ORPHA:33314
Jessner lymphocytic infiltration of the skin
Synonyms: Jessner-Kanof lymphocytic infiltration of the skin
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
A rare chronic benign cutaneous disease characterized by asymptomatic non-scaly erythematous papules or plaques on the face and neck.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Jessner lymphocytic infiltration of the skin | Jessner-Kanof lymphocytic infiltration of the skin |
| fr | Infiltration lymphocytaire cutanée de Jessner | Infiltration lymphocytaire cutanée bénigne de Jessner · Infiltration lymphocytaire cutanée de Jessner-Kanof |
| de | Jessner-Lymphozyteninfiltration der Haut | JLIS · Lymphozytische Infiltration Jessner-Kanof · Lymphozytäre Infiltration der Haut Jessner-Kanof |
| es | Infiltración linfocítica cutánea de Jessner | Infiltración linfocítica cutánea de Jessner-Kanof · Infiltración linfocítica cutánea de Jessner-Kanof |
| it | Infiltrazione linfocitaria cutanea di Jessner | |
| nl | Lymfocytaire infiltratie van huid, Jessner-type | Lymfocytaire infiltratie van huid, Jessner-Kanof-type |
| pt | Infiltração linfocítica Jessner na pele | |
| pl | Limfocytarny naciek skóry Jessnera | Limfocytarny naciek skóry Jessnera-Kanofi |
| cs | Jessnerova lymfocytární infiltrace kůže | Jessnerova benigní lymfocytární infiltrace kůže · Lymfocytární infiltrát kůže Jessner-Kanof |
| uk | Лімфоцитарна інфільтрація шкіри Джесснера | Лімфоцитарна інфільтрація шкіри Джесснера-Канофа |
| zh | 皮肤Jessner淋巴细胞浸润症 | 皮肤Jessner-Kanof淋巴细胞浸润症 |
| tr | Jessner lenfositik cilt infiltrasyonu | Jessner-Kanof cildin lenfositik infiltrasyonu |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.6 | NTBT | attributed | validated |
| ICD-11 | EE90 | E | specific | validated |
| MONDO | 0018051 | E | validated | |
| UMLS | C0580181 | E | validated | |
| GARD | 6940 | E | validated | |
| MedDRA | 10063628 | 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:90077Other acquired skin 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet 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.
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HPO phenotypes
6 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0010783 | Erythema | |
| HP:0200034 | Papule | |
| HP:0200035 | Skin plaque | |
| Frequent (79-30%) | ||
| HP:0004332 | Abnormal lymphocyte morphology | |
| HP:0000992 | Cutaneous photosensitivity | |
| HP:0000989 | Pruritus | |
Run the differential on the 3 obligate / very frequent terms
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/33314
- This record as JSON: /data/d/33314.json