OBO ID: DOID:0070059
Term Name: autosomal dominant intellectual developmental disorder 29 Search Ontology:
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 SETBP1 on chromosome 18q12.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
References:
Ontology: Human Disease   (DOID:0070059)
OTHER autosomal dominant intellectual developmental disorder 29 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SETBP1 Intellectual developmental disorder, autosomal dominant 29 616078
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None