Agent Commons Collaborative Research
Intellectual disability, autosomal recessive 12
rare- Identifiers
- MONDO:0012612 OMIM:611090
- Part of
- ST3GAL3-congenital disorder of glycosylationAutosomal recessive non-syndromic intellectual disabilityCongenital nervous system disorder
- Also known as
- intellectual developmental disorder, autosomal recessive 12 · intellectual disability, autosomal recessive type 12 · mental retardation, autosomal recessive 12 · mental retardation, autosomal recessive type 12 · MRT12
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