Intellectual disability, autosomal recessive 27

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LINS1 gene.

Identifiers: MONDO:0013702 OMIM:614340
Causal genes: LINS1
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in LINS1 · intellectual developmental disorder, autosomal recessive 27 · intellectual disability, autosomal recessive type 27 · LINS1 autosomal recessive non-syndromic intellectual disability · mental retardation, autosomal recessive 27

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