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- Homocystinuria abstract "Classical Homocystinuria, also known as cystathionine beta synthase deficiency or CBS deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving cystathionine beta synthase. It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.".
- Homocystinuria diseasesdb "5991".
- Homocystinuria emedicineSubject "derm".
- Homocystinuria emedicineTopic "708".
- Homocystinuria icd10 "E72.1".
- Homocystinuria icd9 "270.4".
- Homocystinuria medlineplus "001199".
- Homocystinuria meshId "D006712".
- Homocystinuria omim "236200".
- Homocystinuria thumbnail L-Homocysteine.svg?width=300.
- Homocystinuria wikiPageExternalLink viewer?a=v&pid=sites&srcid=ZGVmYXVsdGRvbWFpbnxtdWx0aWZhY3RvcmhlYWx0aHxneDoyMjRkY2I4NmI2MDZlNTc4.
- Homocystinuria wikiPageExternalLink diet.htm.
- Homocystinuria wikiPageExternalLink NBK1524.
- Homocystinuria wikiPageID "662647".
- Homocystinuria wikiPageRevisionID "599640474".
- Homocystinuria caption Homocysteine.
- Homocystinuria diseasesdb "5991".
- Homocystinuria emedicinesubj "derm".
- Homocystinuria emedicinetopic "708".
- Homocystinuria genereviewsname "Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency".
- Homocystinuria genereviewsnbk "NBK1524".
- Homocystinuria hasPhotoCollection Homocystinuria.
- Homocystinuria icd "270.4".
- Homocystinuria icd "E72.1".
- Homocystinuria medlineplus "1199".
- Homocystinuria meshid "D006712".
- Homocystinuria name "Homocystinuria".
- Homocystinuria omim "236200".
- Homocystinuria wordnet_type synset-disease-noun-1.
- Homocystinuria subject Category:Abnormalities_of_dermal_fibrous_and_elastic_tissue.
- Homocystinuria subject Category:Amino_acid_metabolism_disorders.
- Homocystinuria subject Category:Autosomal_recessive_disorders.
- Homocystinuria type AbnormalitiesOfDermalFibrousAndElasticTissue.
- Homocystinuria type Abnormality114501726.
- Homocystinuria type Abstraction100002137.
- Homocystinuria type AminoAcidMetabolismDisorders.
- Homocystinuria type Attribute100024264.
- Homocystinuria type AutosomalRecessiveDisorders.
- Homocystinuria type Condition113920835.
- Homocystinuria type Disorder114052403.
- Homocystinuria type PhysicalCondition114034177.
- Homocystinuria type State100024720.
- Homocystinuria type Disease.
- Homocystinuria type AilmentCondition.
- Homocystinuria type Situation.
- Homocystinuria comment "Classical Homocystinuria, also known as cystathionine beta synthase deficiency or CBS deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving cystathionine beta synthase. It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.".
- Homocystinuria label "Homocistinuria".
- Homocystinuria label "Homocistinúria".
- Homocystinuria label "Homocystinuria".
- Homocystinuria label "Homocystinurie".
- Homocystinuria label "Homocystinurie".
- Homocystinuria label "Homocystinurie".
- Homocystinuria label "Homocystynuria".
- Homocystinuria label "Omocistinuria".
- Homocystinuria label "بيلة هوموسيستينية".
- Homocystinuria label "ホモシスチン尿症".
- Homocystinuria label "高胱胺酸尿症".
- Homocystinuria sameAs Homocystinurie.
- Homocystinuria sameAs Homocistinuria.
- Homocystinuria sameAs Homocystinurie.
- Homocystinuria sameAs Omocistinuria.
- Homocystinuria sameAs ホモシスチン尿症.
- Homocystinuria sameAs Homocystinurie.
- Homocystinuria sameAs Homocystynuria.
- Homocystinuria sameAs Homocistinúria.
- Homocystinuria sameAs m.030sd6.
- Homocystinuria sameAs Q994859.
- Homocystinuria sameAs Q994859.
- Homocystinuria sameAs 522.
- Homocystinuria sameAs Homocystinuria.
- Homocystinuria wasDerivedFrom Homocystinuria?oldid=599640474.
- Homocystinuria depiction L-Homocysteine.svg.
- Homocystinuria isPrimaryTopicOf Homocystinuria.
- Homocystinuria name "Homocystinuria".