SLC17A8

solute carrier family 17 member 8
OMIM: 607557
PanelMode of inheritanceDetails
1 panel
R-numbers: R67
Signed-off version 3.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
hearing loss, Nonsyndromic Hearing Loss, Dominant, Deafness, autosomal dominant 25, 605583