ORPHA:280065
Calciphylaxis cutis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
A rare, life-threatening, non-inflammatory vasculopathy characterized clinically by progressive and painful skin lesions associated with calcification of cutaneous arterial microvessels. Calciphylaxis predominantly affects patients with end-stage kidney disease (ESKD) on dialysis.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Calciphylaxis cutis | |
| fr | Calciphylaxie cutanée | |
| de | Kalziphylaxie, kutane | |
| es | Calcifilaxis cutánea | |
| it | Calcifilassi cutanea | |
| nl | Calciphylaxis cutis | Cutane calcifylaxie |
| pt | Calcifilaxia cutis | |
| pl | Kalcyfilaksja skóry | |
| cs | Calciphylaxis cutis | |
| uk | Кальцифілаксія шкіри | |
| zh | 皮肤钙化防御 | |
| tr | Kalsifilaksi kutis |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E83.5 | NTBT | attributed | validated |
| ICD-11 | EB90.42 | NTBT | attributed | validated |
| MONDO | 0017216 | E | validated | |
| UMLS | C4274083 | 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 (2):
- ORPHA:280062Calciphylaxis
rare systemic and rheumatological diseases; rare circulatory system diseases - ORPHA:79379Skin vascular disease
rare skin diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/280065
- This record as JSON: /data/d/280065.json