ORPHA:98788
Pitt-Rogers-Danks syndrome
inactive · moved to ORPHA:280Wolf-Hirschhorn syndrome
Synonyms: Intellectual disability-dysmorphism-intrauterine growth retardation syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Wolf-Hirschhorn syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pitt-Rogers-Danks syndrome | Intellectual disability-dysmorphism-intrauterine growth retardation syndrome |
| fr | Syndrome de Pitt-Rogers-Danks | Syndrome de déficience intellectuelle-dysmorphie-retard de croissance intra-utérin |
| de | Pitt-Rogers-Danks-Syndrom | Intelligenzminderung - Dysmorphien - intrauterine Wachstumsretardierung · Intelligenzminderung-Dysmorphie-intrauterine Wachstumsverzögerung-Syndrom |
| es | Síndrome de Pitt-Rogers-Danks | Síndrome de discapacidad intelectual-dismorfia-retraso del crecimiento intrauterino |
| it | Sindrome di Pitt-Rogers-Danks | Sindrome disabilità intellettiva-dismorfismi-ritardo della crescita intrauterina |
| nl | Syndroom van Pitt-Rogers-Danks | Intellectuele achterstand - dysmorfie - intra-uteriene groeiretardatie-syndroom |
| pt | Síndrome Pitt-Rogers-Danks | Síndrome de perturbação do desenvolvimento intelectual-dismorfia-atraso do crescimento intrauterino |
| pl | Zespół Pitta, Rogersa i Danksa | = en |
| cs | Pittův-Rogersův-Danksův syndrom | Syndrom zahrnující mentální retardaci, dysmorfismus a intrauterinní růstovou retardaci · Pitt-Rogers-Danksův syndrom |
| uk | Синдром Пітта-Роджерса-Данкса | Синдром інтелектуальної недостатності-дизморфізму- затримки внутрішньоутробного розвитку |
| zh | Pitt-Rogers-Danks综合征 | 智力障碍-畸形-宫内发育迟缓综合征 |
| tr | Pitt-Rogers-Danks sendromu | Zihinsel yetersizlik-dismorfizm-intrauterin büyüme geriliği sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0796117 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/98788
- This record as JSON: /data/d/98788.json