ORPHA:477808
Other genetic dermis disorder
- 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 dermis disorder | |
| fr | Autre anomalie génétique du derme | |
| de | Hautkrankheit, genetisch bedingte, sonstige | |
| es | Otros trastornos genéticos de la dermis | |
| it | Altra malattia genetica del derma | |
| nl | Andere genetische aandoening van dermis | |
| pt | Outra doença genética da derme | |
| pl | Inne genetyczne zaburzenia naskórka | |
| cs | Jiné geneticky podmíněné nemoci dermis | |
| uk | Інше генетично обумовлене захворювання дерми | |
| zh | 其他遗传性皮肤病 | |
| tr | Diğer genetik dermis bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18798 | E | validated | |
| UMLS | C5681256 | 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:183472Genetic dermis disorder
rare genetic diseases
Children (13):
- ORPHA:2987Antecubital pterygium syndrome
- ORPHA:90340Blau syndrome
- ORPHA:1555Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome
- ORPHA:79149Dermochondrocorneal dystrophy
- ORPHA:1764Familial dysautonomia
- ORPHA:353220Familial primary localized cutaneous amyloidosis
- ORPHA:468666Isolated generalized anhidrosis with normal sweat glands
- ORPHA:2028Juvenile hyaline fibromatosis
- ORPHA:140933Linear atrophoderma of Moulin
- ORPHA:530Lipoid proteinosis
- ORPHA:2796Pachydermoperiostosis
- ORPHA:357225Primary non-essential cutis verticis gyrata
- ORPHA:2762Progressive osseous heteroplasia
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/477808
- This record as JSON: /data/d/477808.json