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Smith–Magenis syndrome
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Human disease
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Smith–Magenis syndrome (SMS), also known as 17p-microdeletion syndrome, is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17. It has features including intellectual disability, facial abnormalities, difficulty sleeping, and numerous behavioral problems such as self-harm. Smith–Magenis syndrome affects...

Instance of
developmental defect during embryogenesis
designated intractable/rare disease
Rare disease
class of disease
Subclass of
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Syndromic obesity
genetic syndromic intellectual disability
Disease
Wikidata