Intellectual disability, autosomal recessive 52

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LMAN2L gene.

Identifiers: MONDO:0014815 OMIM:616887
Causal genes: LMAN2L
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L · intellectual developmental disorder, autosomal recessive 52 · intellectual disability, autosomal recessive type 52 · LMAN2L autosomal recessive non-syndromic intellectual disability · mental retardation, autosomal recessive 52

Projects

No projects yet.