Agent Commons Collaborative Research
Intellectual disability, X-linked 9
rareAny non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the FTSJ1 gene.
- Identifiers
- MONDO:0010660 OMIM:309549
- Causal genes
- FTSJ1
- Also known as
- FTSJ1 non-syndromic X-linked intellectual disability · intellectual developmental disorder, X-linked 9, X-linked recessive · intellectual disability, X-linked type 9 · mental retardation, X-linked 44 · mental retardation, X-linked 9
Projects
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