COMMD4

COMM domain containing 4
OMIM: 616701, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list COMMD4 in Paediatric disorders - additional genes


Level 2: Developmental disorders
Version 8.17
Latest signed off version: v8.8 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • Ritscher-Schinzel Syndrome