Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3961678> ?p ?o }
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- Q3961678 subject Q6500135.
- Q3961678 subject Q6853484.
- Q3961678 subject Q6902466.
- Q3961678 subject Q8482266.
- Q3961678 abstract "Laurence–Moon syndrome (LMS) is a rare autosomal recessive genetic disorder associated with retinitis pigmentosa, extra digits, spastic paraplegia, hypogonadism and mental retardation.".
- Q3961678 icd10 "Q87.8".
- Q3961678 icd9 "759.89".
- Q3961678 meshId "D007849".
- Q3961678 omim "245800".
- Q3961678 thumbnail Autosomal_recessive_-_en.svg?width=300.
- Q3961678 wikiPageExternalLink mr_dx_ing.asp?mr=203.
- Q3961678 wikiPageExternalLink dz-035.html.
- Q3961678 wikiPageWikiLink Q104053.
- Q3961678 wikiPageWikiLink Q106016.
- Q3961678 wikiPageWikiLink Q117060.
- Q3961678 wikiPageWikiLink Q1425030.
- Q3961678 wikiPageWikiLink Q1678281.
- Q3961678 wikiPageWikiLink Q183560.
- Q3961678 wikiPageWikiLink Q186380.
- Q3961678 wikiPageWikiLink Q200779.
- Q3961678 wikiPageWikiLink Q2754563.
- Q3961678 wikiPageWikiLink Q5940334.
- Q3961678 wikiPageWikiLink Q6500135.
- Q3961678 wikiPageWikiLink Q6531938.
- Q3961678 wikiPageWikiLink Q6853484.
- Q3961678 wikiPageWikiLink Q6902466.
- Q3961678 wikiPageWikiLink Q847057.
- Q3961678 wikiPageWikiLink Q8482266.
- Q3961678 wikiPageWikiLink Q938107.
- Q3961678 icd "759.89".
- Q3961678 icd "Q87.8".
- Q3961678 meshid "D007849".
- Q3961678 name "Laurence–Moon syndrome".
- Q3961678 omim "245800".
- Q3961678 type Disease.
- Q3961678 type Thing.
- Q3961678 type Q12136.
- Q3961678 comment "Laurence–Moon syndrome (LMS) is a rare autosomal recessive genetic disorder associated with retinitis pigmentosa, extra digits, spastic paraplegia, hypogonadism and mental retardation.".
- Q3961678 label "Laurence–Moon syndrome".
- Q3961678 depiction Autosomal_recessive_-_en.svg.
- Q3961678 name "Laurence–Moon syndrome".