≈ 193 relations sortantes
- en:inborn error of lipoprotein metabolism --
r_associated #0: 43 / 1 ->
en:carbohydrate metabolism, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:carbohydrate metabolism, inborn errors | rel=r_associated | relid=0 | w=43
- en:inborn error of lipoprotein metabolism --
r_associated #0: 41 / 0.953 ->
en:inborn errors of porphyrin metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn errors of porphyrin metabolism | rel=r_associated | relid=0 | w=41
- en:inborn error of lipoprotein metabolism --
r_associated #0: 40 / 0.93 ->
en:inborn lipid/lipoprotein disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn lipid/lipoprotein disorder | rel=r_associated | relid=0 | w=40
- en:inborn error of lipoprotein metabolism --
r_associated #0: 39 / 0.907 ->
en:ehlers-danlos syndrome, arthrochalasia type
n1=en:inborn error of lipoprotein metabolism | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=39
- en:inborn error of lipoprotein metabolism --
r_associated #0: 39 / 0.907 ->
en:neuronal ceroid lipofuscinosis
n1=en:inborn error of lipoprotein metabolism | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=39
- en:inborn error of lipoprotein metabolism --
r_associated #0: 37 / 0.86 ->
en:inborn errors of steroid synthesis
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn errors of steroid synthesis | rel=r_associated | relid=0 | w=37
- en:inborn error of lipoprotein metabolism --
r_associated #0: 36 / 0.837 ->
en:dyslipidemia
n1=en:inborn error of lipoprotein metabolism | n2=en:dyslipidemia | rel=r_associated | relid=0 | w=36
- en:inborn error of lipoprotein metabolism --
r_associated #0: 36 / 0.837 ->
en:wolman disease
n1=en:inborn error of lipoprotein metabolism | n2=en:wolman disease | rel=r_associated | relid=0 | w=36
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:gamma-glutamyltransferase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:hereditary hyperbilirubinemia
n1=en:inborn error of lipoprotein metabolism | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:lysosomal storage disease
n1=en:inborn error of lipoprotein metabolism | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:methionine adenosyltransferase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:methylmalonic acidemia
n1=en:inborn error of lipoprotein metabolism | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 35 / 0.814 ->
en:pancreatic colipase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:pancreatic colipase deficiency | rel=r_associated | relid=0 | w=35
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:amino acid transport disorders, inborn
n1=en:inborn error of lipoprotein metabolism | n2=en:amino acid transport disorders, inborn | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:aminomethyltransferase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:arakawa syndrome ii
n1=en:inborn error of lipoprotein metabolism | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:congenital
n1=en:inborn error of lipoprotein metabolism | n2=en:congenital | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:disorder of glycoprotein metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of glycoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:disorder of glycosaminoglycan metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of glycosaminoglycan metabolism | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:fructose-1,6-bisphosphatase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:hyperprolinemia type 1
n1=en:inborn error of lipoprotein metabolism | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:metal metabolism, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:metal metabolism, inborn errors | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:organic acid metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:organic acid metabolism disorder | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:ornithine carbamoyltransferase deficiency disease
n1=en:inborn error of lipoprotein metabolism | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:peroxisomal disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:peroxisomal disorder | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:pyridoxine dependency syndrome
n1=en:inborn error of lipoprotein metabolism | n2=en:pyridoxine dependency syndrome | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:renal tubular transport, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:renal tubular transport, inborn errors | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 34 / 0.791 ->
en:urea cycle metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=34
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:17-beta-hydroxysteroid dehydrogenase 3 deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:5-oxoprolinase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:adrenal gland hyperplasia ii
n1=en:inborn error of lipoprotein metabolism | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:alpha, alpha-trehalase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:biotinidase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:congenital adrenal hyperplasia
n1=en:inborn error of lipoprotein metabolism | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:congenital sucrase-isomaltase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:hereditary fructose intolerance
n1=en:inborn error of lipoprotein metabolism | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:hereditary orotic aciduria
n1=en:inborn error of lipoprotein metabolism | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:holocarboxylase synthetase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:inborn error of glutathione metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn error of glutathione metabolism | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:inborn immunodeficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn immunodeficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:inherited metabolic disorder of nervous system
n1=en:inborn error of lipoprotein metabolism | n2=en:inherited metabolic disorder of nervous system | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:placental steroid sulfatase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 32 / 0.744 ->
en:severe steroid 21-hydroxylase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=32
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:aldosterone synthase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:aldosterone synthase deficiency | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:amino acid/carbohydrate metabolic disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:amino acid/carbohydrate metabolic disorder | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:brain diseases, metabolic, inborn
n1=en:inborn error of lipoprotein metabolism | n2=en:brain diseases, metabolic, inborn | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:glucose-6-phosphate dehydrogenase deficiency anemia
n1=en:inborn error of lipoprotein metabolism | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:hmg-coa lyase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:hnsha due to hexokinase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:hnsha due to hexokinase deficiency | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:hnsha due to nadh diaphorase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:hnsha due to nadh diaphorase deficiency | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:hypophosphatasia
n1=en:inborn error of lipoprotein metabolism | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:inborn errors of bilirubin metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn errors of bilirubin metabolism | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:intermediary metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:intermediary metabolism disorder | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:myoglobinuria, recurrent
n1=en:inborn error of lipoprotein metabolism | n2=en:myoglobinuria, recurrent | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:primary hyperoxaluria
n1=en:inborn error of lipoprotein metabolism | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:progeria
n1=en:inborn error of lipoprotein metabolism | n2=en:progeria | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:purine-pyrimidine metabolism, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:purine-pyrimidine metabolism, inborn errors | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 31 / 0.721 ->
en:sarcosinemia
n1=en:inborn error of lipoprotein metabolism | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=31
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:acetyl-coa: carboxylase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:acetyl-coa: carboxylase deficiency | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:classical phenylketonuria
n1=en:inborn error of lipoprotein metabolism | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:cystathionine beta-synthase deficiency disease
n1=en:inborn error of lipoprotein metabolism | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:cytochrome-c oxidase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:disorder of creatine synthesis
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of creatine synthesis | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:familial amyloidosis
n1=en:inborn error of lipoprotein metabolism | n2=en:familial amyloidosis | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:fatty acid metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:fatty acid metabolism disorder | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:glutamate-cysteine ligase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:histidinemia
n1=en:inborn error of lipoprotein metabolism | n2=en:histidinemia | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:hyperlipoproteinemia type i
n1=en:inborn error of lipoprotein metabolism | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:inherited disorder of bilirubin metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inherited disorder of bilirubin metabolism | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:phosphoglycerate kinase 1 deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:propionic acidemia
n1=en:inborn error of lipoprotein metabolism | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 30 / 0.698 ->
en:storage disease
n1=en:inborn error of lipoprotein metabolism | n2=en:storage disease | rel=r_associated | relid=0 | w=30
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:5 alpha steroid reductase 2 deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:albinism
n1=en:inborn error of lipoprotein metabolism | n2=en:albinism | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:carbamoyl-phosphate synthetase i deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:disorder of lipoprotein storage and metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of lipoprotein storage and metabolism | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:enterokinase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:glycine dehydrogenase (decarboxylating) deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:inborn biological transport disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn biological transport disorder | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:inherited disorder of thyroid metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inherited disorder of thyroid metabolism | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:phenylketonuria ii
n1=en:inborn error of lipoprotein metabolism | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:steroid metabolism, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:steroid metabolism, inborn errors | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 29 / 0.674 ->
en:tyrosinemia type ii
n1=en:inborn error of lipoprotein metabolism | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=29
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:17 alpha-hydroxyprogesterone aldolase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:17 alpha-hydroxyprogesterone aldolase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:alpha-1 antitrypsin deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:amino acid metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:amino acid metabolism disorder | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:argininosuccinic aciduria
n1=en:inborn error of lipoprotein metabolism | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:defect in post-translational modification of lysosomal enzymes
n1=en:inborn error of lipoprotein metabolism | n2=en:defect in post-translational modification of lysosomal enzymes | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:galactosemia
n1=en:inborn error of lipoprotein metabolism | n2=en:galactosemia | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:gaucher disease
n1=en:inborn error of lipoprotein metabolism | n2=en:gaucher disease | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:hypolipoproteinemias
n1=en:inborn error of lipoprotein metabolism | n2=en:hypolipoproteinemias | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:lipid metabolism disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:lipid metabolism disorder | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:lipid metabolism, inborn errors
n1=en:inborn error of lipoprotein metabolism | n2=en:lipid metabolism, inborn errors | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:methylcrotonyl-coa carboxylase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:moderate steroid 21-hydroxylase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:pancreatic trypsinogen deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:pancreatic trypsinogen deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:pentosuria
n1=en:inborn error of lipoprotein metabolism | n2=en:pentosuria | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:porphobilinogen synthase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:pyruvate dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:pyruvate kinase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:pyruvate kinase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:succinic semialdehyde dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:urocanase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 28 / 0.651 ->
en:valinemia
n1=en:inborn error of lipoprotein metabolism | n2=en:valinemia | rel=r_associated | relid=0 | w=28
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:dihydropyrimidine dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:erythropoietic protoporphyria
n1=en:inborn error of lipoprotein metabolism | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:ethanolaminosis
n1=en:inborn error of lipoprotein metabolism | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:fat overload syndrome
n1=en:inborn error of lipoprotein metabolism | n2=en:fat overload syndrome | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:folinic acid responsive seizure syndrome
n1=en:inborn error of lipoprotein metabolism | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:inherited disorder of folate metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:inherited disorder of folate metabolism | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:isovaleric acidemia
n1=en:inborn error of lipoprotein metabolism | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:lecithin acyltransferase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:methylmalonyl-coenzyme a mutase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:multiple acyl-coa dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 27 / 0.628 ->
en:vrozené poruchy metabolismu nec in mdrcze18_1
n1=en:inborn error of lipoprotein metabolism | n2=en:vrozené poruchy metabolismu nec in mdrcze18_1 | rel=r_associated | relid=0 | w=27
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:2-hydroxyglutaric aciduria
n1=en:inborn error of lipoprotein metabolism | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:disorder of lipid storage and metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of lipid storage and metabolism | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:disorder of pyruvate metabolism and mitochondrial respiratory chain
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:disorder of sialic acid metabolism
n1=en:inborn error of lipoprotein metabolism | n2=en:disorder of sialic acid metabolism | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:familial renal iminoglycinuria
n1=en:inborn error of lipoprotein metabolism | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:glucose-6-phosphate dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:glutathione synthetase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:glycogen storage disease
n1=en:inborn error of lipoprotein metabolism | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:glycogen storage disease type x
n1=en:inborn error of lipoprotein metabolism | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:hereditary methemoglobinemia, enzymatic type
n1=en:inborn error of lipoprotein metabolism | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:inborn errors of carbohydrate metabolism (excl glucose)
n1=en:inborn error of lipoprotein metabolism | n2=en:inborn errors of carbohydrate metabolism (excl glucose) | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:lipofuscinosis
n1=en:inborn error of lipoprotein metabolism | n2=en:lipofuscinosis | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:lipoid congenital adrenal hyperplasia
n1=en:inborn error of lipoprotein metabolism | n2=en:lipoid congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:maple syrup urine disease
n1=en:inborn error of lipoprotein metabolism | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:n-acetylglutamate synthase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:premature aging syndrome
n1=en:inborn error of lipoprotein metabolism | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:prolidase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:pseudohypoparathyroidism
n1=en:inborn error of lipoprotein metabolism | n2=en:pseudohypoparathyroidism | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:sulfite oxidase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
en:unclassified metabolic disorder
n1=en:inborn error of lipoprotein metabolism | n2=en:unclassified metabolic disorder | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 26 / 0.605 ->
erreur innée du métabolisme des lipoprotéines
n1=en:inborn error of lipoprotein metabolism | n2=erreur innée du métabolisme des lipoprotéines | rel=r_associated | relid=0 | w=26
- en:inborn error of lipoprotein metabolism --
r_associated #0: 25 / 0.581 ->
protéine
n1=en:inborn error of lipoprotein metabolism | n2=protéine | rel=r_associated | relid=0 | w=25
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
albinisme
n1=en:inborn error of lipoprotein metabolism | n2=albinisme | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception
n1=en:inborn error of lipoprotein metabolism | n2=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
cétoacidurie à chaînes ramifiées
n1=en:inborn error of lipoprotein metabolism | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
congénital
n1=en:inborn error of lipoprotein metabolism | n2=congénital | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
congenital
n1=en:inborn error of lipoprotein metabolism | n2=congenital | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
congénitale
n1=en:inborn error of lipoprotein metabolism | n2=congénitale | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en biotinidase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en céto-acide décarboxylase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en cytochrome oxydase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en cytochrome-c oxydase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en prolidase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
déficit en semialdéhyde succinique-déshydrogénase
n1=en:inborn error of lipoprotein metabolism | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:bisphosphoglycerate mutase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:bisphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:branched-chain ketoaciduria
n1=en:inborn error of lipoprotein metabolism | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:classical maple syrup urine disease
n1=en:inborn error of lipoprotein metabolism | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:erythrocyte enolase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:erythrocyte enolase deficiency | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:hexose-6-phosphate dehydrogenase deficiency
n1=en:inborn error of lipoprotein metabolism | n2=en:hexose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:histidinaemia
n1=en:inborn error of lipoprotein metabolism | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:hyperlipoproteinemia type I
n1=en:inborn error of lipoprotein metabolism | n2=en:hyperlipoproteinemia type I | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:leucinosis
n1=en:inborn error of lipoprotein metabolism | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:maple-tree syrup disease
n1=en:inborn error of lipoprotein metabolism | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:thiamin-responsive maple syrup urine disease
n1=en:inborn error of lipoprotein metabolism | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:wolman's disease
n1=en:inborn error of lipoprotein metabolism | n2=en:wolman's disease | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
en:Wolman's disease
n1=en:inborn error of lipoprotein metabolism | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
glycogénose
n1=en:inborn error of lipoprotein metabolism | n2=glycogénose | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
histidinémie
n1=en:inborn error of lipoprotein metabolism | n2=histidinémie | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
hyperoxalurie primaire
n1=en:inborn error of lipoprotein metabolism | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
hyperoxalurie primitive
n1=en:inborn error of lipoprotein metabolism | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
hyperplasie congénitale des surrénales
n1=en:inborn error of lipoprotein metabolism | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
intolérance au fructose
n1=en:inborn error of lipoprotein metabolism | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
leucinose
n1=en:inborn error of lipoprotein metabolism | n2=leucinose | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
lipofuscinose
n1=en:inborn error of lipoprotein metabolism | n2=lipofuscinose | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
lipofuscinose neuronale céroïde
n1=en:inborn error of lipoprotein metabolism | n2=lipofuscinose neuronale céroïde | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
lipofuscinose neuronale céroïde infantile finlandaise
n1=en:inborn error of lipoprotein metabolism | n2=lipofuscinose neuronale céroïde infantile finlandaise | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie de Wolman
n1=en:inborn error of lipoprotein metabolism | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie de wolman
n1=en:inborn error of lipoprotein metabolism | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
Maladie de Wolman
n1=en:inborn error of lipoprotein metabolism | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie des urines à l'odeur de sirop d'érable
n1=en:inborn error of lipoprotein metabolism | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie des urines avec odeur de sirop erable
n1=en:inborn error of lipoprotein metabolism | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie du sirop d'érable
n1=en:inborn error of lipoprotein metabolism | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
maladie lysosomique de surcharge
n1=en:inborn error of lipoprotein metabolism | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
nystagmus congénital isolé
n1=en:inborn error of lipoprotein metabolism | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
oxalose
n1=en:inborn error of lipoprotein metabolism | n2=oxalose | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
oxalose primitive
n1=en:inborn error of lipoprotein metabolism | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
oxaloses
n1=en:inborn error of lipoprotein metabolism | n2=oxaloses | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
progeria
n1=en:inborn error of lipoprotein metabolism | n2=progeria | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
progéria
n1=en:inborn error of lipoprotein metabolism | n2=progéria | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
protoproporphyrie érythropoïétique
n1=en:inborn error of lipoprotein metabolism | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
pseudo-hypoparathyroïdie
n1=en:inborn error of lipoprotein metabolism | n2=pseudo-hypoparathyroïdie | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
pseudo-hypoparathyroïdisme
n1=en:inborn error of lipoprotein metabolism | n2=pseudo-hypoparathyroïdisme | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
pseudohypoparathyroïdie
n1=en:inborn error of lipoprotein metabolism | n2=pseudohypoparathyroïdie | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
pseudohypoparathyroïdisme
n1=en:inborn error of lipoprotein metabolism | n2=pseudohypoparathyroïdisme | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
semialdéhyde succinique-déshydrogénase (déficit en)
n1=en:inborn error of lipoprotein metabolism | n2=semialdéhyde succinique-déshydrogénase (déficit en) | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
sirop d'érable (urine à odeur de)
n1=en:inborn error of lipoprotein metabolism | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
- en:inborn error of lipoprotein metabolism --
r_associated #0: 20 / 0.465 ->
Wolman (maladie de)
n1=en:inborn error of lipoprotein metabolism | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
| ≈ 275 relations entrantes
- en:maple syrup urine disease ---
r_associated #0: 699 -->
en:inborn error of lipoprotein metabolism
n1=en:maple syrup urine disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=699
- leucinose ---
r_associated #0: 609.18 -->
en:inborn error of lipoprotein metabolism
n1=leucinose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=609.18
- maladie du sirop d'érable ---
r_associated #0: 604.37 -->
en:inborn error of lipoprotein metabolism
n1=maladie du sirop d'érable | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=604.37
- en:branched-chain ketoaciduria ---
r_associated #0: 520 -->
en:inborn error of lipoprotein metabolism
n1=en:branched-chain ketoaciduria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=520
- en:classical maple syrup urine disease ---
r_associated #0: 280 -->
en:inborn error of lipoprotein metabolism
n1=en:classical maple syrup urine disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=280
- en:thiamin-responsive maple syrup urine disease ---
r_associated #0: 280 -->
en:inborn error of lipoprotein metabolism
n1=en:thiamin-responsive maple syrup urine disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=280
- déficit en céto-acide décarboxylase ---
r_associated #0: 275 -->
en:inborn error of lipoprotein metabolism
n1=déficit en céto-acide décarboxylase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=275
- maladie des urines à l'odeur de sirop d'érable ---
r_associated #0: 275 -->
en:inborn error of lipoprotein metabolism
n1=maladie des urines à l'odeur de sirop d'érable | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=275
- maladie des urines avec odeur de sirop erable ---
r_associated #0: 270 -->
en:inborn error of lipoprotein metabolism
n1=maladie des urines avec odeur de sirop erable | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=270
- en:wolman disease ---
r_associated #0: 158 -->
en:inborn error of lipoprotein metabolism
n1=en:wolman disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=158
- maladie de Wolman ---
r_associated #0: 156 -->
en:inborn error of lipoprotein metabolism
n1=maladie de Wolman | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=156
- hyperoxalurie primaire ---
r_associated #0: 151 -->
en:inborn error of lipoprotein metabolism
n1=hyperoxalurie primaire | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=151
- oxaloses ---
r_associated #0: 151 -->
en:inborn error of lipoprotein metabolism
n1=oxaloses | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=151
- hyperoxalurie primitive ---
r_associated #0: 150 -->
en:inborn error of lipoprotein metabolism
n1=hyperoxalurie primitive | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=150
- en:primary hyperoxaluria ---
r_associated #0: 149 -->
en:inborn error of lipoprotein metabolism
n1=en:primary hyperoxaluria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=149
- oxalose primitive ---
r_associated #0: 146 -->
en:inborn error of lipoprotein metabolism
n1=oxalose primitive | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=146
- oxalose ---
r_associated #0: 140 -->
en:inborn error of lipoprotein metabolism
n1=oxalose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=140
- déficit en cytochrome oxydase ---
r_associated #0: 103 -->
en:inborn error of lipoprotein metabolism
n1=déficit en cytochrome oxydase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=103
- en:cytochrome-c oxidase deficiency ---
r_associated #0: 103 -->
en:inborn error of lipoprotein metabolism
n1=en:cytochrome-c oxidase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=103
- déficit en cytochrome-c oxydase ---
r_associated #0: 95 -->
en:inborn error of lipoprotein metabolism
n1=déficit en cytochrome-c oxydase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=95
- progeria ---
r_associated #0: 90 -->
en:inborn error of lipoprotein metabolism
n1=progeria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=90
- en:progeria ---
r_associated #0: 86 -->
en:inborn error of lipoprotein metabolism
n1=en:progeria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=86
- progéria ---
r_associated #0: 82 -->
en:inborn error of lipoprotein metabolism
n1=progéria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=82
- albinisme ---
r_associated #0: 77 -->
en:inborn error of lipoprotein metabolism
n1=albinisme | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=77
- en:albinism ---
r_associated #0: 76 -->
en:inborn error of lipoprotein metabolism
n1=en:albinism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=76
- congénitale ---
r_associated #0: 65 -->
en:inborn error of lipoprotein metabolism
n1=congénitale | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=65
- en:congenital ---
r_associated #0: 61 -->
en:inborn error of lipoprotein metabolism
n1=en:congenital | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=61
- pseudo-hypoparathyroïdie ---
r_associated #0: 61 -->
en:inborn error of lipoprotein metabolism
n1=pseudo-hypoparathyroïdie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=61
- pseudo-hypoparathyroïdisme ---
r_associated #0: 60 -->
en:inborn error of lipoprotein metabolism
n1=pseudo-hypoparathyroïdisme | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=60
- congenital ---
r_associated #0: 58 -->
en:inborn error of lipoprotein metabolism
n1=congenital | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=58
- pseudohypoparathyroïdie ---
r_associated #0: 58 -->
en:inborn error of lipoprotein metabolism
n1=pseudohypoparathyroïdie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=58
- en:pseudohypoparathyroidism ---
r_associated #0: 56 -->
en:inborn error of lipoprotein metabolism
n1=en:pseudohypoparathyroidism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=56
- congénital ---
r_associated #0: 55 -->
en:inborn error of lipoprotein metabolism
n1=congénital | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=55
- pseudohypoparathyroïdisme ---
r_associated #0: 55 -->
en:inborn error of lipoprotein metabolism
n1=pseudohypoparathyroïdisme | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=55
- en:Wolman's disease ---
r_associated #0: 50 -->
en:inborn error of lipoprotein metabolism
n1=en:Wolman's disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=50
- sirop d'érable (urine à odeur de) ---
r_associated #0: 48 -->
en:inborn error of lipoprotein metabolism
n1=sirop d'érable (urine à odeur de) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=48
- en:hypolipoproteinemias ---
r_associated #0: 42 -->
en:inborn error of lipoprotein metabolism
n1=en:hypolipoproteinemias | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=42
- déficit en prolidase ---
r_associated #0: 41 -->
en:inborn error of lipoprotein metabolism
n1=déficit en prolidase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=41
- en:hereditary hyperbilirubinemia ---
r_associated #0: 41 -->
en:inborn error of lipoprotein metabolism
n1=en:hereditary hyperbilirubinemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=41
- maladie de wolman ---
r_associated #0: 41 -->
en:inborn error of lipoprotein metabolism
n1=maladie de wolman | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=41
- en:leucinosis ---
r_associated #0: 40 -->
en:inborn error of lipoprotein metabolism
n1=en:leucinosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=40
- déficit en semialdéhyde succinique-déshydrogénase ---
r_associated #0: 39 -->
en:inborn error of lipoprotein metabolism
n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=39
- en:maple-tree syrup disease ---
r_associated #0: 39 -->
en:inborn error of lipoprotein metabolism
n1=en:maple-tree syrup disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=39
- en:prolidase deficiency ---
r_associated #0: 39 -->
en:inborn error of lipoprotein metabolism
n1=en:prolidase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=39
- en:hereditary methemoglobinemia, enzymatic type ---
r_associated #0: 37 -->
en:inborn error of lipoprotein metabolism
n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=37
- en:lipoid congenital adrenal hyperplasia ---
r_associated #0: 37 -->
en:inborn error of lipoprotein metabolism
n1=en:lipoid congenital adrenal hyperplasia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=37
- en:succinic semialdehyde dehydrogenase deficiency ---
r_associated #0: 37 -->
en:inborn error of lipoprotein metabolism
n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=37
- lipofuscinose ---
r_associated #0: 37 -->
en:inborn error of lipoprotein metabolism
n1=lipofuscinose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=37
- en:arakawa syndrome ii ---
r_associated #0: 36 -->
en:inborn error of lipoprotein metabolism
n1=en:arakawa syndrome ii | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=36
- Wolman (maladie de) ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=Wolman (maladie de) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:argininosuccinic aciduria ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:argininosuccinic aciduria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:hereditary fructose intolerance ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:hereditary fructose intolerance | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:inborn errors of porphyrin metabolism ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn errors of porphyrin metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:lipofuscinosis ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:lipofuscinosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:purine-pyrimidine metabolism, inborn errors ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:purine-pyrimidine metabolism, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:sulfite oxidase deficiency ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:sulfite oxidase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:vrozené poruchy metabolismu nec in mdrcze18_1 ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=en:vrozené poruchy metabolismu nec in mdrcze18_1 | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- erreur innée du métabolisme des lipoprotéines ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=erreur innée du métabolisme des lipoprotéines | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- intolérance au fructose ---
r_associated #0: 35 -->
en:inborn error of lipoprotein metabolism
n1=intolérance au fructose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=35
- en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:dihydropyrimidine dehydrogenase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:hnsha due to nadh diaphorase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:hnsha due to nadh diaphorase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:holocarboxylase synthetase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:holocarboxylase synthetase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:porphobilinogen synthase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:porphobilinogen synthase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:pyruvate kinase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:pyruvate kinase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:tyrosinemia type ii ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:tyrosinemia type ii | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:unclassified metabolic disorder ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:unclassified metabolic disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:urocanase deficiency ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=en:urocanase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- lipofuscinose neuronale céroïde ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=lipofuscinose neuronale céroïde | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- nystagmus congénital isolé ---
r_associated #0: 34 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus congénital isolé | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=34
- en:neuronal ceroid lipofuscinosis ---
r_associated #0: 33 -->
en:inborn error of lipoprotein metabolism
n1=en:neuronal ceroid lipofuscinosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=33
- en:2-hydroxyglutaric aciduria ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:2-hydroxyglutaric aciduria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:disorder of pyruvate metabolism and mitochondrial respiratory chain ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of pyruvate metabolism and mitochondrial respiratory chain | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:gamma-glutamyltransferase deficiency ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:gamma-glutamyltransferase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:gaucher disease ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:gaucher disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:glucose-6-phosphate dehydrogenase deficiency anemia ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:glycogen storage disease type x ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:glycogen storage disease type x | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:inherited disorder of folate metabolism ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:inherited disorder of folate metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:inherited disorder of thyroid metabolism ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:inherited disorder of thyroid metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:intermediary metabolism disorder ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:intermediary metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:lipid metabolism disorder ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:lipid metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:methionine adenosyltransferase deficiency ---
r_associated #0: 32 -->
en:inborn error of lipoprotein metabolism
n1=en:methionine adenosyltransferase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=32
- en:amino acid transport disorders, inborn ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:amino acid transport disorders, inborn | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:hereditary orotic aciduria ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:hereditary orotic aciduria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:hmg-coa lyase deficiency ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:hmg-coa lyase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:hnsha due to hexokinase deficiency ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:hnsha due to hexokinase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:hyperprolinemia type 1 ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:hyperprolinemia type 1 | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:lipid metabolism, inborn errors ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:lipid metabolism, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- en:ornithine carbamoyltransferase deficiency disease ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- maladie lysosomique de surcharge ---
r_associated #0: 31 -->
en:inborn error of lipoprotein metabolism
n1=maladie lysosomique de surcharge | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=31
- cétoacidurie à chaînes ramifiées ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=cétoacidurie à chaînes ramifiées | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:congenital adrenal hyperplasia ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:congenital adrenal hyperplasia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:glucose-6-phosphate dehydrogenase deficiency ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:multiple acyl-coa dehydrogenase deficiency ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:premature aging syndrome ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:premature aging syndrome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:pyridoxine dependency syndrome ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:pyridoxine dependency syndrome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:sarcosinemia ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:sarcosinemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- en:wolman's disease ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=en:wolman's disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- hyperplasie congénitale des surrénales ---
r_associated #0: 30 -->
en:inborn error of lipoprotein metabolism
n1=hyperplasie congénitale des surrénales | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=30
- Maladie de Wolman ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=Maladie de Wolman | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:5 alpha steroid reductase 2 deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:5 alpha steroid reductase 2 deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:alpha, alpha-trehalase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:alpha, alpha-trehalase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:biotinidase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:biotinidase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:disorder of glycosaminoglycan metabolism ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of glycosaminoglycan metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:erythrocyte enolase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:erythrocyte enolase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:ethanolaminosis ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:ethanolaminosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:familial renal iminoglycinuria ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:familial renal iminoglycinuria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:glutathione synthetase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:glutathione synthetase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:hyperlipoproteinemia type I ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:hyperlipoproteinemia type I | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:hyperlipoproteinemia type i ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:hyperlipoproteinemia type i | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:phenylketonuria ii ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:phenylketonuria ii | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:placental steroid sulfatase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:placental steroid sulfatase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:severe steroid 21-hydroxylase deficiency ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:severe steroid 21-hydroxylase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:urea cycle metabolism disorder ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:urea cycle metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- en:valinemia ---
r_associated #0: 29 -->
en:inborn error of lipoprotein metabolism
n1=en:valinemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=29
- déficit en biotinidase ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=déficit en biotinidase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:aminomethyltransferase deficiency ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:aminomethyltransferase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:bisphosphoglycerate mutase deficiency ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:bisphosphoglycerate mutase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:brain diseases, metabolic, inborn ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:brain diseases, metabolic, inborn | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:cystathionine beta-synthase deficiency disease ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:cystathionine beta-synthase deficiency disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:enterokinase deficiency ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:enterokinase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:glutamate-cysteine ligase deficiency ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:glutamate-cysteine ligase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:isovaleric acidemia ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:isovaleric acidemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:moderate steroid 21-hydroxylase deficiency ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:myoglobinuria, recurrent ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=en:myoglobinuria, recurrent | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- lipofuscinose neuronale céroïde infantile finlandaise ---
r_associated #0: 28 -->
en:inborn error of lipoprotein metabolism
n1=lipofuscinose neuronale céroïde infantile finlandaise | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=28
- en:carbamoyl-phosphate synthetase i deficiency ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:fatty acid metabolism disorder ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:fatty acid metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:glycine dehydrogenase (decarboxylating) deficiency ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:glycogen storage disease ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:glycogen storage disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:hexose-6-phosphate dehydrogenase deficiency ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:hexose-6-phosphate dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:inborn errors of bilirubin metabolism ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn errors of bilirubin metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:lysosomal storage disease ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:lysosomal storage disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:n-acetylglutamate synthase deficiency ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:n-acetylglutamate synthase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:peroxisomal disorder ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:peroxisomal disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:pyruvate dehydrogenase deficiency ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:pyruvate dehydrogenase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- en:steroid metabolism, inborn errors ---
r_associated #0: 27 -->
en:inborn error of lipoprotein metabolism
n1=en:steroid metabolism, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=27
- albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:alpha-1 antitrypsin deficiency ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:alpha-1 antitrypsin deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:amino acid metabolism disorder ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:amino acid metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:congenital sucrase-isomaltase deficiency ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:congenital sucrase-isomaltase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:defect in post-translational modification of lysosomal enzymes ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:defect in post-translational modification of lysosomal enzymes | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:disorder of sialic acid metabolism ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of sialic acid metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:erythropoietic protoporphyria ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:erythropoietic protoporphyria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:folinic acid responsive seizure syndrome ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:folinic acid responsive seizure syndrome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:histidinaemia ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:histidinaemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:histidinemia ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:histidinemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:inborn errors of steroid synthesis ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn errors of steroid synthesis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:methylmalonyl-coenzyme a mutase deficiency ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- en:propionic acidemia ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=en:propionic acidemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- glycogénose ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=glycogénose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- histidinémie ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=histidinémie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- protoproporphyrie érythropoïétique ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=protoproporphyrie érythropoïétique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- semialdéhyde succinique-déshydrogénase (déficit en) ---
r_associated #0: 26 -->
en:inborn error of lipoprotein metabolism
n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=26
- albinisme avec pigmentation minime ---
r_associated #0: 25 -->
en:inborn error of lipoprotein metabolism
n1=albinisme avec pigmentation minime | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=25
- dyslipémie ---
r_associated #0: 25 -->
en:inborn error of lipoprotein metabolism
n1=dyslipémie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=25
- contractures congénitales et arachnodactylie ---
r_associated #0: 23 -->
en:inborn error of lipoprotein metabolism
n1=contractures congénitales et arachnodactylie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=23
- déficit en sulfite-oxydase ---
r_associated #0: 23 -->
en:inborn error of lipoprotein metabolism
n1=déficit en sulfite-oxydase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=23
- en:oxalosis ---
r_associated #0: 23 -->
en:inborn error of lipoprotein metabolism
n1=en:oxalosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=23
- en:Gaucher disease ---
r_associated #0: 22 -->
en:inborn error of lipoprotein metabolism
n1=en:Gaucher disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=22
- acidurie argininosuccinique ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=acidurie argininosuccinique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- acidémie isovalérique ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=acidémie isovalérique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- albinisme oculocutané de type mutant jaune ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=albinisme oculocutané de type mutant jaune | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- déficit enzymatique partiel de la surrénale ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=déficit enzymatique partiel de la surrénale | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- en:nystagmus ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=en:nystagmus | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- en:tyrosinemia type II ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=en:tyrosinemia type II | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- idiosyncrasie au fructose ---
r_associated #0: 21 -->
en:inborn error of lipoprotein metabolism
n1=idiosyncrasie au fructose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=21
- en:17 alpha-hydroxyprogesterone aldolase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:17 alpha-hydroxyprogesterone aldolase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:17-beta-hydroxysteroid dehydrogenase 3 deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:17-beta-hydroxysteroid dehydrogenase 3 deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:5-oxoprolinase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:5-oxoprolinase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:acetyl-coa: carboxylase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:acetyl-coa: carboxylase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:adrenal gland hyperplasia ii ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:adrenal gland hyperplasia ii | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:aldosterone synthase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:aldosterone synthase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:amino acid/carbohydrate metabolic disorder ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:amino acid/carbohydrate metabolic disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:carbohydrate metabolism, inborn errors ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:carbohydrate metabolism, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:classical phenylketonuria ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:classical phenylketonuria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:disorder of creatine synthesis ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of creatine synthesis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:disorder of glycoprotein metabolism ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of glycoprotein metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:disorder of lipid storage and metabolism ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of lipid storage and metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:disorder of lipoprotein storage and metabolism ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:disorder of lipoprotein storage and metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:dyslipidemia ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:dyslipidemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:ehlers-danlos syndrome, arthrochalasia type ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:familial amyloidosis ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:familial amyloidosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:fat overload syndrome ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:fat overload syndrome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:fructose-1,6-bisphosphatase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:galactosemia ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:galactosemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:hypophosphatasia ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:hypophosphatasia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inborn biological transport disorder ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn biological transport disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inborn error of glutathione metabolism ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn error of glutathione metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inborn errors of carbohydrate metabolism (excl glucose) ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn errors of carbohydrate metabolism (excl glucose) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inborn immunodeficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn immunodeficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inborn lipid/lipoprotein disorder ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inborn lipid/lipoprotein disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inherited disorder of bilirubin metabolism ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inherited disorder of bilirubin metabolism | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:inherited metabolic disorder of nervous system ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:inherited metabolic disorder of nervous system | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:lecithin acyltransferase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:lecithin acyltransferase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:metal metabolism, inborn errors ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:metal metabolism, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:methylcrotonyl-coa carboxylase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:methylmalonic acidemia ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:methylmalonic acidemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:organic acid metabolism disorder ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:organic acid metabolism disorder | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:pancreatic colipase deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:pancreatic colipase deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:pancreatic trypsinogen deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:pancreatic trypsinogen deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:pentosuria ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:pentosuria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:phosphoglycerate kinase 1 deficiency ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:phosphoglycerate kinase 1 deficiency | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:renal tubular transport, inborn errors ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:renal tubular transport, inborn errors | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- en:storage disease ---
r_associated #0: 20 -->
en:inborn error of lipoprotein metabolism
n1=en:storage disease | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=20
- Albert (position d') ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=Albert (position d') | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- His (faisceau de) ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=His (faisceau de) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- Hyperplasie congénitale des surrénales ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=Hyperplasie congénitale des surrénales | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- Intolérance au fructose ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=Intolérance au fructose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- hypophosphatasie ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=hypophosphatasie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- troubles héréditaires du transport tubulaire rénal ---
r_associated #0: 15 -->
en:inborn error of lipoprotein metabolism
n1=troubles héréditaires du transport tubulaire rénal | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=15
- Albinisme ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=Albinisme | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- CONGÉNITALE ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=CONGÉNITALE | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- Glycogénose ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=Glycogénose | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- Histidinémie ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=Histidinémie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- Progéria ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=Progéria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- cornée et tyrosinose de type II ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=cornée et tyrosinose de type II | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- déficit en phosphatases alcalines ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=déficit en phosphatases alcalines | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:Albert's position ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:Albert's position | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:HHH syndrome ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:HHH syndrome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:contractural arachnodactyly ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:contractural arachnodactyly | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:dyslipaemia ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:dyslipaemia | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:glycogenosis ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:glycogenosis | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:hyperornithinemia hyperammoniemia homocitrullinuria ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:infantile finnish type ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:infantile finnish type | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- en:minimal pigment type ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=en:minimal pigment type | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- glycogénique (surcharge et infiltration) ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=glycogénique (surcharge et infiltration) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- hyperlipoprotéinémie de type I ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=hyperlipoprotéinémie de type I | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- hypophosphatasies ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=hypophosphatasies | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- maladie de Gaucher ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=maladie de Gaucher | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- nystagmus ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- nystagmus héréditaire vertical ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus héréditaire vertical | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- nystagmus lié au sexe ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus lié au sexe | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- nystagmus myoclonies ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus myoclonies | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- profondeur de l'anesthésie (stade de) ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=profondeur de l'anesthésie (stade de) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- prolidase (déficit en) ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=prolidase (déficit en) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- sirtuine ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=sirtuine | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- sisi-test ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=sisi-test | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- sismothérapie ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=sismothérapie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- syndrome de Rathbun ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=syndrome de Rathbun | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- xanthomatose familiale primitive ---
r_associated #0: 10 -->
en:inborn error of lipoprotein metabolism
n1=xanthomatose familiale primitive | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=10
- albinisme avec immunodéficience et troubles hématologiques ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- albinisme avec surdité ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=albinisme avec surdité | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- faisceau de His ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=faisceau de His | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminergie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminergie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminergique ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminergique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminique ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminolibération ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminolibération | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminolytique ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminolytique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminopexie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminopexie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminurie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminurie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histaminémie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histaminémie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidase ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidinase ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidinase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidine ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidine | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidine-ammoniac-lyase ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidine-ammoniac-lyase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidine-décarboxylase ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidine-décarboxylase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- histidine-désaminase ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=histidine-désaminase | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- hyperostose vertébrale ankylosante ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=hyperostose vertébrale ankylosante | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- hyperoxalurie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=hyperoxalurie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- hyperoxalémie ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=hyperoxalémie | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- lipodystrophies (manifestations rénales des) ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=lipodystrophies (manifestations rénales des) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- nystagmus (zone de moindre) ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=nystagmus (zone de moindre) | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- semidominance ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=semidominance | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- semiquinone ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=semiquinone | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminal ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminal | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminifère ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminifère | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminomateux ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminomateux | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminome ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminome | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminome de l'ovaire ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminome de l'ovaire | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminome du médiastin ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminome du médiastin | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- séminome spermatocytaire ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=séminome spermatocytaire | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- sémiochimique ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=sémiochimique | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
- sémiologie extrapyramidale ---
r_associated #0: 5 -->
en:inborn error of lipoprotein metabolism
n1=sémiologie extrapyramidale | n2=en:inborn error of lipoprotein metabolism | rel=r_associated | relid=0 | w=5
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