An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein.

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dbo:abstract
  • MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein. (en)
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  • ddb34533
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  • Q87.8
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  • 300260 (xsd:integer)
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  • 85281
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dbp:caption
  • This condition is due to MECP2 overexpression (en)
dbp:diseasesdb
  • ddb34533 (en)
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dbp:icd
  • Q87.8 (en)
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  • 537723.0
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  • MECP2 duplication syndrome (en)
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  • 300260 (xsd:integer)
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  • 85281 (xsd:integer)
dbp:synonyms
  • X-linked intellectual disability-hypotonia-recurrent Infections syndrome (en)
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  • MECP2 duplication syndrome (M2DS) is a rare disease that is characterized by severe intellectual disability and impaired motor function. It is an X-linked genetic disorder caused by the overexpression of MeCP2 protein. (en)
rdfs:label
  • MECP2 duplication syndrome (en)
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  • MECP2 duplication syndrome (en)
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