|
OMIM:614256 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 10; MRD10
Xenbase Genes: cacng2
Human Disease Resource: OMIM
MONDO:0013657 - intellectual disability, autosomal dominant 10 |
MONDO:0100172 - intellectual disability, autosomal dominant |
DOID:0070040 - autosomal dominant non-syndromic intellectual disability 10 |