Familial Glucocorticoid Deficiency Type 3

Preferred Label : Familial Glucocorticoid Deficiency Type 3;

NCIt related terms : GCCD3; Non-classic CLAH (FGD variant);

Alternative definition : NICHD: A variant of familial glucocorticoid deficiency caused by a defect in the steroidogenic acute regulatory protein; it may mimic lipoid congenital adrenal hyperplasia.;

Details

Origin ID

C131451;

UMLS CUI

C1836621;

Automatic exact mappings (from CISMeF team)
- Glucocorticoid deficiency 3 [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glucocorticoid deficiency 3 [OMIM Phenotype]
- glucocorticoid deficiency 3 [MeSH Supplementary Concept]
- glucocorticoid deficiency 3 [MeSH concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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