FAM92A

family with sequence similarity 92 member A
OMIM: 617273, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FAM92A in Limb disorders


Level 2: Musculoskeletal
Version 7.20
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • postaxial polydactyly type A9