SPG21

SPG21, maspardin
OMIM: 608181
PanelMode of inheritanceDetails
4 panels
R-numbers: R60
Signed-off version 3.21
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mast syndrome, 248900, Spastic Paraplegia, autosomal recessive
R-numbers: R62
Signed-off version 3.23
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mast syndrome, MIM# 248900
R-numbers: R58
Signed-off version 4.41
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic Paraplegia, Recessive
R-numbers: R61
Signed-off version 4.28
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic Paraplegia, Recessive, Mast syndrome, 248900