specific language impairment 5
MONDO:0014184Mondo
Findings
No curated finding names specific language impairment 5 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A communication disorder that involves the processing of linguistic information.
Definition from the Mondo Disease Ontology (MONDO:0014184), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance · Typified by incomplete penetrance
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Delayed speech and language developmentHPOHP:0000750
- 26 of 26 reported patients
- Hyperintensity of cerebral white matter on MRIHPOHP:0030890
- 22 of 31 reported patients
- Autistic behaviorHPOHP:0000729
- 4 of 15 reported patients
- Global developmental delayHPOHP:0001263
- 4 of 15 reported patients
- Language impairmentHPOHP:0002463
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- TM4SF20HGNC:26230
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
- Limited · G2P · Autosomal dominant · 2015
Where it sits
- A kind of
Other names
2 names
Resolves to: specific language impairment 5
- Also called
- SLI5specific language impairment type 5