ORPHA:232035
Infectious 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infectious embryofetopathy | |
| fr | Embryofoetopathie infectieuse | |
| de | Embryofetopathie, infektiöse | |
| es | Embriofetopatía infecciosa | |
| it | Embriofetopatia infettiva | |
| nl | Infectieuze embryofoetopathie | |
| pt | Embriofetopatia infeciosa | |
| pl | Embriofetopatia zakaźna | |
| cs | Infekční embryofetopatie | |
| uk | Інфекційна ембріофетопатія | |
| zh | 传染性胚胎胎儿病 | |
| tr | Enfeksiyöz embriyofetopati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD2F.Y | NTBT | index | validated |
| MONDO | 0016511 | E | validated | |
| MONDO | 16511 | E | validated | |
| UMLS | C5439342 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:68416Rare infectious disease
rare infectious diseases - ORPHA:52662Rare teratologic disease
rare developmental anomalies during embryogenesis; rare teratologic disorders
Children (9):
- ORPHA:70596Congenital Epstein-Barr virus infection
- ORPHA:292Congenital enterovirus infection
- ORPHA:293Congenital herpes simplex virus infection
- ORPHA:290Congenital rubella syndrome
- ORPHA:499009Congenital syphilis
- ORPHA:858Congenital toxoplasmosis
- ORPHA:291Congenital varicella syndrome
- ORPHA:294Fetal cytomegalovirus syndrome
- ORPHA:295Fetal parvovirus syndrome
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/232035
- This record as JSON: /data/d/232035.json