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Details
Link-It Detail - Disease - Hyperandrogenism
Debug Stats
  • ### Total Build Time: 130 ms 40.661 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 389 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 463 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=16 ms Completed: 16 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=34 ms Completed: 34 ms rowSize= 6.711 KB
  • CONCEPT_RELATIONSHIPS gt=31 ms Completed: 31 ms rowSize= 12.214 KB
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 18.990 KB
  • CONCEPT_XREFS gt=13 ms Completed: 13 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hyperandrogenism C0206081
Hyperandrogenisation syndrome
Definition (1)
A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Adrenogenital Syndrome C0302280
Ancestral Roots
RootRoot Plus OneDepthParent
img Male Urogenital Diseases C1720894img Urogenital Abnormalities C00420635img Adrenogenital Syndrome C0302280
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007686img Adrenogenital Syndrome C0302280
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208876img Adrenogenital Syndrome C0302280
img Endocrine System Diseases C0014130img Gonadal Disorders C00180505img Adrenogenital Syndrome C0302280
img Mental Disorders C0004936img Sexual and Gender Disorders C05250475img Adrenogenital Syndrome C0302280
Relationships (31)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 8
diso_​to_​diso : 16
diso_​to_​phen : 2


Relationships:
none : 27
isa : 3
mapped_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO126img Polycystic Ovary Syndrome C0032460
DISO_to_DISO79img Polycystic Ovary Syndrome C0032460
DISO_to_ANAT71img In Blood C0005768
DISO_to_DISO58img Complication Aspects C1171258
DISO_to_DISO54img Complication Aspects C1171258
DISO_to_ANAT40img In Blood C0005768
DISO_to_PHEN36img genetic aspects C0017399
DISO_to_CHEM29img Androgens C0002844
DISO_to_PHEN29img genetic aspects C0017399
DISO_to_CHEM28img Testosterone C0039601
DISO_to_DISO23img Insulin Resistance C0021655
DISO_to_DISO19img Hirsutism C0019572
DISO_to_DISO19img Insulin Resistance C0021655
DISO_to_DISO17img HYPERINSULINEMIA C0020459
DISO_to_CHEM16img 1,1-Dimethylbiguanide C0025598
DISO_to_DISO15img Obesity C0028754
DISO_to_CHEM14img ANDROGEN ANTAG C0002842
DISO_to_CHEM14img Agents, Antihyperglycemic C0020616
DISO_to_CHEM14img Androgens C0002844
DISO_to_ANAT13img Ovary C0029939
DISO_to_DISO13img HYPERINSULINEMIA C0020459
DISO_to_ANAT12img Ovary C0029939
DISO_to_CHEM11img 2-Methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide C0016384
DISO_to_ANAT10img Female genitalia C0017421
DISO_to_CHEM10img ANDROGEN ANTAG C0002842
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanRETN56729resistin
img GENERIF, Score=827, Pubmed Id: 15886251, UMLKSK CUI: C0206081
HumanWNT454361wingless-type MMTV integration site family, member 4
img OMIM, Score=1000, UMLKSK CUI: C0206081
HumanSORBS110580sorbin and SH3 domain containing 1
img GENERIF, Score=1000, Pubmed Id: 12849814, UMLKSK CUI: C0206081
HumanNAMPT10135nicotinamide phosphoribosyltransferase
img GENERIF, Score=1000, Pubmed Id: 17582143, UMLKSK CUI: C0206081
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
img GENERIF, Score=1000, Pubmed Id: 12161545, UMLKSK CUI: C0206081
HumanSRD5A16715steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)
img GAD, Score=1000, Pubmed Id: 16100771, UMLKSK CUI: C0206081
HumanSERPINE15054serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
img GENERIF, Score=827, Pubmed Id: 11809921, UMLKSK CUI: C0206081
HumanMC4R4160melanocortin 4 receptor
img GENERIF, Score=1000, Pubmed Id: 15533382, UMLKSK CUI: C0206081
HumanINSR3643insulin receptor
img GENERIF, Score=861, Pubmed Id: 18556968, UMLKSK CUI: C0206081
HumanINSL33640insulin-like 3 (Leydig cell)
img GENERIF, Score=812, Pubmed Id: 17356050, UMLKSK CUI: C0206081
HumanINS3630insulin
img GENERIF, Score=1000, Pubmed Id: 11937112, UMLKSK CUI: C0206081
HumanIL63569interleukin 6 (interferon, beta 2)
img GAD, Score=1000, Pubmed Id: 11889177, UMLKSK CUI: C0206081
img GENERIF, Score=1000, Pubmed Id: 11889177, UMLKSK CUI: C0206081
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
img GENERIF, Score=861, Pubmed Id: 12240900, UMLKSK CUI: C0206081
HumanCYP21A21589cytochrome P450, family 21, subfamily A, polypeptide 2
img GENERIF, Score=1000, Pubmed Id: 12050257, UMLKSK CUI: C0206081
HumanCYP19A11588cytochrome P450, family 19, subfamily A, polypeptide 1
img GENERIF, Score=827, Pubmed Id: 15802318, UMLKSK CUI: C0206081
img GAD, Score=1000, Pubmed Id: 15802318, UMLKSK CUI: C0206081
HumanAR367androgen receptor
img GAD, Score=833, Pubmed Id: 12843184, UMLKSK CUI: C0206081
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206081Hyperandrogenism0self