kallmann syndrome 4

Preferred Label : kallmann syndrome 4;

MeSH note : mutation in PROK2;

Origin ID

C565696;

UMLS CUI

C1857720;

Automatic exact mappings (from CISMeF team)
- Hypogonadotropic hypogonadism 4 with or without anosmia [OMIM Phenotype]
MeSH term(s) associated for indexing
- kallmann syndrome [MeSH Descriptor]
Record concept(s)
- kallmann syndrome 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]