1. Genes and Genomic Entities
  2. HOXD10

HOXD10

homeobox D10
OMIM: 142984, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red HOXD10 in Hereditary neuropathy

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.506

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • NHS GMS
  • South West GLH
  • Expert Review Red
  • Emory Genetics Laboratory
  • UKGTN
  • Radboud University Medical Center, Nijmegen
  • Expert list
Phenotypes
  • Charcot Marie Tooth disease, foot deformity of, 192950
  • Charcot Marie Tooth disease, foot deformity of, 192950
Red HOXD10 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
    Red HOXD10 in Hereditary neuropathy or pain disorder


    Level 2: Neurology
    Version 7.36
    Latest signed off version: v7.0 (30 Apr 2025)

    		review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Radboud University Medical Center, Nijmegen
    • South West GLH
    • Expert Review Red
    • UKGTN
    • Emory Genetics Laboratory
    • Expert list
    • NHS GMS
    • NHS GMS
    • South West GLH
    Phenotypes
    • Charcot Marie Tooth disease, foot deformity of, 192950