SLC35A3

solute carrier family 35 member A3
OMIM: 605632
PanelMode of inheritanceDetails
2 panels
R-numbers: R83
Signed-off version 10.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis, impaired intellectual development, and seizures, OMIM:615553
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis, impaired intellectual development, and seizures, OMIM:615553