Term Name: | autosomal dominant intellectual developmental disorder 10 |
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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. |
Ontology: | Human Disease [DOID:0070040] ( DOID:0070040 ) |