autosomal dominant intellectual developmental disorder 10 (DOID:0070040)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 10; autosomal dominant non-syndromic intellectual disability 10; MRD10
Alt IDs: OMIM:614256
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CACNG2 gene on chromosome 22q12.3.