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Human Disease

autosomal dominant intellectual developmental disorder 3

Term ID
DOID:0070033
Synonyms
  • autosomal dominant mental retardation 3
  • autosomal dominant non-syndromic intellectual disability 3
  • MRD3
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CDH15 gene on chromosome 16q24.3. https://www.ncbi.nlm.nih.gov/pubmed/19012874
References
Ontology
Human Disease   ( DOID:0070033 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models