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bn:00000292n
Noun Concept
Categories: Lipid metabolism disorders, Syndromes, Rare diseases, All articles needing additional references, Autosomal recessive disorders
EN
abetalipoproteinemia  abetalipoproteinaemia  ABETALIPOPROTEINEMIA; ABL  Abetalipoproteinemia neuropathy  ABL
EN
A rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels WordNet 3.0
Definitions
Relations
Sources
EN
A rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels WordNet 3.0 & Open English WordNet
Abetalipoproteinemia is a disorder characterized by abnormal absorption of fat and fat-soluble vitamins from food. Wikipedia
A rare genetic disorder Wikipedia Disambiguation
Human disease Wikidata
A rare autosomal recessive disorder that interferes with the normal absorption of fat and fat-soluble vitamins from food. Wiktionary
Rare disorder. Wiktionary (translation)
IS A
genetic disease
hypobetalipoproteinemia
lipidosis
rare disease
hypolipoproteinemia
+2 relations
GENETIC ASSOCIATION
microsomal triglyceride transfer protein
HEALTH SPECIALTY
endocrinology
WordNet 3.0 & Open English WordNet
EN
abetalipoproteinemia
Wikipedia
EN
abetalipoproteinemia
Wikidata
EN
abetalipoproteinemia
Wiktionary
EN
abetalipoproteinemia
Wikipedia Redirections
EN
abetalipoproteinaemia, Abetalipoproteinemia neuropathy, Bassen-Kornzweig syndrome, Bassen–Kornzweig syndrome, Betalipoprotein Deficiency Disease, Congenital betalipoprotein deficiency syndrome, Familial hypobetalipoproteinemia, microsomal triglyceride transfer protein deficiency disease
Wikidata Alias
EN
ABETALIPOPROTEINEMIA, ABETALIPOPROTEINEMIA; ABL, ABL, Acanthocytosis, Bassen-Kornzweig disease, Bassen-Kornzweig Syndrome, familial hypobetalipoproteinemia, Homozygous familial hypobetalipoproteinemia, Microsomal Triglyceride Transfer Protein Deficiency, microsomal triglyceride transfer protein deficiency disease, Mtp Deficiency

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