Category:Abetalipoproteinemia

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<nowiki>abetalipoproteinemia; A-bêta-lipoprotéinémie; Abetalipoproteinemija; Abetalipoproteinämie; síndrome de bassen-kornzweig; 無β脂蛋白血症; Abetalipoproteinemija; Abetalipoproteinemi; 無β・リポタンパク血症; abetalipoproteinemia; Abetalipoproteinemia; אבטאליפופרוטאינמיה; Abetalipoproteinemia; 無β脂蛋白血癥; 無β脂蛋白血症; Abetalipoproteinemia; Abetalipoproteinemia; abetalipoproteinemia; فقد البروتين الشحمي بيتا من الدم; 無β脂蛋白血症; Бассен-Корнзвейг синдромы; rara malattia metabolica ereditaria, a trasmissione autosomica recessiva, causata dal deficit di una proteina; doença humana; хвороба людини; Krankheit; مرض يصيب الإنسان; Human disease; մարդու հիվանդություն; síndrome humana; homa malsano; Síndrome de Bassen Kornzweig; Carencia de Lipoproteína; Síndrome de Lipoproteína Beta de Baja Densidad; Carencia de lipoproteína; Sindrome de Lipoproteina Beta de Baja Densidad; Carencia de lipoproteina; Carencia de Lipoproteina; Sindrome de Bassen Kornzweig; Sindrome de Lipoproteína Beta de Baja Densidad; Bassen-Kornzweig-Syndrom; Akanthozytose; A beta lipoprotéinémie; A-beta-lipoproteinemie; Syndrome de Bassen et Kornzweig; Syndrome de Bassen-Kornzweig; Síndrome de bassen-kornzweig; familial hypobetalipoproteinemia; microsomal triglyceride transfer protein deficiency disease; Bassen-Kornzweig Syndrome; Microsomal Triglyceride Transfer Protein Deficiency; Bassen-Kornzweig disease; Homozygous familial hypobetalipoproteinemia; Mtp Deficiency; ABETALIPOPROTEINEMIA; ABL; ABETALIPOPROTEINEMIA; ABL; Acanthocytosis; sindromo de Bassen-Kornzweig; Abetalipoprotenemia; Zespół Bassena-Kornzweiga; Zespół Bassena i Kornzweiga</nowiki>
abetalipoproteinemia 
Human disease
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Subclass of
  • hypolipoproteinemia
  • autosomal recessive metabolic cerebellar ataxia
  • metabolic disease with dementia
  • metabolic disease with intestinal involvement
  • hypobetalipoproteinemia
  • neurometabolic disease
  • developmental anomaly of metabolic origin
  • syndromic dyslipidemia
  • constitutional hemolytic anemia due to acanthocytosis
  • rare hereditary metabolic disease with peripheral neuropathy
  • metabolic disease with pigmentary retinitis
  • intestinal disease due to fat malabsorption
  • genetic disease
  • autosomal recessive disease
  • disease
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