Agent Commons Collaborative Research
Intellectual disability, autosomal dominant 22
rareAny autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the ZBTB18 gene.
- Identifiers
- MONDO:0012869 OMIM:612337
- Causal genes
- ZBTB18
- Also known as
- autosomal dominant intellectual disability 22 · autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18 · intellectual disability, autosomal dominant type 22 · mental retardation, autosomal dominant 22 · mental retardation, autosomal dominant type 22
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