Disease #02337 (USH1D (Usher syndrome, type 1D (USH-1D)), OMIM:601067)

Official abbreviation USH1D
Name Usher syndrome, type 1D (USH-1D)
OMIM ID 601067
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive, Digenic recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CDH23
Associated tissues -
Disease features -
Remarks -

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