(Q50349625)
English
autosomal dominant non-syndromic intellectual disability 21
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of CTCF on chromosome 16q22.1.
- MRD21
- autosomal dominant mental retardation 21
- Mental Retardation, Autosomal Dominant type 21
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 21; MRD21
Statements
1 reference
1 reference
1 reference
3 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference