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Human Disease

autosomal dominant intellectual developmental disorder 26

Term ID
DOID:0070056
Synonyms
  • autosomal dominant mental retardation 26
  • autosomal dominant non-syndromic intellectual disability 26
  • MRD26
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the AUTS2 gene on chromosome 7q11.22. https://www.ncbi.nlm.nih.gov/pubmed/23332918
References
Ontology
Human Disease   ( DOID:0070056 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models