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Human Disease

autosomal dominant intellectual developmental disorder 33

Term ID
DOID:0070063
Synonyms
  • autosomal dominant mental retardation 33
  • autosomal dominant non-syndromic intellectual disability 33
  • MRD33
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DPP6 gene on chromosome 7q36.2. https://www.ncbi.nlm.nih.gov/pubmed/23832105
References
Ontology
Human Disease   ( DOID:0070063 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models