KIAA0825

KIAA0825
OMIM: 617266, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green KIAA0825 in Limb disorders


Level 2: Musculoskeletal
Version 8.7
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 Green
    • Literature
    Phenotypes
    • Polydactyly, postaxial, type A10 OMIM:618498
    • polydactyly, postaxial, type a10 MONDO:0032785
    Amber KIAA0825 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.11
    Latest signed off version: v7.0 (6 May 2026)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Amber
    Phenotypes
    • Polydactyly, postaxial, type A10, OMIM:618498