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Details
Link-It Detail - Disease - Glucocorticoid deficiency
Debug Stats
  • ### Total Build Time: 85 ms 17.092 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 348 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=59 ms Completed: 59 ms rowSize= 11.987 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 3.535 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Glucocorticoid deficiency C1955741
Relationships (27)

Relation Types:
diso_​to_​diso : 27


Relationships:
expanded_​form_​of : 1
mapped_​to : 26
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmapped_toimg ACTH DEFICIENCY, ISOLATED C0271583
DISO_to_DISOmapped_toimg ADDISON DISEASE, CONGENITAL C0271740
DISO_to_DISOmapped_toimg ADRENAL HAEMORRHAGE C0151693
DISO_to_DISOmapped_toimg ADRENAL SUPPRESSION C0271738
DISO_to_DISOmapped_toimg ATROPHY ADRENAL C0342490
DISO_to_DISOmapped_toimg Acyl-CoA oxidase deficiency C0342871
DISO_to_DISOmapped_toimg Addison Disease C0001403
DISO_to_DISOmapped_toimg Addison disease with adrenoleucodystrophy C0342477
DISO_to_DISOmapped_toimg Addison melanoderma (disorder) C1279223
DISO_to_DISOmapped_toimg Addisonian crisis C0151467
DISO_to_DISOmapped_toimg Adrenal Insufficiency C0001623
DISO_to_DISOmapped_toimg Adrenal calcification C0271750
DISO_to_DISOmapped_toimg Adrenal cortical hypofunction C0405580
DISO_to_DISOmapped_toimg Adrenal gland haematoma C0347638
DISO_to_DISOmapped_toimg Adrenal infarction C0271751
DISO_to_DISOmapped_toimg Adrenocortical haemorrhage C0342484
DISO_to_DISOmapped_toimg Adrenocorticotropic hormone (ACTH) deficiency (disorder) C0342388
DISO_to_DISOmapped_toimg Classic pseudohypoaldosteronism C0268437
DISO_to_DISOmapped_toimg Drug-induced adrenocortical insufficiency C0348943
DISO_to_DISOmapped_toimg Familial Addison disease C0271739
DISO_to_DISOexpanded_form_ofimg Glucocorticoid deficiency C1955741
DISO_to_DISOmapped_toimg Hereditary adrenal unresponsiveness to corticotropin C0271741
DISO_to_DISOmapped_toimg Hyperreninemic hypoaldosteronism C0342483
DISO_to_DISOmapped_toimg Iatrogenic adrenal insufficiency C0342480
DISO_to_DISOmapped_toimg Idiopathic ACTH deficiency C0342389
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanMC2R4158melanocortin 2 receptor (adrenocorticotropic hormone)
img GENERIF, Score=673, Pubmed Id: 18492762, UMLKSK CUI: C1955741
img GAD, Score=1000, Pubmed Id: 8227361, UMLKSK CUI: C1955741
HumanCYP3A41576cytochrome P450, family 3, subfamily A, polypeptide 4
img GENERIF, Score=901, Pubmed Id: 18957504, UMLKSK CUI: C1955741
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1955741Glucocorticoid deficiency0self