Search Ontology:
Human Disease
Coffin-Siris syndrome 4
- Term ID
- DOID:0070046
- Synonyms
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- autosomal dominant mental retardation 16
- CSS4
- MRD16
- Definition
- A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the SMARCA4 gene on chromosome 19p13.2. https://www.ncbi.nlm.nih.gov/pubmed/22426308
- References
- Ontology
- Human Disease ( DOID:0070046 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models