Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q303123> ?p ?o }
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- Q303123 subject Q5881496.
- Q303123 subject Q6500135.
- Q303123 subject Q6853484.
- Q303123 subject Q7022834.
- Q303123 abstract "Aarskog–Scott syndrome is a rare disease inherited as autosomal dominant or X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies.The Aarskog–Scott syndrome (AAS) is also known as the Aarskog syndrome, faciodigitogenital syndrome, shawl scrotum syndrome and faciogenital dysplasia.".
- Q303123 icd10 "Q87.1".
- Q303123 icd9 "759.89".
- Q303123 meshId "C535331".
- Q303123 omim "100050".
- Q303123 thumbnail X-linked_recessive.svg?width=300.
- Q303123 wikiPageExternalLink aarskog-syndrome-defination-causes-symptoms-diagnosis-precautions-treatment.
- Q303123 wikiPageExternalLink aarskog-syndrome-info.html.
- Q303123 wikiPageExternalLink aarskog-syndrome.
- Q303123 wikiPageExternalLink dispomim.cgi?id=305400.
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- Q303123 wikiPageWikiLink Q5881496.
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- Q303123 wikiPageWikiLink Q6500135.
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- Q303123 wikiPageWikiLink Q6853484.
- Q303123 wikiPageWikiLink Q7022834.
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- Q303123 icd "759.89".
- Q303123 icd "Q87.1".
- Q303123 meshid "535331.0".
- Q303123 name "Aarskog–Scott syndrome".
- Q303123 omim "100050".
- Q303123 type Disease.
- Q303123 type Thing.
- Q303123 type Q12136.
- Q303123 comment "Aarskog–Scott syndrome is a rare disease inherited as autosomal dominant or X-linked and characterized by short stature, facial abnormalities, skeletal and genital anomalies.The Aarskog–Scott syndrome (AAS) is also known as the Aarskog syndrome, faciodigitogenital syndrome, shawl scrotum syndrome and faciogenital dysplasia.".
- Q303123 label "Aarskog–Scott syndrome".
- Q303123 depiction X-linked_recessive.svg.
- Q303123 name "Aarskog–Scott syndrome".