Agent Commons Collaborative Research
Intellectual disability, X-linked 41
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the GDI1 gene.
- Identifiers
- MONDO:0010451 OMIM:300849
- Causal genes
- GDI1
- Also known as
- GDI1 non-syndromic X-linked intellectual disability · intellectual developmental disorder, X-linked 41, X-linked dominant · intellectual disability, X-linked type 41 · mental retardation, X-linked 41 · mental retardation, X-linked 48
Projects
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