ORPHA:251529
Toxic or drug-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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Toxic or drug-related embryofetopathy | |
| fr | Embryofoetopathie d'exposition toxique ou médicamenteuse | |
| de | Embryopathie, toxische oder Medikamenten-induzierte | |
| es | Embriofetopatía tóxica o asociada a fármacos | Embriofetopatía tóxica o asociada a medicamentos |
| it | Embriofetopatia da esposizione tossica o farmacologica | |
| nl | Toxische of medicatiegerelateerde embryofoetopathie | |
| pt | Embriofetopatia tóxica ou relacionada com fármacos | |
| pl | Embriofetopatia związana z zatruciem lub lekiem | |
| cs | Embryofetopatie vázaná s drogami nebo léky | |
| uk | Токсична або медикаментозна ембріофетопатія | |
| zh | 毒物或药物相关胚胎胎儿病 | |
| tr | Toksik veya ilaç-ilişkili embriyofetopati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LD2F.0 | E | specific | validated |
| MONDO | 0016677 | E | validated | |
| MONDO | 16677 | E | validated | |
| UMLS | C5680710 | 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:108999Rare disorder due to toxic effects
rare disorders due to toxic effects - ORPHA:52662Rare teratologic disease
rare developmental anomalies during embryogenesis; rare teratologic disorders
Children (17):
- ORPHA:40366Acitretin/etretinate embryopathy
- ORPHA:1908Aminopterin/methotrexate embryofetopathy
- ORPHA:1911Cocaine embryofetopathy
- ORPHA:1916Diethylstilbestrol syndrome
- ORPHA:1915Fetal alcohol syndrome
- ORPHA:370068Fetal anticonvulsant syndrome
- ORPHA:1910Fetal iodine syndrome
- ORPHA:1917Fetal methylmercury syndrome
- ORPHA:1918Fetal minoxidil syndrome
- ORPHA:1909Indomethacin embryofetopathy
- ORPHA:2305Isotretinoin syndrome
- ORPHA:1923Methimazole embryofetopathy
- ORPHA:268249Mycophenolate mofetil embryopathy
- ORPHA:485358Propylthiouracil embryofetopathy
- ORPHA:3312Thalidomide embryopathy
- ORPHA:1920Toluene embryopathy
- ORPHA:1914Vitamin K antagonist embryofetopathy
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/251529
- This record as JSON: /data/d/251529.json