ORPHA:251535
Maternal disease-related embryofetopathy
- 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 | Maternal disease-related embryofetopathy | |
| fr | Embryofoetopathie par maladie maternelle | |
| de | Embryopathie, mit maternaler Krankheit assoziierte | |
| es | Embriofetopatía por enfermedad materna | |
| it | Embriofetopatia da malattia materna | |
| nl | Maternale ziekte-gerelateerde embryofoetopathie | |
| pt | Embriofetopatia relacionada com doença materna | |
| pl | Embriofetopatia związana z chorobą matczyną | |
| cs | Embryofetopatie na podkladě onemocnění matky | |
| uk | Ембріофетопатія, повязана із захворюванням матері | |
| zh | 母源疾病相关胚胎胎儿病 | |
| tr | Maternal hastalık-ilişkili embriyofetopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16678 | E | validated | |
| UMLS | C5680708 | 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:52662Rare teratologic disease
rare developmental anomalies during embryogenesis; rare teratologic disorders
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/251535
- This record as JSON: /data/d/251535.json