Birt-hogg-dube syndrome 2 - CISMeF

" /> Birt-hogg-dube syndrome 2 - CISMeF

CISMeF

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Birt-hogg-dube syndrome 2OMIM Phenotype

Preferred Label : Birt-hogg-dube syndrome 2;

Symbol : BHD2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620459;

Details

Origin ID

620459;

UMLS CUI

C5830676;

Genes related to phenotype
- Pr domain-containing protein 10 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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09/05/2025

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