ORPHA:673568
Eccrine angiomatous hamartoma
Synonyms: EAH · Eccrine angiomatous nevus
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Eccrine angiomatous hamartoma | EAH · Eccrine angiomatous nevus |
| fr | Hamartome angio-eccrine | HAE |
| de | Hamartom, ekkrin-angiomatöses | EAH · Ekkriner angiomatöser Nävus |
| es | Hamartoma angiomatoso ecrino | Nevus angiomatoso ecrino |
| it | Amartoma angiomatoso eccrino | EAH · Nevo angiomatoso eccrino |
| nl | Eccrien angiomateus hamartoom | EAH · Eccriene angiomateuze naevus |
| pt | Hamartoma angiomatoso écrino | EAH · Nevus angiomatoso écrino |
| pl | Eccrine angiomatous hamartoma | = en |
| cs | Ekrinní angiomatózní hamartom | = en |
| uk | Еккринна ангіоматозна гамартома | EAH · Екринний ангіоматозний невус |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D18.0 | NTBT | attributed | validated |
| ICD-11 | LC0Y | NTBT | index | validated |
| MONDO | 975755 | E | validated | |
| UMLS | C0406801 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:673470Benign vascular tumor
rare developmental anomalies during embryogenesis; rare circulatory system diseases; rare neoplastic diseases - ORPHA:79386Rare skin tumor or hamartoma
rare skin diseases; rare neoplastic diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/673568
- This record as JSON: /data/d/673568.json