1. Genes and Genomic Entities
  2. SMPDL3A

SMPDL3A

sphingomyelin phosphodiesterase acid like 3A
OMIM: 610728, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list SMPDL3A in Pain syndromes

Level 3: Channelopathies
Level 2: Neurology and neurodevelopmental disorders
Version 1.12

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Sensory neuropathy