kallmann syndrome 5

Preferred Label : kallmann syndrome 5;

MeSH note : mutation in CHD7;

Origin ID

C567220;

UMLS CUI

C2675302;

Automatic exact mappings (from CISMeF team)
- Hypogonadotropic hypogonadism 5 with or without anosmia [OMIM Phenotype]
MeSH term(s) associated for indexing
- kallmann syndrome [MeSH Descriptor]
Record concept(s)
- kallmann syndrome 5 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]