C3orf58

chromosome 3 open reading frame 58
OMIM: 612200, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red C3orf58 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review Not set
    Sources
    • Victorian Clinical Genetics Services
    Tags
    • new-gene-name