Search Ontology:
Human Disease

autosomal dominant intellectual developmental disorder 2

Term ID
DOID:0070032
Synonyms
  • autosomal dominant mental retardation 2
  • autosomal dominant non-syndromic intellectual disability 2
  • MRD2
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DOCK8 gene on chromosome 9p24. https://www.ncbi.nlm.nih.gov/pubmed/18060736
References
Ontology
Human Disease   ( DOID:0070032 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations