hyperandrogenism, nonclassic type, due to 21-Hydroxylase deficiency

Preferred Label : hyperandrogenism, nonclassic type, due to 21-Hydroxylase deficiency;

MeSH note : mutation in CYP21A2;

Origin ID

C565977;

UMLS CUI

C1859995;

Automatic exact mappings (from CISMeF team)
- Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [OMIM Phenotype]
- Hyperandrogenism due to non-classic type of 21-hydroxylase deficiency (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- hyperandrogenism [MeSH Descriptor]
Record concept(s)
- hyperandrogenism, nonclassic type, due to 21-Hydroxylase deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]