SPG21

SPG21, maspardin
OMIM: 608181
PanelMode of inheritanceDetails
4 panels
Component of the following Super Panels:
  • - Adult-onset neurological disorders
Signed-off version 6.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mast syndrome, 248900, Spastic Paraplegia, autosomal recessive
R-numbers: R61
Signed-off version 9.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic Paraplegia, Recessive, Mast syndrome, 248900
R-numbers: R62
Signed-off version 7.8
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mast syndrome, MIM# 248900
Component of the following Super Panels:
  • - Adult-onset neurological disorders
Signed-off version 9.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spastic Paraplegia, Recessive