TPH2

tryptophan hydroxylase 2
OMIM: 607478, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TPH2 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003

Red TPH2 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • {Attention deficit-hyperactivity disorder, susceptibility to, 7} 613003