SPG21

SPG21, maspardin
OMIM: 608181
PanelMode of inheritanceDetails
2 panels
R-numbers: R60
Signed-off version 1.27
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mast syndrome, 248900, Spastic Paraplegia, autosomal recessive
R-numbers: R61
Signed-off version 2.18
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic Paraplegia, Recessive, Mast syndrome, 248900