Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q20707211> ?p ?o }
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- Q20707211 subject Q7824736.
- Q20707211 abstract "Hoyeraal-Hreidarsson syndrome (HHS) is a very rare multisystem X-linked recessive disorder characterized by excessively short telomeres and is considered a severe form of dyskeratosis congenita. Being an X-linked disorder, HHS primarily affects males. Patients with HHS typically present in early childhood with cerebellar hypoplasia, immunodeficiency, progressive bone marrow failure, and intrauterine growth retardation. The primary cause of death in HHS is bone marrow failure, but mortality from cancer and pulmonary fibrosis is also significant.".
- Q20707211 icd10 "Q82.8".
- Q20707211 icd9 "757.39".
- Q20707211 meshId "C536068".
- Q20707211 omim "305000".
- Q20707211 wikiPageExternalLink OC_Exp.php?Lng=EN&Expert=3322.
- Q20707211 wikiPageWikiLink Q1142188.
- Q20707211 wikiPageWikiLink Q12078.
- Q20707211 wikiPageWikiLink Q1671598.
- Q20707211 wikiPageWikiLink Q183560.
- Q20707211 wikiPageWikiLink Q185057.
- Q20707211 wikiPageWikiLink Q2003151.
- Q20707211 wikiPageWikiLink Q2214869.
- Q20707211 wikiPageWikiLink Q32446.
- Q20707211 wikiPageWikiLink Q3709312.
- Q20707211 wikiPageWikiLink Q431643.
- Q20707211 wikiPageWikiLink Q5319553.
- Q20707211 wikiPageWikiLink Q641307.
- Q20707211 wikiPageWikiLink Q7824736.
- Q20707211 wikiPageWikiLink Q7882181.
- Q20707211 wikiPageWikiLink Q838145.
- Q20707211 wikiPageWikiLink Q846316.
- Q20707211 icd "757.39".
- Q20707211 icd "Q82.8".
- Q20707211 meshid "536068.0".
- Q20707211 name "Hoyeraal-Hreidarsson syndrome".
- Q20707211 omim "305000".
- Q20707211 type Disease.
- Q20707211 type Thing.
- Q20707211 type Q12136.
- Q20707211 comment "Hoyeraal-Hreidarsson syndrome (HHS) is a very rare multisystem X-linked recessive disorder characterized by excessively short telomeres and is considered a severe form of dyskeratosis congenita. Being an X-linked disorder, HHS primarily affects males. Patients with HHS typically present in early childhood with cerebellar hypoplasia, immunodeficiency, progressive bone marrow failure, and intrauterine growth retardation.".
- Q20707211 label "Hoyeraal-Hreidarsson syndrome".
- Q20707211 name "Hoyeraal-Hreidarsson syndrome".