Intellectual disability, autosomal recessive 1

rare

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PRSS12 gene.

Identifiers: MONDO:0009580 OMIM:249500
Causal genes: PRSS12
Part of: Autosomal recessive non-syndromic intellectual disability
Also known as: autosomal recessive non-syndromic intellectual disability caused by mutation in PRSS12 · intellectual disability, autosomal recessive type 1 · mental retardation, autosomal recessive 1 · mental retardation, autosomal recessive type 1 · MRT1

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