FAT3

FAT atypical cadherin 3
OMIM: 612483, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list FAT3 in Hereditary neuropathy or pain disorder


Level 2: Neurology
Version 7.45
Latest signed off version: v7.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
Phenotypes
  • axonal sensory and motor peripheral neuropathy
  • cranial neuropathy
  • scoliosis
  • respiratory failure
  • pseudoobstruction