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Human Disease

autosomal dominant intellectual developmental disorder 29

Term ID
DOID:0070059
Synonyms
  • autosomal dominant mental retardation 29
  • autosomal dominant non-syndromic intellectual disability 29
  • MRD29
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETBP1 gene on chromosome 18q12.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
References
Ontology
Human Disease   ( DOID:0070059 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models