ORPHA:178503
Dursun syndrome
inactive · moved to ORPHA:331176Severe congenital neutropenia due to G6PC3 deficiency
Synonyms: Pulmonary arterial hypertension-leukopenia-atrial septal defect 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 Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dursun syndrome | Pulmonary arterial hypertension-leukopenia-atrial septal defect syndrome |
| fr | Syndrome de Dursun | Syndrome d'hypertension artérielle pulmonaire-leucopénie-communication interauriculaire |
| de | Dursun-Syndrom | Pulmonale arterielle Hypertonie - Leukopenie - Vorhofseptumdefekt |
| es | Síndrome de Dursun | Hipertensión arterial pulmonar-leucopenia-defecto septal atrial |
| it | Sindrome di Dursun | Ipertensione arteriosa polmonare - leucopenia - difetto del setto atriale · Sindrome di Dursun |
| nl | Syndroom van Dursun | Pulmonale arteriële hypertensie - leukopenie - atriumseptumdefect-syndroom |
| pt | Hipertensão arterial pulmonar - leucopenia - comunicação inter-auricular | |
| pl | Zespół Dursuna | Nadciśnienie płucne - leukopenia - wada przegrody międzyprzedsionkowej |
| cs | Dursunův syndrom | Syndrom zahrnující plicní arteriální hypertenzi, leukopenii a defekt síňového septa |
| uk | Синдром Дурсуна | Синдром легеневої артеріальної гіпертензії-лейкопенії- дефекту міжпередсердної перегородки |
| zh | Dursun 综合征 | 肺动脉高压-白细胞减少-房间隔缺损综合征 |
| tr | Dursun sendromu | Pulmoner arteriyel hipertansiyon-lökopeni-atriyal septal defekt sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C2751630 | 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/178503
- This record as JSON: /data/d/178503.json