ORPHA:79468
Acanthokeratolytic verrucous nevus
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Acanthokeratolytic verrucous nevus | |
| fr | Naevus verruqueux acantho-kératolytique | |
| de | Naevus, akanthokeratolytischer verruköser | |
| es | Nevo verrugoso acantoqueratolítico | |
| it | Nevo verrucoso acanto-cheratolitico | |
| nl | Acanthokeratolytische verruceuze naevus | |
| pt | Nevo verrugoso acantoqueratolítico | |
| pl | Znamię brodawkowate akantokeratolityczne | |
| cs | Akantokeratolytický verukózní névus | |
| uk | Акантокератолітичний верукозний невус | |
| zh | 棘状角化松解疣状痣 | |
| tr | Akantokeratolitik verrüköz nevüs |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q82.5 | NTBT | attributed | validated |
| MONDO | 0019320 | E | validated | |
| UMLS | C5681486 | E | validated | |
| GARD | 5485 | 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 (1):
- ORPHA:2611Linear verrucous nevus syndrome
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/79468
- This record as JSON: /data/d/79468.json