ORPHA:163988
OBSOLETE: Developmental delay-deafness syndrome, Hildebrand type
inactive · referred to ORPHA:1435Xq21 microdeletion 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 Xq21 microdeletion syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Developmental delay-deafness syndrome, Hildebrand type | |
| fr | OBSOLETE : Syndrome de retard de développement-surdité, type Hildebrand | |
| de | OBSOLET: Entwicklungsverzögerung - Schwerhörigkeit, Typ Hildebrand | |
| es | OBSOLETO: Síndrome de retraso del desarrollo-sordera, tipo Hildebrand | |
| it | OBSOLETO: Ritardo dello sviluppo - sordità, tipo Hildebrand | |
| nl | OBSOLEET: Ontwikkelingsachterstand - doofheid-syndroom, Hildebrand-type | |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento-surdez, tipo Hildebrand | |
| pl | NIEAKTUALNE: Opóznienienie rozwoju - gluchota, typ Hildebranda | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující opožděný vývoj a hluchotu, Hildebrandův typ | |
| uk | ЗАСТАРІЛО: Синдром затримки розвитку-глухоти, тип Гільдебранда | |
| zh | 弃用: Hildebrand 型发育迟缓性耳聋综合征 | |
| tr | Eski adı: gelişme geriliği-sağırlık sendromu, Hildebrand tipi |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/163988
- This record as JSON: /data/d/163988.json