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 8.4
Latest signed off version: v8.0 (6 May 2026)

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