(Q50349613)
English
autosomal dominant non-syndromic intellectual disability 9
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of KIF1A on chromosome 2q37.3.
- autosomal dominant mental retardation 9
- MRD9
- mental retardation, autosomal dominant 9
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9
- Mental Retardation, Autosomal Dominant type 9
- NESCAV syndrome
Statements
1 reference
3 references
C133742
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C133742
1 reference
1 reference
Identifiers
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1 reference
1 reference
1 reference