Waardenburg syndrome, type 2f - CISMeF

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CISMeF

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Waardenburg syndrome, type 2fOMIM Phenotype

Preferred Label : Waardenburg syndrome, type 2f;

Symbol : WS2F;

Type : Phenotype, molecular basis known;

Prefixed ID : #619947;

Details

Origin ID

619947;

UMLS CUI

C5677013;

Genes related to phenotype
- Kit ligand [OMIM gene]
ORDO concept(s)
- Waardenburg syndrome type 2 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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31/05/2025

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