FITM2

fat storage inducing transmembrane protein 2
OMIM: 612029, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green FITM2 in Childhood onset dystonia or chorea or related movement disorder


Version 1.246
Latest signed off version: v1.137 (5 Aug 2021)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Siddiqi syndrome OMIM:618635
  • siddiqi syndrome MONDO:0032842