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Human Disease

autosomal dominant intellectual developmental disorder 13

Term ID
DOID:0070043
Synonyms
  • autosomal dominant mental retardation 13
  • autosomal dominant non-syndromic intellectual disability 13
  • mental retardation, autosomal dominant 13, with neuronal migration defects
  • MRD13
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31. https://www.ncbi.nlm.nih.gov/pubmed/21076407
References
Ontology
Human Disease   ( DOID:0070043 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models