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Usher syndrome type 1C
rareA form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding harmonin on chromosome 11p15. It is inherited in an autosomal recessive manner.
- Identifiers
- MONDO:0010171 OMIM:276904
- Causal genes
- USH1C
- Part of
- Usher syndrome type 1
- Also known as
- USH1C · Usher syndrome, Acadian variety · Usher syndrome, type 1C · USHER syndrome, type IC
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