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 8.6
Latest signed off version: v8.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • ?Polydactyly, postaxial, type A9, OMIM:618219
    • polydactyly, postaxial, type A9, MONDO:0032603
    Tags
    • new-gene-name
    • Q2_26_promote_green