Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Carnitine_palmitoyltransferase_II_deficiency> ?p ?o }
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- Carnitine_palmitoyltransferase_II_deficiency abstract "Carnitine palmitoyltransferase II deficiency (CPT-II) is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source. The adult myopathic form of this disease was first characterized in 1973 by DiMauro and DiMauro. It is the most common inherited disorder of lipid metabolism affecting the skeletal muscle of adults. CPT II deficiency is also the most frequent cause of hereditary myoglobinuria. Symptoms of this disease are commonly provoked by prolonged exercise or periods without food.".
- Carnitine_palmitoyltransferase_II_deficiency icd10 "E71.3".
- Carnitine_palmitoyltransferase_II_deficiency icd9 "277.85".
- Carnitine_palmitoyltransferase_II_deficiency omim "255110".
- Carnitine_palmitoyltransferase_II_deficiency thumbnail Carnitine_structure.png?width=300.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageExternalLink ghr.nlm.nih.gov.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageExternalLink br.fcgi?book=gene&part=cpt2.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageID "2525632".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageLength "22872".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageOutDegree "45".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageRevisionID "672640702".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Arrhythmia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Cardiac_arrest.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Cardiac_arrhythmia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Cardiomegaly.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Cardiomyopathy.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Carnitine.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Carnitine_O-palmitoyltransferase.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Carnitine_palmitoyltransferase_II.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Carnitine_palmitoyltransferase_I_deficiency.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Category:Fatty-acid_metabolism_disorders.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Category:Hepatology.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Creatine_kinase.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Dominance_(genetics).
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Epileptic_seizure.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Fasciculation.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Fatty_acid.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Fibroblast.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink File:Autorecessive.svg.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Gene.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Hepatomegaly.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Hyperammonemia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Hypoglycemia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Hypoketotic_hypoglycemia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Infant.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Kidney_failure.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Long-chain_fatty_acid.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Lymphocyte.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Medium-chain_triglyceride.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Micelle.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Mitochondria.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Mitochondrion.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myalgia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myoglobin.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myoglobinuria.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myokymia.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myopathic.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Myopathy.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Neonatal.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Primary_carnitine_deficiency.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Renal_failure.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Rhabdomyolysis.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Seizure.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Skeletal_muscle.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Sudden_infant_death_syndrome.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Systemic_primary_carnitine_deficiency.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Tandem_mass_spectrometry.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink Triheptanoin.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLink File:Acyl-CoA_from_cytosol_to_the_mitochondrial_matrix.svg.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLinkText "CPT-II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLinkText "Carnitine palmitoyltransferase II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLinkText "Carnitine_palmitoyltransferase_II_deficiency".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLinkText "II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageWikiLinkText "carnitine palmitoyltransferase II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency caption Carnitine.
- Carnitine_palmitoyltransferase_II_deficiency diseasesdb "32534".
- Carnitine_palmitoyltransferase_II_deficiency emedicinesubj "ped".
- Carnitine_palmitoyltransferase_II_deficiency emedicinetopic "321".
- Carnitine_palmitoyltransferase_II_deficiency hasPhotoCollection Carnitine_palmitoyltransferase_II_deficiency.
- Carnitine_palmitoyltransferase_II_deficiency icd "277.85".
- Carnitine_palmitoyltransferase_II_deficiency icd "E71.3".
- Carnitine_palmitoyltransferase_II_deficiency name "Carnitine palmitoyltransferase II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency omim "255110".
- Carnitine_palmitoyltransferase_II_deficiency wikiPageUsesTemplate Template:Fatty-acid_metabolism_disorders.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageUsesTemplate Template:Lipidemias.
- Carnitine_palmitoyltransferase_II_deficiency wikiPageUsesTemplate Template:Reflist.
- Carnitine_palmitoyltransferase_II_deficiency subject Category:Autosomal_recessive_disorders.
- Carnitine_palmitoyltransferase_II_deficiency subject Category:Fatty-acid_metabolism_disorders.
- Carnitine_palmitoyltransferase_II_deficiency subject Category:Hepatology.
- Carnitine_palmitoyltransferase_II_deficiency hypernym Autosomal.
- Carnitine_palmitoyltransferase_II_deficiency type Disease.
- Carnitine_palmitoyltransferase_II_deficiency type Disorder.
- Carnitine_palmitoyltransferase_II_deficiency type Error.
- Carnitine_palmitoyltransferase_II_deficiency type Specialty.
- Carnitine_palmitoyltransferase_II_deficiency type Thing.
- Carnitine_palmitoyltransferase_II_deficiency type Q12136.
- Carnitine_palmitoyltransferase_II_deficiency comment "Carnitine palmitoyltransferase II deficiency (CPT-II) is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source. The adult myopathic form of this disease was first characterized in 1973 by DiMauro and DiMauro. It is the most common inherited disorder of lipid metabolism affecting the skeletal muscle of adults.".
- Carnitine_palmitoyltransferase_II_deficiency label "Carnitine palmitoyltransferase II deficiency".
- Carnitine_palmitoyltransferase_II_deficiency sameAs Deficiencia_de_carnitina_palmitoiltransferasa_tipo_II.
- Carnitine_palmitoyltransferase_II_deficiency sameAs Déficit_en_carnitine_palmitoyltransférase_II.
- Carnitine_palmitoyltransferase_II_deficiency sameAs m.07ky7f.
- Carnitine_palmitoyltransferase_II_deficiency sameAs Q2033861.
- Carnitine_palmitoyltransferase_II_deficiency sameAs Q2033861.
- Carnitine_palmitoyltransferase_II_deficiency wasDerivedFrom Carnitine_palmitoyltransferase_II_deficiency?oldid=672640702.
- Carnitine_palmitoyltransferase_II_deficiency depiction Carnitine_structure.png.
- Carnitine_palmitoyltransferase_II_deficiency isPrimaryTopicOf Carnitine_palmitoyltransferase_II_deficiency.
- Carnitine_palmitoyltransferase_II_deficiency name "Carnitine palmitoyltransferase II deficiency".