OBO ID: DOID:0080238
Term Name: autosomal dominant mental retardation 47 Search Ontology:
Synonyms:
Definition: An autosomal dominant non-syndromic intellectual disability that has_material_basis_in heterozygous mutation in the STAG1 gene on chromosome 3q22. https://pubmed.ncbi.nlm.nih.gov/28119487/
References:
Ontology: Human Disease   (DOID:0080238)
OTHER autosomal dominant mental retardation 47 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
STAG1 Mental retardation, autosomal dominant 47 617635
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None