Usher syndrome type 1C

Term ID

DOID:0110830

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. https://www.ncbi.nlm.nih.gov/pubmed/10973247

References

• ICD10CM:H35.5
• OMIM:276904

Ontology

Human Disease   ( DOID:0110830 )