ORPHA:79386
Rare 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 | Rare skin tumor or hamartoma | |
| fr | Tumeur ou hamartome de la peau rare | |
| de | Hauttumor oder Hamartom, seltene Formen | |
| es | Tumor cutáneo raro | |
| it | Tumore cutaneo raro | |
| nl | Zeldzame tumor van huid of hamartoom | |
| pt | Tumor de pele, raro | |
| pl | Rzadki guz skóry lub harmatoma | |
| cs | Vzácné kožní nádory nebo hamartomy | |
| uk | Рідкісна пухлина шкіри або гамартома | |
| zh | 罕见皮肤肿瘤或错构瘤 | |
| tr | Nadir cilt tümörü veya hamartom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19300 | E | validated | |
| UMLS | C5681474 | 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:89826Rare skin disease
rare skin diseases - ORPHA:98057Rare tumor
rare neoplastic diseases
Children (39):
- ORPHA:569164Angiomatoid fibrous histiocytoma
- ORPHA:113Bazex-Dupré-Christol syndrome
- ORPHA:122Birt-Hogg-Dubé syndrome
- ORPHA:79493Brooke-Spiegler syndrome
- ORPHA:263435Congenital smooth muscle hamartoma
- ORPHA:723286Cutaneous epithelioid angiomatous nodule
- ORPHA:79140Cutaneous neuroendocrine carcinoma
- ORPHA:31112Dermatofibrosarcoma protuberans
- ORPHA:673568Eccrine angiomatous hamartoma
- ORPHA:2396Encephalocraniocutaneous lipomatosis
- ORPHA:2800Extramammary Paget disease
- 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:411777Generalized eruptive keratoacanthoma
- ORPHA:377Gorlin syndrome
- ORPHA:276280Hemihyperplasia-multiple lipomatosis syndrome
- ORPHA:523Hereditary leiomyomatosis and renal cell cancer
- ORPHA:2591Infantile myofibromatosis
- ORPHA:673525Intravascular papillary endothelial hyperplasia
- ORPHA:168999Malignant melanoma of the mucosa
- ORPHA:65748Multiple self-healing squamous epithelioma
- ORPHA:636Neurofibromatosis type 1
- ORPHA:638Neurofibromatosis-Noonan syndrome
- ORPHA:306498PTEN hamartoma tumor syndrome
- ORPHA:499182Pilomatrix carcinoma
- ORPHA:91414Pilomatrixoma
- ORPHA:542Primary cutaneous lymphoma
- ORPHA:492Proliferating trichilemmal cyst
- ORPHA:300515Rare nail tumor
- ORPHA:294057Rare nevus
- ORPHA:3110Rombo syndrome
- ORPHA:199257Superficial fibromatosis
- ORPHA:840Syringocystadenoma papilliferum
- ORPHA:864Trichofolliculoma
- ORPHA:805Tuberous sclerosis complex
Codes that Orphanet moved or referred to this one:
- ORPHA:98701OBSOLETE: Phakomatosis with eye involvement referred to · inactive
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/79386
- This record as JSON: /data/d/79386.json