DCAF8

DDB1 and CUL4 associated factor 8
OMIM: 615820, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red DCAF8 in Hereditary neuropathy

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.476

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • South West GLH
  • Expert Review Red
  • Expert Review
Phenotypes
  • ?Giant axonal neuropathy 2, autosomal dominant, 610100
Red DCAF8 in Hereditary neuropathy or pain disorder


Version 3.87
Latest signed off version: v3.24 (15 May 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • South West GLH
  • Expert Review Red
  • Expert Review
  • NHS GMS
  • NHS GMS
  • South West GLH
Phenotypes
  • ?Giant axonal neuropathy 2, autosomal dominant, 610100