PPIA

peptidylprolyl isomerase A
OMIM: 123840, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list PPIA in Early onset dementia (encompassing fronto-temporal dementia and prion disease)

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.83

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