ORPHA:163953
X-linked intellectual disability, Raymond type
inactive · moved to ORPHA:776Lujan-Fryns syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Lujan-Fryns syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | X-linked intellectual disability, Raymond type | |
| fr | Déficience intellectuelle liée à l'X type Raymond | |
| de | Intelligenzminderung, X-chromosomale, Typ Raymond | |
| es | Discapacidad intelectual ligada al cromosoma X tipo Raymond | |
| it | Disabilità intellettiva legata all'X, tipo Raymond | |
| nl | X-gebonden intellectuele achterstand, Raymond-type | |
| pt | Perturbação do desenvolvimento intelectual ligada ao X, tipo Raymond | |
| pl | Niepełnosprawność intelektualna sprzężona z chromosomem X, typ Raymonda | |
| cs | X-vázaná mentální retardace, Raymondové typ | |
| uk | Х-зчеплена розумова відсталість, тип Реймонда | |
| zh | Raymond 型X连锁型智力障碍综合征 | |
| tr | X'e bağlı zihinsel yetersizlik, Raymond tipi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 300799 | 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/163953
- This record as JSON: /data/d/163953.json