adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone

Preferred Label : adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0566276;

UMLS CUI

C1859978;

Automatic exact mappings (from CISMeF team)
- Adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone [OMIM Phenotype]
Related record
- adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone [OMIM Phenotype]
- Familial adrenal hypoplasia with absent pituitary luteinizing hormone [ORDO Disease]

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