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- Abetalipoproteinemia abstract "Abetalipoproteinemia, or Bassen-Kornzweig syndrome, is a rare autosomal recessive disorder that interferes with the normal absorption of fat and fat-soluble vitamins from food. It is caused by a mutation in microsomal triglyceride transfer protein resulting in deficiencies in the apolipoproteins B-48 and B-100, which are used in the synthesis and exportation of chylomicrons and VLDL respectively. It is not to be confused with familial dysbetalipoproteinemia.".
- Abetalipoproteinemia diseasesdb "17".
- Abetalipoproteinemia emedicineSubject "med".
- Abetalipoproteinemia emedicineTopic "1117".
- Abetalipoproteinemia icd10 "E78.6".
- Abetalipoproteinemia icd9 "272.5".
- Abetalipoproteinemia medlineplus "001666".
- Abetalipoproteinemia meshId "D000012".
- Abetalipoproteinemia omim "200100".
- Abetalipoproteinemia thumbnail Abetalipoproteinemia_-_very_high_mag.jpg?width=300.
- Abetalipoproteinemia wikiPageExternalLink bassen-kornzweig-syndrome-info.html.
- Abetalipoproteinemia wikiPageID "68451".
- Abetalipoproteinemia wikiPageRevisionID "605889430".
- Abetalipoproteinemia caption "Micrograph showing enterocytes with a clear cytoplasm characteristic of abetalipoproteinemia. Duodenal biopsy. H&E stain.".
- Abetalipoproteinemia diseasesdb "17".
- Abetalipoproteinemia emedicinesubj "med".
- Abetalipoproteinemia emedicinetopic "1117".
- Abetalipoproteinemia hasPhotoCollection Abetalipoproteinemia.
- Abetalipoproteinemia icd "272.5".
- Abetalipoproteinemia icd "E78.6".
- Abetalipoproteinemia medlineplus "1666".
- Abetalipoproteinemia meshid "D000012".
- Abetalipoproteinemia name "Abetalipoproteinemia".
- Abetalipoproteinemia omim "200100".
- Abetalipoproteinemia width "175".
- Abetalipoproteinemia wordnet_type synset-disease-noun-1.
- Abetalipoproteinemia subject Category:Autosomal_recessive_disorders.
- Abetalipoproteinemia subject Category:Lipid_metabolism_disorders.
- Abetalipoproteinemia subject Category:Rare_diseases.
- Abetalipoproteinemia type Disease.
- Abetalipoproteinemia type AilmentCondition.
- Abetalipoproteinemia type Situation.
- Abetalipoproteinemia comment "Abetalipoproteinemia, or Bassen-Kornzweig syndrome, is a rare autosomal recessive disorder that interferes with the normal absorption of fat and fat-soluble vitamins from food. It is caused by a mutation in microsomal triglyceride transfer protein resulting in deficiencies in the apolipoproteins B-48 and B-100, which are used in the synthesis and exportation of chylomicrons and VLDL respectively. It is not to be confused with familial dysbetalipoproteinemia.".
- Abetalipoproteinemia label "A-beta-lipoprotéinémie".
- Abetalipoproteinemia label "Abetalipoproteinemia".
- Abetalipoproteinemia label "Abetalipoproteinemia".
- Abetalipoproteinemia label "Abetalipoproteinemia".
- Abetalipoproteinemia label "Abetalipoproteinemia".
- Abetalipoproteinemia label "Abetalipoproteinämie".
- Abetalipoproteinemia label "Síndrome de Bassen-Kornzweig".
- Abetalipoproteinemia sameAs Abetalipoproteinämie.
- Abetalipoproteinemia sameAs Abetalipoproteinemia.
- Abetalipoproteinemia sameAs A-beta-lipoprotéinémie.
- Abetalipoproteinemia sameAs Abetalipoproteinemia.
- Abetalipoproteinemia sameAs Abetalipoproteinemia.
- Abetalipoproteinemia sameAs Síndrome_de_Bassen-Kornzweig.
- Abetalipoproteinemia sameAs m.0hw_d.
- Abetalipoproteinemia sameAs Q319812.
- Abetalipoproteinemia sameAs Q319812.
- Abetalipoproteinemia sameAs 13.
- Abetalipoproteinemia sameAs 1300.
- Abetalipoproteinemia wasDerivedFrom Abetalipoproteinemia?oldid=605889430.
- Abetalipoproteinemia depiction Abetalipoproteinemia_-_very_high_mag.jpg.
- Abetalipoproteinemia isPrimaryTopicOf Abetalipoproteinemia.
- Abetalipoproteinemia name "Abetalipoproteinemia".
