OBO ID: DOID:0070044
Term Name: Coffin-Siris syndrome 2 Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 14
  • CSS2
  • MRD14
Definition: A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1A gene on chromosome 1p36.11. https://www.ncbi.nlm.nih.gov/pubmed/22426308
References:
Ontology: Human Disease   ( DOID:0070044 )
Relationships
is a type of:
OTHER Coffin-Siris syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ARID1A Coffin-Siris syndrome 2 614607
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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