Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Hoyeraal-Hreidarsson_syndrome> ?p ?o }
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- Hoyeraal-Hreidarsson_syndrome 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.".
- Hoyeraal-Hreidarsson_syndrome icd10 "Q82.8".
- Hoyeraal-Hreidarsson_syndrome icd9 "757.39".
- Hoyeraal-Hreidarsson_syndrome meshId "C536068".
- Hoyeraal-Hreidarsson_syndrome omim "305000".
- Hoyeraal-Hreidarsson_syndrome wikiPageExternalLink OC_Exp.php?Lng=EN&Expert=3322.
- Hoyeraal-Hreidarsson_syndrome wikiPageID "46872856".
- Hoyeraal-Hreidarsson_syndrome wikiPageLength "3433".
- Hoyeraal-Hreidarsson_syndrome wikiPageOutDegree "24".
- Hoyeraal-Hreidarsson_syndrome wikiPageRevisionID "696316213".
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Aplastic_anemia.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Bone_marrow_failure.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Cancer.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Category:X-linked_recessive_disorders.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Cerebellar_hypoplasia.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Dyskeratosis_congenita.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Dysplastic_nail.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Immunodeficiency.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Intellectual_disability.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Intrauterine_growth_restriction.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Leukoplakia.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Livedo_reticularis.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Microcephaly.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Pulmonary_fibrosis.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Sex_linkage.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLink Telomere.
- Hoyeraal-Hreidarsson_syndrome wikiPageWikiLinkText "Hoyeraal-Hreidarsson syndrome".
- Hoyeraal-Hreidarsson_syndrome diseasesdb "32955".
- Hoyeraal-Hreidarsson_syndrome icd "757.39".
- Hoyeraal-Hreidarsson_syndrome icd "Q82.8".
- Hoyeraal-Hreidarsson_syndrome meshid "536068.0".
- Hoyeraal-Hreidarsson_syndrome name "Hoyeraal-Hreidarsson syndrome".
- Hoyeraal-Hreidarsson_syndrome omim "305000".
- Hoyeraal-Hreidarsson_syndrome wikiPageUsesTemplate Template:Disease-stub.
- Hoyeraal-Hreidarsson_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Hoyeraal-Hreidarsson_syndrome wikiPageUsesTemplate Template:Reflist.
- Hoyeraal-Hreidarsson_syndrome subject Category:X-linked_recessive_disorders.
- Hoyeraal-Hreidarsson_syndrome type Disease.
- Hoyeraal-Hreidarsson_syndrome type Thing.
- Hoyeraal-Hreidarsson_syndrome type Q12136.
- Hoyeraal-Hreidarsson_syndrome 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.".
- Hoyeraal-Hreidarsson_syndrome label "Hoyeraal-Hreidarsson syndrome".
- Hoyeraal-Hreidarsson_syndrome sameAs Q20707211.
- Hoyeraal-Hreidarsson_syndrome sameAs m.013cdytb.
- Hoyeraal-Hreidarsson_syndrome sameAs Q20707211.
- Hoyeraal-Hreidarsson_syndrome wasDerivedFrom Hoyeraal-Hreidarsson_syndrome?oldid=696316213.
- Hoyeraal-Hreidarsson_syndrome isPrimaryTopicOf Hoyeraal-Hreidarsson_syndrome.
- Hoyeraal-Hreidarsson_syndrome name "Hoyeraal-Hreidarsson syndrome".