adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone

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

Origin ID

C565976;

UMLS CUI

C1859978;

Automatic exact mappings (from CISMeF team)
- Adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone [OMIM Phenotype]
MeSH term(s) associated for indexing
- adrenal insufficiency [MeSH Descriptor]
- luteinizing hormone [MeSH Descriptor]
Record concept(s)
- adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone [MeSH 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]