Version: 8.0.0
Date: Tue Jan 28 2025
autosomal dominant congenital deafness with onychodystrophy
DOID:0080720
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

autosomal dominant congenital deafness with onychodystrophy

Definition
A syndrome that is characterized by autosomal dominant inheritance of congenital deafness and onychodystrophy and that has_material_basis_in heterozygous mutation in the ATP6V1B2 gene on chromosome 8p21.
Synonyms
None
Cross References
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Sources of Associations

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      Associated Models

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