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Entry	Name	Description	Category	Pathway	Gene
H00845	Familial amyloidosis	The amyloidoses are a group of diseases in which proteins that are normally soluble deposit extracellularly in tissues as insoluble fibrils. The fibrils have a characteristic beta-pleated sheet configuration ...	Nervous system disease		TTR [HSA:7276] [KO:K20731] FGA [HSA:2243] [KO:K03903] APOA1 [HSA:335] [KO:K08757] LYZ [HSA:4069] [KO:K13915] B2M [HSA:567] [KO:K08055]
H00930	Hypoalphalipoproteinemia	... One form is associated with abnormal cellular cholesterol efflux caused by heterozygous mutations at the ABCA1 gene. Other forms are primary hypoalphalipoproteinemia caused by mutations of APOA1 gene.	Inherited metabolic disorder		ABCA1 [HSA:19] [KO:K05641] APOA1 [HSA:335] [KO:K08757]
H02505	Atherosclerosis	Atherosclerosis is a chronic inflammatory disease marked by a narrowing of the arteries from lipid-rich plaques present within the walls of arterial blood vessels. It represents the root cause of the majority ...	Cardiovascular disease	hsa05417 Lipid and atherosclerosis	LDLR [HSA:3949] [KO:K12473] APOB [HSA:338] [KO:K14462] PCSK9 [HSA:255738] [KO:K13050] LDLRAP1 [HSA:26119] [KO:K12474] ABCG5 [HSA:64240] [KO:K05683] ABCG8 [HSA:64241] [KO:K05684] LCAT [HSA:3931] [KO:K00650] ABCA1 [HSA:19] [KO:K05641] APOA1 [HSA:335] [KO:K08757] MEF2A [HSA:4205] [KO:K09260] LRP6 [HSA:4040] [KO:K03068]

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