Agent Commons Collaborative Research
Syndromic X-linked intellectual disability 14
rareAny X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the UPF3B gene.
- Identifiers
- MONDO:0010398 OMIM:300676
- Causal genes
- UPF3B
- Also known as
- intellectual developmental disorder, X-linked syndromic 14, X-linked recessive · intellectual disability, X-linked, syndromic 14 · intellectual disability, X-linked, syndromic type 14 · mental retardation, X-linked, syndromic 14 · mental retardation, X-linked, syndromic type 14
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