ORPHA:79360
Other genetic epidermal disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Other genetic epidermal disease | |
| fr | Autre maladie génétique de l'épiderme | |
| de | Hautkrankheit, genetische, unklassifizierte | |
| es | Enfermedad epidérmica génetica sin clasificar | |
| it | Malattie genetice dell'epidermide non classificate | |
| nl | Genetische niet-geclasificeerde epidermale ziekte | |
| pt | Doença epidérmica, sindrómica | |
| pl | Genetyczne niesklasyfikowane zaburzenia naskórka | |
| cs | Jiné geneticky podmíněné postižení epidermis | |
| uk | Інші генетичні епідермальні захворювання | |
| zh | 其他遗传性表皮疾病 | |
| tr | Diğer genetik epidermal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19275 | E | validated | |
| UMLS | C5681490 | 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:183426Genetic epidermal disorder
rare genetic diseases
Children (17):
- ORPHA:1658Absence of fingerprints-congenital milia syndrome
- ORPHA:90301Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome
- ORPHA:163931Acrodermatitis continua of Hallopeau
- ORPHA:2388Choreoacanthocytosis
- ORPHA:218Darier disease
- ORPHA:247353Generalized pustular psoriasis
- ORPHA:1867Hereditary bullous dystrophy, macular type
- ORPHA:409Hyperkeratosis lenticularis perstans
- ORPHA:50943Keratolytic winter erythema
- ORPHA:2339Keratosis follicularis-dwarfism-cerebral atrophy syndrome
- ORPHA:498Keratosis pilaris atrophicans
- ORPHA:158687Lethal acantholytic erosive disorder
- ORPHA:294023Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome
- ORPHA:163927Pustulosis palmaris et plantaris
- ORPHA:85165Severe achondroplasia-developmental delay-acanthosis nigricans syndrome
- ORPHA:369992Severe dermatitis-multiple allergies-metabolic wasting syndrome
- ORPHA:482606X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79360
- This record as JSON: /data/d/79360.json