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This Concept Map, created with IHMC CmapTools, has information related to: Tangiers Disease, high cellular cholesterol in tonsils leads to enlarged tonsils, high cellular cholesterol in tonsils leads to yellow orange tonsiliar plaques, Tangier Disease can manifest as Heterozygous ABCA1 mutation, Tangier Disease can present as Thrombocytopenia, Tangier Disease can present as Hepatomegaly, Tangier Disease can present as enlarged tonsils, Tangier Disease can manifest as Homozygous ABCA1 mutation, Tangier Disease is biochemically inherited as autosomal codominant trait, loss of ABCA1 activity prevents production of nascent HDL, Tangier Disease is clinically inherited as autosomal recessive trait, Tangier Disease is diagnosed according to family history, Tangier Disease can present as peripheral neuropathy, VLDL has TAG, Tangier Disease can present as Lymphadenopathy, Tangier Disease can present as Splenomegaly, Tangier Disease is diagnosed according to clinical signs and symptoms, Tangier Disease is diagnosed according to sequencing ABCA1 gene, Apo C-II located on nascent HDL