Deafness, autosomal recessive 123

Preferred Label : Deafness, autosomal recessive 123;

Symbol : DFNB123;

Type : Phenotype, molecular basis known;

Prefixed ID : #620745;

Details

Origin ID

620745;

UMLS CUI

C5935588;

Genes related to phenotype
- Syntaxin 4 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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