Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms
disease diseaseOn this page
Summary
Localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms (MONDO:0019584) is a disease. A subtype of atypical lichen myxedematosus — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: <1 / 1 000 000 (Worldwide) [Orphanet-validated]
Clinical features
Epidemiology
Prevalence records
2 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Cases/families | 5 | Worldwide | Validated | |
| Point prevalence | <1 / 1 000 000 | Worldwide | Validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms |
| Mondo ID | MONDO:0019584 |
| Orphanet | 90399 |
| UMLS | C5681466 |
| MedGen | 1843442 |
| GARD | 0019143 |
| Is cancer (heuristic) | no |
Disease family
Classification path: disease › human disease › disease by body system or component › integumentary system disorder › skin disorder › cutaneous mucinosis › lichen myxedematosus › atypical lichen myxedematosus › localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms
Related subtypes (2): localized lichen myxedematosus with mixed features of different subtypes, scleromyxedema without monoclonal gammopathy
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.