(Q50349643)
English
autosomal dominant non-syndromic intellectual disability 39
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MYT1L on chromosome 2p25.3.
- autosomal dominant mental retardation 39
- MRD39
- Chromosome 2P25.3 Deletion Syndrome
- Chromosome 2P25.3 Duplication Syndrome
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
- Mental Retardation, Autosomal Dominant type 39
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 39; MRD39
Statements
1 reference
5 references
C156309
0 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference