COMMD4

COMM domain containing 4
OMIM: 616701, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red COMMD4 in Mendeliome


Version 1.3793

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ritscher-Schinzel syndrome, MONDO:0019078, COMMD4-related

Red COMMD4 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.575

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ritscher-Schinzel syndrome, MONDO:0019078, COMMD4-related

Red COMMD4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.496

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ritscher-Schinzel syndrome, MONDO:0019078, COMMD4-related