ORPHA:90649
Orofaciodigital syndrome type 7
inactive · moved to ORPHA:2750Orofaciodigital syndrome type 1
Synonyms: OFD7 · Oral-facial-digital syndrome type 7 · Whelan 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 Orofaciodigital syndrome type 1
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Orofaciodigital syndrome type 7 | OFD7 · Oral-facial-digital syndrome type 7 · Whelan syndrome |
| fr | Syndrome oro-facio-digital de type 7 | OFD7 · Syndrome de Whelan · Syndrome orofaciodigital de type 7 |
| de | Oro-fazio-digitales Syndrom Typ 7 | OFD7 · Whelan-Syndrom |
| es | Síndrome orofaciodigital tipo 7 | OFD7 · Síndrome de Whelan |
| it | Sindrome orofaciodigitale, tipo 7 | OFD7 · Sindrome di Whelan · Sindrome oro-facio-digitale, tipo 7 |
| nl | Orofaciodigitaal syndroom type 7 | OFD7 · Oraal-faciaal-digitaal syndroom type 7 · Syndroom van Whelan |
| pt | Síndrome orofaciodigital tipo 7 | |
| pl | Zespół ustno-twarzowo-palcowy typu 7 | Zespół ustno-twarzowo-palcowy typu 7 · OFD7 · Zespół Whelana |
| cs | Orofaciodigitální syndrom, typ 7 | OFD7 · Orální-faciální-digitální syndrom, typ 7 · Whelanův syndrom |
| uk | Орофаціодигітальний синдром, тип 7 | OFD7 · Орально-лицево-пальцевий синдром, тип 7 · Синдром Вілана |
| zh | 口面指综合征7型 | 口-面-指综合征7型 |
| tr | Orofasiyodijital sendromu tip 7 | OFD7 · Whelan sendromu · Oral-fasiyal-dijital sendromu tip 7 |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 608518 | E | validated | |
| UMLS | C0796100 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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/90649
- This record as JSON: /data/d/90649.json