PPIA

peptidylprolyl isomerase A
OMIM: 123840, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red PPIA in Early-onset Dementia


Level 2: Neurology and neurodevelopmental disorders
Version 1.24

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • amyotrophic lateral sclerosis, MONDO:0004976, PPIA-associated

    Red PPIA in Mendeliome


    Version 1.1891

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • amyotrophic lateral sclerosis, MONDO:0004976