USH1C

USH1 protein network component harmonin
OMIM: 605242
PanelMode of inheritanceDetails
2 panels
R-numbers: R67
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nonsyndromic Hearing Loss, Recessive, Acadian and Samaritan variety Usher syndrome, type 1C, 276904, hearing loss, Deafness, autosomal recessive 18A, 602092
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders