PCDHA9

protocadherin alpha 9
OMIM: 606315, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber PCDHA9 in Motor Neurone Disease


Level 2: Neurology and neurodevelopmental disorders
Version 1.38

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • amyotrophic lateral sclerosis MONDO:0004976

    Amber PCDHA9 in Incidentalome


    Version 0.349

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • amyotrophic lateral sclerosis MONDO:0004976

    Red PCDHA9 in Mendeliome


    Version 1.3382

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Hirschsprung disease MONDO:0018309
    • root resorption MONDO:0001997