Term Name: | Usher syndrome type 1C |
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Synonyms: | USH1C, Usher syndrome type I Acadian variety, Usher syndrome type IC |
Definition: | An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15. |
Ontology: | Human Disease [DOID:0110830] ( DOID:0110830 ) |