intellectual disability, autosomal recessive 42

Rare Disease

MONDO:0014348

Also known as:

PGAP1 autosomal recessive non-syndromic intellectual disabilityautosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1intellectual disability, autosomal recessive 42

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

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Companies Active in intellectual disability, autosomal recessive 42

1 company

Organizations with orphan designations or approved therapies for this disease

Prestwick Pharmaceuticals, Inc

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