Disease Index
9,486 diseasesdisorder of folate metabolism and transport
human disease
disorder of fructose metabolism
human disease
disorder of fucoglycosan synthesis
human disease
disorder of galactose metabolism
human disease
disorder of glutamine metabolism
human disease
disorder of glycolysis
human disease
disorder of glyoxylate metabolism
human disease
disorder of ketone body transport
human disease
disorder of lipid absorption and transport
human disease
disorder of lysine and hydroxylysine metabolism
human disease
disorder of lysosomal-related organelles
human disease
disorder of magnesium metabolism
human disease
ICD: E83.4
disorder of medulla oblongata
human disease
disorder of melanin metabolism
human disease
disorder of metabolite absorption and transport
human disease
disorder of multiple glycosylation
human disease
disorder of neutral amino acid transport
acquired metabolic disease that is has its basis in the disruption of neutral amino acid transport
disorder of O-mannosylglycan synthesis
human disease
disorder of O-N-acetylgalactosaminylglycan synthesis
human disease
disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis
human disease
disorder of O-xylosylglycan synthesis
human disease
disorder of ornithine metabolism
human disease
disorder of other vitamins and cofactors metabolism and transport
human disease
disorder of peroxisomal alpha-, beta- and omega-oxidation
human disease
disorder of phenylalanine metabolism
human disease
disorder of phospholipids, sphingolipids and fatty acids biosynthesis
human disease
disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement
human disease
disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement
human disease
disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement
human disease
disorder of plasmalogens biosynthesis
human disease