Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 5
- Term ID
- DOID:0070035
- Synonyms
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- autosomal dominant mental retardation 5
- autosomal dominant non-syndromic intellectual disability 5
- MRD5
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SYNGAP1 gene on chromosome 6p21.32. https://www.ncbi.nlm.nih.gov/pubmed/19196676
- References
- Ontology
- Human Disease ( DOID:0070035 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models