Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Pearson_syndrome> ?p ?o. }
Showing items 1 to 59 of
59
with 100 items per page.
- Pearson_syndrome abstract "Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure to thrive, pancreatic fibrosis with insulin-dependent diabetes and exocrine pancreatic deficiency, muscle and neurologic impairment, and, frequently, early death. It is usually fatal in infancy. The few patients who survive into adulthood often develop symptoms of Kearns-Sayre syndrome. It is caused by a deletion in mitochondrial DNA. Pearson syndrome is very rare, less than hundred cases have been reported in medical literature worldwide. The syndrome was first described by Pearson in 1979, the deletions causing it were discovered a decade later.".
- Pearson_syndrome diseasesdb "32159".
- Pearson_syndrome emedicineSubject "ped".
- Pearson_syndrome emedicineTopic "1750".
- Pearson_syndrome omim "557000".
- Pearson_syndrome wikiPageExternalLink mt-overview.
- Pearson_syndrome wikiPageExternalLink index.html.
- Pearson_syndrome wikiPageID "12041898".
- Pearson_syndrome wikiPageRevisionID "548308636".
- Pearson_syndrome diseasesdb "32159".
- Pearson_syndrome emedicinesubj "ped".
- Pearson_syndrome emedicinetopic "1750".
- Pearson_syndrome genereviewsname "Mitochondrial DNA Deletion Syndromes".
- Pearson_syndrome genereviewsnbk "NBK1203".
- Pearson_syndrome hasPhotoCollection Pearson_syndrome.
- Pearson_syndrome name "Pearson syndrome".
- Pearson_syndrome omim "557000".
- Pearson_syndrome wordnet_type synset-disease-noun-1.
- Pearson_syndrome subject Category:Mitochondrial_diseases.
- Pearson_syndrome subject Category:Rare_diseases.
- Pearson_syndrome subject Category:Syndromes.
- Pearson_syndrome type Abstraction100002137.
- Pearson_syndrome type Attribute100024264.
- Pearson_syndrome type Cognition100023271.
- Pearson_syndrome type Complex105870365.
- Pearson_syndrome type Concept105835747.
- Pearson_syndrome type Condition113920835.
- Pearson_syndrome type Content105809192.
- Pearson_syndrome type Disease114070360.
- Pearson_syndrome type Idea105833840.
- Pearson_syndrome type IllHealth114052046.
- Pearson_syndrome type Illness114061805.
- Pearson_syndrome type PathologicalState114051917.
- Pearson_syndrome type PhysicalCondition114034177.
- Pearson_syndrome type PsychologicalFeature100023100.
- Pearson_syndrome type State100024720.
- Pearson_syndrome type Syndrome105870790.
- Pearson_syndrome type Syndromes.
- Pearson_syndrome type Whole105869584.
- Pearson_syndrome type Disease.
- Pearson_syndrome type AilmentCondition.
- Pearson_syndrome type Situation.
- Pearson_syndrome comment "Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure to thrive, pancreatic fibrosis with insulin-dependent diabetes and exocrine pancreatic deficiency, muscle and neurologic impairment, and, frequently, early death. It is usually fatal in infancy. The few patients who survive into adulthood often develop symptoms of Kearns-Sayre syndrome. It is caused by a deletion in mitochondrial DNA.".
- Pearson_syndrome label "Morbus Pearson".
- Pearson_syndrome label "Pearson syndrome".
- Pearson_syndrome label "Syndrome de Pearson".
- Pearson_syndrome label "Síndrome de Pearson".
- Pearson_syndrome label "Zespół Pearsona".
- Pearson_syndrome sameAs Morbus_Pearson.
- Pearson_syndrome sameAs Síndrome_de_Pearson.
- Pearson_syndrome sameAs Syndrome_de_Pearson.
- Pearson_syndrome sameAs Zespół_Pearsona.
- Pearson_syndrome sameAs m.02vmxng.
- Pearson_syndrome sameAs Q9081107.
- Pearson_syndrome sameAs Q9081107.
- Pearson_syndrome sameAs Pearson_syndrome.
- Pearson_syndrome wasDerivedFrom Pearson_syndrome?oldid=548308636.
- Pearson_syndrome isPrimaryTopicOf Pearson_syndrome.
- Pearson_syndrome name "Pearson syndrome".