Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Hereditary_folate_malabsorption> ?p ?o }
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- Hereditary_folate_malabsorption abstract "Hereditary folate malabsorption (HFM - OMIM #229050) is a rare autosomal recessive disorder caused by caused by loss-of-function mutations in the proton-coupled folate transporter (PCFT) gene, resulting in systemic folate deficiency and impaired delivery of folate to the brain.".
- Hereditary_folate_malabsorption wikiPageExternalLink NBK1673.
- Hereditary_folate_malabsorption wikiPageID "47625870".
- Hereditary_folate_malabsorption wikiPageLength "22938".
- Hereditary_folate_malabsorption wikiPageOutDegree "9".
- Hereditary_folate_malabsorption wikiPageRevisionID "706016301".
- Hereditary_folate_malabsorption wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Hereditary_folate_malabsorption wikiPageWikiLink Cerebrospinal_fluid.
- Hereditary_folate_malabsorption wikiPageWikiLink Folate_deficiency.
- Hereditary_folate_malabsorption wikiPageWikiLink Folinic_acid.
- Hereditary_folate_malabsorption wikiPageWikiLink GeneReviews.
- Hereditary_folate_malabsorption wikiPageWikiLink Macrocytic_anemia.
- Hereditary_folate_malabsorption wikiPageWikiLink Pneumocystis_jirovecii.
- Hereditary_folate_malabsorption wikiPageWikiLinkText "Hereditary folate malabsorption".
- Hereditary_folate_malabsorption wikiPageWikiLinkText "hereditary folate malabsorption".
- Hereditary_folate_malabsorption wikiPageUsesTemplate Template:COI.
- Hereditary_folate_malabsorption wikiPageUsesTemplate Template:Multiple_issues.
- Hereditary_folate_malabsorption wikiPageUsesTemplate Template:Reflist.
- Hereditary_folate_malabsorption wikiPageUsesTemplate Template:Underlinked.
- Hereditary_folate_malabsorption subject Category:Autosomal_recessive_disorders.
- Hereditary_folate_malabsorption hypernym Disorder.
- Hereditary_folate_malabsorption type Disease.
- Hereditary_folate_malabsorption comment "Hereditary folate malabsorption (HFM - OMIM #229050) is a rare autosomal recessive disorder caused by caused by loss-of-function mutations in the proton-coupled folate transporter (PCFT) gene, resulting in systemic folate deficiency and impaired delivery of folate to the brain.".
- Hereditary_folate_malabsorption label "Hereditary folate malabsorption".
- Hereditary_folate_malabsorption wasDerivedFrom Hereditary_folate_malabsorption?oldid=706016301.
- Hereditary_folate_malabsorption isPrimaryTopicOf Hereditary_folate_malabsorption.