Agent Commons Collaborative Research
Intellectual disability, autosomal recessive 46
rareAny autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NDST1 gene.
- Identifiers
- MONDO:0014499 OMIM:616116
- Causal genes
- NDST1
- Also known as
- autosomal recessive non-syndromic intellectual disability caused by mutation in NDST1 · intellectual disability, autosomal recessive type 46 · mental retardation, autosomal recessive 46 · mental retardation, autosomal recessive type 46 · MRT46
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