Erythema palmare hereditarium
Synonyms: Lane disease · Red palms disease
- Type
- Disease
- Group
- Disorder
- Inheritance
- Autosomal dominant
- Age of onset
- Infancy, Neonatal
- Status
- active
Erythema palmare hereditarium is a rare, benign, congenital genetic skin disorder characterized by permanent and asymptomatic erythema of the palmar and, less frequently, the solar surfaces. In most cases, it presents with sharply demarcated redness of the thenar and hypothenar eminences, as well as the palmar aspect of the phalanges, with scattered telangiectasia spots that do not cause any discomfort (pain, itching or burning) to the patient.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Erythema palmare hereditarium | Lane disease · Red palms disease |
| fr | Erythème palmaire héréditaire | Erythème palmoplantaire symétrique héréditaire · Maladie de Lane · Syndrome des paumes rouges |
| de | Erythema palmare hereditarium | Hereditäres Erythem der Handinnenfläche · Lane-Krankheit · Syndrom der roten Palmae |
| es | Eritema palmar hereditario | Enfermedad de Lane · Síndrome de las palmas rojas |
| it | Eritema palmare ereditario | Malattia dei palmi rossi · Malattia di Lane |
| nl | Erythema palmare hereditarium | Erfelijk erytheem van handpalm · Rode palmen-ziekte · Ziekte van Lane |
| pt | Eritema palmar hereditário | |
| pl | Dziedziczny rumień dłoniowy | Choroba Lane'a · Choroba czerwonych dłoni |
| cs | Erythema palmaris hereditarium | Laneova nemoc · Nemoc červených dlaní |
| uk | Спадкова еритема долонь | Хвороба Лейна · Хвороба червоних долонь |
| zh | 遗传性掌红斑 | 红掌病 |
| tr | Eritema palmare hereditarium | Lane hastalığı · Kırmızı avuç içi hastalığı |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 133000 | E | validated | |
| ICD-10 | L98.8 | NTBT | attributed | validated |
| ICD-11 | EM0Y | NTBT | attributed | validated |
| MONDO | 0007570 | E | validated | |
| MeSH | C565041 | E | validated | |
| UMLS | C1851502 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:79385Unclassified genetic skin disorder
rare genetic diseases; rare skin diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
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.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/231031
- This record as JSON: /data/d/231031.json