SLC26A5

solute carrier family 26 member 5
OMIM: 604943
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
#613865:?Deafness, autosomal recessive 61, Nonsyndromic Hearing Loss, Recessive, Deafness, autosomal recessive 61, 613865, hearing loss