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

amyloidosis, primary localized cutaneous, 1 | RareConnect | RareConnect.io

/familial primary localized cutaneous amyloidosis

/amyloidosis, primary localized cutaneous, 1

amyloidosis, primary localized cutaneous, 1

Rare Disease

MONDO:0024522

Also Known As

OSMR primary cutaneous amyloidosisPLCA1amyloidosis 9amyloidosis, primary cutaneous, 1amyloidosis, primary localised cutaneous, type 1amyloidosis, primary localized cutaneous, 1amyloidosis, primary localized cutaneous, type 1primary cutaneous amyloidosis caused by mutation in OSMRPCAamyloidosis, familial cutaneous lichenlichen amyloidosis, familial

Definition

Any primary cutaneous amyloidosis in which the cause of the disease is a mutation in the OSMR 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:105250 ↗

GARD

Related Diseases

amyloidosis, primary localized cutaneous, 2

MONDO:0013502

amyloidosis, primary localized cutaneous, 3

MONDO:0054765

← Back to All Diseases