SLC9A1

solute carrier family 9 member A1
OMIM: 107310
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Lichtenstein-Knorr syndrome OMIM:616291, Lichtenstein-Knorr syndrome MONDO:0014572