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Details
Link-It Detail - Disease - Adrenogenital disorder due to 21-hydroxylase deficiency
Debug Stats
  • ### Total Build Time: 80 ms 7.675 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=54 ms Completed: 54 ms rowSize= 3.317 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 2.700 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.188 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Adrenogenital disorder due to 21-hydroxylase deficiency C0268287
Relationships (6)

Relation Types:
diso_​to_​chem : 1
diso_​to_​diso : 5


Relationships:
associated_​with : 2
isa : 4
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMassociated_withimg Steroid 21-Hydroxylase C0038304
DISO_to_DISOisaimg 21-hydroxylase deficiency, salt wasting type C0268291
DISO_to_DISOassociated_withimg 270 CONGENITAL DEFICIENCIES C0333006
DISO_to_DISOisaimg Mild steroid 21-hydroxylase deficiency C0268288
DISO_to_DISOisaimg Moderate steroid 21-hydroxylase deficiency C0268289
DISO_to_DISOisaimg Severe steroid 21-hydroxylase deficiency C0268290
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanCYP21A21589cytochrome P450, family 21, subfamily A, polypeptide 2
img GAD, Score=926, Pubmed Id: 1406709, UMLKSK CUI: C0268287
HumanAR367androgen receptor
img GENERIF, Score=1000, Pubmed Id: 12050225, UMLKSK CUI: C0268287
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268287Adrenogenital disorder due to 21-hydroxylase deficiency0self