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Human Disease

autosomal dominant intellectual developmental disorder 10

Term ID
DOID:0070040
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 the CACNG2 gene on chromosome 22q12.3. https://www.ncbi.nlm.nih.gov/pubmed/21376300
References
Ontology
Human Disease   ( DOID:0070040 )
Relationships
is a type of
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Genes Involved
Zebrafish Models