SPTSSA:Ensemblv115

serine palmitoyltransferase small subunit A
OMIM: 613540, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber SPTSSA in Hereditary Spastic Paraplegia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • Spastic paraplegia 90B, autosomal recessive , MIM# 620417
  • Spastic paraplegia 90A, autosomal dominant, MIM# 620416