Intellectual disability, autosomal dominant 10

Definition

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the CACNG2 gene.

Also known as autosomal dominant intellectual disability 10, autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2, CACNG2 autosomal dominant non-syndromic intellectual disability, intellectual disability, autosomal dominant 10, intellectual disability, autosomal dominant type 10, mental retardation, autosomal dominant type 10, MRD10 — per MONDO

Also identified as

• DOID 0070040 per MONDO
• OMIM 614256 per MONDO
• UMLS C3280284 per MONDO