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- Alkaptonuria abstract "Alkaptonuria (black urine disease or alcaptonuria) is a rare inherited genetic disorder of phenylalanine and tyrosine metabolism. This is an autosomal recessive condition that is due to a defect in the enzyme homogentisate 1,2-dioxygenase (EC 1.13.11.5), which participates in the degradation of tyrosine. As a result, homogentisic acid and its oxide, called alkapton, accumulate in the blood and are excreted in urine in large amounts (hence -uria). Excessive homogentisic acid causes damage to cartilage (ochronosis, leading to osteoarthritis) and heart valves as well as precipitating as kidney stones. Treatment with nitisinone, which suppresses homogentisic acid production, is being studied. Alkaptonuria is more common in Slovakia and the Dominican Republic than in other countries.".
- Alkaptonuria diseasesdb "409".
- Alkaptonuria emedicineSubject "ped".
- Alkaptonuria emedicineTopic "64".
- Alkaptonuria icd10 "E70.2 (ILDS E70.210)".
- Alkaptonuria icd9 "270.2".
- Alkaptonuria medlineplus "001200".
- Alkaptonuria meshId "D000474".
- Alkaptonuria omim "203500".
- Alkaptonuria thumbnail Homogentisic_acid.svg?width=300.
- Alkaptonuria wikiPageExternalLink www.akusociety.org.
- Alkaptonuria wikiPageExternalLink www.developAKUre.eu.
- Alkaptonuria wikiPageExternalLink watch?v=nuVn7QGkv-I.
- Alkaptonuria wikiPageID "148249".
- Alkaptonuria wikiPageRevisionID "605412937".
- Alkaptonuria caption Homogentisic_acid.
- Alkaptonuria diseasesdb "409".
- Alkaptonuria emedicinesubj "ped".
- Alkaptonuria emedicinetopic "64".
- Alkaptonuria genereviewsname "Alkaptonuria".
- Alkaptonuria genereviewsnbk "NBK1454".
- Alkaptonuria hasPhotoCollection Alkaptonuria.
- Alkaptonuria icd "270.2".
- Alkaptonuria icd "E70.2".
- Alkaptonuria medlineplus "1200".
- Alkaptonuria meshid "D000474".
- Alkaptonuria name "Alkaptonuria".
- Alkaptonuria omim "203500".
- Alkaptonuria width "180".
- Alkaptonuria wordnet_type synset-disease-noun-1.
- Alkaptonuria subject Category:Amino_acid_metabolism_disorders.
- Alkaptonuria subject Category:Autosomal_recessive_disorders.
- Alkaptonuria subject Category:Skin_conditions_resulting_from_errors_in_metabolism.
- Alkaptonuria type Disease.
- Alkaptonuria type AilmentCondition.
- Alkaptonuria type Situation.
- Alkaptonuria comment "Alkaptonuria (black urine disease or alcaptonuria) is a rare inherited genetic disorder of phenylalanine and tyrosine metabolism. This is an autosomal recessive condition that is due to a defect in the enzyme homogentisate 1,2-dioxygenase (EC 1.13.11.5), which participates in the degradation of tyrosine. As a result, homogentisic acid and its oxide, called alkapton, accumulate in the blood and are excreted in urine in large amounts (hence -uria).".
- Alkaptonuria label "Alcaptonuria".
- Alkaptonuria label "Alcaptonuria".
- Alkaptonuria label "Alcaptonurie".
- Alkaptonuria label "Alcaptonúria".
- Alkaptonuria label "Alkaptonuria".
- Alkaptonuria label "Alkaptonuria".
- Alkaptonuria label "Alkaptonurie".
- Alkaptonuria label "Alkaptonurie".
- Alkaptonuria label "Алкаптонурия".
- Alkaptonuria label "黑尿症".
- Alkaptonuria sameAs Alkaptonurie.
- Alkaptonuria sameAs Alcaptonuria.
- Alkaptonuria sameAs Alcaptonurie.
- Alkaptonuria sameAs Alcaptonuria.
- Alkaptonuria sameAs Alkaptonurie.
- Alkaptonuria sameAs Alkaptonuria.
- Alkaptonuria sameAs Alcaptonúria.
- Alkaptonuria sameAs m.012_rz.
- Alkaptonuria sameAs Q651680.
- Alkaptonuria sameAs Q651680.
- Alkaptonuria sameAs 60.
- Alkaptonuria wasDerivedFrom Alkaptonuria?oldid=605412937.
- Alkaptonuria depiction Homogentisic_acid.svg.
- Alkaptonuria isPrimaryTopicOf Alkaptonuria.
- Alkaptonuria name "Alkaptonuria".