Disease #02745 (DFNA41 (deafness, autosomal dominant, type 41 (DFNA-41)), OMIM:608224)

Official abbreviation DFNA41
Name deafness, autosomal dominant, type 41 (DFNA-41)
OMIM ID 608224
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene P2RX2
Associated tissues -
Disease features -
Remarks -

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