Disease #00160

Official abbreviation 500004
Name RETINITIS PIGMENTOSA-DEAFNESS SYNDROME
OMIM ID 500004
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 10 genes CDH23, CLRN1, DFNB31, GPR98, MT-TS2, MYO7A, PCDH15, USH1C, USH1G, USH2A
Associated tissues -
Disease features -
Remarks -

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