PanelApp (test)
  1. Genes and Genomic Entities
  2. FAM92A

FAM92A

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber FAM92A in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Polydactyly, postaxial, type A9, MIM# 618219

Amber FAM92A in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.276

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Polydactyly, postaxial, type A9, MIM# 618219

    Amber FAM92A in Fetal anomalies


    Version 1.255

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Polydactyly, postaxial, type A9 - MIM#618219