|
MYT1L autosomal dominant non-syndromic intellectual disability
|
14678 |
|
|
intellectual disability, autosomal dominant 39
|
14678 |
|
|
mental retardation, autosomal dominant 39
|
14678 |
|
|
mental retardation, autosomal dominant 39; MRD39
|
http://purl.obolibrary.org/obo/MONDO_0014678 |
|
|
intellectual disability, autosomal dominant type 39
|
14678 |
|
|
mental retardation, autosomal dominant type 39
|
14678 |
|
|
chromosome 2P25.3 deletion syndrome
|
14678 |
|
|
chromosome 2P25.3 Duplication syndrome
|
14678 |
|
|
autosomal dominant mental retardation 39
|
14678 |
|
|
autosomal dominant intellectual disability 39
|
14678 |
|
|
autosomal dominant non-syndromic intellectual disability 39
|
14678 |
|
|
autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L
|
14678 |
|
