ORPHA:719931
Angiokeratoma circumscriptum
Synonyms: AKC · Angiokeratoma circumscriptum neviforme
- Type
- Morphological anomaly
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Angiokeratoma circumscriptum | AKC · Angiokeratoma circumscriptum neviforme |
| fr | Angiokératome circonscrit | AKC · Angiokératose circonscrite naeviforme |
| de | Angiokeratoma circumscriptum | AKC · Angiokeratoma circumscriptum naeviforme |
| es | Angioqueratoma circunscrito | AKC · Angioqueratoma circunscrito neviforme |
| it | Angiocheratoma circoscritto | AKC · Angiocheratoma circoscritto neviforme |
| nl | Angiokeratoma circumscriptum | AKC · Angiokeratoma circumscriptum naeviforme |
| pt | Angiokeratoma circumscriptum | |
| pl | Angiokeratoma circumscriptum | = en |
| cs | Angiokeratoma circumscriptum | = en |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:2415Rare lymphatic malformation
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 100 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/719931
- This record as JSON: /data/d/719931.json