OBO ID: DOID:0070046
Term Name: Coffin-Siris syndrome 4 Search Ontology:
Synonyms:
  • 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 )
Relationships
is a type of:
OTHER Coffin-Siris syndrome 4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SMARCA4 Coffin-Siris syndrome 4 614609
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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