(Q50349626)
English
autosomal dominant non-syndromic intellectual disability 22
autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ZBTB18 on chromosome 1q44
- autosomal dominant mental retardation 22
- MRD22
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 22
- Chromosome 1Qter Deletion Syndrome
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22
- Chromosome 1Q43-Q44 Deletion Syndrome
- Mental Retardation, Autosomal Dominant type 22
Statements
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