ORPHA:1678
Dincsoy-Salih-Patel syndrome
inactive · moved to ORPHA:3157Septo-optic dysplasia spectrum
Synonyms: Facial dysmorphism-ambiguous genitalia-hypopituitarism-short limbs 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 Septo-optic dysplasia spectrum
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dincsoy-Salih-Patel syndrome | Facial dysmorphism-ambiguous genitalia-hypopituitarism-short limbs syndrome |
| fr | Syndrome de Dincsoy-Salih-Patel | Syndrome de dysmorphie-ambiguïté génitale-hypopituitarisme-membres courts |
| de | Dincsoy-Salih-Patel-Syndrom | Faziale Dysmorphien - intersexuelles Genitale - Hypopituitarismus - kurze Extremitäten |
| es | Síndrome de Dincsoy-Salih-Patel | |
| it | Sindrome di Dincsoy-Salih-Patel | Dismorfismi facciali - genitali ambigui - ipopituitarismo - arti corti |
| nl | Syndroom van Dincsoy-Salih-Patel | Faciale dysmorfie - ambigue genitaliën - hypopituïtarisme - korte ledematen-syndroom |
| pt | Síndrome Dincsoy-Salih-Patel | Dismorfia facial-ambiguidade dos genitais-hipopituitarismo-membros curtos |
| pl | Zespół Dincsoy'a, Saliha i Patela | Dysmorfia twarzy - obojnacze narządy płciowe - hipopituitaryzm - krótkie kończyny |
| cs | Dincsoyův-Salihův-Patelův syndrom | Syndrom zahrnující faciální dysmorfismus, obojetný genitál, hypopituitarismus a krátké končetiny · Dincsoy-Salih-Patelův syndrom |
| uk | Синдром Дінчоя-Саліха-Пателя | Синдром дисморфізму обличчя - неоднозначних геніталій - гіпопітуїтаризма - коротких кінцівок |
| zh | Dincsoy-Salih-Patel综合征 | 面部畸形-两性畸形-垂体功能低下-短肢综合征 |
| tr | Dincsoy-Salih-Patel sendromu | Fasiyal dismorfizmi-belirsiz cinsel organ-hipopituitarizm-kısa ekstremiteler sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 601016 | E | validated | |
| UMLS | C1832874 | 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/1678
- This record as JSON: /data/d/1678.json