ORPHA:138059
Teratogenic Pierre Robin syndrome
Synonyms: Teratogenic Pierre Robin sequence
- 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 | Teratogenic Pierre Robin syndrome | Teratogenic Pierre Robin sequence |
| fr | Syndrome de Pierre Robin d'origine tératogène | Séquence de Pierre Robin d'origine tératogène |
| de | Pierre-Robin-Sequenz, teratogene | Pierre-Robin-Syndrom durch teratogene Substanzen |
| es | Síndrome de Pierre Robin teratogénico | Secuencia de Pierre Robin teratogénica |
| it | Sindrome teratogenica di Pierre Robin | Sequenza teratogenica di Pierre Robin |
| nl | Teratogeen syndroom van Pierre Robin | Teratogene Pierre Robin sequentie |
| pt | Sequência de Pierre Robin teratogénica | |
| pl | Teratogenny zespół Pierre' a Robina | Teratogenna sekwencja Pierre' a Robina |
| cs | Pierre Robinův syndrom způsobený teratogeny | Teratogenní Pierre Robinova sekvence · Pierre Robinova sekvence způsobená teratogeny |
| uk | Тератогенний синдром Пєра Робена | Тератогенна послідовність Пєра Робіна |
| zh | 致畸性Pierre Robin综合征 | 致畸性Pierre-Robin序列征 |
| tr | Teratojenik Pierre Robin sendromu | Teratojenik Pierre Robin dizisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15323 | E | validated | |
| UMLS | C5679603 | E | validated | |
| GARD | 19899 | 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 (1):
- ORPHA:138044Rare disease with Pierre Robin syndrome
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases; rare surgical maxillo-facial diseases
Children (20):
- ORPHA:1908Aminopterin/methotrexate embryofetopathy
- ORPHA:1911Cocaine embryofetopathy
- ORPHA:1926Diabetic embryopathy
- ORPHA:1915Fetal alcohol syndrome
- ORPHA:1912Fetal hydantoin syndrome
- ORPHA:1910Fetal iodine syndrome
- ORPHA:1917Fetal methylmercury syndrome
- ORPHA:1918Fetal minoxidil syndrome
- ORPHA:295Fetal parvovirus syndrome
- ORPHA:1913Fetal trimethadione syndrome
- ORPHA:1906Fetal valproate spectrum disorder
- ORPHA:1909Indomethacin embryofetopathy
- ORPHA:2305Isotretinoin syndrome
- ORPHA:2216Maternal hyperthermia-induced birth defects
- ORPHA:2209Maternal phenylketonuria syndrome
- ORPHA:1923Methimazole embryofetopathy
- ORPHA:1919Phenobarbital embryopathy
- ORPHA:485358Propylthiouracil embryofetopathy
- 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/138059
- This record as JSON: /data/d/138059.json