Intellectual disability, autosomal recessive 42

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PGAP1 gene.

Identifiers: MONDO:0014348 OMIM:615802
Causal genes: PGAP1
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1 · intellectual disability, autosomal recessive type 42 · mental retardation, autosomal recessive 42 · mental retardation, autosomal recessive type 42 · MRT42

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