Skip to main content

RareConnect.ioRare Intelligence

Explore Data Discover Patient Groups News Partner

Sign In Sign Up

Explore Data Patient Groups News Partner

RareConnect.ioRare Intelligence

Combining the speed of AI with the wisdom of the community to build the world's most accurate disease registry.

Explore

Disease Directory
Patient Groups
News
FAQ
MONDO Ontology ↗

Get Involved

Partner with Us
Register Your PAG
Community
Pricing

Legal

Privacy Policy
Terms of Service
Accessibility
Contact Us

© 2025 RareConnect.io. Powered by MONDO Ontology

pigmented nodular adrenocortical disease, primary, 3 | RareConnect | RareConnect.io

/primary pigmented nodular adrenocortical disease

/pigmented nodular adrenocortical disease, primary, 3

pigmented nodular adrenocortical disease, primary, 3

Rare Disease

MONDO:0013616

Also Known As

PDE8B primary pigmented nodular adrenocortical diseasepigmented nodular adrenocortical disease, primary, 3pigmented nodular adrenocortical disease, primary, type 3primary pigmented nodular adrenocortical disease caused by mutation in PDE8BCushing syndrome, adrenal, due to PPNAD3PPNAD3

Definition

Any primary pigmented nodular adrenocortical disease in which the cause of the disease is a mutation in the PDE8B gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614190 ↗

GARD

Related Diseases

pigmented nodular adrenocortical disease, primary, 2

MONDO:0012505

pigmented nodular adrenocortical disease, primary, 1

MONDO:0012509

pigmented nodular adrenocortical disease, primary, 4

MONDO:0014359

isolated primary pigmented nodular adrenocortical disease

MONDO:0958262

← Back to All Diseases