Disease #06859 (DFNX7 (?Deafness, X-linked 7), OMIM:301018)

Official abbreviation DFNX7
Name ?Deafness, X-linked 7
OMIM ID 301018
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GPRASP2
Associated tissues -
Disease features -
Remarks -

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