CCDC174

coiled-coil domain containing 174
OMIM: 616735, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CCDC174 in Intellectual disability


Level 2: Developmental disorders
Version 9.281
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Hypotonia, infantile, with psychomotor retardation - IHPMR, 616816
    Tags
    • founder-effect