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
Press Enter · cited answer in seconds
0 sources
abetalipoproteinemia
Summary
abetalipoproteinemia is a developmental defect during embryogenesis[1]. abetalipoproteinemia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- abetalipoproteinemia's instance of is recorded as developmental defect during embryogenesis[3].
- abetalipoproteinemia's instance of is recorded as designated intractable/rare disease[4].
- abetalipoproteinemia's instance of is recorded as rare disease[5].
- abetalipoproteinemia's instance of is recorded as class of disease[6].
- abetalipoproteinemia's instance of is recorded as symptom or sign[7].
- abetalipoproteinemia's instance of is recorded as genetic disease[8].
- abetalipoproteinemia is a type of hypolipoproteinemia[9].
- abetalipoproteinemia is a type of autosomal recessive metabolic cerebellar ataxia[10].
- abetalipoproteinemia is a type of metabolic disease with dementia[11].
- abetalipoproteinemia is a type of metabolic disease with intestinal involvement[12].
- abetalipoproteinemia is a type of hypobetalipoproteinemia[13].
- abetalipoproteinemia is a type of neurometabolic disease[14].
- abetalipoproteinemia is a type of developmental anomaly of metabolic origin[15].
- abetalipoproteinemia is a type of syndromic dyslipidemia[16].
- abetalipoproteinemia is a type of constitutional hemolytic anemia due to acanthocytosis[17].
- abetalipoproteinemia is a type of rare hereditary metabolic disease with peripheral neuropathy[18].
- abetalipoproteinemia is a type of metabolic disease with pigmentary retinitis[19].
- abetalipoproteinemia is a type of intestinal disease due to fat malabsorption[20].
- abetalipoproteinemia is a type of genetic disease[21].
- abetalipoproteinemia is a type of autosomal recessive disease[22].
- abetalipoproteinemia is a type of disease[23].
- abetalipoproteinemia's Commons category is recorded as Abetalipoproteinemia[24].
- abetalipoproteinemia's ICPC 2 ID is recorded as T93[25].
- abetalipoproteinemia's described at URL is recorded as https://www.ncbi.nlm.nih.gov/books/NBK513355/[26].
- abetalipoproteinemia's described at URL is recorded as https://medlineplus.gov/genetics/condition/abetalipoproteinemia/[27].
Why It Matters
abetalipoproteinemia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] abetalipoproteinemia is known by 31 alternative names across languages and contexts.[28]