TDO2:Ensemblv115

tryptophan 2,3-dioxygenase
OMIM: 191070, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TDO2 in Miscellaneous Metabolic Disorders


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Red
Phenotypes
  • Hypertryptophanemia MIM#600627
  • Disorders of histidine, tryptophan or lysine metabolism

Red TDO2 in Aminoacidopathy


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • ClinGen
  • Expert Review Red
Phenotypes
  • familial hypertryptophanemia MONDO:0010907