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

• OMIM:614256

Ontology

Human Disease   ( DOID:0070040 )