ORPHA:79382
Subcutaneous tissue 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 | Subcutaneous tissue disease | |
| fr | Maladie du tissu sous-cutané | |
| de | Gewebekrankheit, subkutane | |
| es | Enfermedad del tejido subcutáneo | |
| it | Malattia del tessuto sottocutaneo | |
| nl | Aandoening van subcutis | |
| pt | Doença do tecido subcutâneo | |
| pl | Choroba tkanki podskórnej | |
| cs | Nemoci podkoží | |
| uk | Захворювання підшкірної клітковини | |
| zh | 皮下组织疾病 | |
| tr | Deri altı doku hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019296 | E | validated | |
| MONDO | 19296 | E | validated | |
| UMLS | C1290008 | 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:89826Rare skin disease
rare skin diseases
Children (20):
- ORPHA:36397Adiposis dolorosa
- ORPHA:404454Alacrimia-choreoathetosis-liver dysfunction syndrome
- ORPHA:140944CLOVES syndrome
- ORPHA:909Cerebrotendinous xanthomatosis
- ORPHA:94087Cytophagic histiocytic panniculitis
- ORPHA:345Dissecting cellulitis of the scalp
- ORPHA:2396Encephalocraniocutaneous lipomatosis
- ORPHA:730401Erythema induratum of Bazin
- ORPHA:199279Familial angiolipomatosis
- ORPHA:199276Familial multiple lipomatosis
- ORPHA:333Farber disease
- ORPHA:337Fibrodysplasia ossificans progressiva
- ORPHA:468666Isolated generalized anhidrosis with normal sweat glands
- ORPHA:2398Multiple symmetric lipomatosis
- ORPHA:699678Necrotizing cellulitis
- ORPHA:699697Necrotizing fasciitis
- ORPHA:477742Nodular fasciitis
- ORPHA:33577Nodular non-suppurative panniculitis
- ORPHA:90970Primary lipodystrophy
- ORPHA:529Roch-Leri mesosomatous lipomatosis
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/79382
- This record as JSON: /data/d/79382.json