specific language impairment
Information
- Disease name
- specific language impairment
- Disease ID
- DOID:0060244
- Description
- "A language disorder characterized by difficulty in language acquisition despite otherwise normal development and in the absence of any obvious explanatory factors." [url:http\://en.wikipedia.org/wiki/Specific_language_impairment, url:https\://www.ncbi.nlm.nih.gov/pubmed/19646677]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05325333 | Active, not recruiting | N/A | Retrieval-Based Word Learning in Developmental Language Disorder | March 16, 2022 | December 9, 2025 |
| NCT04141332 | Completed | Specific Language Impairment (SLI) in Children May Caused by Epileptic Brain Activity | February 1, 2018 | March 1, 2019 | |
| NCT01829360 | Completed | N/A | Accelerating Word Learning in Children With Language Impairment | March 2013 | August 2018 |
| NCT06001866 | Completed | N/A | Retrieval-Based Word Learning in Developmental Language Disorder: Verb Learning | March 1, 2023 | January 25, 2024 |
| NCT06026124 | Recruiting | N/A | Retrieval-Based Word Learning in Developmental Language Disorder During Book Reading | October 31, 2022 | July 31, 2026 |
| NCT04531514 | Recruiting | N/A | A Framework For Linking Sequential Pattern Rules in DLD: Perception in Toddlers | August 3, 2020 | July 2026 |
| NCT04558541 | Recruiting | N/A | A Developmental Framework For Linking Phonological And Morpho-syntactic Sequential Pattern Rules In DLD: Production | August 7, 2022 | July 31, 2026 |
| NCT04996472 | Recruiting | N/A | A Framework For Linking Sequential Pattern Rules in DLD: Perception in Adults | August 3, 2020 | July 2026 |
| NCT03438760 | Terminated | N/A | Improving STEM Outcomes for Young Children With Language Learning Disabilities | November 3, 2017 | August 30, 2020 |
- Disase is a (Disease Ontology)
- DOID:93
- Cross Reference ID (Disease Ontology)
- MIM:606711
- Cross Reference ID (Disease Ontology)
- MIM:606712
- Cross Reference ID (Disease Ontology)
- MIM:607134
- Cross Reference ID (Disease Ontology)
- MIM:612514
- Cross Reference ID (Disease Ontology)
- MIM:615432
- OMIM Phenotype Series Number (OMIM)
- PS606711
- MedGen concept unique identifier (MedGen Concept name)
- C0454651
- MedGen unique identifier (MedGen Concept name)
- 627772