ORPHA:656085
Benign atrophic papulosis
Synonyms: BAP
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Benign atrophic papulosis | BAP |
| fr | Papulose atrophiante bénigne | |
| de | Benigne atrophische Papulose | = en |
| es | Papulosis atrófica benigna | PAB |
| it | Papulosi atrofica benigna | PAB |
| nl | Benigne atrofische papulose | BAP · Goedaardige papulosis atrophicans |
| pt | Papulose atrófica benigna | = en |
| pl | Łagodna grudkowatość zanikowa | = en |
| cs | Benigní atrofická papulóza | = en |
| uk | Доброякісний атрофічний папулез | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0958274 | E | validated | |
| UMLS | C5891170 | 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:656071Atrophic papulosis
rare genetic diseases; rare skin diseases
No children.
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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/656085
- This record as JSON: /data/d/656085.json