ORPHA:93555
Mixed cryoglobulinemia type III
Synonyms: MC type III
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Age of onset
- All ages
- Status
- active
A clinico-serological subtype of mixed cryoglobulinemia syndrome, is an immune complex disorder, characterized by purpura, weakness and arthralgia and defined immunochemically by cryoglobulins containing both polyclonal IgGs and polyclonal IgMs.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mixed cryoglobulinemia type III | MC type III |
| fr | Cryoglobulinémie mixte type III | = en |
| de | Kryoglobulinämie, gemischte, Typ III | MC vom Typ II I |
| es | Crioglobulinemia mixta tipo III | Crioglobulinemia mixta tipo 3 |
| it | Crioglobulinemia mista, tipo III | MC, tipo III |
| nl | Gemengde cryoglobulinemie type III | = en |
| pt | Crioglobulinemia mista tipo III | |
| pl | Mieszana krioglobulinemia typu III | = en |
| cs | Smíšená kryoglobulinemie, typ III | MC typ III |
| uk | Змішана кріоглобулінемія, тип III | MC тип III |
| zh | 混合性冷沉球蛋白血症III型 | MC III型 |
| tr | Karma kriyoglobulinemi tip III | MC tip III |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D89.1 | NTBT | attributed | validated |
| ICD-11 | 4A44.90 | NTBT | attributed | validated |
| MONDO | 0019727 | E | validated | |
| UMLS | C5680263 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:91138Cryoglobulinemic vasculitis
rare neurological diseases; rare respiratory diseases; rare renal diseases; rare systemic and rheumatological diseases; rare circulatory system diseases; rare systemic or rheumatologic diseases of childhood; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93555
- This record as JSON: /data/d/93555.json