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

• OMIM:612580

Ontology

Human Disease   ( DOID:0070033 )