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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   kennedy disease
  

Disease ID 887
Disease kennedy disease
Definition
This gene plays a role in the transcriptional activation of androgen responsive genes.
Synonym
kennedy disease) gene
spinal and bulbar muscular atrophy
testicular feminization
androgen receptor (dihydrotestosterone receptor
androgen receptor gene
ar gene
dhtr
dihydrotestosterone receptor
nr3c4
nuclear receptor subfamily 3, group c, member 4
smax1
Orphanet
OMIM
DOID
UMLS
C1367578
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:106)
C0032460  |  polycystic ovary  |  6
C0032460  |  polycystic ovary syndrome  |  6
C0024530  |  malaria  |  6
C0751651  |  mitochondrial disorder  |  5
C0039585  |  androgen insensitivity syndrome  |  5
C0751651  |  mitochondrial disorders  |  5
C0376358  |  prostate cancer  |  4
C0011847  |  diabetes  |  4
C0004096  |  asthma  |  4
C0028754  |  obesity  |  3
C0006142  |  breast cancer  |  3
C0002395  |  alzheimer's disease  |  2
C0021400  |  influenza  |  2
C0042769  |  virus infection  |  2
C1621895  |  adrenal hyperplasia  |  2
C0017636  |  glioblastoma  |  2
C0149931  |  migraine  |  2
C0011570  |  depression  |  2
C0035334  |  retinitis pigmentosa  |  2
C0025202  |  melanomas  |  2
C0035333  |  retinitis  |  2
C0018799  |  heart disease  |  2
C0010068  |  coronary heart disease  |  2
C1261473  |  sarcomas  |  2
C0001627  |  congenital adrenal hyperplasia  |  2
C0007115  |  thyroid ca  |  1
C0027868  |  neuromuscular disease  |  1
C0020619  |  hypogonadism  |  1
C0021364  |  male infertility  |  1
C0024299  |  lymphoma  |  1
C0021359  |  infertility  |  1
C0003873  |  rheumatoid arthritis  |  1
C0006111  |  brain disorder  |  1
C0010068  |  coronary artery disease  |  1
C0028754  |  adiposity  |  1
C0019069  |  hemophilia  |  1
C0037317  |  sleep disturbance  |  1
C0003467  |  anxiety  |  1
C1279296  |  chronic leukemia  |  1
C0206644  |  fibrous histiocytoma  |  1
C0029124  |  optic atrophy  |  1
C0043117  |  idiopathic thrombocytopenic purpura  |  1
C0004153  |  atherosclerosis  |  1
C0029463  |  osteosarcoma  |  1
C0014544  |  epilepsy  |  1
C0039101  |  synovial sarcoma  |  1
C0042373  |  vascular disease  |  1
C1140680  |  ovarian ca  |  1
C0040053  |  thrombosis  |  1
C0010346  |  crohn's disease  |  1
C0028960  |  oligozoospermia  |  1
C0010036  |  corneal dystrophy  |  1
C0855197  |  testicular germ cell cancer  |  1
C0023467  |  acute myeloid leukemia  |  1
C0020757  |  ichthyosis  |  1
C0004096  |  bronchial asthma  |  1
C0023418  |  leukaemia  |  1
C0024439  |  macular corneal dystrophy  |  1
C0751651  |  mitochondrial disease  |  1
C0009402  |  colorectal cancer  |  1
C0007138  |  transitional cell carcinoma  |  1
C0016952  |  galactosemia  |  1
C0001418  |  adenocarcinoma  |  1
C0238462  |  medullary thyroid carcinoma  |  1
C0041296  |  tuberculosis  |  1
C0041696  |  major depression  |  1
C0028960  |  oligospermia  |  1
C1261473  |  sarcoma  |  1
C0220633  |  uveal melanoma  |  1
C0020456  |  hyperglycaemia  |  1
C0024623  |  gastric cancer  |  1
C0002453  |  amenorrhea  |  1
C0020501  |  primary hyperoxaluria  |  1
C0021359  |  infertile  |  1
C1261473  |  soft tissue sarcoma  |  1
C0023449  |  acute lymphoblastic leukaemia  |  1
C0020538  |  hypertension  |  1
C0242379  |  lung cancer  |  1
C0002170  |  alopecia  |  1
C0149931  |  migraine headache  |  1
C0000786  |  spontaneous abortion  |  1
C0002736  |  amyotrophic lateral sclerosis  |  1
C0026986  |  myelodysplastic syndromes  |  1
C0004509  |  azoospermia  |  1
C1509147  |  histiocytoma  |  1
C0162359  |  hypohidrotic ectodermal dysplasia  |  1
C0040100  |  thymoma  |  1
C0007137  |  squamous cell carcinoma  |  1
C0035335  |  retinoblastoma  |  1
C0037317  |  sleep disturbances  |  1
C0004352  |  autism  |  1
C0034150  |  purpura  |  1
C0011881  |  diabetic nephropathy  |  1
C0022116  |  ischemia  |  1
C0549473  |  thyroid carcinoma  |  1
C0016627  |  avian influenza  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0752354  |  proximal myotonic myopathy  |  1
C1261473  |  soft tissue sarcomas  |  1
C0023418  |  leukemias  |  1
C1140680  |  ovarian cancer  |  1
C0007113  |  rectal cancer  |  1
C0019048  |  hemoglobinuria  |  1
C0028945  |  oligodendrogliomas  |  1
C0007134  |  renal cell cancer  |  1
C0011854  |  type 1 diabetes  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
367  |  AR  |  OMIM;UNIPROT
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus
Symbol | Locus(Total Locus:1)
AR  |  Xq12
Disease ID 887
Disease kennedy disease
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:13)
HP:0005978  |  Type II diabetes mellitus
HP:0001618  |  Dysphonia
HP:0000771  |  Gynecomastia
HP:0001288  |  Gait disturbance
HP:0000029  |  Testicular atrophy
HP:0100639  |  Erectile abnormalities
HP:0003119  |  Abnormality of lipid metabolism
HP:0100022  |  Abnormality of movement
HP:0001265  |  Hyporeflexia
HP:0001252  |  Muscular hypotonia
HP:0000144  |  Decreased fertility
HP:0001260  |  Dysarthria
HP:0003202  |  Skeletal muscle atrophy
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:89)
HP:0002664  |  Neoplasia  |  12
HP:0000147  |  Sclerocystic ovaries  |  6
HP:0003002  |  Breast carcinoma  |  4
HP:0012125  |  Prostate cancer  |  4
HP:0002099  |  Asthma  |  4
HP:0001513  |  Obesity  |  3
HP:0008221  |  Enlarged adrenal glands  |  3
HP:0008258  |  Congenital adrenal hyperplasia  |  2
HP:0100843  |  Glioblastoma  |  2
HP:0000718  |  Aggressive behaviour  |  2
HP:0000789  |  Infertility  |  2
HP:0002076  |  Migraine headaches  |  2
HP:0000716  |  Depression  |  2
HP:0000510  |  Retinitis pigmentosa  |  2
HP:0030731  |  Carcinoma  |  1
HP:0012315  |  Histiocytoma  |  1
HP:0000252  |  Small head circumference  |  1
HP:0002380  |  Muscle twitch  |  1
HP:0030448  |  Soft tissue sarcoma  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0000135  |  Hypogonadism  |  1
HP:0000648  |  Optic-nerve degeneration  |  1
HP:0007716  |  Intraocular melanoma  |  1
HP:0009919  |  Retinoblastoma  |  1
HP:0001399  |  Liver failure  |  1
HP:0100710  |  Impulsivity  |  1
HP:0200055  |  Small hand  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0003159  |  Hyperoxaluria  |  1
HP:0002018  |  Nausea  |  1
HP:0000979  |  Purpura  |  1
HP:0001131  |  Corneal dystrophy  |  1
HP:0200067  |  Recurrent spontaneous abortion  |  1
HP:0000822  |  Hypertension  |  1
HP:0000365  |  Hearing impairment  |  1
HP:0000855  |  Insulin resistance  |  1
HP:0012570  |  Synovial sarcoma  |  1
HP:0100242  |  Sarcoma  |  1
HP:0001370  |  Rheumatoid arthritis  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0002665  |  Lymphoma  |  1
HP:0012126  |  Gastric cancer  |  1
HP:0005558  |  Chronic leukemia  |  1
HP:0001596  |  Hair loss  |  1
HP:0100805  |  Precocious menopause  |  1
HP:0004936  |  Blood clot in vein  |  1
HP:0011999  |  Paranoia  |  1
HP:0005268  |  Spontaneous abortion  |  1
HP:0000717  |  Autism  |  1
HP:0004416  |  Precocious atherosclerosis  |  1
HP:0007529  |  Hidrotic ectodermal dysplasia  |  1
HP:0001677  |  Coronary artery disease  |  1
HP:0002865  |  Medullary thyroid carcinoma  |  1
HP:0008689  |  Bilateral cryptorchidism  |  1
HP:0012142  |  Pancreatic squamous cell carcinoma  |  1
HP:0007607  |  Hypohidrotic ectodermal dysplasia  |  1
HP:0000027  |  Azoospermia  |  1
HP:0003689  |  Multiple mtDNA deletions  |  1
HP:0000786  |  Primary amenorrhea  |  1
HP:0006554  |  Acute hepatic failure  |  1
HP:0012531  |  Pain  |  1
HP:0002625  |  Blood clot in a deep vein  |  1
HP:0002098  |  Respiratory distress  |  1
HP:0002890  |  Thyroid carcinoma  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0100013  |  Tumours of the breast  |  1
HP:0000047  |  Hypospadias  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0100522  |  Thymoma  |  1
HP:0000544  |  CPEO  |  1
HP:0008064  |  Ichthyosis  |  1
HP:0002669  |  Osteosarcoma  |  1
HP:0000798  |  Oligospermia  |  1
HP:0000028  |  Cryptorchidism  |  1
HP:0001250  |  Seizures  |  1
HP:0002621  |  Atherosclerosis  |  1
HP:0003641  |  Hemoglobin in urine  |  1
HP:0000141  |  Abnormal absence of menstruation  |  1
HP:0000739  |  Anxiety  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0000689  |  Misalignment of upper and lower dental arches  |  1
HP:0003251  |  Male infertility  |  1
HP:0000952  |  Yellow skin  |  1
HP:0000054  |  Short penis  |  1
HP:0100723  |  Gastrointestinal stroma tumor  |  1
HP:0008669  |  Abnormal spermatogenesis  |  1
HP:0002360  |  Sleep disturbance  |  1
HP:0007354  |  Amyotrophic lateral sclerosis  |  1
HP:0002597  |  Abnormality of blood vessels  |  1
Disease ID 887
Disease kennedy disease
Manually Symptom
UMLS  | Name(Total Manually Symptoms:2)
C0392678  |  swallowing impairment
C0011168  |  dysphagia
Text Mined Symptom(Waiting for update.)
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:7)
HP ID HP Name MP ID MP Name Annotation
HP:0003202Skeletal muscle atrophyMP:0014068abnormal muscle glycogen levelthe normal concentration of a readily converted carbohydrate reserve in muscle tissue
HP:0003119Abnormality of lipid metabolismMP:0009536abnormal interstitial cell of Cajal morphologyany structural anomaly in the type of cell found in the gastrointestinal tract and serving as a pacemaker that triggers gut contraction; ICCs mediate inputs from the enteric nervous system to smooth muscle cells and are thought to be the cells from which
HP:0100022Abnormality of movementMP:0005223abnormal dorsal-ventral polarity of the somitesanomalous development or formation of the pattern of somites along the axis that runs from the front (ventral) to the back (dorsal) surface of the body
HP:0001252Muscular hypotoniaMP:0004144hypotoniadecreased muscle tension resulting in limpness of the muscles in the resting state, not to be confused with weakness
HP:0000144Decreased fertilityMP:0008975delayed male fertilityability of a male organism to produce live offspring occurring at a later than expected age
HP:0000029Testicular atrophyMP:0011346renal tubule atrophyacquired diminution of the size of the loops of Henle, the proximal convoluted tubule or the distal convoluted tubule associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure,
HP:0005978Type II diabetes mellitusMP:0004803increased susceptibility to autoimmune diabetesgreater likelihood that an organism will develop inflammatory pancreatic disease resulting from the body attacking and destroying the insulin-producing beta islet cells of the pancreas
Mapped by homologous gene(Total Items:13)
HP ID HP Name MP ID MP Name Annotation
HP:0001252Muscular hypotoniaMP: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:0100022Abnormality of movementMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0001265HyporeflexiaMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000029Testicular atrophyMP:0020316decreased vascular endothelial cell proliferationdecrease in the expansion rate of any vascular endothelial cell population by cell division
HP:0001618DysphoniaMP:0013659abnormal erythroid lineage cell morphologyany structural anomaly of an immature or mature cell in the lineage leading to and including erythrocytes
HP:0001288Gait disturbanceMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0001260DysarthriaMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0003119Abnormality of lipid metabolismMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
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:0005978Type II diabetes mellitusMP:0020137decreased bone mineralizationdecrease in the rate at which minerals are deposited into bone
HP:0003202Skeletal muscle atrophyMP:0020329decreased capillary densityreduction in the number of capillaries in a given cross-sectional area of a tissue
HP:0000771GynecomastiaMP: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: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 887
Disease kennedy disease
Case(Waiting for update.)