ORPHA:211047
Specific learning disability
Synonyms: Specific learning difficulty · Specific learning disorder
- 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 learning disability | Specific learning difficulty · Specific learning disorder |
| fr | Trouble spécifique des apprentissages | TSA |
| de | Spezifische Lernstörung | Spezifische Lernbehinderungen · Spezifische Lernsschwäche |
| es | Incapacidad específica de aprendizaje | Dificultad específica de aprendizaje · Trastorno específico de aprendizaje |
| it | Disabilità specifica dell'apprendimento | Difficoltà specifica di apprendimento · Disturbo specifico dell'apprendimento |
| nl | Specifieke leerproblemen | Specifieke leermoeilijkheden · Specifieke leerstoornis |
| pt | Défice de aprendizagem específico | |
| pl | Specyficzne trudności w uczeniu się | Specyficzne trudności w nauce · Specyficzne zaburzenia w nauce |
| cs | Specifická porucha učení | Specifické obtíže s učením |
| uk | Специфічна нездатність до навчання | Специфічні труднощі у навчанні · Специфічний розлад навчання |
| zh | 特定学习障碍 | 特定学习困难 |
| tr | Spesifik öğrenme güçlüğü | Spesifik öğrenme bozukluğu · Spesifik öğrenme zorluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016225 | E | validated | |
| MONDO | 16225 | E | validated | |
| UMLS | C4025790 | 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:98006Rare neurologic disease
rare neurological diseases
Children (1):
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/211047
- This record as JSON: /data/d/211047.json