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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   cushing syndrome
  

Disease ID 480
Disease cushing syndrome
Definition
A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent.
Synonym
cushing syndrome [disease/finding]
cushing's basophilism
cushing's syndrome
cushing's syndrome (disorder)
cushing's syndrome iii
cushing's syndrome nos
cushing's syndrome nos (disorder)
cushings syndrome
itsenko disease
itsenko-cushing syndrome
pituitary basophilism
suprarenogenic syndrome
syndrome cushing's
syndrome, cushing
syndrome, cushing's
Orphanet
DOID
UMLS
C0010481
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:83)
C0020538  |  hypertension  |  10
C0001430  |  adenoma  |  8
C0011847  |  diabetes  |  7
C0206667  |  adrenocortical adenoma  |  6
C0001622  |  hypercortisolism  |  6
C1384514  |  primary aldosteronism  |  5
C0028754  |  obesity  |  5
C1621895  |  adrenal hyperplasia  |  5
C0020428  |  aldosteronism  |  4
C0878544  |  cardiomyopathy  |  4
C0598639  |  hypercortisolemia  |  3
C0007193  |  dilated cardiomyopathy  |  3
C0334684  |  renal adenoma  |  3
C0206667  |  adrenal adenoma  |  3
C0020456  |  hyperglycemia  |  3
C0342494  |  adrenocortical hyperplasia  |  3
C0011849  |  diabetes mellitus  |  3
C0001623  |  adrenal insufficiency  |  2
C0398623  |  hypercoagulable state  |  2
C0032000  |  pituitary adenoma  |  2
C0206686  |  adrenocortical carcinoma  |  2
C1565489  |  renal insufficiency  |  2
C0242379  |  lung cancer  |  2
C0032285  |  pneumonia  |  2
C0276688  |  cryptococcal pneumonia  |  2
C0398623  |  hypercoagulability  |  2
C0011860  |  type 2 diabetes  |  2
C0206667  |  adrenocortical adenomas  |  2
C0235660  |  galactorrhea  |  1
C0409974  |  lupus erythematosus  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0022658  |  renal diseases  |  1
C0025267  |  multiple endocrine neoplasia type i  |  1
C0034013  |  precocious puberty  |  1
C0022658  |  kidney disease  |  1
C0679466  |  cognitive deficits  |  1
C0406810  |  carney complex  |  1
C0015300  |  exophthalmos  |  1
C0342494  |  adrenal cortical hyperplasia  |  1
C0040053  |  thrombosis  |  1
C0011854  |  insulin-dependent diabetes  |  1
C0376358  |  prostate cancer  |  1
C0007115  |  thyroid ca  |  1
C0011860  |  diabetes mellitus type 2  |  1
C0001206  |  acromegaly  |  1
C0018021  |  goiter  |  1
C0011854  |  insulin-dependent diabetes mellitus  |  1
C0027819  |  neuroblastoma  |  1
C0549473  |  thyroid carcinoma  |  1
C0221406  |  cushing's disease  |  1
C0035078  |  kidney failure  |  1
C0020598  |  hypoglycemia  |  1
C0948265  |  metabolic syndrome  |  1
C0022658  |  renal disease  |  1
C0023903  |  tumor of liver  |  1
C0001621  |  adrenal disease  |  1
C0242343  |  panhypopituitarism  |  1
C0018920  |  cavernous hemangioma  |  1
C0022661  |  chronic kidney failure  |  1
C0033975  |  psychosis  |  1
C0018916  |  hemangioma  |  1
C1140680  |  ovarian ca  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0022661  |  chronic kidney disease  |  1
C0242379  |  lung cancers  |  1
C0025268  |  multiple endocrine neoplasia type ii  |  1
C0029456  |  osteoporosis  |  1
C0020428  |  hyperaldosteronism  |  1
C0238462  |  medullary thyroid carcinoma  |  1
C0007222  |  cardiovascular disease  |  1
C0206695  |  neuroendocrine carcinoma  |  1
C0936282  |  blastoma  |  1
C0206717  |  olfactory neuroblastoma  |  1
C0034150  |  purpura  |  1
C0004153  |  atherosclerosis  |  1
C0002395  |  alzheimer's disease  |  1
C0042373  |  vascular disease  |  1
C0027662  |  multiple endocrine neoplasia  |  1
C0029925  |  ovarian carcinoma  |  1
C0149925  |  small cell lung cancer  |  1
C0031511  |  pheochromocytoma  |  1
C0235461  |  androgen excess  |  1
C0024141  |  systemic lupus erythematosus  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:9)
2778  |  GNAS  |  UniProtKB-KW
5443  |  POMC  |  CTD_human
5573  |  PRKAR1A  |  CTD_human;UniProtKB-KW
9049  |  AIP  |  UniProtKB-KW
5566  |  PRKACA  |  UniProtKB-KW
79798  |  ARMC5  |  UniProtKB-KW
1392  |  CRH  |  CTD_human
8622  |  PDE8B  |  UniProtKB-KW
50940  |  PDE11A  |  UniProtKB-KW;UNIPROT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:5)
3290  |  HSD11B1  |  CIPHER
7450  |  VWF  |  CIPHER
5443  |  POMC  |  CTD_human
5573  |  PRKAR1A  |  CTD_human
1392  |  CRH  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:73)
9370  |  ADIPOQ  |  1.955  |  DISEASES
480  |  ATP1A4  |  1.19  |  DISEASES
551  |  AVP  |  3.53  |  DISEASES
553  |  AVPR1B  |  2.962  |  DISEASES
632  |  BGLAP  |  3.134  |  DISEASES
796  |  CALCA  |  3.383  |  DISEASES
8573  |  CASK  |  1.337  |  DISEASES
92211  |  CDHR1  |  1.029  |  DISEASES
1056  |  CEL  |  1.21  |  DISEASES
1114  |  CHGB  |  1.039  |  DISEASES
23122  |  CLASP2  |  1.432  |  DISEASES
1325  |  CORT  |  2.296  |  DISEASES
1394  |  CRHR1  |  2.344  |  DISEASES
401262  |  CRIP3  |  2.661  |  DISEASES
1499  |  CTNNB1  |  1.674  |  DISEASES
1528  |  CYB5A  |  2.164  |  DISEASES
1585  |  CYP11B2  |  4.103  |  DISEASES
1586  |  CYP17A1  |  4.097  |  DISEASES
1589  |  CYP21A2  |  2.913  |  DISEASES
1555  |  CYP2B6  |  1.769  |  DISEASES
1576  |  CYP3A4  |  2.773  |  DISEASES
1813  |  DRD2  |  1.57  |  DISEASES
2159  |  F10  |  1.448  |  DISEASES
2152  |  F3  |  1.467  |  DISEASES
2157  |  F8  |  1.306  |  DISEASES
114907  |  FBXO32  |  1.071  |  DISEASES
2271  |  FH  |  1.081  |  DISEASES
2289  |  FKBP5  |  1.971  |  DISEASES
2520  |  GAST  |  2.835  |  DISEASES
2641  |  GCG  |  2.775  |  DISEASES
51738  |  GHRL  |  2.536  |  DISEASES
2695  |  GIP  |  3.746  |  DISEASES
2696  |  GIPR  |  3.787  |  DISEASES
2778  |  GNAS  |  3.609  |  DISEASES
9446  |  GSTO1  |  1.935  |  DISEASES
9563  |  H6PD  |  1.107  |  DISEASES
3066  |  HDAC2  |  1.125  |  DISEASES
3283  |  HSD3B1  |  3.582  |  DISEASES
3284  |  HSD3B2  |  2.862  |  DISEASES
3360  |  HTR4  |  3.066  |  DISEASES
3363  |  HTR7  |  1.357  |  DISEASES
3481  |  IGF2  |  2.445  |  DISEASES
3601  |  IL15RA  |  1.029  |  DISEASES
3645  |  INSRR  |  1.107  |  DISEASES
3762  |  KCNJ5  |  2.412  |  DISEASES
4158  |  MC2R  |  4.357  |  DISEASES
4221  |  MEN1  |  3.748  |  DISEASES
2315  |  MLANA  |  1.259  |  DISEASES
117194  |  MRGPRX2  |  1.308  |  DISEASES
594857  |  NPS  |  1.917  |  DISEASES
7182  |  NR2C2  |  2.12  |  DISEASES
7025  |  NR2F1  |  1.802  |  DISEASES
4306  |  NR3C2  |  2.804  |  DISEASES
3164  |  NR4A1  |  2.077  |  DISEASES
2516  |  NR5A1  |  1.339  |  DISEASES
100630918  |  PARTICL  |  2.773  |  DISEASES
5241  |  PGR  |  1.71  |  DISEASES
5573  |  PRKAR1A  |  5.459  |  DISEASES
9232  |  PTTG1  |  1.887  |  DISEASES
6005  |  RHAG  |  1.215  |  DISEASES
866  |  SERPINA6  |  4.286  |  DISEASES
462  |  SERPINC1  |  1.448  |  DISEASES
6462  |  SHBG  |  2.286  |  DISEASES
23583  |  SMUG1  |  2.565  |  DISEASES
26800  |  SNORD49A  |  2.108  |  DISEASES
6752  |  SSTR2  |  3.46  |  DISEASES
6753  |  SSTR3  |  1.076  |  DISEASES
246744  |  STH  |  2.11  |  DISEASES
8859  |  STK19  |  1.094  |  DISEASES
9095  |  TBX19  |  4.022  |  DISEASES
51506  |  UFC1  |  1.176  |  DISEASES
7432  |  VIP  |  1.897  |  DISEASES
163223  |  ZNF676  |  2.108  |  DISEASES
Locus(Waiting for update.)
Disease ID 480
Disease cushing syndrome
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:41)
HP:0001061  |  Acne
HP:0001065  |  Striae distensae
HP:0000787  |  Nephrolithiasis
HP:0010978  |  Abnormality of immune system physiology
HP:0000518  |  Cataract
HP:0012378  |  Fatigue
HP:0100639  |  Erectile abnormalities
HP:0000978  |  Bruising susceptibility
HP:0002027  |  Abdominal pain
HP:0100585  |  Telangiectasia of the skin
HP:0001644  |  Dilated cardiomyopathy
HP:0003124  |  Hypercholesterolemia
HP:0003198  |  Myopathy
HP:0004295  |  Abnormality of the gastric mucosa
HP:0000869  |  Secondary amenorrhea
HP:0000963  |  Thin skin
HP:0002902  |  Hyponatremia
HP:0000822  |  Hypertension
HP:0004372  |  Reduced consciousness/confusion
HP:0000979  |  Purpura
HP:0000858  |  Menstrual irregularities
HP:0000739  |  Anxiety
HP:0001510  |  Growth delay
HP:0007552  |  Abnormal subcutaneous fat tissue distribution
HP:0002900  |  Hypokalemia
HP:0002757  |  Recurrent fractures
HP:0000939  |  Osteoporosis
HP:0000709  |  Psychosis
HP:0002230  |  Generalized hirsutism
HP:0001578  |  Hypercortisolism
HP:0000311  |  Round face
HP:0002360  |  Sleep disturbance
HP:0003072  |  Hypercalcemia
HP:0100631  |  Neoplasm of the adrenal gland
HP:0001324  |  Muscle weakness
HP:0000819  |  Diabetes mellitus
HP:0001956  |  Truncal obesity
HP:0000716  |  Depression
HP:0000737  |  Irritability
HP:0010885  |  Aseptic necrosis
HP:0000144  |  Decreased fertility
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:66)
HP:0000822  |  Hypertension  |  10
HP:0100570  |  Carcinoid tumor  |  9
HP:0002664  |  Neoplasia  |  7
HP:0001578  |  Hypercortisolism  |  6
HP:0008256  |  Adrenocortical adenomas  |  6
HP:0008221  |  Enlarged adrenal glands  |  5
HP:0030731  |  Carcinoma  |  5
HP:0001513  |  Obesity  |  5
HP:0001638  |  Cardiomyopathy  |  4
HP:0003074  |  High blood glucose  |  4
HP:0001907  |  Thromboembolic disease  |  4
HP:0001644  |  Congestive cardiomyopathy  |  3
HP:0000819  |  Diabetes mellitus  |  3
HP:0000708  |  Behavioral problems  |  3
HP:0100543  |  Cognitive deficits  |  3
HP:0000855  |  Insulin resistance  |  3
HP:0011734  |  Central adrenal insufficiency  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0002900  |  Hypokalemia  |  2
HP:0030445  |  Lung carcinoid tumor  |  2
HP:0000939  |  Osteoporosis  |  2
HP:0012743  |  Central obesity  |  2
HP:0002893  |  Pituitary adenoma  |  2
HP:0100724  |  Hypercoagulability  |  2
HP:0000846  |  Hypoadrenalism  |  2
HP:0002090  |  Pneumonia  |  2
HP:0006744  |  Adrenal carcinoma  |  2
HP:0008231  |  Macronodular adrenal hyperplasia  |  2
HP:0003256  |  Coagulopathy  |  1
HP:0100615  |  Neoplasm of the ovary  |  1
HP:0000709  |  Psychosis  |  1
HP:0000979  |  Purpura  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0002621  |  Atherosclerosis  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0010783  |  Erythema  |  1
HP:0002668  |  Paragangliomas  |  1
HP:0000871  |  Panhypopituitarism  |  1
HP:0000845  |  Acromegalic growth  |  1
HP:0001519  |  Dolichostenomelia  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0100523  |  Hepatic abscess  |  1
HP:0000859  |  Mineralocorticoid excess  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0100829  |  Galactorrhoea  |  1
HP:0001048  |  Cavernous angioma  |  1
HP:0100568  |  Endocrine neoplasia  |  1
HP:0003006  |  Neuroblastoma  |  1
HP:0012722  |  Heart block  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0002725  |  Systemic lupus erythematosus  |  1
HP:0001943  |  Hypoglycemia  |  1
HP:0012378  |  Fatigue  |  1
HP:0200114  |  Metabolic alkalosis  |  1
HP:0001649  |  Tachycardia  |  1
HP:0012622  |  Chronic kidney disease  |  1
HP:0000520  |  Anterior bulging of the globe of eye  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0000825  |  Hyperinsulinaemic hypoglycaemia  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0030357  |  Small cell lung carcinoma  |  1
HP:0012432  |  Chronic fatigue  |  1
HP:0000853  |  Goitre  |  1
HP:0002666  |  Pheochromocytoma  |  1
HP:0002865  |  Medullary thyroid carcinoma  |  1
HP:0000826  |  Precocious puberty  |  1
Disease ID 480
Disease cushing syndrome
Manually Symptom
UMLS  | Name(Total Manually Symptoms:22)
C2707258  |  infections
C2364072  |  depression
C1963274  |  vasculitis
C1963138  |  hypertension
C1442863  |  third nerve paresis
C1392499  |  cholesterolemia
C1384514  |  primary aldosteronism
C1336746  |  carcinoid tumor of the thymus
C0858734  |  insulin hypoglycemia
C0598639  |  hypercortisolemia
C0376293  |  stigmata
C0280089  |  pulmonary carcinoid tumor
C0271650  |  glucose intolerance
C0233401  |  psychiatric symptoms
C0206667  |  adrenal adenoma
C0155616  |  secondary hypertension
C0032000  |  adenoma of pituitary gland
C0030552  |  muscle pareses
C0027709  |  nephrocalcinosis
C0016065  |  polyostotic fibrous dysplasia
C0014013  |  pyothorax
C0004936  |  mental disorders
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:23)
C0020538  |  hypertension  |  10
C0001430  |  adenoma  |  7
C0001622  |  hypercortisolism  |  6
C0206667  |  adrenal adenoma  |  4
C0028754  |  obesity  |  4
C0020456  |  hyperglycemia  |  4
C0206667  |  adrenocortical adenoma  |  4
C0598639  |  hypercortisolemia  |  3
C0398623  |  hypercoagulable state  |  2
C0029456  |  osteoporosis  |  2
C0398623  |  hypercoagulability  |  2
C0342494  |  adrenocortical hyperplasia  |  2
C0242343  |  panhypopituitarism  |  1
C0020598  |  hypoglycemia  |  1
C1384514  |  primary aldosteronism  |  1
C1336746  |  carcinoid tumor of the thymus  |  1
C0031511  |  pheochromocytoma  |  1
C0033975  |  psychosis  |  1
C0002949  |  dissecting aneurysm  |  1
C0007222  |  cardiovascular disease  |  1
C0342494  |  adrenal cortical hyperplasia  |  1
C0032000  |  pituitary adenoma  |  1
C0001231  |  ectopic acth secretion  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:14)
HP ID HP Name MP ID MP Name Annotation
HP:0000963Thin skinMP:0010678abnormal skin adnexa morphologyany structural anomaly of the tissue or structures associated with or embedded in the skin such as hair and hair follicles, sweat glands, sebaceous glands and claws or nails
HP:0000311Round faceMP:0012546triangular facea face whose lower half becomes relatively thin, approaching an appearance of a triangle with a tip facing downwards; usually associated with a prominent forehead and micrognathia
HP:0007552Abnormal subcutaneous fat tissue distributionMP:0002086abnormal extraembryonic tissue morphologyany structural anomaly of the membranes involved with embryonic protection and nutrition
HP:0001956Truncal obesityMP:0005659decreased susceptibility to diet-induced obesityless likely to become excessively overweight or to increase fat in the subcutaneous connective tissue as a result of consuming a diet geared to increase body fat
HP:0004295Abnormality of the gastric mucosaMP:0004500increased incidence of tumors by ionizing radiation inductionhigher than normal frequency of tumor incidence induced by radiation in which the individual particle or photon carries sufficient energy to completely remove an electron from its orbit; common types of this radiation include gamma-rays and X-rays
HP:0001324Muscle weaknessMP:0000746weaknessstate of being infirm or less strong than normal
HP:0000144Decreased fertilityMP:0008975delayed male fertilityability of a male organism to produce live offspring occurring at a later than expected age
HP:0100631Neoplasm of the adrenal glandMP:0011205excessive folding of visceral yolk sacthe appearance of wrinkles or folds on the surface of the visceral yolk sac
HP:0001644Dilated cardiomyopathyMP:0005330cardiomyopathydiseases of the heart (myocardium); may result from many causes
HP:0010978Abnormality of immune system physiologyMP:0011205excessive folding of visceral yolk sacthe appearance of wrinkles or folds on the surface of the visceral yolk sac
HP:0010885Aseptic necrosisMP:0001654hepatic necrosismorphological changes resulting from pathological death of liver tissue; usually due to irreversible damage
HP:0100585Telangiectasia of the skinMP:0011022abnormal circadian regulation of systemic arterial blood pressureany anomaly in the process in which an organism modulates its blood pressure at different values with a regularity of approximately 24 hours
HP:0000978Bruising susceptibilityMP:0005596increased susceptibility to type I hypersensitivity reactiongreater likelihood of developing a response manifested by localized or generalized reaction that occurs immediately (minutes) after exposure to an antigen to which the person/animal was previously sensitized; it is IgE-mediated, and mast cell activation a
HP:0002757Recurrent fracturesMP:0004675rib fracturesa crack or break in the bones forming the bony wall of the chest
Mapped by homologous gene(Total Items:41)
HP ID HP Name MP ID MP Name Annotation
HP:0001578HypercortisolismMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0000739AnxietyMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000978Bruising susceptibilityMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0007552Abnormal subcutaneous fat tissue distributionMP:0013293embryonic lethality prior to tooth bud stagedeath prior to the appearance of tooth buds (Mus: E12-E12.5)
HP:0100639Erectile abnormalitiesMP:0014198absent pituitary infundibular stalkabsence of the apical portion of the tubular structure extending from the hypothalamus to the posterior lobe of the pituitary gland
HP:0002360Sleep disturbanceMP:0020169increased thyroid gland weighthigher than average weight of the thyroid gland
HP:0001061AcneMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0004372Reduced consciousness/confusionMP:0013405increased circulating lactate levelgreater amount of lactate in the blood which is produced from pyruvate by lactate dehydrogenase
HP:0002900HypokalemiaMP:0014206decreased intestinal epithelial sodium ion transmembrane transport
HP:0004295Abnormality of the gastric mucosaMP:0020154impaired humoral immune responseimpaired response of the immune system that mediates secreted antibodies produced in B cells
HP:0000518CataractMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0001510Growth delayMP:0020169increased thyroid gland weighthigher than average weight of the thyroid gland
HP:0003072HypercalcemiaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0000819Diabetes mellitusMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0100631Neoplasm of the adrenal glandMP:0012498abnormal cardiogenic plate morphologyany structural anomaly of the splanchnic mesodermal thickening which forms cranial and lateral to the developing neural plate; angiogenic cell clusters (aka angioblastic cords) located in a horse-shoe shape configuration in the cardiogenic plate coalesce
HP:0000939OsteoporosisMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0001324Muscle weaknessMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
HP:0012378FatigueMP:0013659abnormal erythroid lineage cell morphologyany structural anomaly of an immature or mature cell in the lineage leading to and including erythrocytes
HP:0002230Generalized hirsutismMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0001644Dilated cardiomyopathyMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0002757Recurrent fracturesMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0010885Aseptic necrosisMP:0013501increased fibroblast apoptosisincrease in the timing or the number of fibroblast cells undergoing programmed cell death
HP:0001065Striae distensaeMP:0020039increased bone ossificationincrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0000963Thin skinMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0003198MyopathyMP:0020280increased creatine kinase levelincreased level of the enzyme that catalyzes the reversible transfer of creatine to phosphocreatine
HP:0000737IrritabilityMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0002027Abdominal painMP:0020220decreased tear productiondecreased production of the amount of fluid produced in the eye
HP:0000787NephrolithiasisMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0000709PsychosisMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0001956Truncal obesityMP:0014169decreased brown adipose tissue massdecreased physical bulk or volume of brown adipose tissue
HP:0000311Round faceMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000869Secondary amenorrheaMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0010978Abnormality of immune system physiologyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0000979PurpuraMP:0020216decreased circulating complement protein levelless than normal levels of the serum proteins that act sequentially to allow for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes
HP:0000716DepressionMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000858Menstrual irregularitiesMP:0014167ectopic bonethe appearance of an extra bone structure at an atypical location
HP:0003124HypercholesterolemiaMP:0014169decreased brown adipose tissue massdecreased physical bulk or volume of brown adipose tissue
HP:0100585Telangiectasia of the skinMP:0014127increased thymoma incidencegreater than the expected number of a malignant neoplasm originating from the epithelial cells of the thymus, occurring in a specific population in a given time period; thymoma is an uncommon tumor linked with myasthenia gravis and other autoimmune diseas
HP:0002902HyponatremiaMP:0020215impaired blood coagulationimpaired ability of the blood to clot
HP:0000822HypertensionMP:0020216decreased circulating complement protein levelless than normal levels of the serum proteins that act sequentially to allow for the direct killing of microbes, the disposal of immune complexes, and the regulation of other immune processes
HP:0000144Decreased fertilityMP:0014198absent pituitary infundibular stalkabsence of the apical portion of the tubular structure extending from the hypothalamus to the posterior lobe of the pituitary gland
Disease ID 480
Disease cushing syndrome
Case(Waiting for update.)