SLC16A13

solute carrier family 16 member 13
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC16A13 in Mendeliome


Version 2.78

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Lactic acidosis MONDO:0006040, SLC16A13-related

Red SLC16A13 in Mitochondrial disease


Level 2: Metabolic disorders
Version 2.1

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Literature
    Phenotypes
    • Lactic acidosis MONDO:0006040, SLC16A13-related