hypogonadotropic hypogonadism and anosmia, autosomal dominant

Preferred Label : hypogonadotropic hypogonadism and anosmia, autosomal dominant;

Origin ID

C538534;

UMLS CUI

C2931874;

MeSH term(s) associated for indexing
- kallmann syndrome [MeSH Descriptor]
Record concept(s)
- Hypogonadotropic hypogonadism and anosmia, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]