ORPHA:622914
Rare genetic nevus
- 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
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare genetic nevus | |
| fr | Naevus rare d'origine génétique | |
| de | Seltener Nävus, genetisch bedingter | |
| es | Nevo genético raro | |
| it | Nevo genetico raro | |
| nl | Zeldzame genetische naevus | |
| pt | Nevus genético raro | |
| pl | Rzadkie znamię uwarunkowane genetycznie | |
| cs | Vzácný genetický névus | |
| uk | Рідкісний генетично обумовлений невус |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681828 | 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:183487Genetic skin tumor or hamartoma
rare genetic diseases
Children (17):
- ORPHA:64755Becker nevus syndrome
- ORPHA:139CHILD syndrome
- ORPHA:140944CLOVES syndrome
- ORPHA:201Cowden syndrome
- ORPHA:35125Epidermal nevus syndrome
- ORPHA:497737Epidermolytic nevus
- ORPHA:626Large/giant congenital melanocytic nevus
- ORPHA:2612Linear nevus sebaceus syndrome
- ORPHA:497757MME-related autosomal dominant Charcot Marie Tooth disease type 2
- ORPHA:64754Nevus comedonicus syndrome
- ORPHA:313936PENS syndrome
- ORPHA:2874Phakomatosis pigmentokeratotica
- ORPHA:166286Porokeratotic eccrine ostial and dermal duct nevus
- ORPHA:744Proteus syndrome
- ORPHA:2969Proteus-like syndrome
- ORPHA:137608Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
- ORPHA:171723White sponge nevus
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/622914
- This record as JSON: /data/d/622914.json