ORPHA:641343
Imprinting disorders
- 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 | Imprinting disorders | |
| fr | Maladies liées à des anomalies de l'empreinte génétique | |
| de | Imprintingerkrankung | |
| es | Trastornos de la impronta | |
| it | Malattie da alterato imprinting | |
| nl | Imprintingsstoornissen | |
| pt | Doenças de imprinting | |
| pl | Zaburzenia piętnowania | |
| cs | Poruchy imprintingu | |
| uk | Порушення імпринтингу |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | D000096803 | E | validated | |
| UMLS | C5816793 | 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:98053Rare genetic disease
rare genetic diseases
Children (12):
- ORPHA:72Angelman syndrome
- ORPHA:116Beckwith-Wiedemann syndrome
- ORPHA:254519Kagami-Ogata syndrome
- ORPHA:739Prader-Willi syndrome
- ORPHA:79443Pseudohypoparathyroidism type 1A
- ORPHA:94089Pseudohypoparathyroidism type 1B
- ORPHA:79444Pseudohypoparathyroidism type 1C
- ORPHA:79445Pseudopseudohypoparathyroidism
- ORPHA:398069Schaaf-Yang syndrome
- ORPHA:813Silver-Russell syndrome
- ORPHA:254516Temple syndrome
- ORPHA:99886Transient neonatal diabetes mellitus
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/641343
- This record as JSON: /data/d/641343.json