abetalipoproteinemia
rare genetic disease involving failure of synthesis or assembly of plasma lipoproteins that contain apo-protein B (chylomicrons, VLDL, and LDL); characterized by severe vitamin E deficiency, leading to serious neurological damage
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abetalipoproteinemia
Summary
abetalipoproteinemia is a designated intractable/rare disease[1]. abetalipoproteinemia draws 134 Wikipedia views per month (designated_intractable_rare_disease category, ranking #41 of 201).[2]
Key Facts
- abetalipoproteinemia's instance of is recorded as designated intractable/rare disease[3].
- abetalipoproteinemia's instance of is recorded as rare disease[4].
- abetalipoproteinemia's instance of is recorded as class of disease[5].
- abetalipoproteinemia's instance of is recorded as symptom or sign[6].
- abetalipoproteinemia is a type of hypolipoproteinemia[7].
- abetalipoproteinemia is a type of autosomal recessive metabolic cerebellar ataxia[8].
- abetalipoproteinemia is a type of metabolic disease with dementia[9].
- abetalipoproteinemia is a type of metabolic disease with intestinal involvement[10].
- abetalipoproteinemia is a type of hypobetalipoproteinemia[11].
- abetalipoproteinemia is a type of neurometabolic disease[12].
- abetalipoproteinemia is a type of developmental anomaly of metabolic origin[13].
- abetalipoproteinemia is a type of syndromic dyslipidemia[14].
- abetalipoproteinemia is a type of constitutional hemolytic anemia due to acanthocytosis[15].
- abetalipoproteinemia is a type of rare hereditary metabolic disease with peripheral neuropathy[16].
- abetalipoproteinemia is a type of metabolic disease with pigmentary retinitis[17].
- abetalipoproteinemia is a type of intestinal disease due to fat malabsorption[18].
- abetalipoproteinemia is a type of genetic disease[19].
- abetalipoproteinemia is a type of autosomal recessive disease[20].
- abetalipoproteinemia is a type of developmental defect during embryogenesis[21].
- abetalipoproteinemia is a type of genetic disease[22].
- abetalipoproteinemia's Commons category is recorded as Abetalipoproteinemia[23].
- abetalipoproteinemia's ICPC 2 ID is recorded as T93[24].
- abetalipoproteinemia's described at URL is recorded as https://www.ncbi.nlm.nih.gov/books/NBK513355/[25].
- abetalipoproteinemia's described at URL is recorded as https://medlineplus.gov/genetics/condition/abetalipoproteinemia/[26].
- abetalipoproteinemia's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4573[27].
Why It Matters
abetalipoproteinemia draws 134 Wikipedia views per month (designated_intractable_rare_disease category, ranking #41 of 201).[2] abetalipoproteinemia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] abetalipoproteinemia is known by 41 alternative names across languages and contexts.[29]