ORPHA:183487
Genetic skin tumor or hamartoma
- 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 | Genetic skin tumor or hamartoma | |
| fr | Tumeur ou hamartome génétique de la peau | |
| de | Genetisch bedingter Hauttumor oder Hamartom | |
| es | Tumor de la piel genético o hamartoma | |
| it | Neoplasia genetica della cute o amartoma | |
| nl | Genetische huidtumor of hamartoom | |
| pt | Tumor ou hamartoma da pele genético | |
| pl | Guz skóry uwarunkowany genetycznie | Genetycznie uwarunkowany guz skóry lub hamartoma |
| cs | Geneticky podmíněné nádory kůže nebo hamartomy | |
| uk | Генетично обумовлена пухлина шкіри або гамартома | |
| zh | 遗传性皮肤肿瘤 | |
| tr | Genetik deri tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15950 | E | validated | |
| UMLS | C5680571 | 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 (2):
- ORPHA:68346Rare genetic skin disease
rare genetic diseases - ORPHA:68336Rare genetic tumor
rare genetic diseases
Children (23):
- ORPHA:113Bazex-Dupré-Christol syndrome
- ORPHA:122Birt-Hogg-Dubé syndrome
- ORPHA:79493Brooke-Spiegler syndrome
- ORPHA:31112Dermatofibrosarcoma protuberans
- ORPHA:2396Encephalocraniocutaneous lipomatosis
- ORPHA:404560Familial atypical multiple mole melanoma syndrome
- ORPHA:493Familial keratoacanthoma
- ORPHA:618Familial melanoma
- ORPHA:538756Familial multiple discoid fibromas
- ORPHA:53715Familial tumoral calcinosis
- ORPHA:168632Generalized basaloid follicular hamartoma syndrome
- ORPHA:377Gorlin syndrome
- ORPHA:276280Hemihyperplasia-multiple lipomatosis syndrome
- ORPHA:523Hereditary leiomyomatosis and renal cell cancer
- ORPHA:2591Infantile myofibromatosis
- ORPHA:65748Multiple self-healing squamous epithelioma
- ORPHA:636Neurofibromatosis type 1
- ORPHA:638Neurofibromatosis-Noonan syndrome
- ORPHA:306498PTEN hamartoma tumor syndrome
- ORPHA:622914Rare genetic nevus
- ORPHA:3110Rombo syndrome
- ORPHA:840Syringocystadenoma papilliferum
- ORPHA:805Tuberous sclerosis complex
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/183487
- This record as JSON: /data/d/183487.json