"Coffin-Lowry Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A rare, X-linked INTELLECTUAL DISABILITY syndrome that results from mutations in the RIBOSOMAL PROTEIN S6 KINASE gene. Typical manifestations of the disease include an intelligence quotient of less than 50, facial anomalies, and other malformations.
- Coffin-Lowry Syndrome
- Coffin Lowry Syndrome
- Syndrome, Coffin-Lowry
- Coffin Syndrome
- Syndrome, Coffin
- Mental Retardation with Osteocartilaginous Abnormalities
Below are MeSH descriptors whose meaning is more general than "Coffin-Lowry Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Coffin-Lowry Syndrome".
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