1. Genes and Genomic Entities
  2. FAM92A

FAM92A

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber FAM92A in Limb disorders


Level 2: Musculoskeletal
Version 8.16
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
    Amber FAM92A in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.26
    Latest signed off version: v7.0 (6 May 2026)

    		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