ORPHA:2626
OBSOLETE: Hypopituitarism-short stature-skeletal anomalies syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Blethen-Wenick-Hawkins syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hypopituitarism-short stature-skeletal anomalies syndrome | OBSOLETE: Blethen-Wenick-Hawkins syndrome |
| fr | OBSOLETE : Syndrome de nanisme hypophysaire-anomalies squelettiques | OBSOLETE : Syndrome de Blethen-Wenick-Hawkins |
| de | OBSOLET: Hypopituitarismus-Kleinwuchs-Skelettanomalien-Syndrom | OBSOLET: Blethen-Wenick-Hawkins-Syndrom |
| es | OBSOLETO: Síndrome de hipopituitarismo-talla baja-anomalías esqueléticas | OBSOLETO: Síndrome de Blethen-Wenick-Hawkins |
| it | OBSOLETO: Sindrome ipopituitarismo-bassa statura-anomalie scheletriche | OBSOLETO: Sindrome di Blethen-Wenick-Hawkins |
| nl | OBSOLEET: Hypopituïtarisme - kleine gestalte - skeletanomalieën-syndroom | OBSOLEET: Syndroom van Blethen-Wenick-Hawkins |
| pt | OBSOLETO: Síndrome de hipopituitarismo-baixa estatura-anomalias esqueléticas | OBSOLETO: Síndrome Blethen-Wenick-Hawkins |
| pl | NIEAKTUALNE: Niedoczynnosc przysadki - niski wzrost - anomalie szkieletowe | NIEAKTUALNE: Zespół Blethena, Wenicka i Hawkinsa |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující hypopituitarismus, malý vzrůst a kosterní anomálie | = en |
| uk | ЗАСТАРІЛО: Синдром гіпопітуїтаризму-низькорослості-скелетних аномалій | ЗАСТАРІЛО: Синдром Блетена-Веніка-Хокінса |
| zh | 弃用：垂体功能减退-身材矮小-骨骼畸形综合征 | Blethen-Wenick-Hawkins 综合征 |
| tr | Eski adı: Hipopituitarizm-kısa boy-iskelet anomalileri sendromu | Blethen-Wenick-Hawkins sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/2626
- This record as JSON: /data/d/2626.json