Familial Glucocorticoid Deficiency Type 4

Preferred Label : Familial Glucocorticoid Deficiency Type 4;

NCIt related terms : GCCD4;

Alternative definition : NICHD: Familial glucocorticoid deficiency caused by mutation(s) in the NNT gene encoding nicotinamide nucleotide transhydrogenase.;

Details

Origin ID

C131452;

UMLS CUI

C3553587;

Automatic exact mappings (from CISMeF team)
- Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency [OMIM Phenotype]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]

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