OBO ID: DOID:0070038
Term Name: autosomal dominant non-syndromic intellectual disability 8 Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 8
  • MRD8
Definition: An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3. https://www.ncbi.nlm.nih.gov/pubmed/21376300
References:
Ontology: Human Disease   (DOID:0070038)
OTHER autosomal dominant non-syndromic intellectual disability 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GRIN1 Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant 614254
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None