pigmented nodular adrenocortical disease, primary, 3
MONDO:0013616Mondo
Findings
No curated finding names pigmented nodular adrenocortical disease, primary, 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE8B gene.
Definition from the Mondo Disease Ontology (MONDO:0013616), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- PDE8BHGNC:8794
- Strong · Genomics England PanelApp · Autosomal dominant · 2020
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
Where it sits
Other names
3 names
Resolves to: pigmented nodular adrenocortical disease, primary, 3
- Also called
- PDE8B primary pigmented nodular adrenocortical diseasepigmented nodular adrenocortical disease, primary, type 3primary pigmented nodular adrenocortical disease caused by mutation in PDE8B