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- Multiple_carboxylase_deficiency abstract "Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.The deficiency can be in biotinidase or holocarboxylase synthetase.These conditions respond to biotin.Forms include: Holocarboxylase synthetase deficiency - neonatal; Biotinidase deficiency - late onset;If left untreated, the symptoms can include feeding problems, hypotonia, generalised erythematous rash with skin exfoliation and alopecia, failure to thrive, seizure, coma, developmental delay, foul smelling urine, metabolic acidosis, ketosis and hyperammonemia.".
- Multiple_carboxylase_deficiency meshId "D009100".
- Multiple_carboxylase_deficiency wikiPageExternalLink mcd_prof.htm.
- Multiple_carboxylase_deficiency wikiPageID "17921514".
- Multiple_carboxylase_deficiency wikiPageLength "1760".
- Multiple_carboxylase_deficiency wikiPageOutDegree "17".
- Multiple_carboxylase_deficiency wikiPageRevisionID "679636709".
- Multiple_carboxylase_deficiency wikiPageWikiLink Alopecia.
- Multiple_carboxylase_deficiency wikiPageWikiLink Biotin.
- Multiple_carboxylase_deficiency wikiPageWikiLink Biotinidase.
- Multiple_carboxylase_deficiency wikiPageWikiLink Biotinidase_deficiency.
- Multiple_carboxylase_deficiency wikiPageWikiLink Carboxylation.
- Multiple_carboxylase_deficiency wikiPageWikiLink Category:Vitamin,_coenzyme,_and_cofactor_metabolism_disorders.
- Multiple_carboxylase_deficiency wikiPageWikiLink Coma.
- Multiple_carboxylase_deficiency wikiPageWikiLink Developmental_delay.
- Multiple_carboxylase_deficiency wikiPageWikiLink Epileptic_seizure.
- Multiple_carboxylase_deficiency wikiPageWikiLink Erythema.
- Multiple_carboxylase_deficiency wikiPageWikiLink Failure_to_thrive.
- Multiple_carboxylase_deficiency wikiPageWikiLink Hair_loss.
- Multiple_carboxylase_deficiency wikiPageWikiLink Holocarboxylase_synthetase.
- Multiple_carboxylase_deficiency wikiPageWikiLink Holocarboxylase_synthetase_deficiency.
- Multiple_carboxylase_deficiency wikiPageWikiLink Hyperammonemia.
- Multiple_carboxylase_deficiency wikiPageWikiLink Hypotonia.
- Multiple_carboxylase_deficiency wikiPageWikiLink Ketosis.
- Multiple_carboxylase_deficiency wikiPageWikiLink Metabolic_acidosis.
- Multiple_carboxylase_deficiency wikiPageWikiLink Seizure.
- Multiple_carboxylase_deficiency wikiPageWikiLink Specific_developmental_disorder.
- Multiple_carboxylase_deficiency wikiPageWikiLinkText "Multiple carboxylase deficiency".
- Multiple_carboxylase_deficiency wikiPageWikiLinkText "Multiple-CoA carboxylase deficiency".
- Multiple_carboxylase_deficiency wikiPageWikiLinkText "multiple carboxylase deficiency".
- Multiple_carboxylase_deficiency hasPhotoCollection Multiple_carboxylase_deficiency.
- Multiple_carboxylase_deficiency meshid "D009100".
- Multiple_carboxylase_deficiency name "Multiple carboxylase deficiency".
- Multiple_carboxylase_deficiency wikiPageUsesTemplate Template:Endocrine-disease-stub.
- Multiple_carboxylase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- Multiple_carboxylase_deficiency wikiPageUsesTemplate Template:Metabolic_disorders_of_vitamins,_coenzymes,_and_cofactors.
- Multiple_carboxylase_deficiency wikiPageUsesTemplate Template:Reflist.
- Multiple_carboxylase_deficiency subject Category:Vitamin,_coenzyme,_and_cofactor_metabolism_disorders.
- Multiple_carboxylase_deficiency hypernym Form.
- Multiple_carboxylase_deficiency type Disease.
- Multiple_carboxylase_deficiency type Error.
- Multiple_carboxylase_deficiency type Thing.
- Multiple_carboxylase_deficiency type Q12136.
- Multiple_carboxylase_deficiency comment "Multiple carboxylase deficiency is a form of metabolic disorder involving failures of carboxylation enzymes.The deficiency can be in biotinidase or holocarboxylase synthetase.These conditions respond to biotin.Forms include: Holocarboxylase synthetase deficiency - neonatal; Biotinidase deficiency - late onset;If left untreated, the symptoms can include feeding problems, hypotonia, generalised erythematous rash with skin exfoliation and alopecia, failure to thrive, seizure, coma, developmental delay, foul smelling urine, metabolic acidosis, ketosis and hyperammonemia.".
- Multiple_carboxylase_deficiency label "Multiple carboxylase deficiency".
- Multiple_carboxylase_deficiency sameAs m.047t24j.
- Multiple_carboxylase_deficiency sameAs Q6934914.
- Multiple_carboxylase_deficiency sameAs Q6934914.
- Multiple_carboxylase_deficiency wasDerivedFrom Multiple_carboxylase_deficiency?oldid=679636709.
- Multiple_carboxylase_deficiency isPrimaryTopicOf Multiple_carboxylase_deficiency.
- Multiple_carboxylase_deficiency name "Multiple carboxylase deficiency".