About: Arakawa's syndrome II

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Arakawa's syndrome II is an autosomal dominant metabolic disorder that causes a deficiency of the enzyme tetrahydrofolate-methyltransferase; affected individuals cannot properly metabolize methylcobalamin, a type of Vitamin B12.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalDominantDisorders yago:WikicatMetabolicDisorders yago:Abstraction100002137 yago:Attribute100024264 yago:AutosomalDominantDisease114162025 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Disease114070360 yago:Disorder114052403 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:MetabolicDisorder114084502 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisorders disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes umbel-rc:AilmentCondition
rdfs:label	Arakawa's syndrome II (en) Niedobór syntazy metioninowej (pl) Синдром Аракава II (uk)
rdfs:comment	Arakawa's syndrome II is an autosomal dominant metabolic disorder that causes a deficiency of the enzyme tetrahydrofolate-methyltransferase; affected individuals cannot properly metabolize methylcobalamin, a type of Vitamin B12. (en) Niedobór syntazy metioninowej, niedobór metylotransferazy homocysteinowej, zespół Arakawy II (ang. methionine synthase deficiency, tetrahydrofolate-methyltransferase deficiency syndrome, N5-methylhomocysteine transferase deficiency, Arakawa syndrome II) to genetycznie uwarunkowana choroba metaboliczna wynikająca z niedoboru enzymu metylotransferazy homocysteinowej. Dotknięte nią osoby nie mogą właściwie metabolizować metylokobalaminy, jednej z postaci witaminy B12. (pl) Синдром Аракава II (англ. Arakawa's syndrome II; також англ. Methionine synthase deficiency, Tetrahydrofolate-methyltransferase deficiency syndrome, N5-methylhomocysteine transferase deficiency, синдром дефіциту метіонінсинтази, синдром дефіциту тетрагідрофолатметилтрансферази, синдром дефіциту N5-метилгомоцистеїнтрансферази) — клінічний синдром, аутосомно-домінантне порушення обміну речовин, яке спричинює дефіцит ферменту тетрагідрофолатметилтрансферази. (uk)
foaf:name	Arakawa's syndrome II (en)
name	Arakawa's syndrome II (en)
foaf:depiction
dcterms:subject	Vitamin, coenzyme, and cofactor metabolism disorders Syndromes affecting the nervous system Syndromes with intellectual disability Syndromes affecting blood Autosomal dominant disorders
Wikipage page ID	4211737 (xsd:integer)
Wikipage revision ID	1061928871 (xsd:integer)
Link from a Wikipage to another Wikipage	Scoliosis Epilepsy dbr:Methionine_synthase Delayed milestone Megaloblastic anemia Ventricular system Myoclonus Pectus excavatum Vitamin, coenzyme, and cofactor metabolism disorders Cyanocobalamin Diarrhea Vomiting Syndromes affecting the nervous system Syndromes with intellectual disability Hepatosplenomegaly Atrophy Hypotonia Syndromes affecting blood Autosomal dominant disorders Dominance (genetics) Autosome Metabolic disorder Intellectual disability Methylcobalamin Neurology Tetrahydrofolate-methyltransferase Glutamate formiminotransferase
sameAs	Arakawa's syndrome II Arakawa's syndrome II Arakawa's syndrome II Arakawa's syndrome II Arakawa's syndrome II Arakawa's syndrome II
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Clear dbt:Cn dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:RareDiseases
thumbnail	wiki-commons:Special:FilePath/Mecobalamin.svg?width=300
DiseasesDB	32787 (xsd:integer)
OMIM	156570 (xsd:integer)
caption	Methylcobalamin
synonyms	Methionine synthase deficiency, Tetrahydrofolate-methyltransferase deficiency syndrome, and N5-methylhomocysteine transferase deficiency. (en)
has abstract	Arakawa's syndrome II is an autosomal dominant metabolic disorder that causes a deficiency of the enzyme tetrahydrofolate-methyltransferase; affected individuals cannot properly metabolize methylcobalamin, a type of Vitamin B12. (en) Niedobór syntazy metioninowej, niedobór metylotransferazy homocysteinowej, zespół Arakawy II (ang. methionine synthase deficiency, tetrahydrofolate-methyltransferase deficiency syndrome, N5-methylhomocysteine transferase deficiency, Arakawa syndrome II) to genetycznie uwarunkowana choroba metaboliczna wynikająca z niedoboru enzymu metylotransferazy homocysteinowej. Dotknięte nią osoby nie mogą właściwie metabolizować metylokobalaminy, jednej z postaci witaminy B12. (pl) Синдром Аракава II (англ. Arakawa's syndrome II; також англ. Methionine synthase deficiency, Tetrahydrofolate-methyltransferase deficiency syndrome, N5-methylhomocysteine transferase deficiency, синдром дефіциту метіонінсинтази, синдром дефіциту тетрагідрофолатметилтрансферази, синдром дефіциту N5-метилгомоцистеїнтрансферази) — клінічний синдром, аутосомно-домінантне порушення обміну речовин, яке спричинює дефіцит ферменту тетрагідрофолатметилтрансферази. (uk)
gold:hypernym	Disorder
dbp:wordnet_type	http://www.w3.org/2006/03/wn/wn20/instances/synset-disease-noun-1
prov:wasDerivedFrom	wikipedia-en:Arakawa's_syndrome_II?oldid=1061928871&ns=0
page length (characters) of wiki page	3239 (xsd:nonNegativeInteger)

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