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Human Disease

autosomal dominant intellectual developmental disorder 42

Term ID
DOID:0070072
Synonyms
  • autosomal dominant mental retardation 42
  • autosomal dominant non-syndromic intellectual disability 42
  • MRD42
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GNB1 gene on chromosome 1p36.33. https://www.ncbi.nlm.nih.gov/pubmed/27108799
References
Ontology
Human Disease   ( DOID:0070072 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models