LRTOMT

leucine rich transmembrane and O-methyltransferase domain containing
OMIM: 612414
PanelMode of inheritanceDetails
1 panel
R-numbers: R67
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nonsyndromic Hearing Loss, Recessive, Deafness, autosomal recessive 63, 611451, hearing loss