abetalipoproteinemia

Summary

abetalipoproteinemia is a developmental defect during embryogenesis^[1]. abetalipoproteinemia draws 254 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #41 of 308).^[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's subclass of is recorded as hypolipoproteinemia^[9].
• abetalipoproteinemia's subclass of is recorded as autosomal recessive metabolic cerebellar ataxia^[10].
• abetalipoproteinemia's subclass of is recorded as metabolic disease with dementia^[11].
• abetalipoproteinemia's subclass of is recorded as metabolic disease with intestinal involvement^[12].
• abetalipoproteinemia's subclass of is recorded as hypobetalipoproteinemia^[13].
• abetalipoproteinemia's subclass of is recorded as neurometabolic disease^[14].
• abetalipoproteinemia's subclass of is recorded as developmental anomaly of metabolic origin^[15].
• abetalipoproteinemia's subclass of is recorded as syndromic dyslipidemia^[16].
• abetalipoproteinemia's subclass of is recorded as constitutional hemolytic anemia due to acanthocytosis^[17].
• abetalipoproteinemia's subclass of is recorded as rare hereditary metabolic disease with peripheral neuropathy^[18].
• abetalipoproteinemia's subclass of is recorded as metabolic disease with pigmentary retinitis^[19].
• abetalipoproteinemia's subclass of is recorded as intestinal disease due to fat malabsorption^[20].
• abetalipoproteinemia's subclass of is recorded as genetic disease^[21].
• abetalipoproteinemia's subclass of is recorded as autosomal recessive disease^[22].
• abetalipoproteinemia's subclass of is recorded as disease^[23].
• abetalipoproteinemia's Commons category is recorded as Abetalipoproteinemia^[24].
• abetalipoproteinemia's MeSH descriptor ID is recorded as D000012^[25].
• abetalipoproteinemia's OMIM ID is recorded as 200100^[26].
• abetalipoproteinemia's ICD-9 ID is recorded as 272.5^[27].

Why It Matters

abetalipoproteinemia draws 254 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #41 of 308).^[2] abetalipoproteinemia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.^[28] abetalipoproteinemia is known by 31 alternative names across languages and contexts.^[29]