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Biological Sciences and Healthcare, part 4

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... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of lipoprotein AND/OR lipid metabolism > Disorder of lipoprotein storage and metabolism > Hyperlipidemia > Hypercholesterolemia > Primary hypercholesterolemia > Familial hypercholesterolemia (disorder) > Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations
... > Increased lipid > Hyperlipidemia > Hypercholesterolemia > Primary hypercholesterolemia > Familial hypercholesterolemia (disorder) > Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations
... > Serum cholesterol abnormal > Serum cholesterol raised > Hypercholesterolemia > Primary hypercholesterolemia > Familial hypercholesterolemia (disorder) > Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of lipoprotein AND/OR lipid metabolism > Disorder of lipoprotein storage and metabolism > Low density lipoprotein receptor mutation (disorder) > Low density lipoprotein receptor adaptor protein 1 mutation > Combined heterozygous low density lipoprotein receptor co-occurrent with low density lipoprotein receptor adaptor protein 1 mutations > Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations

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Familial hypercholesterolaemia co-occurrent and due to combined heterozygous low density lipoprotein receptor and low density lipoprotein receptor adaptor protein 1 mutations  

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http://www.irandoc.acir/onto/irandoc/767133009

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