ORPHA:211053
Specific language disorder
Synonyms: Dysphasia
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Specific language disorder | Dysphasia |
| fr | Dysphasie | |
| de | Spezifische Sprachentwicklungsstörung | Dysphasie |
| es | Trastorno específico del lenguaje | Disfasia |
| it | Disturbo specifico del linguaggio | Disfasia |
| nl | Specifieke taalstoornis | Dysfasie |
| pt | Dificuldade específica de linguagem | |
| pl | Specyficzne zaburzenia językowe | Dysfazja |
| cs | Specifická porucha řeči | Dysfázie |
| uk | Специфічні мовні розлади | Дисфазія |
| zh | 特定语言障碍 | 语言障碍 |
| tr | Spesifik dil bozukluğu | Disfazi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016226 | E | validated | |
| MONDO | 16226 | E | validated | |
| MeSH | D000080888 | E | validated | |
| UMLS | C0454651 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:211047Specific learning disability
rare neurological diseases
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/211053
- This record as JSON: /data/d/211053.json