'en:udpglucose 4-epimerase deficiency disease'
(id=7057566 ; fe=en:udpglucose 4-epimerase deficiency disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=17496 creation date=2017-06-25 touchdate=2025-08-27 17:07:06.000)

≈ 188 relations sortantes en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 36 / 1 -> déficit en galactose épimérase n1=en:udpglucose 4-epimerase deficiency disease | n2=déficit en galactose épimérase | rel=r_associated | relid=0 | w=36 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 34 / 0.944 -> en:galactosemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:galactosemia | rel=r_associated | relid=0 | w=34 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 30 / 0.833 -> en:congenital disorder of glycosylation type ia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=30 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 30 / 0.833 -> en:cystathionine beta-synthase deficiency disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=30 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 30 / 0.833 -> en:interleukin-1 receptor-associated kinase 4 deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=30 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 30 / 0.833 -> en:leukotriene c4 synthase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=30 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 29 / 0.806 -> déficit en udp galactose 4-épimérase n1=en:udpglucose 4-epimerase deficiency disease | n2=déficit en udp galactose 4-épimérase | rel=r_associated | relid=0 | w=29 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 29 / 0.806 -> en:porphobilinogen synthase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=29 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 29 / 0.806 -> galactosémies n1=en:udpglucose 4-epimerase deficiency disease | n2=galactosémies | rel=r_associated | relid=0 | w=29 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:alpha, alpha-trehalase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:histidinemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:histidinemia | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:mental retardation n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mental retardation | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:sly syndrome n1=en:udpglucose 4-epimerase deficiency disease | n2=en:sly syndrome | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:splenomegaly n1=en:udpglucose 4-epimerase deficiency disease | n2=en:splenomegaly | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:tay-sachs disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 28 / 0.778 -> en:vomiting n1=en:udpglucose 4-epimerase deficiency disease | n2=en:vomiting | rel=r_associated | relid=0 | w=28 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:argininemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:argininemia | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:congenital sucrase-isomaltase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:deficiency of glucosyltransferase 1 n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:hereditary angioedema n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:propionic acidemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> en:xanthinuria, type i n1=en:udpglucose 4-epimerase deficiency disease | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> galactosémie n1=en:udpglucose 4-epimerase deficiency disease | n2=galactosémie | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> galactosémie type iii n1=en:udpglucose 4-epimerase deficiency disease | n2=galactosémie type iii | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> maladie n1=en:udpglucose 4-epimerase deficiency disease | n2=maladie | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 27 / 0.75 -> vomissement n1=en:udpglucose 4-epimerase deficiency disease | n2=vomissement | rel=r_associated | relid=0 | w=27 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:glutamate-cysteine ligase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:lesch-nyhan syndrome n1=en:udpglucose 4-epimerase deficiency disease | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:methionine adenosyltransferase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:methylmalonyl-coenzyme a mutase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:mucopolysaccharidosis type i n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 26 / 0.722 -> en:pseudocholinesterase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=26 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 25 / 0.694 -> en:21-hydroxylase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=25 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 25 / 0.694 -> en:adenylosuccinate lyase deficiency (disorder) n1=en:udpglucose 4-epimerase deficiency disease | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=25 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 25 / 0.694 -> en:enterokinase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=25 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 25 / 0.694 -> en:fucosidosis n1=en:udpglucose 4-epimerase deficiency disease | n2=en:fucosidosis | rel=r_associated | relid=0 | w=25 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 25 / 0.694 -> glucose n1=en:udpglucose 4-epimerase deficiency disease | n2=glucose | rel=r_associated | relid=0 | w=25 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:angiokeratoma corporis diffusum n1=en:udpglucose 4-epimerase deficiency disease | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:carbamoyl-phosphate synthetase i deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:gaucher disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gaucher disease | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:hereditary fructose intolerance n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:mannosidosis n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mannosidosis | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 24 / 0.667 -> en:niemann-pick disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=24 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 23 / 0.639 -> en:isovaleric acidemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=23 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 23 / 0.639 -> en:sensorineural hearing loss n1=en:udpglucose 4-epimerase deficiency disease | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=23 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 22 / 0.611 -> en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) n1=en:udpglucose 4-epimerase deficiency disease | n2=en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) | rel=r_associated | relid=0 | w=22 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 22 / 0.611 -> en:hmg-coa lyase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=22 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 22 / 0.611 -> en:jaundice n1=en:udpglucose 4-epimerase deficiency disease | n2=en:jaundice | rel=r_associated | relid=0 | w=22 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 22 / 0.611 -> perte d'audition sensorineurale n1=en:udpglucose 4-epimerase deficiency disease | n2=perte d'audition sensorineurale | rel=r_associated | relid=0 | w=22 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:aminoacylase 1 deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:argininosuccinic aciduria n1=en:udpglucose 4-epimerase deficiency disease | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:glycogen storage disease type ii n1=en:udpglucose 4-epimerase deficiency disease | n2=en:glycogen storage disease type ii | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:hepatomegaly n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hepatomegaly | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:hyperprolinemia type 2 n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:hypotonia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hypotonia | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:maroteaux-lamy syndrome n1=en:udpglucose 4-epimerase deficiency disease | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 21 / 0.583 -> en:prolidase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=21 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> absence de croissance n1=en:udpglucose 4-epimerase deficiency disease | n2=absence de croissance | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> angiokeratoma corporis diffusum de Fabry n1=en:udpglucose 4-epimerase deficiency disease | n2=angiokeratoma corporis diffusum de Fabry | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> arriération n1=en:udpglucose 4-epimerase deficiency disease | n2=arriération | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> arriération mentale n1=en:udpglucose 4-epimerase deficiency disease | n2=arriération mentale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> asthénie sénile n1=en:udpglucose 4-epimerase deficiency disease | n2=asthénie sénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> débilité mentale n1=en:udpglucose 4-epimerase deficiency disease | n2=débilité mentale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> débilité sénile n1=en:udpglucose 4-epimerase deficiency disease | n2=débilité sénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> déficience intellectuelle n1=en:udpglucose 4-epimerase deficiency disease | n2=déficience intellectuelle | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> déficit en prolidase n1=en:udpglucose 4-epimerase deficiency disease | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence (sémiologie) n1=en:udpglucose 4-epimerase deficiency disease | n2=démence (sémiologie) | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence dégénérative primaire n1=en:udpglucose 4-epimerase deficiency disease | n2=démence dégénérative primaire | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence forme dépressive ou délirante n1=en:udpglucose 4-epimerase deficiency disease | n2=démence forme dépressive ou délirante | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence présénile n1=en:udpglucose 4-epimerase deficiency disease | n2=démence présénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence sénile n1=en:udpglucose 4-epimerase deficiency disease | n2=démence sénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> démence sénile avec delirium ou état confusionnel aigu n1=en:udpglucose 4-epimerase deficiency disease | n2=démence sénile avec delirium ou état confusionnel aigu | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:acyl-coa dehydrogenase, short-chain deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:age-related physical debility n1=en:udpglucose 4-epimerase deficiency disease | n2=en:age-related physical debility | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:alkaptonuria n1=en:udpglucose 4-epimerase deficiency disease | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:alpha-mannosidosis n1=en:udpglucose 4-epimerase deficiency disease | n2=en:alpha-mannosidosis | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:and microgenitalism n1=en:udpglucose 4-epimerase deficiency disease | n2=en:and microgenitalism | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:and proeminent incisors n1=en:udpglucose 4-epimerase deficiency disease | n2=en:and proeminent incisors | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:Anderson-Fabry's disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:Anderson-Fabry's disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:arginosuccinate lyase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:arginosuccinate lyase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:autosomal recessive inheritance n1=en:udpglucose 4-epimerase deficiency disease | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:biotinidase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:bisphosphoglycerate mutase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:bisphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:butyryl-coa dehydrogenase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:butyryl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:ceruloplasmin deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:ceruloplasmin deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of chymosin n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of chymosin | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of hydroxymethylglutaryl-coa hydrolase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of hydroxymethylglutaryl-coa hydrolase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of inosine nucleosidase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of inosine nucleosidase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of long-chain fatty-acyl-coa hydrolase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of long-chain fatty-acyl-coa hydrolase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of lysine-trna ligase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of lysine-trna ligase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of mitochondrial aspartyl-trna synthetase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of mitochondrial aspartyl-trna synthetase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of phosphoadenylate 3'-nucleotidase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of phosphoadenylate 3'-nucleotidase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:deficiency of sulfotransferase n1=en:udpglucose 4-epimerase deficiency disease | n2=en:deficiency of sulfotransferase | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:dhfr deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:dhfr deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:dwarfism n1=en:udpglucose 4-epimerase deficiency disease | n2=en:dwarfism | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:emesia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:emesia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:enlarged spleen n1=en:udpglucose 4-epimerase deficiency disease | n2=en:enlarged spleen | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:erythrocyte enolase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:erythrocyte enolase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:feeble-mindedness n1=en:udpglucose 4-epimerase deficiency disease | n2=en:feeble-mindedness | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:fumarase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:fumarase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:galactokinase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:galactokinase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:galactosuria n1=en:udpglucose 4-epimerase deficiency disease | n2=en:galactosuria | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, asn34ser n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, asn34ser | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, gly319glu n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, gly319glu | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, gly90glu n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, gly90glu | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, leu183pro n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, leu183pro | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, leu313met n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, leu313met | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:gale, lys257arg n1=en:udpglucose 4-epimerase deficiency disease | n2=en:gale, lys257arg | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:Gaucher disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:Gaucher disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:glucose-6-phosphate dehydrogenase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:glutathione synthetase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:glycogen storage disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:hartnup disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hartnup disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:histidinaemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:homocarnosinosis n1=en:udpglucose 4-epimerase deficiency disease | n2=en:homocarnosinosis | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:hyperlipoproteinemia type i n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hyperlipoproteinemia type i | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:hyperlipoproteinemia type I n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hyperlipoproteinemia type I | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:hypersplenism n1=en:udpglucose 4-epimerase deficiency disease | n2=en:hypersplenism | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:learning disability n1=en:udpglucose 4-epimerase deficiency disease | n2=en:learning disability | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:mental deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mental deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:mental dullness n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mental dullness | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:mental handicap n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mental handicap | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:mucopolysaccharidosis i n1=en:udpglucose 4-epimerase deficiency disease | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:muscular hypotonia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:muscular hypotonia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:Niemann-Pick disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:oligergasia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:oligergasia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:oligopsychia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:oligopsychia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:pediatric failure to thrive n1=en:udpglucose 4-epimerase deficiency disease | n2=en:pediatric failure to thrive | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:phosphoglycerate mutase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:phosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:presenile dementia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:presenile dementia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:pyruvate dehydrogenase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:pyruvate kinase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:pyruvate kinase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:retardation n1=en:udpglucose 4-epimerase deficiency disease | n2=en:retardation | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:senile asthenia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:senile asthenia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:senile dementia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:senile dementia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:senility n1=en:udpglucose 4-epimerase deficiency disease | n2=en:senility | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:Tay-Sachs disease n1=en:udpglucose 4-epimerase deficiency disease | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:thyroid peroxidase deficiency n1=en:udpglucose 4-epimerase deficiency disease | n2=en:thyroid peroxidase deficiency | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:transferase deficiency galactosemia n1=en:udpglucose 4-epimerase deficiency disease | n2=en:transferase deficiency galactosemia | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:tyrosinemia type i n1=en:udpglucose 4-epimerase deficiency disease | n2=en:tyrosinemia type i | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:unspecified senile psychotic condition n1=en:udpglucose 4-epimerase deficiency disease | n2=en:unspecified senile psychotic condition | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:vomitus n1=en:udpglucose 4-epimerase deficiency disease | n2=en:vomitus | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> en:with growth retardation n1=en:udpglucose 4-epimerase deficiency disease | n2=en:with growth retardation | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> faciès anormal, retard de croissance et retard mental n1=en:udpglucose 4-epimerase deficiency disease | n2=faciès anormal, retard de croissance et retard mental | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> fucosidose n1=en:udpglucose 4-epimerase deficiency disease | n2=fucosidose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> galactosurie n1=en:udpglucose 4-epimerase deficiency disease | n2=galactosurie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hépatomégalie n1=en:udpglucose 4-epimerase deficiency disease | n2=hépatomégalie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hérédité autosomale récessive n1=en:udpglucose 4-epimerase deficiency disease | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> histidinémie n1=en:udpglucose 4-epimerase deficiency disease | n2=histidinémie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> homocarnosinose n1=en:udpglucose 4-epimerase deficiency disease | n2=homocarnosinose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hypersplénisme n1=en:udpglucose 4-epimerase deficiency disease | n2=hypersplénisme | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hypothyroïdie (manifestations neuromusculaires dans l') n1=en:udpglucose 4-epimerase deficiency disease | n2=hypothyroïdie (manifestations neuromusculaires dans l') | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hypotonie n1=en:udpglucose 4-epimerase deficiency disease | n2=hypotonie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hypotonie musculaire n1=en:udpglucose 4-epimerase deficiency disease | n2=hypotonie musculaire | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> Hypotonie musculaire n1=en:udpglucose 4-epimerase deficiency disease | n2=Hypotonie musculaire | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> hypotonie, obésité et incisives proéminentes n1=en:udpglucose 4-epimerase deficiency disease | n2=hypotonie, obésité et incisives proéminentes | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> intolérance au fructose n1=en:udpglucose 4-epimerase deficiency disease | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> maladie de Niemann-Pick n1=en:udpglucose 4-epimerase deficiency disease | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> maladie de Tay-Sachs n1=en:udpglucose 4-epimerase deficiency disease | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> maladie de tay-sachs n1=en:udpglucose 4-epimerase deficiency disease | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> maladie de Tay-sachs n1=en:udpglucose 4-epimerase deficiency disease | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> nanisme, retard mental, anomalies oculaires n1=en:udpglucose 4-epimerase deficiency disease | n2=nanisme, retard mental, anomalies oculaires | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> oligophrénie n1=en:udpglucose 4-epimerase deficiency disease | n2=oligophrénie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose n1=en:udpglucose 4-epimerase deficiency disease | n2=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> psychose présénile n1=en:udpglucose 4-epimerase deficiency disease | n2=psychose présénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> psychose sénile n1=en:udpglucose 4-epimerase deficiency disease | n2=psychose sénile | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> retard de croissance n1=en:udpglucose 4-epimerase deficiency disease | n2=retard de croissance | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> retard de croissance staturo-pondérale n1=en:udpglucose 4-epimerase deficiency disease | n2=retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> Retard de croissance staturo-pondérale n1=en:udpglucose 4-epimerase deficiency disease | n2=Retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> retard mental n1=en:udpglucose 4-epimerase deficiency disease | n2=retard mental | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> Retard mental n1=en:udpglucose 4-epimerase deficiency disease | n2=Retard mental | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe n1=en:udpglucose 4-epimerase deficiency disease | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> retardation mentale n1=en:udpglucose 4-epimerase deficiency disease | n2=retardation mentale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> sénescence sans mention de psychose n1=en:udpglucose 4-epimerase deficiency disease | n2=sénescence sans mention de psychose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> sénilité n1=en:udpglucose 4-epimerase deficiency disease | n2=sénilité | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> splénomégalie n1=en:udpglucose 4-epimerase deficiency disease | n2=splénomégalie | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> splénomégalie congénitale n1=en:udpglucose 4-epimerase deficiency disease | n2=splénomégalie congénitale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> syndrome de glissement n1=en:udpglucose 4-epimerase deficiency disease | n2=syndrome de glissement | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> syndrome de Treft-Sanborn-Carey n1=en:udpglucose 4-epimerase deficiency disease | n2=syndrome de Treft-Sanborn-Carey | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> syndrome du retard de développement n1=en:udpglucose 4-epimerase deficiency disease | n2=syndrome du retard de développement | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> trouble psychotique sénile non précisé n1=en:udpglucose 4-epimerase deficiency disease | n2=trouble psychotique sénile non précisé | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> troubles endocriniens, épilepsie et déficience mentale n1=en:udpglucose 4-epimerase deficiency disease | n2=troubles endocriniens, épilepsie et déficience mentale | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> v+ n1=en:udpglucose 4-epimerase deficiency disease | n2=v+ | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> V+ n1=en:udpglucose 4-epimerase deficiency disease | n2=V+ | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> vieillesse sans mention de psychose n1=en:udpglucose 4-epimerase deficiency disease | n2=vieillesse sans mention de psychose | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 20 / 0.556 -> vomissements n1=en:udpglucose 4-epimerase deficiency disease | n2=vomissements | rel=r_associated | relid=0 | w=20 en:udpglucose 4-epimerase deficiency disease -- r_associated #0: 1 / 0.028 -> en:disease or syndrome n1=en:udpglucose 4-epimerase deficiency disease | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1

≈ 372 relations entrantes en:vomiting --- r_associated #0: 450 --> en:udpglucose 4-epimerase deficiency disease n1=en:vomiting | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=450 vomissement --- r_associated #0: 448 --> en:udpglucose 4-epimerase deficiency disease n1=vomissement | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=448 trouble psychotique sénile non précisé --- r_associated #0: 405 --> en:udpglucose 4-epimerase deficiency disease n1=trouble psychotique sénile non précisé | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=405 psychose sénile --- r_associated #0: 404 --> en:udpglucose 4-epimerase deficiency disease n1=psychose sénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=404 asthénie sénile --- r_associated #0: 400 --> en:udpglucose 4-epimerase deficiency disease n1=asthénie sénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=400 démence forme dépressive ou délirante --- r_associated #0: 400 --> en:udpglucose 4-epimerase deficiency disease n1=démence forme dépressive ou délirante | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=400 démence sénile avec delirium ou état confusionnel aigu --- r_associated #0: 400 --> en:udpglucose 4-epimerase deficiency disease n1=démence sénile avec delirium ou état confusionnel aigu | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=400 en:senility --- r_associated #0: 400 --> en:udpglucose 4-epimerase deficiency disease n1=en:senility | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=400 sénescence sans mention de psychose --- r_associated #0: 400 --> en:udpglucose 4-epimerase deficiency disease n1=sénescence sans mention de psychose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=400 débilité sénile --- r_associated #0: 395 --> en:udpglucose 4-epimerase deficiency disease n1=débilité sénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=395 démence dégénérative primaire --- r_associated #0: 395 --> en:udpglucose 4-epimerase deficiency disease n1=démence dégénérative primaire | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=395 psychose présénile --- r_associated #0: 395 --> en:udpglucose 4-epimerase deficiency disease n1=psychose présénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=395 en:senile asthenia --- r_associated #0: 390 --> en:udpglucose 4-epimerase deficiency disease n1=en:senile asthenia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=390 en:unspecified senile psychotic condition --- r_associated #0: 390 --> en:udpglucose 4-epimerase deficiency disease n1=en:unspecified senile psychotic condition | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=390 vieillesse sans mention de psychose --- r_associated #0: 390 --> en:udpglucose 4-epimerase deficiency disease n1=vieillesse sans mention de psychose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=390 en:age-related physical debility --- r_associated #0: 375 --> en:udpglucose 4-epimerase deficiency disease n1=en:age-related physical debility | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=375 démence présénile --- r_associated #0: 351 --> en:udpglucose 4-epimerase deficiency disease n1=démence présénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=351 en:presenile dementia --- r_associated #0: 340 --> en:udpglucose 4-epimerase deficiency disease n1=en:presenile dementia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=340 syndrome de glissement --- r_associated #0: 340 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome de glissement | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=340 démence sénile --- r_associated #0: 330 --> en:udpglucose 4-epimerase deficiency disease n1=démence sénile | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=330 sénilité --- r_associated #0: 321 --> en:udpglucose 4-epimerase deficiency disease n1=sénilité | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=321 retard de croissance staturo-pondérale --- r_associated #0: 156 --> en:udpglucose 4-epimerase deficiency disease n1=retard de croissance staturo-pondérale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=156 absence de croissance --- r_associated #0: 155 --> en:udpglucose 4-epimerase deficiency disease n1=absence de croissance | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=155 syndrome du retard de développement --- r_associated #0: 147 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome du retard de développement | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=147 en:pediatric failure to thrive --- r_associated #0: 145 --> en:udpglucose 4-epimerase deficiency disease n1=en:pediatric failure to thrive | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=145 Retard de croissance staturo-pondérale --- r_associated #0: 135 --> en:udpglucose 4-epimerase deficiency disease n1=Retard de croissance staturo-pondérale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=135 en:mental retardation --- r_associated #0: 134 --> en:udpglucose 4-epimerase deficiency disease n1=en:mental retardation | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=134 retardation mentale --- r_associated #0: 131 --> en:udpglucose 4-epimerase deficiency disease n1=retardation mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=131 Retard mental --- r_associated #0: 130 --> en:udpglucose 4-epimerase deficiency disease n1=Retard mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=130 retard mental --- r_associated #0: 130 --> en:udpglucose 4-epimerase deficiency disease n1=retard mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=130 splénomégalie --- r_associated #0: 123 --> en:udpglucose 4-epimerase deficiency disease n1=splénomégalie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=123 en:hypersplenism --- r_associated #0: 120 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypersplenism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=120 en:splenomegaly --- r_associated #0: 120 --> en:udpglucose 4-epimerase deficiency disease n1=en:splenomegaly | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=120 splénomégalie congénitale --- r_associated #0: 120 --> en:udpglucose 4-epimerase deficiency disease n1=splénomégalie congénitale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=120 hypersplénisme --- r_associated #0: 115 --> en:udpglucose 4-epimerase deficiency disease n1=hypersplénisme | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=115 vomissements --- r_associated #0: 114 --> en:udpglucose 4-epimerase deficiency disease n1=vomissements | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=114 en:hypotonia --- r_associated #0: 87 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=87 hypotonie --- r_associated #0: 85 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=85 hépatomégalie --- r_associated #0: 79 --> en:udpglucose 4-epimerase deficiency disease n1=hépatomégalie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=79 en:hepatomegaly --- r_associated #0: 78 --> en:udpglucose 4-epimerase deficiency disease n1=en:hepatomegaly | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=78 arriération mentale --- r_associated #0: 71 --> en:udpglucose 4-epimerase deficiency disease n1=arriération mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=71 débilité mentale --- r_associated #0: 70 --> en:udpglucose 4-epimerase deficiency disease n1=débilité mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=70 retard de croissance --- r_associated #0: 68 --> en:udpglucose 4-epimerase deficiency disease n1=retard de croissance | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=68 retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 58 --> en:udpglucose 4-epimerase deficiency disease n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=58 en:mucopolysaccharidosis type i --- r_associated #0: 57 --> en:udpglucose 4-epimerase deficiency disease n1=en:mucopolysaccharidosis type i | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=57 en:mucopolysaccharidosis i --- r_associated #0: 55 --> en:udpglucose 4-epimerase deficiency disease n1=en:mucopolysaccharidosis i | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=55 hypotonie musculaire --- r_associated #0: 46 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie musculaire | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=46 hypotonie, obésité et incisives proéminentes --- r_associated #0: 46 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie, obésité et incisives proéminentes | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=46 maladie de Niemann-Pick --- r_associated #0: 46 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de Niemann-Pick | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=46 en:Niemann-Pick disease --- r_associated #0: 45 --> en:udpglucose 4-epimerase deficiency disease n1=en:Niemann-Pick disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=45 en:galactosuria --- r_associated #0: 43 --> en:udpglucose 4-epimerase deficiency disease n1=en:galactosuria | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=43 hérédité autosomale récessive --- r_associated #0: 43 --> en:udpglucose 4-epimerase deficiency disease n1=hérédité autosomale récessive | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=43 déficit en prolidase --- r_associated #0: 41 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en prolidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=41 en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 41 --> en:udpglucose 4-epimerase deficiency disease n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=41 v+ --- r_associated #0: 41 --> en:udpglucose 4-epimerase deficiency disease n1=v+ | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=41 V+ --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=V+ | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 en:autosomal recessive inheritance --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=en:autosomal recessive inheritance | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 en:glycogen storage disease --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=en:glycogen storage disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 en:homocarnosinosis --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=en:homocarnosinosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 en:senile dementia --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=en:senile dementia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 intolérance au fructose --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=intolérance au fructose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 40 --> en:udpglucose 4-epimerase deficiency disease n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=40 en:hereditary angioedema --- r_associated #0: 39 --> en:udpglucose 4-epimerase deficiency disease n1=en:hereditary angioedema | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=39 en:prolidase deficiency --- r_associated #0: 39 --> en:udpglucose 4-epimerase deficiency disease n1=en:prolidase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=39 angiokeratoma corporis diffusum de Fabry --- r_associated #0: 38 --> en:udpglucose 4-epimerase deficiency disease n1=angiokeratoma corporis diffusum de Fabry | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=38 faciès anormal, retard de croissance et retard mental --- r_associated #0: 38 --> en:udpglucose 4-epimerase deficiency disease n1=faciès anormal, retard de croissance et retard mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=38 Hypotonie musculaire --- r_associated #0: 36 --> en:udpglucose 4-epimerase deficiency disease n1=Hypotonie musculaire | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=36 en:congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency --- r_associated #0: 36 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=36 en:hereditary fructose intolerance --- r_associated #0: 36 --> en:udpglucose 4-epimerase deficiency disease n1=en:hereditary fructose intolerance | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=36 en:jaundice --- r_associated #0: 36 --> en:udpglucose 4-epimerase deficiency disease n1=en:jaundice | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=36 nanisme, retard mental, anomalies oculaires --- r_associated #0: 36 --> en:udpglucose 4-epimerase deficiency disease n1=nanisme, retard mental, anomalies oculaires | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=36 déficit en galactose épimérase --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en galactose épimérase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:enterokinase deficiency --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:enterokinase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:galactokinase deficiency --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:galactokinase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:gale, leu183pro --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, leu183pro | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:hyperprolinemia type 2 --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:hyperprolinemia type 2 | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:maroteaux-lamy syndrome --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:maroteaux-lamy syndrome | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:mental deficiency --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:mental deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:niemann-pick disease --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:niemann-pick disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:tyrosinemia type i --- r_associated #0: 35 --> en:udpglucose 4-epimerase deficiency disease n1=en:tyrosinemia type i | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=35 en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:arginosuccinate lyase deficiency --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:arginosuccinate lyase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:feeble-mindedness --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:feeble-mindedness | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:gale, leu313met --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, leu313met | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:gaucher disease --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:gaucher disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:glutamate-cysteine ligase deficiency --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:glutamate-cysteine ligase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:glycogen storage disease type ii --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:glycogen storage disease type ii | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:hartnup disease --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:hartnup disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:leukotriene c4 synthase deficiency --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:leukotriene c4 synthase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:sensorineural hearing loss --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=en:sensorineural hearing loss | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 perte d'audition sensorineurale --- r_associated #0: 34 --> en:udpglucose 4-epimerase deficiency disease n1=perte d'audition sensorineurale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=34 en:alpha, alpha-trehalase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:alpha, alpha-trehalase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:aminoacylase 1 deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:aminoacylase 1 deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:bisphosphoglycerate mutase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:bisphosphoglycerate mutase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:butyryl-coa dehydrogenase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:butyryl-coa dehydrogenase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:congenital sucrase-isomaltase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital sucrase-isomaltase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:dhfr deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:dhfr deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:erythrocyte enolase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:erythrocyte enolase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:fucosidosis --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:fucosidosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:gale, gly90glu --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, gly90glu | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:methionine adenosyltransferase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:methionine adenosyltransferase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:phosphoglycerate mutase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:phosphoglycerate mutase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:porphobilinogen synthase deficiency --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:porphobilinogen synthase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 en:sly syndrome --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=en:sly syndrome | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 galactosémie type iii --- r_associated #0: 32 --> en:udpglucose 4-epimerase deficiency disease n1=galactosémie type iii | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=32 déficience intellectuelle --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=déficience intellectuelle | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:Anderson-Fabry's disease --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:Anderson-Fabry's disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:cystathionine beta-synthase deficiency disease --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:cystathionine beta-synthase deficiency disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:deficiency of glucosyltransferase 1 --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of glucosyltransferase 1 | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:deficiency of lysine-trna ligase --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of lysine-trna ligase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:gale, lys257arg --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, lys257arg | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:glutathione synthetase deficiency --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:glutathione synthetase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:isovaleric acidemia --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:isovaleric acidemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 en:mental dullness --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=en:mental dullness | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 fucosidose --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=fucosidose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 galactosurie --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=galactosurie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 galactosémies --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=galactosémies | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 histidinémie --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=histidinémie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 homocarnosinose --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=homocarnosinose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 oligophrénie --- r_associated #0: 31 --> en:udpglucose 4-epimerase deficiency disease n1=oligophrénie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=31 arriération --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=arriération | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 démence (sémiologie) --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=démence (sémiologie) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:21-hydroxylase deficiency --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:21-hydroxylase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:Tay-Sachs disease --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:Tay-Sachs disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:deficiency of phosphoadenylate 3'-nucleotidase --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of phosphoadenylate 3'-nucleotidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:emesia --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:emesia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:gale, gly319glu --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, gly319glu | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:histidinaemia --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:histidinaemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:histidinemia --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:histidinemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:learning disability --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:learning disability | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:lesch-nyhan syndrome --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:lesch-nyhan syndrome | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:mannosidosis --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:mannosidosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:mental handicap --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:mental handicap | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:oligopsychia --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:oligopsychia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:pseudocholinesterase deficiency --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:pseudocholinesterase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:pyruvate dehydrogenase deficiency --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:pyruvate dehydrogenase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:retardation --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:retardation | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:tay-sachs disease --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:tay-sachs disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:xanthinuria, type i --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=en:xanthinuria, type i | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 galactosémie --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=galactosémie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 maladie de Tay-Sachs --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de Tay-Sachs | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 maladie de Tay-sachs --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de Tay-sachs | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 maladie de tay-sachs --- r_associated #0: 30 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de tay-sachs | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=30 en:alkaptonuria --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:alkaptonuria | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:alpha-mannosidosis --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:alpha-mannosidosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:and microgenitalism --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:and microgenitalism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:and proeminent incisors --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:and proeminent incisors | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:argininemia --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:argininemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:biotinidase deficiency --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:biotinidase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:deficiency of sulfotransferase --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of sulfotransferase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:failure of the mind --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:failure of the mind | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:hyperlipoproteinemia type i --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:hyperlipoproteinemia type i | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:muscular hypotonia --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:muscular hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:oligergasia --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:oligergasia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 en:pyruvate kinase deficiency --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=en:pyruvate kinase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 syndrome de Treft-Sanborn-Carey --- r_associated #0: 29 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome de Treft-Sanborn-Carey | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=29 Déficience intellectuelle --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=Déficience intellectuelle | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:Gaucher disease --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:Gaucher disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:ceruloplasmin deficiency --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:ceruloplasmin deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:congenital disorder of glycosylation type ia --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital disorder of glycosylation type ia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:dwarfism --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:dwarfism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:hmg-coa lyase deficiency --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:hmg-coa lyase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:propionic acidemia --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:propionic acidemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 en:with growth retardation --- r_associated #0: 28 --> en:udpglucose 4-epimerase deficiency disease n1=en:with growth retardation | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=28 déficit en udp galactose 4-épimérase --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en udp galactose 4-épimérase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:angiokeratoma corporis diffusum --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:angiokeratoma corporis diffusum | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:argininosuccinic aciduria --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:argininosuccinic aciduria | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:deficiency of chymosin --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of chymosin | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:deficiency of mitochondrial aspartyl-trna synthetase --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of mitochondrial aspartyl-trna synthetase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:enlarged spleen --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:enlarged spleen | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:galactosemia --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:galactosemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:gale, asn34ser --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:gale, asn34ser | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:thyroid peroxidase deficiency --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:thyroid peroxidase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:transferase deficiency galactosemia --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:transferase deficiency galactosemia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:vomitus --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=en:vomitus | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 troubles endocriniens, épilepsie et déficience mentale --- r_associated #0: 27 --> en:udpglucose 4-epimerase deficiency disease n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=27 en:deficiency of hydroxymethylglutaryl-coa hydrolase --- r_associated #0: 26 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of hydroxymethylglutaryl-coa hydrolase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=26 en:deficiency of inosine nucleosidase --- r_associated #0: 26 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of inosine nucleosidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=26 en:deficiency of long-chain fatty-acyl-coa hydrolase --- r_associated #0: 26 --> en:udpglucose 4-epimerase deficiency disease n1=en:deficiency of long-chain fatty-acyl-coa hydrolase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=26 en:fumarase deficiency --- r_associated #0: 26 --> en:udpglucose 4-epimerase deficiency disease n1=en:fumarase deficiency | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=26 en:hyperlipoproteinemia type I --- r_associated #0: 26 --> en:udpglucose 4-epimerase deficiency disease n1=en:hyperlipoproteinemia type I | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=26 Maladie de Tay-Sachs --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=Maladie de Tay-Sachs | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 cataracte-atrophie du cervelet-myopathie --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=cataracte-atrophie du cervelet-myopathie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 en:X-linked --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=en:X-linked | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 en:cerebellar atrophy --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=en:cerebellar atrophy | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 en:deafness --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=en:deafness | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 en:ophthalmoplegia --- r_associated #0: 25 --> en:udpglucose 4-epimerase deficiency disease n1=en:ophthalmoplegia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=25 déficience mentale --- r_associated #0: 24 --> en:udpglucose 4-epimerase deficiency disease n1=déficience mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=24 déficit en biotinidase --- r_associated #0: 24 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en biotinidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=24 en:juvenile cataract --- r_associated #0: 24 --> en:udpglucose 4-epimerase deficiency disease n1=en:juvenile cataract | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=24 mucopolysaccharidose de type I --- r_associated #0: 24 --> en:udpglucose 4-epimerase deficiency disease n1=mucopolysaccharidose de type I | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=24 angiokeratoma corporis diffusum de fabry --- r_associated #0: 23 --> en:udpglucose 4-epimerase deficiency disease n1=angiokeratoma corporis diffusum de fabry | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=23 cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie --- r_associated #0: 23 --> en:udpglucose 4-epimerase deficiency disease n1=cataracte juvénile, atrophie cérébelleuse, retard mental et myopathie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=23 en:enlarged liver --- r_associated #0: 23 --> en:udpglucose 4-epimerase deficiency disease n1=en:enlarged liver | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=23 en:obesity --- r_associated #0: 23 --> en:udpglucose 4-epimerase deficiency disease n1=en:obesity | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=23 en:emesis --- r_associated #0: 22 --> en:udpglucose 4-epimerase deficiency disease n1=en:emesis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=22 en:glycogen storage disease type II --- r_associated #0: 22 --> en:udpglucose 4-epimerase deficiency disease n1=en:glycogen storage disease type II | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=22 en:morosis --- r_associated #0: 22 --> en:udpglucose 4-epimerase deficiency disease n1=en:morosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=22 en:oligophrenia --- r_associated #0: 22 --> en:udpglucose 4-epimerase deficiency disease n1=en:oligophrenia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=22 glycogénose --- r_associated #0: 22 --> en:udpglucose 4-epimerase deficiency disease n1=glycogénose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=22 acidurie argininosuccinique --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=acidurie argininosuccinique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 acidémie isovalérique --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=acidémie isovalérique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 alcaptonurie --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=alcaptonurie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 argininémie --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=argininémie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 déficit en galactokinase --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en galactokinase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 idiosyncrasie au fructose --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=idiosyncrasie au fructose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 mannosidose --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=mannosidose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:udpglucose 4-epimerase deficiency disease n1=mucopolysaccharidose de type 1 | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=21 Splénomégalie --- r_associated #0: 20 --> en:udpglucose 4-epimerase deficiency disease n1=Splénomégalie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=20 Sénilité --- r_associated #0: 20 --> en:udpglucose 4-epimerase deficiency disease n1=Sénilité | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=20 maladie --- r_associated #0: 20 --> en:udpglucose 4-epimerase deficiency disease n1=maladie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=20 Arrhenius (loi d') --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=Arrhenius (loi d') | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 CUD --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=CUD | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 Fuchs (syndrome de) --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=Fuchs (syndrome de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 His (faisceau de) --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=His (faisceau de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 Intolérance au fructose --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=Intolérance au fructose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 Maladie de Niemann-Pick --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=Maladie de Niemann-Pick | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 Vomissement --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=Vomissement | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 en:congenital atrophy of thyroid --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital atrophy of thyroid | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 en:congenital hypothyroidism --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital hypothyroidism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 en:neonatal hypothyroidism --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=en:neonatal hypothyroidism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 handicap mental --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=handicap mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypothyroïdie congénitale --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypothyroïdie congénitale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypothyroïdie et psychisme --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypothyroïdie et psychisme | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypothyroïdie néonatale --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypothyroïdie néonatale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonie plasmatique --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie plasmatique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonie sphinctérienne anale --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie sphinctérienne anale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonie sphinctérienne uréthrale --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie sphinctérienne uréthrale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonie utérine --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie utérine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonie vésicale --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonie vésicale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotonique --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotonique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose congénitale des cils --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose congénitale des cils | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose congénitale simple --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose congénitale simple | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose héréditaire de Marie Unna --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose héréditaire de Marie Unna | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 obésité --- r_associated #0: 15 --> en:udpglucose 4-epimerase deficiency disease n1=obésité | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=15 Déficience mentale --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Déficience mentale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Fucosidose --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Fucosidose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Glycogénose --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Glycogénose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Histidinémie --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Histidinémie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Hypotonie --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Hypotonie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Hépatomégalie --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Hépatomégalie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 MOMO (syndrome) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=MOMO (syndrome) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Manning (score de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Manning (score de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Mannosidose --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Mannosidose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Niemann-Pick (maladie de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Retard de croissance --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Retard de croissance | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Sengstaken-Blakemore (sonde de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Sengstaken-Blakemore (sonde de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Splendore-Hoeppli (corps astéroïdes de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Splendore-Hoeppli (corps astéroïdes de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 VOMISSEMENTS --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=VOMISSEMENTS | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Vomissements --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Vomissements | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 Went (atrophie optique liée au sexe de) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=Went (atrophie optique liée au sexe de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 alcalose métabolique (classification) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=alcalose métabolique (classification) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 atonie de l'utérus --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=atonie de l'utérus | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit en chaînes alpha du récepteur de l'interféron ? --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en chaînes alpha du récepteur de l'interféron ? | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit en cuivre lié à l'X --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en cuivre lié à l'X | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit en cystathionine-bêta-synthase --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en cystathionine-bêta-synthase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit en facteurs du complément --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en facteurs du complément | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit en flux calcique transmembranaire --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en flux calcique transmembranaire | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 déficit intellectuel --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=déficit intellectuel | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence d'Alzheimer --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence d'Alzheimer | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence frontotemporale --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence frontotemporale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence héréditaire et infarctus multiples cérébraux --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence héréditaire et infarctus multiples cérébraux | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence myoclonique --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence myoclonique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence parkinsonienne avec dégénérescence pallidopontonigrée --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence parkinsonienne avec dégénérescence pallidopontonigrée | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence précoce --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence précoce | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence pugilistique --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence pugilistique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence régressive --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence régressive | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 démence sémantique --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=démence sémantique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:Arrhenius'law --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:Arrhenius'law | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:Fabry's disease --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:Fabry's disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:Tay Sachs' disease --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:Tay Sachs' disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:alcaptonuria --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:alcaptonuria | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:anal sphincter hypotonia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:anal sphincter hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:and growth retardation --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:and growth retardation | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:ataxia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:ataxia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:bladder hypotonia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:bladder hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:congenital eyelashes hypotrichosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital eyelashes hypotrichosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:endocrine disorder --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:endocrine disorder | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:eye abnormality --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:eye abnormality | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:glycogenosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:glycogenosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hepatomégalia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hepatomégalia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:homogentisuria --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:homogentisuria | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypacusis and athetosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypacusis and athetosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypothyreosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypothyreosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypothyroidism and psychism --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypothyroidism and psychism | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypotonic --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypotonic | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypotrichosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypotrichosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypotrichosis congenita simplex --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypotrichosis congenita simplex | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:hypotrichosis-anodontic syndrome --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:hypotrichosis-anodontic syndrome | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:intellectual disability --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:intellectual disability | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:optic atrophy --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:optic atrophy | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:phosphatide thesaurismosis | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:plasma hypotonia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:plasma hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:sphincteric hypotony --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:sphincteric hypotony | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:unusual facies --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:unusual facies | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 en:uterine hypotonia --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=en:uterine hypotonia | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 faciale (paralysie du nouveau-né) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=faciale (paralysie du nouveau-né) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=glycogénique (surcharge et infiltration) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 hyperlipoprotéinémie de type I --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=hyperlipoprotéinémie de type I | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 inertie utérine --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=inertie utérine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 macrosomie, obésité, macrocéphalie et anomalies oculaires --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=macrosomie, obésité, macrocéphalie et anomalies oculaires | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 maladie d'Anderson-Fabry --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=maladie d'Anderson-Fabry | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 maladie de Gaucher --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de Gaucher | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 maladie de Pompe --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de Pompe | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 maladie de niemann-pick --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=maladie de niemann-pick | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 nanisme --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=nanisme | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 prolidase (déficit en) --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=prolidase (déficit en) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 surdité --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=surdité | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=trichomégalie avec retard mental, nanisme, et dégénérescence pigmentée de la rétine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:udpglucose 4-epimerase deficiency disease n1=urticaire-surdité-amylose rénale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=10 ARRX --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=ARRX | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 Handicap mental --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=Handicap mental | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 Hypotonique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=Hypotonique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=Tay-Sachs (maladie de) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 arrière-pied --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=arrière-pied | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 atrophie congénitale de la thyroïde --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=atrophie congénitale de la thyroïde | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 crétinismes --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=crétinismes | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 déficit en cytochrome c oxydase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en cytochrome c oxydase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 déficit en céramidase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en céramidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 déficit en facteur von Willebrand --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=déficit en facteur von Willebrand | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence alcoolique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence alcoolique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence aluminique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence aluminique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence sous-corticale --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence sous-corticale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence sénile de type Alzheimer --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence sénile de type Alzheimer | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence sénile mixte --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence sénile mixte | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence traumatique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence traumatique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence vasculaire --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence vasculaire | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence vésanique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence vésanique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démence à corps de Lewy --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démence à corps de Lewy | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 démences et prions --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=démences et prions | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 en:Sachs' disease --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=en:Sachs' disease | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 en:congenital goiter --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=en:congenital goiter | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 faisceau de His --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=faisceau de His | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 fuchsine --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=fuchsine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 fucose --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=fucose | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 fucosidase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=fucosidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 fucoside --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=fucoside | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 goitre congénital --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=goitre congénital | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminergie --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminergie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminergique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminergique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminolibération --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminolibération | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminolytique --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminolytique | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminopexie --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminopexie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminurie --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminurie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histaminémie --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histaminémie | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidinase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidinase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidine --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidine | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidine-ammoniac-lyase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidine-ammoniac-lyase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidine-décarboxylase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidine-décarboxylase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 histidine-désaminase --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=histidine-désaminase | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 hypothyroïdisme congénital --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=hypothyroïdisme congénital | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 hépato-pulmonaire (syndrome) --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=hépato-pulmonaire (syndrome) | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 infantilisme type brissaud --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=infantilisme type brissaud | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 nanisme hypothyroïdien --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=nanisme hypothyroïdien | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 syndrome de Fuchs --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=syndrome de Fuchs | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5 vomitus --- r_associated #0: 5 --> en:udpglucose 4-epimerase deficiency disease n1=vomitus | n2=en:udpglucose 4-epimerase deficiency disease | rel=r_associated | relid=0 | w=5