OBO ID: DOID:0070040
Term Name: autosomal dominant intellectual developmental disorder 10 Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 10
  • autosomal dominant non-syndromic intellectual disability 10
  • MRD10
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of CACNG2 on chromosome 22q12.3. https://www.ncbi.nlm.nih.gov/pubmed/21376300
References:
Ontology: Human Disease   (DOID:0070040)
OTHER autosomal dominant intellectual developmental disorder 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNG2 ?Intellectual developmental disorder, autosomal dominant 10 614256
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None