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- Tyrosinemia_type_III abstract "Type III tyrosinemia is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27), encoded by the gene HPD. This enzyme is abundant in the liver, and smaller amounts are found in the kidneys. It is one of a series of enzymes needed to break down tyrosine. Specifically, 4-hydroxyphenylpyruvate dioxygenase converts a tyrosine byproduct called 4-hydroxyphenylpyruvate to homogentisic acid. Characteristic features of type III tyrosinemia include mild mental retardation, seizures, and periodic loss of balance and coordination (intermittent ataxia). Type III tyrosinemia is very rare; only a few cases have been reported.".
- Tyrosinemia_type_III icd10 "E70.2".
- Tyrosinemia_type_III icd9 "270.2".
- Tyrosinemia_type_III meshId "D020176".
- Tyrosinemia_type_III omim "276710".
- Tyrosinemia_type_III thumbnail L-tyrosine-skeletal.png?width=300.
- Tyrosinemia_type_III wikiPageID "17920716".
- Tyrosinemia_type_III wikiPageLength "1519".
- Tyrosinemia_type_III wikiPageOutDegree "10".
- Tyrosinemia_type_III wikiPageRevisionID "642742251".
- Tyrosinemia_type_III wikiPageWikiLink 4-Hydroxyphenylpyruvate_dioxygenase.
- Tyrosinemia_type_III wikiPageWikiLink 4-Hydroxyphenylpyruvic_acid.
- Tyrosinemia_type_III wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- Tyrosinemia_type_III wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Tyrosinemia_type_III wikiPageWikiLink Epileptic_seizure.
- Tyrosinemia_type_III wikiPageWikiLink Homogentisic_acid.
- Tyrosinemia_type_III wikiPageWikiLink Intellectual_disability.
- Tyrosinemia_type_III wikiPageWikiLink Intermittent_ataxia.
- Tyrosinemia_type_III wikiPageWikiLink Tyrosine.
- Tyrosinemia_type_III wikiPageWikiLink File:Pathophysiology_of_metabolic_disorders_of_phenylalanine_and_tyrosine.png.
- Tyrosinemia_type_III wikiPageWikiLinkText "Tyrosinemia type III".
- Tyrosinemia_type_III caption Tyrosine.
- Tyrosinemia_type_III diseasesdb "29836".
- Tyrosinemia_type_III emedicinesubj "ped".
- Tyrosinemia_type_III emedicinetopic "2339".
- Tyrosinemia_type_III icd "270.2".
- Tyrosinemia_type_III icd "E70.2".
- Tyrosinemia_type_III meshid "D020176".
- Tyrosinemia_type_III name "Tyrosinemia type III".
- Tyrosinemia_type_III omim "276710".
- Tyrosinemia_type_III wikiPageUsesTemplate Template:Amino_acid_metabolic_pathology.
- Tyrosinemia_type_III wikiPageUsesTemplate Template:EC_number.
- Tyrosinemia_type_III wikiPageUsesTemplate Template:Infobox_disease.
- Tyrosinemia_type_III wikiPageUsesTemplate Template:Unreferenced.
- Tyrosinemia_type_III subject Category:Amino_acid_metabolism_disorders.
- Tyrosinemia_type_III subject Category:Autosomal_recessive_disorders.
- Tyrosinemia_type_III hypernym Disorder.
- Tyrosinemia_type_III type Disease.
- Tyrosinemia_type_III type Disorder.
- Tyrosinemia_type_III type Error.
- Tyrosinemia_type_III type Thing.
- Tyrosinemia_type_III type Q12136.
- Tyrosinemia_type_III comment "Type III tyrosinemia is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27), encoded by the gene HPD. This enzyme is abundant in the liver, and smaller amounts are found in the kidneys. It is one of a series of enzymes needed to break down tyrosine. Specifically, 4-hydroxyphenylpyruvate dioxygenase converts a tyrosine byproduct called 4-hydroxyphenylpyruvate to homogentisic acid.".
- Tyrosinemia_type_III label "Tyrosinemia type III".
- Tyrosinemia_type_III sameAs Q7861692.
- Tyrosinemia_type_III sameAs Tirosinemia_tipo_3.
- Tyrosinemia_type_III sameAs تیروزینمی_نوع_سه.
- Tyrosinemia_type_III sameAs m.0g5pqgd.
- Tyrosinemia_type_III sameAs Q7861692.
- Tyrosinemia_type_III wasDerivedFrom Tyrosinemia_type_III?oldid=642742251.
- Tyrosinemia_type_III depiction L-tyrosine-skeletal.png.
- Tyrosinemia_type_III isPrimaryTopicOf Tyrosinemia_type_III.
- Tyrosinemia_type_III name "Tyrosinemia type III".