ORPHA:93554
Mixed cryoglobulinemia type II
Synonyms: MC type II
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Age of onset
- All ages
- Status
- active
A clinico-serological subtype of mixed cryoglobulinemia syndrome, an immune complex disorder, characterized by purpura, weakness and arthralgia and defined immunochemically by cryoglobulins composed of polyclonal IgGs (autoantigens) and monoclonal IgM (autoantibody).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mixed cryoglobulinemia type II | MC type II |
| fr | Cryoglobulinémie mixte type II | = en |
| de | Kryoglobulinämie, gemischte, Typ II | MC vom Typ II |
| es | Crioglobulinemia mixta tipo II | |
| it | Crioglobulinemia mista, tipo II | MC, tipo II |
| nl | Gemengde cryoglobulinemie type II | = en |
| pt | Crioglobulinemia mista tipo II | |
| pl | Mieszana krioglobulinemia typu II | = en |
| cs | Smíšená kryoglobulinemie, typ II | MC typ II |
| uk | Змішана кріоглобулінемія, тип II | MC тип II |
| zh | II型混合性冷沉球蛋白血症 | MC II型 |
| tr | Tip II karma kriyoglobulinemi | MC tip II |
Definition in:
2
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 | 0019726 | E | validated | |
| UMLS | C5680264 | 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/93554
- This record as JSON: /data/d/93554.json