1. Genes and Genomic Entities
  2. C20orf24

C20orf24

chromosome 20 open reading frame 24
Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red C20orf24 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.1
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • ?Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2, OMIM:616994
    Tags
    • new-gene-name