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- Carbamoyl_phosphate_synthetase_I_deficiency abstract "Carbamoyl phosphate synthetase I deficiency (CPS I deficiency) is an autosomal recessive metabolic disorder that causes ammonia to accumulate in the blood due to a lack of the enzyme carbamoyl phosphate synthetase I. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Carbamoyl_phosphate_synthetase_I_deficiency diseasesdb "32671".
- Carbamoyl_phosphate_synthetase_I_deficiency emedicineSubject "ped".
- Carbamoyl_phosphate_synthetase_I_deficiency emedicineTopic "314".
- Carbamoyl_phosphate_synthetase_I_deficiency icd9 "270.6".
- Carbamoyl_phosphate_synthetase_I_deficiency meshId "D020165".
- Carbamoyl_phosphate_synthetase_I_deficiency omim "237300".
- Carbamoyl_phosphate_synthetase_I_deficiency thumbnail Autorecessive.jpg?width=300.
- Carbamoyl_phosphate_synthetase_I_deficiency wikiPageExternalLink NBK1217.
- Carbamoyl_phosphate_synthetase_I_deficiency wikiPageID "6531143".
- Carbamoyl_phosphate_synthetase_I_deficiency wikiPageRevisionID "578768899".
- Carbamoyl_phosphate_synthetase_I_deficiency diseasesdb "32671".
- Carbamoyl_phosphate_synthetase_I_deficiency emedicinesubj "ped".
- Carbamoyl_phosphate_synthetase_I_deficiency emedicinetopic "314".
- Carbamoyl_phosphate_synthetase_I_deficiency hasPhotoCollection Carbamoyl_phosphate_synthetase_I_deficiency.
- Carbamoyl_phosphate_synthetase_I_deficiency icd "270.6".
- Carbamoyl_phosphate_synthetase_I_deficiency meshid "D020165".
- Carbamoyl_phosphate_synthetase_I_deficiency name "Carbamoyl phosphate synthetase I deficiency".
- Carbamoyl_phosphate_synthetase_I_deficiency omim "237300".
- Carbamoyl_phosphate_synthetase_I_deficiency wordnet_type synset-disease-noun-1.
- Carbamoyl_phosphate_synthetase_I_deficiency subject Category:Amino_acid_metabolism_disorders.
- Carbamoyl_phosphate_synthetase_I_deficiency subject Category:Autosomal_recessive_disorders.
- Carbamoyl_phosphate_synthetase_I_deficiency type Abstraction100002137.
- Carbamoyl_phosphate_synthetase_I_deficiency type AminoAcidMetabolismDisorders.
- Carbamoyl_phosphate_synthetase_I_deficiency type Attribute100024264.
- Carbamoyl_phosphate_synthetase_I_deficiency type AutosomalRecessiveDisorders.
- Carbamoyl_phosphate_synthetase_I_deficiency type Condition113920835.
- Carbamoyl_phosphate_synthetase_I_deficiency type Disorder114052403.
- Carbamoyl_phosphate_synthetase_I_deficiency type PhysicalCondition114034177.
- Carbamoyl_phosphate_synthetase_I_deficiency type State100024720.
- Carbamoyl_phosphate_synthetase_I_deficiency type Disease.
- Carbamoyl_phosphate_synthetase_I_deficiency type AilmentCondition.
- Carbamoyl_phosphate_synthetase_I_deficiency type Situation.
- Carbamoyl_phosphate_synthetase_I_deficiency comment "Carbamoyl phosphate synthetase I deficiency (CPS I deficiency) is an autosomal recessive metabolic disorder that causes ammonia to accumulate in the blood due to a lack of the enzyme carbamoyl phosphate synthetase I. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Carbamoyl_phosphate_synthetase_I_deficiency label "Carbamoyl phosphate synthetase I deficiency".
- Carbamoyl_phosphate_synthetase_I_deficiency sameAs m.0g9424.
- Carbamoyl_phosphate_synthetase_I_deficiency sameAs Q5037834.
- Carbamoyl_phosphate_synthetase_I_deficiency sameAs Q5037834.
- Carbamoyl_phosphate_synthetase_I_deficiency sameAs 191.
- Carbamoyl_phosphate_synthetase_I_deficiency sameAs Carbamoyl_phosphate_synthetase_I_deficiency.
- Carbamoyl_phosphate_synthetase_I_deficiency wasDerivedFrom Carbamoyl_phosphate_synthetase_I_deficiency?oldid=578768899.
- Carbamoyl_phosphate_synthetase_I_deficiency depiction Autorecessive.jpg.
- Carbamoyl_phosphate_synthetase_I_deficiency isPrimaryTopicOf Carbamoyl_phosphate_synthetase_I_deficiency.
- Carbamoyl_phosphate_synthetase_I_deficiency name "Carbamoyl phosphate synthetase I deficiency".