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- Q2295338 subject Q6500135.
- Q2295338 subject Q8280463.
- Q2295338 abstract "Smith–Magenis Syndrome (SMS) is a developmental disorder that affects many parts of the body. The major features of this condition include mild to moderate intellectual disability, distinctive facial features, sleep disturbances, and behavioral problems. Smith–Magenis syndrome affects an estimated 1 in 25,000 individuals.It is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17 and is sometimes called the 17p- syndrome.".
- Q2295338 icd10 "Q93.5".
- Q2295338 icd9 "758.33".
- Q2295338 omim "182290".
- Q2295338 wikiPageExternalLink ghr.nlm.nih.gov.
- Q2295338 wikiPageExternalLink www.prisms.org.
- Q2295338 wikiPageExternalLink www.smith-magenis.dk.
- Q2295338 wikiPageWikiLink Q1052687.
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- Q2295338 wikiPageWikiLink Q1336182.
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- Q2295338 wikiPageWikiLink Q411457.
- Q2295338 wikiPageWikiLink Q412443.
- Q2295338 wikiPageWikiLink Q418857.
- Q2295338 wikiPageWikiLink Q6500135.
- Q2295338 wikiPageWikiLink Q7273611.
- Q2295338 wikiPageWikiLink Q7275716.
- Q2295338 wikiPageWikiLink Q7454850.
- Q2295338 wikiPageWikiLink Q81938.
- Q2295338 wikiPageWikiLink Q8280463.
- Q2295338 icd "758.33".
- Q2295338 icd "Q93.5".
- Q2295338 name "Smith–Magenis syndrome".
- Q2295338 omim "182290".
- Q2295338 type Disease.
- Q2295338 type Thing.
- Q2295338 type Q12136.
- Q2295338 comment "Smith–Magenis Syndrome (SMS) is a developmental disorder that affects many parts of the body. The major features of this condition include mild to moderate intellectual disability, distinctive facial features, sleep disturbances, and behavioral problems. Smith–Magenis syndrome affects an estimated 1 in 25,000 individuals.It is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17 and is sometimes called the 17p- syndrome.".
- Q2295338 label "Smith–Magenis syndrome".
- Q2295338 name "Smith–Magenis syndrome".