TPI1

triosephosphate isomerase 1
OMIM: 190450, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green TPI1 in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.118

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Hemolytic anemia due to triosephosphate isomerase deficiency,615512
  • Enzyme Disorder
Green TPI1 in Rare anaemia


Version 3.8
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • 615512 Hemolytic anemia due to triosephosphate isomerase deficiency
  • Hemolytic anemia due to triosephosphate isomerase deficiency,615512
  • Enzyme Disorder
Green TPI1 in Severe Paediatric Disorders


Version 1.184

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Hemolytic anemia due to triosephosphate isomerase deficiency, 615512