ITFG2

integrin alpha FG-GAP repeat containing 2
OMIM: 617421, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green ITFG2 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental abnormality
  • Intellectual disability
  • Developmental regression
  • Ataxia

Green ITFG2 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental abnormality
  • Intellectual disability
  • Developmental regression
  • Ataxia