kallmann syndrome 4 - CISMeF

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CISMeF

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Kallmann syndrome 4MeSH Supplementary Concept

Preferred Label : kallmann syndrome 4;

MeSH note : mutation in PROK2;

Détails

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]

Position du mot-clé dans l'(les) arborescence(s) :

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27/07/2025

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