FLT3

fms related tyrosine kinase 3
OMIM: 136351, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FLT3 in Cytopenias and congenital anaemias

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

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • BRIDGE consortium (NIHRBR-RD)
Phenotypes
  • Myelodysplastic syndrome (MDS), Paediatric