ORPHA:659387
PRC-2 complex-related overgrowth spectrum
- Type
- Clinical group
- 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 | PRC-2 complex-related overgrowth spectrum | |
| fr | Syndrome d'hypercroissance liée à complexe PRC-2 | |
| de | PRC2-assoziiertes Überwuchsspektrum | PRC2-assoziiertes Großwuchssyndrom |
| es | Espectro de síndromes de sobrecrecimiento asociado al complejo PRC-2 | |
| it | Spettro delliperaccrescimento correlato al complesso PRC-2 | |
| nl | PRC-2-complex-gerelateerd overgroeispectrum | |
| pt | Espetro clínico de sobrecrescimento PRC-2 complexo-relacionado | |
| pl | Spektrum przerostu związanego z kompleksem PRC-2 | |
| cs | Spektrum nadměrného vzrůstu související s komplexem PRC-2 | |
| uk | Спектр надмірного росту, повязаний з комплексом PRC-2 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5925135 | 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 (4):
- ORPHA:611327Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability
rare genetic diseases - ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
rare developmental anomalies during embryogenesis; rare neurological diseases - ORPHA:498448Overgrowth or tall stature syndrome with skeletal involvement
rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases - ORPHA:93460Overgrowth syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:3446Weaver-like syndrome moved 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/659387
- This record as JSON: /data/d/659387.json