PDE8B

phosphodiesterase 8B
OMIM: 603390, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
No list PDE8B in Parkinson Disease and Complex Parkinsonism

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.128

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
Phenotypes
  • Striatal degeneration, autosomal dominant, MIM#609161
Green PDE8B in Primary pigmented nodular adrenocortical disease


Level 2: Endocrinology
Version 1.13
Latest signed off version: v1.12 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Pigmented nodular adrenocortical disease, primary, 3, OMIM:614190
No list PDE8B in Neurodegenerative disorders, adult onset


Level 2: Neurology
Version 9.22
Latest signed off version: v9.4 (12 Aug 2026)

Component of the following Super Panels:

  • Adult-onset neurological disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Research
    Phenotypes
    • striatal degeneration
    • Parkinsonism
    • bradykinesia, rigidity
    • dysarthria