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- Pyruvate_carboxylase_deficiency abstract "Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. This disorder appears to be much more common in some Algonkian Indian tribes in eastern Canada.[citation needed]".
- Pyruvate_carboxylase_deficiency diseasesdb "7378".
- Pyruvate_carboxylase_deficiency emedicineSubject "med".
- Pyruvate_carboxylase_deficiency emedicineTopic "1979".
- Pyruvate_carboxylase_deficiency icd10 "E74.4".
- Pyruvate_carboxylase_deficiency icd9 "271.8".
- Pyruvate_carboxylase_deficiency meshId "D015324".
- Pyruvate_carboxylase_deficiency omim "266150".
- Pyruvate_carboxylase_deficiency thumbnail Oxaloacetic_acid.png?width=300.
- Pyruvate_carboxylase_deficiency wikiPageExternalLink br.fcgi?book=gene&part=pdc.
- Pyruvate_carboxylase_deficiency wikiPageID "6861722".
- Pyruvate_carboxylase_deficiency wikiPageRevisionID "459668718".
- Pyruvate_carboxylase_deficiency caption "Oxaloacetate is the product of pyruvate carboxylase".
- Pyruvate_carboxylase_deficiency diseasesdb "7378".
- Pyruvate_carboxylase_deficiency emedicinesubj "med".
- Pyruvate_carboxylase_deficiency emedicinetopic "1979".
- Pyruvate_carboxylase_deficiency hasPhotoCollection Pyruvate_carboxylase_deficiency.
- Pyruvate_carboxylase_deficiency icd "271.8".
- Pyruvate_carboxylase_deficiency icd "E74.4".
- Pyruvate_carboxylase_deficiency meshid "D015324".
- Pyruvate_carboxylase_deficiency name "Pyruvate carboxylase deficiency".
- Pyruvate_carboxylase_deficiency omim "266150".
- Pyruvate_carboxylase_deficiency wordnet_type synset-disease-noun-1.
- Pyruvate_carboxylase_deficiency subject Category:Autosomal_recessive_disorders.
- Pyruvate_carboxylase_deficiency subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Pyruvate_carboxylase_deficiency type Abstraction100002137.
- Pyruvate_carboxylase_deficiency type Act100030358.
- Pyruvate_carboxylase_deficiency type Attribute100024264.
- Pyruvate_carboxylase_deficiency type AutosomalRecessiveDisorders.
- Pyruvate_carboxylase_deficiency type Condition113920835.
- Pyruvate_carboxylase_deficiency type Disease114070360.
- Pyruvate_carboxylase_deficiency type Disorder114052403.
- Pyruvate_carboxylase_deficiency type Event100029378.
- Pyruvate_carboxylase_deficiency type IllHealth114052046.
- Pyruvate_carboxylase_deficiency type Illness114061805.
- Pyruvate_carboxylase_deficiency type InbornErrorsOfCarbohydrateMetabolism.
- Pyruvate_carboxylase_deficiency type Mistake100070965.
- Pyruvate_carboxylase_deficiency type Nonaccomplishment100066216.
- Pyruvate_carboxylase_deficiency type PathologicalState114051917.
- Pyruvate_carboxylase_deficiency type PhysicalCondition114034177.
- Pyruvate_carboxylase_deficiency type PsychologicalFeature100023100.
- Pyruvate_carboxylase_deficiency type State100024720.
- Pyruvate_carboxylase_deficiency type YagoPermanentlyLocatedEntity.
- Pyruvate_carboxylase_deficiency type Disease.
- Pyruvate_carboxylase_deficiency type AilmentCondition.
- Pyruvate_carboxylase_deficiency type Situation.
- Pyruvate_carboxylase_deficiency comment "Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system. Pyruvate carboxylase deficiency is a rare condition, with an estimated incidence of 1 in 250,000 births worldwide. This disorder appears to be much more common in some Algonkian Indian tribes in eastern Canada.[citation needed]".
- Pyruvate_carboxylase_deficiency label "Pyruvate carboxylase deficiency".
- Pyruvate_carboxylase_deficiency sameAs m.0gt1l3.
- Pyruvate_carboxylase_deficiency sameAs Q7263794.
- Pyruvate_carboxylase_deficiency sameAs Q7263794.
- Pyruvate_carboxylase_deficiency sameAs Pyruvate_carboxylase_deficiency.
- Pyruvate_carboxylase_deficiency wasDerivedFrom Pyruvate_carboxylase_deficiency?oldid=459668718.
- Pyruvate_carboxylase_deficiency depiction Oxaloacetic_acid.png.
- Pyruvate_carboxylase_deficiency isPrimaryTopicOf Pyruvate_carboxylase_deficiency.
- Pyruvate_carboxylase_deficiency name "Pyruvate carboxylase deficiency".