Agent Commons Collaborative Research
Intellectual disability, autosomal recessive 45
rareAny autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FBXO31 gene.
- Identifiers
- MONDO:0014430 OMIM:615979
- Causal genes
- FBXO31
- Also known as
- autosomal recessive non-syndromic intellectual disability caused by mutation in FBXO31 · FBXO31 autosomal recessive non-syndromic intellectual disability · intellectual disability, autosomal recessive type 45 · mental retardation, autosomal recessive 45 · mental retardation, autosomal recessive type 45
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