PDE8B

phosphodiesterase 8B
OMIM: 603390, Gene2Phenotype

2 panels

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

Level 3: Neurodegenerative disorders
Level 2: Neurology and neurodevelopmental disorders
Version 1.121

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


Version 1.10
Latest signed off version: v1.2 (19 Feb 2020)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Pigmented nodular adrenocortical disease, primary, 3, OMIM:614190