |  myocardial infarct  |  20
C0023470  |  myeloid leukemia  |  20
C0010068  |  coronary heart disease  |  18
C0019158  |  hepatitis  |  18
C0009319  |  colitis  |  18
C0032460  |  polycystic ovary  |  18
C0178664  |  glomerulosclerosis  |  17
C0017658  |  glomerulonephritis  |  17
C0022658  |  renal disease  |  16
C0020456  |  hyperglycemia  |  16
C0020676  |  hypothyroidism  |  15
C0003864  |  arthritis  |  15
C0005586  |  bipolar disorder  |  15
C0007222  |  cardiovascular diseases  |  15
C0376358  |  prostate cancer  |  14
C0409974  |  lupus erythematosus  |  14
C0018099  |  gout  |  14
C0040034  |  thrombocytopenia  |  14
C0017668  |  focal segmental glomerulosclerosis  |  13
C0271650  |  glucose intolerance  |  13
C0022660  |  acute renal failure  |  13
C0149925  |  small cell lung cancer  |  13
C0027697  |  nephritis  |  12
C0004352  |  autism  |  11
C0242350  |  erectile dysfunction  |  11
C0002726  |  amyloidosis  |  10
C0014544  |  epilepsy  |  10
C0017661  |  iga nephropathy  |  10
C0004096  |  asthma  |  10
C0007113  |  rectal cancer  |  9
C0155626  |  acute myocardial infarction  |  9
C0009402  |  colorectal cancer  |  9
C0019163  |  hepatitis b  |  9
C0007134  |  renal cell carcinoma  |  9
C0011854  |  type 1 diabetes  |  8
C0020456  |  hyperglycaemia  |  8
C0027947  |  neutropenia  |  8
C0042384  |  vasculitis  |  8
C0019196  |  hepatitis c  |  8
C0041296  |  tuberculosis  |  8
C0040100  |  thymoma  |  8
C0085253  |  adult-onset still's disease  |  8
C0031090  |  periodontal disease  |  8
C0003467  |  anxiety  |  8
C0878544  |  cardiomyopathy  |  8
C0020443  |  hypercholesterolemia  |  8
C0019204  |  hepatocellular carcinoma  |  8
C0032285  |  pneumonia  |  7
C0035078  |  kidney failure  |  7
C0009324  |  ulcerative colitis  |  7
C0022116  |  ischemia  |  7
C0027819  |  neuroblastoma  |  7
C0029408  |  osteoarthritis  |  7
C0442874  |  neuropathy  |  7
C0079731  |  b-cell lymphoma  |  7
C0031099  |  periodontitis  |  7
C0008350  |  gallstone  |  7
C0004943  |  behcet's disease  |  7
C0002395  |  alzheimer's disease  |  7
C0007785  |  cerebral infarct  |  7
C0029456  |  osteoporosis  |  7
C0149931  |  migraine  |  7
C0206141  |  idiopathic hypereosinophilic syndrome  |  6
C0035309  |  retinopathy  |  6
C0023895  |  liver diseases  |  6
C0011991  |  diarrhea  |  6
C0021053  |  immune disease  |  6
C0398623  |  hypercoagulable state  |  6
C0270612  |  leukoencephalopathy  |  6
C0023890  |  cirrhosis  |  6
C0085580  |  essential hypertension  |  6
C1561644  |  chronic kidney disease (ckd)  |  6
C0042769  |  virus infection  |  6
C0001815  |  myelofibrosis  |  6
C0020619  |  hypogonadism  |  6
C0032285  |  pneumoniae  |  6
C0002878  |  hemolytic anemia  |  6
C0007785  |  cerebral infarction  |  6
C0042870  |  vitamin d defic  |  5
C0033838  |  kimura's disease  |  5
C0030305  |  pancreatitis  |  5
C0376545  |  hematologic malignancies  |  5
C0042769  |  viral infection  |  5
C0011991  |  diarrhoea  |  5
C0028756  |  morbid obesity  |  5
C0010068  |  coronary disease  |  5
C0024117  |  chronic obstructive pulmonary disease  |  5
C0034150  |  purpura  |  5
C0033953  |  sexual dysfunction  |  5
C0031154  |  peritonitis  |  5
C0042870  |  vitamin d deficiency  |  5
C0149985  |  secondary syphilis  |  5
C0040053  |  thrombus  |  5
C0024143  |  lupus nephritis  |  5
C0085207  |  gestational diabetes  |  5
C0030312  |  pancytopenia  |  5
C0035579  |  hypovitaminosis d  |  5
C0030312  |  bone marrow failure  |  5
C0600260  |  obstructive pulmonary disease  |  5
C0004936  |  mental disorders  |  4
C0037769  |  west syndrome  |  4
C1384514  |  primary aldosteronism  |  4
C0022661  |  chronic renal failure  |  4
C0085207  |  gestational diabetes mellitus  |  4
C0206695  |  neuroendocrine carcinoma  |  4
C0022661  |  end-stage renal disease  |  4
C0002871  |  anaemia  |  4
C0040188  |  tic disorders  |  4
C0392525  |  nephrolithiasis  |  4
C0037315  |  sleep apnea syndrome  |  4
C0155765  |  microangiopathy  |  4
C0032914  |  preeclampsia  |  4
C0024537  |  vivax malaria  |  4
C0476089  |  endometrial cancer  |  4
C0264716  |  chronic heart failure  |  4
C0001430  |  adenoma  |  4
C0010346  |  crohn's disease  |  4
C0398623  |  hypercoagulability  |  4
C1565489  |  renal insufficiency  |  4
C0039730  |  thalassemia  |  4
C0039841  |  thiamine deficiency  |  4
C0520679  |  obstructive sleep apnea syndrome  |  4
C0024623  |  gastric cancer  |  4
C0014038  |  encephalitis  |  4
C0020538  |  high blood pressure  |  4
C0010481  |  cushing's syndrome  |  4
C0008350  |  gallstones  |  4
C0039128  |  syphilis  |  4
C0011881  |  diabetic nephropathy  |  4
C0476089  |  endometrial ca  |  4
C0030567  |  parkinson's disease  |  4
C0001815  |  bone marrow fibrosis  |  4
C0035435  |  rheumatic disease  |  4
C0002170  |  alopecia  |  4
C0007570  |  coeliac disease  |  4
C0497327  |  dementia  |  4
C0024537  |  plasmodium vivax malaria  |  4
C0021831  |  bowel disease  |  4
C0018802  |  congestive heart failure  |  3
C0205969  |  thymic carcinoma  |  3
C0852949  |  arterial disease  |  3
C0009241  |  cognitive disorders  |  3
C0020538  |  vascular hypertension  |  3
C0003850  |  arteriosclerosis  |  3
C0003864  |  inflammatory arthritis  |  3
C0042373  |  vascular disorder  |  3
C0025958  |  microcephaly  |  3
C0014118  |  endocarditis  |  3
C0020428  |  aldosteronism  |  3
C0042133  |  uterine leiomyoma  |  3
C0019829  |  hodgkin's lymphoma  |  3
C0022661  |  end stage renal disease  |  3
C0008350  |  cholelithiasis  |  3
C0001418  |  adenocarcinoma  |  3
C0031117  |  peripheral neuropathy  |  3
C1257763  |  overnutrition  |  3
C0034065  |  pulmonary embolism  |  3
C0679466  |  cognitive deficits  |  3
C0085253  |  adult-onset still disease  |  3
C0879615  |  stromal tumor  |  3
C0035455  |  rhinitis  |  3
C0021359  |  infertility  |  3
C0030421  |  paraganglioma  |  3
C0022679  |  cystic kidney  |  3
C0235618  |  proliferative glomerulonephritis  |  3
C0684249  |  lung carcinoma  |  3
C0085413  |  autosomal dominant polycystic kidney disease  |  3
C0024115  |  pulmonary disease  |  3
C1140680  |  ovarian ca  |  3
C0007131  |  non-small cell lung cancer  |  3
C0023787  |  lipodystrophy  |  3
C0024530  |  malaria  |  3
C0042769  |  viral infections  |  3
C0033975  |  psychosis  |  3
C1302401  |  colorectal adenoma  |  3
C0042721  |  viral hepatitis  |  3
C0017601  |  glaucoma  |  3
C0008370  |  cholestasis  |  3
C0238198  |  gastrointestinal stromal tumor  |  3
C0022116  |  ischaemia  |  3
C0152013  |  lung adenocarcinoma  |  3
C0346109  |  peritoneal mesothelioma  |  3
C0278678  |  metastatic renal cell carcinoma  |  3
C0085413  |  autosomal dominant polycystic kidney  |  3
C0159069  |  impaired glucose tolerance  |  3
C0018799  |  cardiac disease  |  3
C0011854  |  type 1 diabetes mellitus  |  3
C1261473  |  sarcoma  |  3
C0042373  |  vascular disorders  |  3
C0026691  |  kawasaki disease  |  3
C0030326  |  panniculitis  |  3
C0020545  |  renovascular hypertension  |  3
C0039263  |  takayasu arteritis  |  3
C0003872  |  psoriatic arthritis  |  3
C0007222  |  cardiovascular disorders  |  3
C0007137  |  squamous cell carcinoma  |  3
C0037315  |  sleep apnoea  |  3
C0020542  |  pulmonary hypertension  |  3
C0013473  |  eating disorder  |  3
C0242231  |  coronary stenosis  |  3
C1510471  |  hypovitaminosis  |  3
C0032460  |  polycystic ovarian syndrome  |  3
C0152021  |  congenital heart disease  |  3
C0149521  |  chronic pancreatitis  |  3
C0023473  |  chronic myeloid leukemia  |  3
C0012739  |  disseminated intravascular coagulation  |  3
C0031511  |  pheochromocytoma  |  3
C0010054  |  coronary atherosclerosis  |  3
C0022658  |  renal diseases  |  2
C0005684  |  bladder cancer  |  2
C0023281  |  leishmaniasis  |  2
C0598608  |  hyperhomocysteinemia  |  2
C0079744  |  diffuse large b-cell lymphoma  |  2
C0376545  |  hematological malignancy  |  2
C0006017  |  pertussis  |  2
C0687720  |  central diabetes insipidus  |  2
C0162871  |  abdominal aneurysm  |  2
C0031347  |  pharyngeal cancer  |  2
C0032269  |  streptococcus pneumoniae infection  |  2
C0019655  |  histoplasmosis  |  2
C0085652  |  pyoderma gangrenosum  |  2
C0206081  |  hyperandrogenism  |  2
C0021831  |  intestinal disease  |  2
C0028326  |  noonan syndrome  |  2
C0008354  |  vibrio cholerae  |  2
C0004623  |  bacterial infection  |  2
C0027707  |  interstitial nephritis  |  2
C0036472  |  scrub typhus  |  2
C0205969  |  malignant thymoma  |  2
C1136085  |  monoclonal gammopathy  |  2
C0004114  |  astrocytoma  |  2
C0024302  |  large cell lymphoma  |  2
C0011127  |  pressure ulcers  |  2
C0036337  |  schizoaffective disorder  |  2
C0007642  |  cellulitis  |  2
C0031069  |  familial mediterranean fever  |  2
C0026848  |  muscular diseases  |  2
C0011860  |  diabetes mellitus type 2  |  2
C0010414  |  cryptococcosis  |  2
C0019829  |  hodgkin lymphoma  |  2
C0339204  |  staphyloma  |  2
C0085096  |  peripheral vascular disease  |  2
C0029132  |  optic neuropathy  |  2
C0027121  |  myositis  |  2
C0038436  |  posttraumatic stress disorder  |  2
C0034212  |  pyoderma  |  2
C0031511  |  pheochromocytomas  |  2
C0302592  |  carcinoma of the cervix  |  2
C0011633  |  dermatomyositis  |  2
C1704436  |  peripheral arterial disease  |  2
C0028756  |  severe obesity  |  2
C0008312  |  biliary cirrhosis  |  2
C0021390  |  inflammatory bowel disease  |  2
C0014130  |  endocrine disease  |  2
C0001824  |  agranulocytosis  |  2
C0003486  |  aortic aneurysm  |  2
C0870082  |  hyperkeratosis  |  2
C0017178  |  gastrointestinal disease  |  2
C0011603  |  dermatitis  |  2
C0002880  |  autoimmune hemolytic anemia  |  2
C0031090  |  periodontal diseases  |  2
C0020757  |  ichthyosis  |  2
C0036202  |  sarcoidosis  |  2
C0010692  |  cystitis  |  2
C0021400  |  influenza  |  2
C0023448  |  lymphocytic leukemia  |  2
C0008312  |  primary biliary cirrhosis  |  2
C0221765  |  chronic schizophrenia  |  2
C0013537  |  eclampsia  |  2
C0206180  |  anaplastic large cell lymphoma  |  2
C0206141  |  idiopathic hypereosinophilic syndrome (hes)  |  2
C0280131  |  ovarian teratoma  |  2
C0017178  |  gastrointestinal diseases  |  2
C0751967  |  relapsing-remitting multiple sclerosis  |  2
C0026640  |  oral cancer  |  2
C0003469  |  anxiety disorder  |  2
C1334699  |  mesenchymal tumor  |  2
C0023646  |  lichen planus  |  2
C0024305  |  non-hodgkin's lymphoma  |  2
C0018784  |  sensorineural deafness  |  2
C0026769  |  multiple sclerosis  |  2
C0033975  |  psychotic disorders  |  2
C0152276  |  myeloid sarcoma  |  2
C0007785  |  cerebral infarctions  |  2
C0007570  |  celiac disease  |  2
C0520679  |  obstructive sleep apnoea  |  2
C0836924  |  thrombocytosis  |  2
C1332977  |  childhood leukemia  |  2
C0524851  |  neurodegenerative disease  |  2
C0151744  |  myocardial ischemia  |  2
C0281963  |  red cell aplasia  |  2
C0007194  |  hypertrophic cardiomyopathy  |  2
C0024305  |  non-hodgkin lymphoma  |  2
C0038013  |  ankylosing spondylitis  |  2
C0740394  |  hyperuricaemia  |  2
C0027868  |  neuromuscular diseases  |  2
C0026946  |  mycosis  |  2
C0006017  |  bordetella pertussis  |  2
C0151744  |  ischaemic heart disease  |  2
C0023473  |  chronic myelogenous leukemia  |  2
C0017168  |  oesophageal reflux  |  2
C0026850  |  muscular dystrophy  |  2
C0041696  |  major depression  |  2
C0026718  |  mucormycosis  |  2
C0014868  |  esophagitis  |  2
C0017168  |  gastroesophageal reflux  |  2
C0022660  |  acute kidney failure  |  2
C0040100  |  thymomas  |  2
C0027868  |  neuromuscular disease  |  2
C0023290  |  visceral leishmaniasis  |  2
C0027662  |  multiple endocrine neoplasia  |  2
C0242966  |  systemic inflammatory response syndrome  |  2
C0024236  |  lymphedema  |  2
C0524851  |  neurodegenerative diseases  |  2
C0221002  |  primary hyperparathyroidism  |  2
C0349530  |  early gastric cancer  |  2
C0085113  |  neurofibromatosis  |  2
C0017168  |  esophageal reflux  |  2
C0034902  |  pure red cell aplasia  |  2
C1136084  |  plasma cell dyscrasia  |  2
C0021831  |  intestinal diseases  |  2
C0010051  |  coronary aneurysm  |  2
C0025362  |  mental retardation  |  2
C0037198  |  sinus thrombosis  |  2
C0004623  |  bacterial infections  |  2
C0011884  |  diabetic retinopathy  |  2
C0041471  |  typhus  |  2
C0023448  |  lymphoblastic leukemia  |  2
C0023895  |  hepatic disease  |  2
C0007129  |  merkel cell carcinoma  |  2
C0206180  |  anaplastic large-cell lymphoma  |  2
C0010051  |  coronary aneurysms  |  2
C0017665  |  membranous glomerulopathy  |  2
C0040147  |  thyroiditis  |  2
C0015625  |  fanconi anemia  |  2
C0023903  |  liver cancer  |  2
C0017665  |  membranous glomerulonephritis  |  2
C0037317  |  sleep disturbance  |  2
C0035435  |  rheumatic diseases  |  2
C0011848  |  diabetes insipidus  |  2
C0085669  |  acute leukaemia  |  2
C0024117  |  chronic obstructive pulmonary disease (copd)  |  2
C0155550  |  neural deafness  |  2
C0152025  |  polyneuropathy  |  2
C0153452  |  gallbladder ca  |  2
C1527336  |  sjogren's syndrome  |  2
C0024299  |  lymphomas  |  2
C0000889  |  acanthosis nigricans  |  2
C0033975  |  psychotic disorder  |  2
C0006625  |  cachexia  |  2
C0003873  |  rheumatoid disease  |  1
C0042345  |  varicose veins  |  1
C0027765  |  nervous disorders  |  1
C0015519  |  factor x deficiency  |  1
C0013421  |  dystonia  |  1
C0039445  |  osler-weber-rendu disease  |  1
C0038436  |  post-traumatic stress disorder  |  1
C0003507  |  aortic stenosis  |  1
C0001815  |  myeloid metaplasia  |  1
C0006060  |  mediterranean spotted fever  |  1
C0023434  |  chronic lymphocytic leukemia  |  1
C0149925  |  small cell lung carcinoma  |  1
C0033581  |  prostatitis  |  1
C0007137  |  squamous carcinoma  |  1
C1619734  |  pulmonary arterial hypertension  |  1
C0268713  |  congenital nephrotic syndrome  |  1
C0699791  |  gastric carcinoma  |  1
C0042345  |  varicose vein  |  1
C0041696  |  major depressive disorder  |  1
C0162836  |  hidradenitis suppurativa  |  1
C0035204  |  respiratory disease  |  1
C0699885  |  bladder carcinoma  |  1
C0002986  |  fabry's disease  |  1
C2717836  |  steroid sulfatase deficiency  |  1
C0000809  |  recurrent miscarriage  |  1
C0020503  |  secondary hyperparathyroidism  |  1
C0001363  |  acute mesenteric ischemia  |  1
C0549473  |  thyroid carcinoma  |  1
C0015190  |  sick euthyroid syndrome  |  1
C0003969  |  vitamin c deficiency  |  1
C0007138  |  urothelial carcinoma  |  1
C0034152  |  henoch-schonlein purpura  |  1
C1527249  |  colorectal cancers  |  1
C0085655  |  polymyositis  |  1
C0242429  |  sore throat  |  1
C0037054  |  sickle cell trait  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C0162529  |  ischemic colitis  |  1
C0015645  |  fasciitis  |  1
C0040137  |  thyroid nodules  |  1
C0033626  |  protein deficiency  |  1
C0238111  |  lennox-gastaut syndrome  |  1
C0024586  |  serotonin syndrome  |  1
C0024115  |  lung diseases  |  1
C0021845  |  intestinal perforation  |  1
C0001818  |  agoraphobia  |  1
C0151650  |  renal fibrosis  |  1
C0014527  |  epidermolysis bullosa  |  1
C0013473  |  eating disorders  |  1
C0007785  |  cerebral ischemia  |  1
C0149931  |  migraine headache  |  1
C0032302  |  mycoplasma pneumonia  |  1
C0006012  |  borderline personality disorder  |  1
C0020676  |  hypothyroid  |  1
C0021053  |  immune disorders  |  1
C0021831  |  enteropathy  |  1
C0018799  |  heart diseases  |  1
C0376545  |  hematological malignancies  |  1
C0153452  |  gallbladder cancer  |  1
C0524851  |  neurodegenerative disorders  |  1
C0302592  |  cervical ca  |  1
C0023470  |  myelogenous leukemia  |  1
C0012739  |  consumption coagulopathy  |  1
C0598894  |  monocytic leukemia  |  1
C0023470  |  myelocytic leukemia  |  1
C0022658  |  kidney diseases  |  1
C0268450  |  gitelman's syndrome  |  1
C0024535  |  falciparum malaria  |  1
C0027022  |  myeloproliferative disorder  |  1
C0553723  |  cutaneous squamous cell carcinoma  |  1
C0007131  |  non-small-cell lung carcinoma  |  1
C1527336  |  sjogren syndrome  |  1
C0003504  |  aortic valve insufficiency  |  1
C0022573  |  keratoconjunctivitis  |  1
C0035309  |  retinal disorders  |  1
C0027708  |  wilms' tumour  |  1
C1140680  |  ovarian cancers  |  1
C0041341  |  tuberous sclerosis complex  |  1
C0376300  |  dengue shock syndrome  |  1
C0040034  |  thrombopenia  |  1
C0025202  |  melanoma  |  1
C0007273  |  carotid artery disease  |  1
C0270853  |  juvenile myoclonic epilepsy  |  1
C0023195  |  lcat deficiency  |  1
C0699790  |  colon carcinoma  |  1
C1800706  |  idiopathic pulmonary fibrosis  |  1
C0017574  |  gingivitis  |  1
C0038041  |  spotted fever  |  1
C0032305  |  pneumocystis jiroveci pneumonia  |  1
C0153382  |  oropharyngeal cancer  |  1
C0221355  |  macrocephaly  |  1
C0268390  |  muckle-wells syndrome  |  1
C0235782  |  gallbladder carcinoma  |  1
C0042164  |  uveitis  |  1
C0017168  |  esophageal reflux disease  |  1
C0023364  |  leptospirosis  |  1
C0011860  |  type ii diabetes mellitus  |  1
C0022575  |  keratoconjunctivitis sicca  |  1
C0268407  |  cardiac amyloidosis  |  1
C0006309  |  brucellosis  |  1
C0242363  |  islet cell tumour  |  1
C0151620  |  hypertensive encephalopathy  |  1
C0001623  |  adrenal insufficiency  |  1
C0025162  |  toxic megacolon  |  1
C0035302  |  retinal artery occlusion  |  1
C0220647  |  carcinoma of unknown primary  |  1
C0013595  |  eczema  |  1
C0026975  |  myelitis  |  1
C1262481  |  eosinophilic gastroenteritis  |  1
C0026948  |  mycosis fungoides  |  1
C0015458  |  facial hemiatrophy  |  1
C0079731  |  b cell lymphoma  |  1
C0035305  |  retinal detachment  |  1
C0334579  |  anaplastic astrocytoma  |  1
C0043207  |  wolfram syndrome  |  1
C0007177  |  pericardial tamponade  |  1
C0011615  |  atopic dermatitis  |  1
C0162568  |  erythropoietic protoporphyria  |  1
C0031485  |  phenylketonuria  |  1
C0553980  |  endomyocardial fibrosis  |  1
C0024419  |  waldenstrom's macroglobulinaemia  |  1
C0019360  |  herpes zoster  |  1
C0037293  |  skin tags  |  1
C0152020  |  gastroparesis  |  1
C0041696  |  unipolar depression  |  1
C0015230  |  exanthem  |  1
C0011334  |  cavities  |  1
C0021775  |  intermittent claudication  |  1
C0032285  |  pneumonitis  |  1
C0007785  |  cerebral infarcts  |  1
C0031046  |  pericarditis  |  1
C0917713  |  becker muscular dystrophy  |  1
C0009326  |  rheumatologic disorder  |  1
C0009447  |  common variable immunodeficiency  |  1
C0021053  |  immune dysfunction  |  1
C0024419  |  macroglobulinaemia  |  1
C0037315  |  sleep apnoea syndrome  |  1
C0017160  |  gastroenteritis  |  1
C0023473  |  chronic myelogenous leukemia (cml)  |  1
C0007138  |  transitional cell carcinoma  |  1
C0019048  |  hemoglobinuria  |  1
C0153392  |  nasopharyngeal cancer  |  1
C0018378  |  guillain-barre syndrome  |  1
C0221056  |  adult dermatomyositis  |  1
C0154916  |  rubeosis iridis  |  1
C1145670  |  respiratory failure  |  1
C0280317  |  squamous cell carcinoma of the tonsil  |  1
C0014130  |  endocrine disorders  |  1
C0025267  |  multiple endocrine neoplasia type 1  |  1
C0034155  |  thrombotic thrombocytopenic purpura  |  1
C1704214  |  xanthogranuloma  |  1
C0149649  |  atheroembolism  |  1
C0018799  |  cardiac diseases  |  1
C0085580  |  primary hypertension  |  1
C0015190  |  euthyroid sick syndrome  |  1
C0037280  |  infestation  |  1
C0024291  |  hemophagocytic lymphohistiocytosis  |  1
C0079584  |  ichthyosis vulgaris  |  1
C0023418  |  leukaemia  |  1
C0027813  |  neuritis  |  1
C0020179  |  huntington's disease  |  1
C0021141  |  syndrome of inappropriate antidiuretic hormone secretion  |  1
C0014869  |  reflux esophagitis  |  1
C0272126  |  evan's syndrome  |  1
C0524988  |  schnitzler syndrome  |  1
C0001418  |  adenocarcinomas  |  1
C0035204  |  respiratory diseases  |  1
C0014848  |  achalasia  |  1
C0023467  |  acute myelocytic leukemia  |  1
C0041349  |  tubulointerstitial nephritis  |  1
C0020659  |  hypothalamic neoplasms  |  1
C0079731  |  b-cell lymphomas  |  1
C0018023  |  nodular goiter  |  1
C0022672  |  acute tubular necrosis  |  1
C0151295  |  mononeuritis multiplex  |  1
C0023418  |  leukaemias  |  1
C0079774  |  peripheral t cell lymphoma  |  1
C0027708  |  wilms tumor  |  1
C0007688  |  central retinal artery occlusion  |  1
C0015974  |  periodic fever  |  1
C0242379  |  lung malignancy  |  1
C0027022  |  myeloproliferative neoplasms  |  1
C0007115  |  thyroid ca  |  1
C0085293  |  hepatitis e  |  1
C0019069  |  haemophilia  |  1
C0014057  |  japanese encephalitis  |  1
C0001175  |  acquired immunodeficiency syndrome  |  1
C0700594  |  radiculopathy  |  1
C0019880  |  homocystinuria  |  1
C0027830  |  neurofibroma  |  1
C0021141  |  syndrome of inappropriate secretion of antidiuretic hormone  |  1
C0155616  |  secondary hypertension  |  1
C0178238  |  intestinal infection  |  1
C0023895  |  liver disorders  |  1
C0020538  |  increased blood pressure  |  1
C0017662  |  membranoproliferative glomerulonephritis  |  1
C0600427  |  cocaine dependence  |  1
C0027708  |  wilms' tumor  |  1
C0023449  |  acute lymphoblastic leukemia  |  1
C0001126  |  renal tubular acidosis  |  1
C0007758  |  cerebellar ataxia  |  1
C0003537  |  aphasia  |  1
C0007117  |  basal cell carcinoma  |  1
C0043046  |  wasting disease  |  1
C0016053  |  fibromyalgia  |  1
C0018801  |  cardiac failure  |  1
C0025202  |  malignant melanoma  |  1
C0920350  |  autoimmune thyroiditis  |  1
C0029925  |  ovarian carcinoma  |  1
C1140680  |  ovarian cancer  |  1
C0271623  |  hypogonadotrophic hypogonadism  |  1
C0085576  |  microcytic anemia  |  1
C0026147  |  primary lymphedema  |  1
C0041466  |  typhoid fever  |  1
C0002896  |  sideroblastic anemia  |  1
C0003128  |  anovulation  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria  |  1
C0079588  |  x-linked recessive ichthyosis  |  1
C0036319  |  schistosoma mansoni  |  1
C0023465  |  acute monoblastic leukemia  |  1
C0013384  |  dyskinesia  |  1
C0019360  |  zoster  |  1
C0153381  |  oral cancers  |  1
C0206660  |  germinoma  |  1
C0030486  |  paraplegia  |  1
C0035920  |  rubella  |  1
C1135191  |  systolic heart failure  |  1
C0014859  |  esophageal cancer  |  1
C0018021  |  thyroid enlargement  |  1
C0017658  |  glomerulonephritides  |  1
C0022578  |  keratoconus  |  1
C0036472  |  tsutsugamushi  |  1
C0856761  |  budd-chiari syndrome  |  1
C0008148  |  chlamydia  |  1
C0017551  |  gilbert's syndrome  |  1
C0041466  |  typhoid  |  1
C0206698  |  cholangiocarcinoma  |  1
C0178664  |  glomerular sclerosis  |  1
C0026896  |  myasthenia gravis  |  1
C0345967  |  malignant mesothelioma  |  1
C1522378  |  large granular lymphocytic leukemia  |  1
C0032460  |  polycystic ovaries  |  1
C0019202  |  wilson's disease  |  1
C0085160  |  hidradenitis  |  1
C0018051  |  gonadal dysgenesis  |  1
C0008625  |  chromosomal abnormality  |  1
C0796279  |  osa syndrome  |  1
C0345905  |  intrahepatic cholangiocarcinoma  |  1
C0278652  |  childhood craniopharyngioma  |  1
C0079774  |  peripheral t-cell lymphoma  |  1
C0001622  |  hypercortisolism  |  1
C0278846  |  invasive thymoma  |  1
C0023895  |  liver disorder  |  1
C0242287  |  neuromyotonia  |  1
C0007282  |  carotid artery stenosis  |  1
C0085692  |  hemorrhagic cystitis  |  1
C0008728  |  churg-strauss syndrome  |  1
C0027708  |  nephroblastoma  |  1
C0023890  |  liver cirrhosis  |  1
C0005283  |  beta thalassemia  |  1
C0014038  |  brain inflammation  |  1
C0003469  |  anxiety disorders  |  1
C2607914  |  allergic rhinitis  |  1
C0032302  |  mycoplasma pneumoniae pneumonia  |  1
C0037274  |  dermatoses  |  1
C0302592  |  cervical carcinoma  |  1
C0024115  |  lung disease  |  1
C0022658  |  renal disorders  |  1
C0023449  |  acute lymphoblastic leukaemia  |  1
C0238461  |  anaplastic thyroid carcinoma  |  1
C0242647  |  mucosa-associated lymphoid tissue  |  1
C0007177  |  cardiac tamponade  |  1
C1327709  |  rectosigmoid cancer  |  1
C0019069  |  hemophilia  |  1
C0029442  |  osteomalacia  |  1
C0014553  |  absence seizures  |  1
C0006267  |  bronchiectasis  |  1
C0042721  |  hepatitis viral  |  1
C0031485  |  phenylketonuria (pku)  |  1
C0019348  |  herpes simplex  |  1
C0025290  |  aseptic meningitis  |  1
C0403529  |  pulmonary-renal syndrome  |  1
C0020443  |  hypercholesterolaemia  |  1
C0271650  |  prediabetes  |  1
C0855211  |  testicular seminoma  |  1
C0041228  |  sleeping sickness  |  1
C0038012  |  spondylitis  |  1
C0004106  |  astigmatism  |  1
C0023487  |  acute promyelocytic leukemia  |  1
C0034362  |  q fever  |  1
C0004943  |  behcet disease  |  1
C1621895  |  adrenal hyperplasia  |  1
C0010403  |  cryoglobulinemia  |  1
C0020437  |  hypercalcaemia  |  1
C0279680  |  transitional cell carcinoma of the bladder  |  1
C0023530  |  leukopenia  |  1
C0341950  |  severe pre-eclampsia  |  1
C0026848  |  myopathy  |  1
C0221239  |  rapidly progressive glomerulonephritis  |  1
C0014145  |  endodermal sinus tumor  |  1
C0020540  |  accelerated hypertension  |  1
C0025268  |  multiple endocrine neoplasia type 2  |  1
C0017661  |  iga glomerulonephritis  |  1
C0740302  |  5q- syndrome  |  1
C0026985  |  myelodysplasia  |  1
C0025309  |  meningoencephalitis  |  1
C0018802  |  congestive cardiac failure  |  1
C0014544  |  epilepsies  |  1
C0007789  |  cerebral palsy  |  1
C0008924  |  cleft lip  |  1
C0001768  |  agammaglobulinemia  |  1
C0026848  |  myopathies  |  1
C0033838  |  kimura disease  |  1
C0024299  |  malignant lymphoma  |  1
C0032587  |  polyradiculoneuropathy  |  1
C1260873  |  aortic valve disease  |  1
C0151779  |  cutaneous malignant melanoma  |  1
C0023484  |  plasma cell leukaemia  |  1
C0026934  |  mycoplasma  |  1
C0235974  |  pancreatic cancer  |  1
C0022661  |  end-stage kidney disease  |  1
C0022656  |  renal cortical necrosis  |  1
C0037274  |  skin disease  |  1
C0017150  |  gastrinomas  |  1
C0016977  |  biliary disease  |  1
C0750952  |  biliary tract cancer  |  1
C0751651  |  mitochondrial disease  |  1
C0085278  |  antiphospholipid syndrome  |  1
C0002895  |  sickle cell disease  |  1
C0028797  |  occupational disease  |  1
C0021359  |  infertile  |  1
C0003972  |  atherosclerotic cardiovascular disease  |  1
C0259749  |  autonomic neuropathy  |  1
C0021345  |  infectious mononucleosis  |  1
C0027059  |  myocarditis  |  1
C0206717  |  olfactory neuroblastoma  |  1
C0036220  |  kaposi sarcoma  |  1
C0686619  |  lymph node metastases  |  1
C0007860  |  cervicitis  |  1
C0013338  |  growth hormone deficiency  |  1
C0037317  |  sleep disturbances  |  1
C0087086  |  thrombi  |  1
C0342199  |  iodine deficiency  |  1
C0812413  |  malignant pleural mesothelioma  |  1
C0001621  |  adrenal disorders  |  1
C0034885  |  rectal neoplasms  |  1
C0024314  |  lymphoproliferative disease  |  1
C0006845  |  chronic mucocutaneous candidiasis  |  1
C0242647  |  mucosa-associated lymphoid tissue lymphoma  |  1
C0154251  |  lipid disorders  |  1
C0020538  |  hypertensive disease  |  1
C0085669  |  acute leukemia  |  1
C1704437  |  respiratory distress syndrome  |  1
C0206754  |  neuroendocrine tumour  |  1
C0162568  |  protoporphyria  |  1
C0023234  |  perthes disease  |  1
C0038220  |  status epilepticus  |  1
C0013080  |  g trisomy  |  1
C0024790  |  paroxysmal nocturnal hemoglobinuria (pnh)  |  1
C0028738  |  nystagmus  |  1
C0028797  |  occupational diseases  |  1
C0751498  |  sigmoid cancer  |  1
C0014130  |  endocrine diseases  |  1
C0162429  |  malnourished  |  1
C0022661  |  end-stage renal failure  |  1
C0014084  |  ollier's disease  |  1
C0041956  |  ureteric obstruction  |  1
C0268425  |  alstrom syndrome  |  1
C1377913  |  pleural mesothelioma  |  1
C0013502  |  hydatid cyst  |  1
C0029134  |  optic neuritis  |  1
C0011860  |  type ii diabetes  |  1
C0027022  |  myeloproliferative disease  |  1
C0030499  |  parasitosis  |  1
C0002895  |  sickle cell anemia  |  1
C0021845  |  bowel perforation  |  1
C0023267  |  leiomyomas  |  1
C0017168  |  gastroesophageal reflux disease  |  1
C0010276  |  craniopharyngioma  |  1
C0041341  |  tuberous sclerosis  |  1
C0020514  |  hyperprolactinemia  |  1
C0034050  |  pulmonary alveolar proteinosis  |  1
C0270549  |  generalized anxiety disorder  |  1
C0162429  |  malnutrition  |  1
C0040128  |  thyroid disease  |  1
C0003857  |  arteriovenous malformation  |  1
C0021053  |  immune disorder  |  1
C0242966  |  systemic inflammatory response syndrome (sirs)  |  1
C0042373  |  angiopathy  |  1
C0023891  |  alcoholic liver cirrhosis  |  1
C0018916  |  angioma  |  1
C0206695  |  neuroendocrine carcinomas  |  1
C0036472  |  tsutsugamushi disease  |  1
C0002895  |  sickle cell anaemia  |  1
C0409818  |  nomid  |  1
C0028242  |  nocardiosis  |  1
C0007134  |  hypernephroma  |  1
C0007131  |  nsclc  |  1
C0221026  |  x-linked agammaglobulinemia  |  1
C0040137  |  thyroid nodule  |  1
C0021933  |  intussusception  |  1
C1257763  |  overfed  |  1
C0023434  |  chronic lymphocytic leukaemia  |  1
C0019621  |  langerhans cell histiocytosis  |  1
C0026654  |  moyamoya syndrome  |  1
C0004114  |  astrocytomas  |  1
C0023524  |  progressive multifocal leukoencephalopathy  |  1
C0151744  |  myocardial ischaemia  |  1
C0021345  |  mononucleosis  |  1
C0004134  |  ataxia  |  1
C0019204  |  hepatocarcinoma  |  1
C0015674  |  chronic fatigue syndrome  |  1
C0086543  |  cataract  |  1
C0849777  |  cystic ovaries  |  1
C0030807  |  pemphigus  |  1
C0007102  |  colon cancer  |  1
C0035585  |  rickettsial diseases  |  1
C0006413  |  burkitt's lymphoma  |  1
C0349631  |  richter's transformation  |  1
C0340305  |  inferior myocardial infarction  |  1
C0035222  |  acute respiratory distress syndrome  |  1
C1527411  |  retinal vein thrombosis  |  1
C0266463  |  lissencephaly  |  1
C0000786  |  miscarriage  |  1
C0334254  |  lymphoepithelioma  |  1
C0008925  |  cleft palate  |  1
C0026654  |  moyamoya  |  1
C0151313  |  sensory neuropathy  |  1
C0018995  |  hemochromatosis  |  1
C0023448  |  lymphocytic leukaemia  |  1
C0007786  |  brain ischemia  |  1
C0566602  |  primary sclerosing cholangitis  |  1
C0346647  |  pancreatic cancers  |  1
C0022572  |  keratoacanthomas  |  1
C0035585  |  rickettsial disease  |  1
C0008311  |  cholangitis  |  1
C0205697  |  sarcomatoid carcinoma  |  1
C0041408  |  turner syndrome  |  1
C0030328  |  weber-christian disease  |  1
C0026846  |  muscle wasting  |  1
C0037769  |  infantile spasms  |  1
C0152018  |  esophageal carcinoma  |  1
C0520679  |  obstructive sleep apnoea syndrome  |  1
C0022661  |  chronic renal disease  |  1
C0014733  |  erysipelas  |  1
C0343386  |  clostridium difficile infection  |  1
C0019045  |  hemoglobin disorders  |  1
C0034050  |  alveolar proteinosis  |  1
C0242647  |  malt lymphoma  |  1
C0008313  |  sclerosing cholangitis  |  1
C0032461  |  polycythaemia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
CD96  |  10225  |  CLINVAR;CTD_human;ORPHANET;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus
Symbol | Locus(Total Locus:1)
CD96  |  3q13.13-q13.2
Disease ID 548
Disease c syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:54)
HP:0000960  |  Sacral dimple
HP:0001373  |  Joint dislocation
HP:0001539  |  Omphalocele
HP:0004378  |  Abnormality of the anus
HP:0000343  |  Long philtrum
HP:0000470  |  Short neck
HP:0002983  |  Micromelia
HP:0002019  |  Constipation
HP:0007598  |  Bilateral single transverse palmar creases
HP:0004422  |  Biparietal narrowing
HP:0007370  |  Aplasia/Hypoplasia of the corpus callosum
HP:0007601  |  Midline facial capillary hemangioma
HP:0000085  |  Horseshoe kidney
HP:0000286  |  Epicanthus
HP:0004322  |  Short stature
HP:0008678  |  Renal hypoplasia/aplasia
HP:0000347  |  Micrognathia
HP:0003083  |  Dislocated radial head
HP:0003196  |  Short nose
HP:0000767  |  Pectus excavatum
HP:0010978  |  Abnormality of immune system physiology
HP:0000486  |  Strabismus
HP:0001250  |  Seizures
HP:0004209  |  Clinodactyly of the 5th finger
HP:0000003  |  Multicystic kidney dysplasia
HP:0001252  |  Muscular hypotonia
HP:0000319  |  Smooth philtrum
HP:0001770  |  Toe syndactyly
HP:0010318  |  Aplasia/Hypoplasia of the abdominal wall musculature
HP:0001582  |  Redundant skin
HP:0002564  |  Malformation of the heart and great vessels
HP:0005280  |  Depressed nasal bridge
HP:0000028  |  Cryptorchidism
HP:0001376  |  Limitation of joint mobility
HP:0001531  |  Failure to thrive in infancy
HP:0010720  |  Abnormal hair pattern
HP:0001161  |  Hand polydactyly
HP:0000776  |  Congenital diaphragmatic hernia
HP:0000368  |  Low-set, posteriorly rotated ears
HP:0001561  |  Polyhydramnios
HP:0000212  |  Gingival overgrowth
HP:0000191  |  Accessory oral frenulum
HP:0000252  |  Microcephaly
HP:0001249  |  Intellectual disability
HP:0010458  |  Female pseudohermaphroditism
HP:0000463  |  Anteverted nares
HP:0001883  |  Talipes
HP:0001522  |  Death in infancy
HP:0000175  |  Cleft palate
HP:0000582  |  Upslanted palpebral fissure
HP:0100720  |  Hypoplasia of the ear cartilage
HP:0000218  |  High palate
HP:0000243  |  Trigonocephaly
HP:0000233  |  Thin vermilion border
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:543)
HP:0001513  |  Obesity  |  376
HP:0000855  |  Insulin resistance  |  205
HP:0000822  |  Hypertension  |  140
HP:0001397  |  Hepatic steatosis  |  74
HP:0000093  |  Proteinuria  |  61
HP:0100753  |  Schizophrenia  |  59
HP:0002621  |  Atherosclerosis  |  50
HP:0000819  |  Diabetes mellitus  |  48
HP:0000112  |  Nephropathy  |  45
HP:0001903  |  Anemia  |  44
HP:0001677  |  Coronary artery disease  |  43
HP:0012743  |  Central obesity  |  40
HP:0003765  |  Psoriasis  |  38
HP:0000083  |  Renal insufficiency  |  37
HP:0001909  |  Leukemia  |  30
HP:0002665  |  Lymphoma  |  28
HP:0003002  |  Breast carcinoma  |  28
HP:0001919  |  Acute renal failure  |  27
HP:0002664  |  Neoplasia  |  27
HP:0000716  |  Depression  |  27
HP:0002149  |  Hyperuricemia  |  25
HP:0002104  |  Absence of spontaneous respiration  |  25
HP:0010535  |  Sleep apnea  |  25
HP:0012622  |  Chronic kidney disease  |  25
HP:0001297  |  Cerebral vascular events  |  23
HP:0002870  |  Obstructive sleep apnea  |  23
HP:0001635  |  Congestive heart failure  |  23
HP:0030731  |  Carcinoma  |  23
HP:0012578  |  Membranous glomerulonephritis  |  23
HP:0004808  |  Acute myelogenous leukemia  |  22
HP:0000969  |  Dropsy  |  21
HP:0012324  |  Myeloid leukemia  |  20
HP:0000842  |  Elevated insulin level  |  20
HP:0003077  |  Hyperlipidemia  |  20
HP:0002725  |  Systemic lupus erythematosus  |  20
HP:0001370  |  Rheumatoid arthritis  |  20
HP:0001658  |  Myocardial infarction  |  19
HP:0000147  |  Sclerocystic ovaries  |  19
HP:0001249  |  Mental retardation  |  18
HP:0002155  |  Increased triglycerides  |  17
HP:0012115  |  Liver inflammation  |  17
HP:0000099  |  Glomerular nephritis  |  17
HP:0012531  |  Pain  |  17
HP:0000096  |  Glomerulosclerosis  |  17
HP:0000833  |  Glucose intolerance  |  16
HP:0002583  |  Colitis  |  16
HP:0003074  |  High blood glucose  |  16
HP:0000821  |  Underactive thyroid  |  15
HP:0001873  |  Low platelet count  |  15
HP:0007302  |  Bipolar disorder  |  15
HP:0001369  |  Arthritis  |  15
HP:0001907  |  Thromboembolic disease  |  14
HP:0001824  |  Weight loss  |  14
HP:0001997  |  Gout  |  14
HP:0030357  |  Small cell lung carcinoma  |  14
HP:0000097  |  focal glomerulosclerosis  |  14
HP:0012125  |  Prostate cancer  |  14
HP:0001945  |  Fever  |  13
HP:0100543  |  Cognitive deficits  |  13
HP:0001631  |  Atria septal defect  |  13
HP:0005505  |  Refractory anemia  |  12
HP:0003774  |  End-stage renal failure  |  12
HP:0002721  |  Immunodeficiency  |  12
HP:0012592  |  Albuminuria  |  12
HP:0000123  |  Nephritis  |  12
HP:0200123  |  Chronic liver inflammation  |  11
HP:0012594  |  High urine albumin levels  |  11
HP:0000717  |  Autism  |  11
HP:0012190  |  T cell lymphoma  |  11
HP:0000802  |  Erectile dysfunction  |  11
HP:0002617  |  Aneurysmal dilatation  |  11
HP:0002625  |  Blood clot in a deep vein  |  10
HP:0001250  |  Seizures  |  10
HP:0002099  |  Asthma  |  10
HP:0004936  |  Blood clot in vein  |  10
HP:0005584  |  Renal cell carcinoma  |  9
HP:0001263  |  Developmental retardation  |  9
HP:0002907  |  Microhematuria  |  9
HP:0002960  |  Autoimmune condition  |  9
HP:0001875  |  Neutropenia  |  8
HP:0002633  |  Vasculitis  |  8
HP:0005110  |  Atrial fibrillation  |  8
HP:0012579  |  Minimal change glomerulonephritis  |  8
HP:0011034  |  Amyloid disease  |  8
HP:0000790  |  Hematuria  |  8
HP:0001638  |  Cardiomyopathy  |  8
HP:0001402  |  Hepatocellular carcinoma  |  8
HP:0000739  |  Anxiety  |  8
HP:0003124  |  Elevated serum cholesterol  |  8
HP:0100522  |  Thymoma  |  8
HP:0003006  |  Neuroblastoma  |  7
HP:0000787  |  Renal calculi  |  7
HP:0001081  |  Gallstones  |  7
HP:0000704  |  Pyorrhea  |  7
HP:0100279  |  Ulcerative colitis  |  7
HP:0002076  |  Migraine headaches  |  7
HP:0002758  |  Osteoarthritis  |  7
HP:0000939  |  Osteoporosis  |  7
HP:0002090  |  Pneumonia  |  7
HP:0002014  |  Diarrhea  |  6
HP:0002352  |  Leukoencephalopathy  |  6
HP:0000135  |  Hypogonadism  |  6
HP:0011974  |  Myelofibrosis  |  6
HP:0001712  |  Left ventricular hypertrophy  |  6
HP:0100820  |  Glomerulopathy  |  6
HP:0001394  |  Hepatic cirrhosis  |  6
HP:0002315  |  Headaches  |  6
HP:0003073  |  Hypoalbuminaemia  |  6
HP:0003281  |  Increased ferritin  |  6
HP:0001268  |  Mental deterioration  |  6
HP:0001298  |  Encephalopathy  |  6
HP:0012191  |  B-cell lymphoma  |  6
HP:0000488  |  Noninflammatory retina disease  |  6
HP:0002140  |  Ischemic stroke  |  6
HP:0004322  |  Stature below 3rd percentile  |  5
HP:0012378  |  Fatigue  |  5
HP:0001511  |  Prenatal onset growth retardation  |  5
HP:0000708  |  Behavioral problems  |  5
HP:0002586  |  Peritonitis  |  5
HP:0002383  |  Encephalitis  |  5
HP:0001876  |  Low blood cell count  |  5
HP:0000979  |  Purpura  |  5
HP:0006510  |  Chronic obstructive pulmonary disease  |  5
HP:0001714  |  Ventricular hypertrophy  |  5
HP:0100512  |  Vitamin D deficiency  |  5
HP:0005506  |  Chronic myeloid leukemia  |  5
HP:0003287  |  Abnormality of mitochondrial metabolism  |  5
HP:0005528  |  Bone marrow hypoplasia  |  5
HP:0009800  |  gestational diabetes  |  5
HP:0001733  |  Pancreatic inflammation  |  5
HP:0100724  |  Hypercoagulability  |  4
HP:0001880  |  Eosinophilia  |  4
HP:0100033  |  Tic disorder  |  4
HP:0001399  |  Liver failure  |  4
HP:0001289  |  Confusion  |  4
HP:0001508  |  Weight faltering  |  4
HP:0100280  |  Morbus Crohn  |  4
HP:0001596  |  Hair loss  |  4
HP:0011675  |  Arrhythmias  |  4
HP:0008711  |  Benign prostatic hypertrophy  |  4
HP:0002527  |  Falls  |  4
HP:0000726  |  Dementia  |  4
HP:0003256  |  Coagulopathy  |  4
HP:0012597  |  Heavy proteinuria  |  4
HP:0100806  |  Sepsis  |  4
HP:0012189  |  Hodgkin disease  |  4
HP:0001518  |  Small for gestational age  |  4
HP:0012126  |  Gastric cancer  |  4
HP:0100602  |  Pre-eclampsia  |  4
HP:0000166  |  Severe periodontal disease  |  4
HP:0004943  |  Accelerated atherosclerosis  |  4
HP:0001324  |  Muscular weakness  |  4
HP:0001878  |  Haemolytic anaemia  |  4
HP:0002716  |  Lymph node hyperplasia  |  4
HP:0002647  |  Aortic dissection  |  4
HP:0003418  |  Back pain  |  4
HP:0001395  |  Hepatic fibrosis  |  4
HP:0012089  |  Arteritis  |  3
HP:0002092  |  Pulmonary artery hypertension  |  3
HP:0001541  |  Ascites  |  3
HP:0030078  |  Lung adenocarcinoma  |  3
HP:0002063  |  Muscle rigidity  |  3
HP:0012050  |  Anasarca  |  3
HP:0006280  |  Chronic pancreas inflammation  |  3
HP:0000572  |  Visual loss  |  3
HP:0009830  |  Peripheral neuritis  |  3
HP:0100817  |  Renovascular hypertension  |  3
HP:0000789  |  Infertility  |  3
HP:0010783  |  Erythema  |  3
HP:0100723  |  Gastrointestinal stroma tumor  |  3
HP:0012490  |  Inflammation of fat tissue  |  3
HP:0002666  |  Pheochromocytoma  |  3
HP:0100003  |  Peritoneal mesothelioma  |  3
HP:0000709  |  Psychosis  |  3
HP:0100584  |  Endocarditis  |  3
HP:0100749  |  Thoracic pain  |  3
HP:0100242  |  Sarcoma  |  3
HP:0000113  |  Polycystic kidney dysplasia  |  3
HP:0000252  |  Small head circumference  |  3
HP:0002148  |  Hypophosphataemia  |  3
HP:0002573  |  Bloody diarrhea  |  3
HP:0004929  |  Coronary artherosclerosis  |  3
HP:0009125  |  Lipodystrophy  |  3
HP:0002634  |  Arteriosclerosis  |  3
HP:0002668  |  Paragangliomas  |  3
HP:0000501  |  Glaucoma  |  3
HP:0002860  |  Squamous cell carcinoma  |  3
HP:0002027  |  Abdominal pain  |  3
HP:0001396  |  Cholestasis  |  3
HP:0012384  |  Nasal inflammation  |  3
HP:0100022  |  Movement disorder  |  3
HP:0040154  |  Hidradenitis suppurativa  |  3
HP:0001262  |  Somnolence  |  3
HP:0005202  |  Helicobacter pylori infection  |  3
HP:0006846  |  Acute encephalopathy  |  3
HP:0002013  |  Emesis  |  3
HP:0000131  |  Uterine leiomyoma  |  3
HP:0030358  |  Non-small cell lung carcinoma  |  3
HP:0002910  |  Elevated transaminases  |  3
HP:0000718  |  Aggressive behaviour  |  2
HP:0002360  |  Sleep disturbance  |  2
HP:0012281  |  Chylous ascites  |  2
HP:0002667  |  Wilms tumor  |  2
HP:0004420  |  Arterial thrombosis  |  2
HP:0003233  |  Low HDL-cholesterol  |  2
HP:0002861  |  Melanoma  |  2
HP:0100633  |  Inflammation of the esophagus  |  2
HP:0012132  |  Erythroid hyperplasia  |  2
HP:0001920  |  Renal artery stenosis  |  2
HP:0002204  |  Pulmonary embolism  |  2
HP:0001717  |  Coronary artery calcification  |  2
HP:0012410  |  Pure red cell aplasia  |  2
HP:0004326  |  Cachexia  |  2
HP:0001271  |  Polyneuropathy  |  2
HP:0040213  |  Hypopnea  |  2
HP:0100658  |  Bacterial infection of skin  |  2
HP:0001639  |  Hypertrophic cardiomyopathy  |  2
HP:0012399  |  Bedsore  |  2
HP:0008064  |  Ichthyosis  |  2
HP:0012539  |  Non-Hodgkin lymphoma  |  2
HP:0008200  |  Primary hyperparathyroidism  |  2
HP:0011947  |  Respiratory infection  |  2
HP:0012398  |  Peripheral edema  |  2
HP:0000962  |  Hyperkeratosis  |  2
HP:0001004  |  Lymphatic obstruction  |  2
HP:0100646  |  Thyroiditis  |  2
HP:0001138  |  Damaged optic nerve  |  2
HP:0040171  |  Low serum testosterone levels  |  2
HP:0002613  |  Biliary cirrhosis  |  2
HP:0003259  |  Increased serum creatinine  |  2
HP:0000956  |  Keratosis nigricans  |  2
HP:0002608  |  Celiac disease  |  2
HP:0001548  |  Overgrowth  |  2
HP:0000999  |  Pyoderma  |  2
HP:0001645  |  Sudden cardiac death  |  2
HP:0003764  |  Naevus  |  2
HP:0002591  |  Voracious appetite  |  2
HP:0009725  |  Bladder neoplasm  |  2
HP:0001708  |  Impaired right ventricular function  |  2
HP:0001970  |  Interstitial nephritis  |  2
HP:0001685  |  Myocardial fibrosis  |  2
HP:0001065  |  Purplish striae  |  2
HP:0001894  |  Thrombocytosis  |  2
HP:0000407  |  sensorineural hearing loss  |  2
HP:0004950  |  Peripheral artery disease  |  2
HP:0012226  |  Ovarian teratoma  |  2
HP:0001067  |  Neurofibromas  |  2
HP:0002896  |  Liver cancer  |  2
HP:0012432  |  Chronic fatigue  |  2
HP:0004942  |  Aortic aneurysm  |  2
HP:0030854  |  Scleral staphyloma  |  2
HP:0010442  |  Polydactyly  |  2
HP:0002119  |  Ventricular dilatation  |  2
HP:0001941  |  acidemia  |  2
HP:0012133  |  Erythroid hypoplasia  |  2
HP:0000078  |  Genital abnormalities  |  2
HP:0100614  |  Muscle inflammation  |  2
HP:0002020  |  Heartburn  |  2
HP:0009592  |  Astrocytoma  |  2
HP:0002637  |  Brain ischemia  |  2
HP:0001917  |  Renal amyloidosis  |  2
HP:0012234  |  Agranulocytosis  |  2
HP:0012193  |  Anaplastic large-cell lymphoma  |  2
HP:0001956  |  Centripetal obesity  |  2
HP:0001061  |  Acne  |  2
HP:0003560  |  Muscular dystrophy  |  2
HP:0003419  |  Low back pain  |  2
HP:0100758  |  Gangrene  |  2
HP:0005086  |  Knee osteoarthritis  |  2
HP:0006562  |  Viral hepatitis  |  2
HP:0007359  |  Partial seizures  |  2
HP:0007430  |  Generalized edema  |  2
HP:0100259  |  Postaxial hexadactyly  |  2
HP:0005521  |  Disseminated intravascular coagulation  |  2
HP:0000010  |  Frequent urinary tract infections  |  1
HP:0000024  |  Inflammation of the prostate  |  1
HP:0001924  |  Hypersideremic anemia  |  1
HP:0000044  |  Hypogonadotrophic hypogonadism  |  1
HP:0006380  |  Contractures of knees  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0012469  |  Infantile spasms  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0001605  |  Vocal cord paralysis  |  1
HP:0001701  |  Pericarditis  |  1
HP:0000858  |  Menstrual irregularity  |  1
HP:0100546  |  Narrowing of carotid artery  |  1
HP:0040141  |  Tardive dyskinesia  |  1
HP:0045029  |  Eosinophilic fasciitis  |  1
HP:0001371  |  Flexion contractures of joints  |  1
HP:0100578  |  Lipoatrophy  |  1
HP:0010550  |  Paraplegia  |  1
HP:0000763  |  Sensory neuropathy  |  1
HP:0000793  |  Membranoproliferative glomerulonephritis  |  1
HP:0006685  |  Endocardial fibrosis  |  1
HP:0000230  |  Inflamed gums  |  1
HP:0001901  |  Abnormally shaped erythrocytes  |  1
HP:0100617  |  Testicular seminoma  |  1
HP:0000026  |  Decreased function of male gonad  |  1
HP:0005994  |  Nodular goiter  |  1
HP:0001159  |  Webbed fingers or toes  |  1
HP:0001096  |  Keratoconjunctivitis  |  1
HP:0001838  |  Rocker bottom foot  |  1
HP:0003510  |  Proportionate dwarfism  |  1
HP:0001433  |  Enlarged liver and spleen  |  1
HP:0100582  |  Nasal polyps  |  1
HP:0002321  |  Vertigo  |  1
HP:0008189  |  Insulin insensitivity  |  1
HP:0002460  |  Weakness of distal muscles  |  1
HP:0002121  |  Petit mal seizures  |  1
HP:0001270  |  Motor retardation  |  1
HP:0012486  |  Inflammation of spinal cord  |  1
HP:0001269  |  Hemiparesis  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0002653  |  Bone pain  |  1
HP:0004850  |  Recurrent deep vein thrombosis  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0002094  |  Dyspnea  |  1
HP:0000988  |  Exanthem  |  1
HP:0009795  |  Branchial cleft fistula  |  1
HP:0000824  |  Growth hormone deficiency  |  1
HP:0002619  |  Varicose veins  |  1
HP:0011967  |  Hypocupremia  |  1
HP:0030828  |  Wheezing  |  1
HP:0011331  |  Atrophy of one side of the face  |  1
HP:0001636  |  Tetrology of fallot  |  1
HP:0001251  |  Ataxia  |  1
HP:0003193  |  Allergic rhinitis  |  1
HP:0004828  |  Myelodysplasia with sideroblastosis  |  1
HP:0000752  |  Hyperactive behavior  |  1
HP:0001578  |  Hypercortisolism  |  1
HP:0004417  |  Intermittent claudication  |  1
HP:0004836  |  Acute promyelocytic leukemia  |  1
HP:0000505  |  Poor vision  |  1
HP:0012444  |  Brain wasting  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0000483  |  Astigmatism  |  1
HP:0002862  |  Bladder carcinoma  |  1
HP:0009829  |  Phocomelia  |  1
HP:0002242  |  Enteropathy  |  1
HP:0001050  |  Plethora  |  1
HP:0005952  |  Decreased lung function  |  1
HP:0000738  |  Sensory hallucination  |  1
HP:0001882  |  Decreased blood leukocyte number  |  1
HP:0001974  |  Leukocytosis  |  1
HP:0012721  |  Venous malformations  |  1
HP:0000529  |  Slowly progressive visual loss  |  1
HP:0030760  |  Kidney fibrosis  |  1
HP:0001650  |  Valvular aortic stenosis  |  1
HP:0002202  |  Pleural effusion  |  1
HP:0000554  |  Uveitis  |  1
HP:0000846  |  Hypoadrenalism  |  1
HP:0004755  |  Supraventricular tachycardia  |  1
HP:0100556  |  Hemiatrophy of the body  |  1
HP:0040187  |  Neonatal sepsis  |  1
HP:0004729  |  Acute tubulointerstitial nephritis  |  1
HP:0012213  |  Reduced creatinine clearance  |  1
HP:0011459  |  Esophageal carcinoma  |  1
HP:0100653  |  Optic neuritis  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0004432  |  Agammaglobulinaemia  |  1
HP:0002958  |  Immune dysregulation  |  1
HP:0002153  |  Elevated serum potassium levels  |  1
HP:0007917  |  Tractional retinal detachment  |  1
HP:0001649  |  Tachycardia  |  1
HP:0100001  |  Malignant mesothelioma  |  1
HP:0000541  |  Detached retina  |  1
HP:0100520  |  Oliguria  |  1
HP:0100510  |  Vitamin C deficiency  |  1
HP:0000164  |  Abnormality of the teeth  |  1
HP:0008677  |  Congenital nephrosis  |  1
HP:0000766  |  Pectus deformity  |  1
HP:0001097  |  Keratoconjunctivitis sicca  |  1
HP:0010524  |  Agnosia  |  1
HP:0001908  |  Hypoplastic anemia  |  1
HP:0003075  |  Hypoproteinemia  |  1
HP:0001942  |  Metabolic acidosis  |  1
HP:0000989  |  pruritis  |  1
HP:0002126  |  Polymicrogyria  |  1
HP:0010609  |  Skin tags  |  1
HP:0100295  |  Muscle fibre atrophy  |  1
HP:0004818  |  Paroxysmal nocturnal hemoglobinuria  |  1
HP:0100778  |  Cryoglobulinemia  |  1
HP:0001681  |  Angina pectoris  |  1
HP:0003771  |  Pulp calcifications  |  1
HP:0002597  |  Abnormality of blood vessels  |  1
HP:0001944  |  Dehydration  |  1
HP:0000568  |  Abnormally small globe of eye  |  1
HP:0000964  |  Eczema  |  1
HP:0012817  |  Noncompaction of the ventricular myocardium  |  1
HP:0008682  |  Renal tubular necrosis  |  1
HP:0002384  |  Dyscognitive seizures  |  1
HP:0001531  |  Failure to thrive in infancy  |  1
HP:0012219  |  Erythema nodosum  |  1
HP:0001937  |  Microangiopathic hemolytic anemia  |  1
HP:0002367  |  Visual hallucinations  |  1
HP:0001662  |  Bradycardia  |  1
HP:0000276  |  Long face  |  1
HP:0001947  |  Renal tubular acidosis  |  1
HP:0002835  |  Aspiration  |  1
HP:0030160  |  Uterine cervicitis  |  1
HP:0002576  |  Intussusception  |  1
HP:0002584  |  Intestinal hemorrhage  |  1
HP:0040216  |  Hypoinsulinemia  |  1
HP:0001890  |  Autoimmune hemolytic anemia  |  1
HP:0100660  |  Dyskinesis  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0006517  |  Alveolar proteinosis  |  1
HP:0030833  |  Neck pain  |  1
HP:0000175  |  Palatoschisis  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0002749  |  Osteomalacia  |  1
HP:0012228  |  Tension-type headache  |  1
HP:0005549  |  Low blood neutrophil level since birth  |  1
HP:0005547  |  Myeloproliferative disorder  |  1
HP:0002072  |  Chorea  |  1
HP:0000867  |  Secondary hyperparathyroidism  |  1
HP:0012223  |  Ruptured spleen  |  1
HP:0011779  |  Anaplastic thyroid carcinoma  |  1
HP:0000876  |  Oligomenorrhea  |  1
HP:0000756  |  Fear of open spaces  |  1
HP:0012819  |  Myocarditis  |  1
HP:0030834  |  Shoulder pain  |  1
HP:0004713  |  Reversible renal failure  |  1
HP:0001136  |  Tortuous retinal arterioles  |  1
HP:0001744  |  Splenomegaly  |  1
HP:0001332  |  Dystonia  |  1
HP:0001999  |  Facial dysmorphism  |  1
HP:0002028  |  Chronic diarrhea  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0030062  |  Craniopharyngioma  |  1
HP:0012075  |  Personality disorder  |  1
HP:0100002  |  Pleural mesothelioma  |  1
HP:0002955  |  Granulomatosis  |  1
HP:0030784  |  Anomic aphasia  |  1
HP:0030153  |  Cholangiocarcinoma  |  1
HP:0100601  |  Eclampsia  |  1
HP:0001872  |  Platelet abnormalities  |  1
HP:0030149  |  Cardiovascular shock  |  1
HP:0000639  |  Nystagmus  |  1
HP:0000952  |  Yellow skin  |  1
HP:0011147  |  Typical absence seizures  |  1
HP:0002836  |  Bladder exstrophy  |  1
HP:0002925  |  Increased serum thyroid-stimulating hormone  |  1
HP:0100785  |  Insomnia  |  1
HP:0002571  |  Achalasia  |  1
HP:0002878  |  Respiratory failure  |  1
HP:0003072  |  Hypercalcemia  |  1
HP:0011123  |  Skin inflammation  |  1
HP:0100537  |  Inflammation of the fascia  |  1
HP:0100568  |  Endocrine neoplasia  |  1
HP:0001892  |  Bleeding diathesis  |  1
HP:0001013  |  Eruptive xanthomas  |  1
HP:0000138  |  Ovarian cyst  |  1
HP:0030685  |  Decreased adiponectin level  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0100257  |  Cleft hand  |  1
HP:0012156  |  Hemophagocytosis  |  1
HP:0002326  |  TIA  |  1
HP:0005181  |  Premature coronary artery disease  |  1
HP:0006740  |  Transitional cell bladder carcinoma  |  1
HP:0001520  |  Birthweight > 90th percentile  |  1
HP:0008069  |  Neoplasm of the skin  |  1
HP:0001007  |  Hirsutism  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0002459  |  Dysautonomia  |  1
HP:0000514  |  Slow eye movements  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0003003  |  Colon cancer  |  1
HP:0004845  |  Acute monoblastic leukemia  |  1
HP:0012532  |  Chronic pain  |  1
HP:0000518  |  Cataract  |  1
HP:0001967  |  Diffuse mesangial sclerosis  |  1
HP:0005550  |  Chronic lymphatic leukemia  |  1
HP:0000563  |  Conical cornea  |  1
HP:0000256  |  Macrocrania  |  1
HP:0008609  |  Morphological abnormality of the middle ear  |  1
HP:0000020  |  Bladder incontinence  |  1
HP:0000496  |  Ocular movement abnormalities  |  1
HP:0002239  |  Gastrointestinal hemorrhage  |  1
HP:0030843  |  Cardiac amyloidosis  |  1
HP:0000271  |  Abnormal face  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0002133  |  Status epilepticus  |  1
HP:0004746  |  Dense deposit disease  |  1
HP:0005576  |  Renal interstitial fibrosis  |  1
HP:0004444  |  Spherocytosis  |  1
HP:0002381  |  Aphasia  |  1
HP:0001897  |  Normocytic anemia  |  1
HP:0002804  |  Arthrogryposis multiplex congenita  |  1
HP:0011510  |  Drusen  |  1
HP:0000767  |  Funnel chest  |  1
HP:0002110  |  Bronchiectasis  |  1
HP:0008672  |  Oxalate nephrolithiasis  |  1
HP:0000479  |  Abnormality of the retina  |  1
HP:0100021  |  Cerebral palsy  |  1
HP:0000133  |  Mixed gonadal dysgenesis  |  1
HP:0001047  |  Atopic dermatitis  |  1
HP:0012182  |  Oropharyngeal squamous cell carcinoma  |  1
HP:0004395  |  Malnutrition  |  1
HP:0001627  |  Congenital heart defects  |  1
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  1
HP:0003641  |  Hemoglobin in urine  |  1
HP:0002189  |  Excessive daytime sleepiness  |  1
HP:0200046  |  Cat cry  |  1
HP:0005978  |  Noninsulin dependent diabetes mellitus  |  1
HP:0000713  |  Agitation  |  1
HP:0001259  |  Coma  |  1
HP:0002018  |  Nausea  |  1
HP:0005310  |  Large vessel vasculitis  |  1
HP:0012325  |  Chronic myelomonocytic leukemia  |  1
HP:0002156  |  High urine homocystine levels  |  1
HP:0004415  |  Pulmonary artery stenosis  |  1
HP:0001952  |  Abnormal glucose tolerance  |  1
HP:0003198  |  Myopathic changes  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
HP:0030151  |  Cholangitis  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0002579  |  Gastrointestinal dysmotility  |  1
HP:0001935  |  Microcytic anemia  |  1
HP:0100620  |  Germinoma  |  1
HP:0100548  |  Exstrophy  |  1
HP:0002390  |  Spinal arteriovenous malformation  |  1
HP:0002578  |  Gastroparesis  |  1
HP:0006721  |  Acute lymphocytic leukemia  |  1
HP:0002671  |  Basalioma  |  1
HP:0001896  |  Reticulocytopenia  |  1
HP:0002488  |  Acute leukemias  |  1
HP:0002639  |  Budd-Chiari syndrome  |  1
HP:0006349  |  Agenesis of permanent dentition  |  1
HP:0001680  |  Coarctation of aorta  |  1
HP:0002728  |  Mucocutaneous candidiasis  |  1
HP:0012076  |  Borderline personality disorder  |  1
HP:0001055  |  Erysipelas  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0003228  |  High blood sodium levels  |  1
HP:0006279  |  Beta-cell dysfunction  |  1
HP:0000347  |  Hypoplasia of mandible  |  1
HP:0004313  |  Decreased immunoglobulin level  |  1
HP:0000870  |  Hyperprolactinemia  |  1
HP:0001339  |  Lissencephaly  |  1
HP:0000832  |  Primary hypothyroidism  |  1
Disease ID 548
Disease c syndrome
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs119477056NA10225CD96umls:C0796095CLINVARNA0.480271442NACD963111585362CA,T
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0004209Clinodactyly of the 5th fingerMP:0003694failure of blastocyst to hatch from the zona pellucida;HP:0000175Cleft palate
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002650ScoliosisMP:0010465aberrant origin of the right subclavian artery;HP:0000243Trigonocephaly
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)