'en:hnsha due to diphosphoglycerate mutase deficiency'
(id=6767403 ; fe=en:hnsha due to diphosphoglycerate mutase deficiency ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=22115.280029296875 creation date=2017-06-24 touchdate=2025-08-27 16:50:06.000)

≈ 467 relations sortantes en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 43 / 1 -> en:acrodermatitis enteropathica n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=43 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 43 / 1 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=43 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 41 / 0.953 -> en:autosomal recessive spastic paraplegia type 11 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=41 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 39 / 0.907 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=39 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:adenosine deaminase overproduction n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:adenosine deaminase overproduction | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:argininemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:argininemia | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:ataxia telangiectasia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:classical phenylketonuria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:congenital leptin deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:cutis laxa, autosomal recessive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:deafness, sensorineural, and male infertility n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:deficiency of hexokinase (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deficiency of hexokinase (disorder) | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 35 / 0.814 -> en:ear, patella, short stature syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=35 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal recessive scid n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=34 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 34 / 0.791 -> en:becker generalized myotonia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=34 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 34 / 0.791 -> en:chitty hall baraitser syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=34 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 34 / 0.791 -> en:chylomicron retention disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 34 / 0.791 -> en:congenital adrenal hyperplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=34 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:3-methylglutaconic aciduria type iv n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:autosomal recessive distal osteolysis syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:bietti crystalline corneoretinal dystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:brachydactyly syndrome type b n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:ehlers-danlos syndrome, type vi n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:familial hypoaldosteronism n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:giacci familial neurogenic acroosteolysis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 32 / 0.744 -> en:glucose-6-phosphate dehydrogenase deficiency anemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=32 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:21-hydroxylase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:ateliotic dwarfism without insulinopenia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:childhood hypophosphatasia (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:congenital cataracts, facial dysmorphism, and neuropathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:congenital transferrin deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:deficiency of glucosyltransferase 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:enterokinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 31 / 0.721 -> en:gaze palsy, familial horizontal, with progressive scoliosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=31 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:3-methylglutaconic aciduria type 3 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:5 alpha steroid reductase 2 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:acid phosphatase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:al awadi syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:aminomethyltransferase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:atrophoderma vermiculatum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:autoinflammation, lipodystrophy and dermatosis syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:bothnia retinal dystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:bowen-conradi syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:cerebrotendinous xanthomatosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:cohen syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:ectodermal dysplasia/ skin fragility syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:epiphyseal dysplasia, multiple, 4 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary methemoglobinemia, enzymatic type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:hnsha due to nadh diaphorase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to nadh diaphorase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:hnsha due to nadh-methemoglobin reductase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to nadh-methemoglobin reductase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:hnsha due to phosphoglycerate kinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to phosphoglycerate kinase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:hypospadias-mental retardation syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:jervell and lange nielsen syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:macdermot winter syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:marles greenberg persaud syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:megalencephalic leukoencephalopathy with subcortical cysts n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:microcephaly-capillary malformation syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:mitochondrial dna depletion syndrome 2 (myopathic type) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:naxos disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:naxos disease | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:neutral lipid storage disease with myopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:niemann-pick disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:northern epilepsy syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:oculocutaneous albinism type 4 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:phenylketonuria ii n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:presentey anomaly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:sanfilippo syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:severe steroid 21-hydroxylase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:spondyloenchondrodysplasia with immune dysregulation n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:spondyloepiphyseal dysplasia, omani type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 30 / 0.698 -> en:trichohepatoenteric syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=30 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:adenine phosphoribosyltransferase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:adenylosuccinate lyase deficiency (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:allanson pantzar mcleod syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:arterial tortuosity syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:behr syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:behr syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:cleft lip/palate-ectodermal dysplasia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:congenital disorder of glycosylation type ic n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:congenital pancreatic enterokinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:cystinosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cystinosis | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:dubin-johnson syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:familial c3b inhibitor deficiency syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:familial renal iminoglycinuria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:hnsha due to phosphofructokinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to phosphofructokinase deficiency | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:hyperprolinemia type 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:isaacs syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:laron syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:laron syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:lethal congenital contracture syndrome 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:lissencephaly syndrome, norman-roberts type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:north american indian childhood cirrhosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:prickle1-related progressive myoclonus epilepsy with ataxia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:rna polymerase iii-related leukodystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:sudden infant death with dysgenesis of the testes syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:valinemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:valinemia | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> en:walker-warburg syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 29 / 0.674 -> syndrome de Walker-Warburg n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=29 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:alstrom syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:antley-bixler syndrome, autosomal dominant n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:aspartylglycosaminuria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:ataxia with vitamin e deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal recessive idiopathic familial dystonia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:behrens baumann dust syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:crigler-najjar syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:cystathionine beta-synthase deficiency disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:donnai-barrow syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:encephalopathy due to sulfite oxidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:factor v and factor viii, combined deficiency of n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:fibular hypoplasia and complex brachydactyly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease type x n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:infantile globoid cell leukodystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:kuskokwim disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:methylmalonyl-coenzyme a mutase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:miller-mckusick-malvaux-syndrome (3m syndrome) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:moderate steroid 21-hydroxylase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:netherton syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:neuraminidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:oculocerebral hypopigmentation syndrome type preus n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:odontohypophosphatasia (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:pelizaeus merzbacher like disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:persistent mullerian duct syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:propionic acidemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:pyruvate carboxylase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:spinal muscular atrophy with respiratory distress 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia, autosomal recessive 2 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:thyroid dyshormonogenesis 4 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 28 / 0.651 -> en:wolman disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:wolman disease | rel=r_associated | relid=0 | w=28 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> ahhns par déficit en diphosphoglycérate mutase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=ahhns par déficit en diphosphoglycérate mutase | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:5-oxoprolinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:alpha, alpha-trehalase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:amelogenesis imperfecta - recessive - rough n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:aminoacylase 1 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal recessive ocular albinism n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:brown-vialetto-van laere syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:cerebellar ataxia ectodermal dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:cerebellar ataxia, cayman type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:congenital amegakaryocytic thrombocytopenia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:congenital plasminogen activator inhibitor deficiency type 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:craniodiaphyseal dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:crisponi syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:fryns macrocephaly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:fucosidosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fucosidosis | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:hereditary adrenal unresponsiveness to corticotropin n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:hereditary stomatocytosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:hnsha due to aldolase a deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:hnsha due to glutathione reductase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:hyperprolinemia type 2 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:isolated hypoplasia of the right ventricle n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:lethal congenital contracture syndrome 2 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:maroteaux-lamy syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:methylene thf reductase deficiency and homocystinuria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:muscle amp deaminase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:neurodegeneration with brain iron accumulation 4 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:otoonychoperoneal syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:pancreatic triacylglycerol lipase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:papillon-lefevre syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:peeling skin syndrome, acral type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:pontocerebellar hypoplasia type 2 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:prader-willi habitus, osteopenia, and camptodactyly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:rapadilino syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:richards-rundle syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia with epilepsy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:type ii acrocephalopolysyndactyly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:verloes bourguignon syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:warsaw breakage syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:werdnig-hoffmann disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:xanthinuria, type i n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 27 / 0.628 -> en:xeroderma pigmentosum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=27 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:albinotic fundus n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:alpha-fetoprotein deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:anemia, hypochromic microcytic, with iron overload n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:autosomal recessive muscular dystrophy with limb girdle distribution n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:bardet-biedl syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:carbamoyl-phosphate synthetase i deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:chondrodysplasia punctata syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:congenital dyserythropoietic anemia, type i n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:cytochrome-c oxidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:dicarboxylicaminoaciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:fatal infantile lactic acidosis with methylmalonic aciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:fructose-1,6-bisphosphatase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:hereditary palmoplantar keratoderma gamborg nielsen type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:hnsha due to gamma glutamyl cysteine synthetase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to gamma glutamyl cysteine synthetase deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:hypomagnesemia 1, intestinal n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:neonatal progeroid syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:neuroacanthocytosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:neurodegeneration due to cerebral folate transport deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:primary hyperoxaluria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:prolonged electroretinal response suppression n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:pseudocholinesterase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:pseudohypoaldosteronism, type 1, recessive form n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:renal tubulopathy with encephalopathy and liver failure syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:saito kuba tsuruta syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:smith-mccort dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 26 / 0.605 -> en:spastic paraplegia 15, autosomal recessive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=26 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:corpus callosum agenesis neuronopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:desmosterolosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:dyskeratosis congenita, autosomal recessive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:ethanolaminosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:glycine dehydrogenase (decarboxylating) deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:gurrieri sammito bellussi syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:hypophosphatemic rickets with hypercalciuria, hereditary n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:laurence-moon syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:mannosidosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mannosidosis | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:microcephalic primordial dwarfism toriello type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:microcephaly, amish type (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:morm syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:morm syndrome | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:morquio syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:porphobilinogen synthase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:pseudotrisomy 13 syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 25 / 0.581 -> en:sulfite oxidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=25 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:arginine:glycine amidinotransferase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:brody myopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:brody myopathy | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:citrin deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:cryptophthalmos syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:erythropenia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:erythropenia | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:gamma-glutamyltransferase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:gracile syndrome (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:hereditary factor xi deficiency disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:hereditary fructose intolerance n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:hmg-coa lyase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:knobloch syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:maple syrup urine disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:mucopolysaccharidosis type i n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:myopathy with exercise intolerance, swedish type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:transcobalamin ii deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 24 / 0.558 -> en:zellweger syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=24 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:3-methylglutaconic aciduria type 1 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:allgrove syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:argininosuccinic aciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:baller-gerold syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:charcot-marie-tooth disease type 4 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:congenital disorder of glycosylation type ig n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:fronto-facio-nasal dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:hnsha due to triosephosphate isomerase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:hyperimmunoglobulin e syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:myopathy, early-onset, with fatal cardiomyopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:nathalie syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:nonaka myopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:sinus histiocytosis with massive lymphadenopathy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:sitosterolemia with xanthomatosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:sly syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sly syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:succinic semialdehyde dehydrogenase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 23 / 0.535 -> en:tungland bellman syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=23 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:3-methylglutaconic aciduria type 5 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:alpha-1 antitrypsin deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:alpha-methylacyl-coa racemase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:autosomal recessive primary microcephaly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:autosomal recessive sideroblastic anemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:combined malonic and methylmalonic aciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:congenital disorder of glycosylation type ia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:congenital sucrase-isomaltase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:deafness, progressive, with stapes fixation n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:familial acantholysis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:glutamate formiminotransferase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:glutamate-cysteine ligase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:hemolytic anemia due to pyruvate kinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:hereditary factor x deficiency disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:hereditary spastic paralysis, infantile onset ascending n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:hnsha due to decreased adenosine deaminase activity n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to decreased adenosine deaminase activity | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:hypomyelination and congenital cataract n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:i-cell disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:i-cell disease | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:isolated hyperchlorhidrosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:isovaleric acidemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:leukotriene c4 synthase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:multicentric osteolysis nodulosis arthropathy spectrum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:multiple sulfatase deficiency disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:prolidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:severe early childhood onset retinal dystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:spondylo-ocular syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:spondyloepiphyseal dysplasia tarda, toledo type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 22 / 0.512 -> en:thomas syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=22 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:2-hydroxyglutaric aciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:acrocallosal syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:childhood myocerebrohepatopathy spectrum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:congenital bowing of long bone n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:congenital dyserythropoietic anemia, type ii n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:epidermolysis bullosa simplex with pyloric atresia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:fatty acid hydroxylase-associated neurodegeneration n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:geroderma osteodysplastica n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:histidinemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:histidinemia | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:hyperphosphatasia with mental retardation n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:hypokalemia, familial n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:infantile hypophosphatasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:interleukin-1 receptor-associated kinase 4 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:jankovic rivera syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:lethal congenital contracture syndrome type 3 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:macular corneal dystrophy n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:majeed syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:microcephaly cervical spine fusion anomalies n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:n-acetylglutamate synthase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:purine-nucleoside phosphorylase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:reardon hall slaney syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:retinitis punctata albescens (disorder) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:sarcosinemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:sonoda syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:spastic ataxia, charlevoix-saguenay type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:spondylocarpotarsal synostosis syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:spondyloenchondrodysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:syndrome of apparent mineralocorticoid excess n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:tay-sachs disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:tyrosinemia type ii n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:tyrosinemia, type iii n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:urocanase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 21 / 0.488 -> en:waardenburg anophthalmia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=21 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> adénite sinusale cytophagique n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=adénite sinusale cytophagique | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> cétoacidurie à chaînes ramifiées n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit congénital en mégacaryocytes n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en biotinidase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en neuraminidase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en prolidase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:adenosine deaminase superactivity n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:adenosine deaminase superactivity | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:alkaptonuria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:anemia due to pentose phosphate pathway defect n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:anemia due to pentose phosphate pathway defect | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:autosomal recessive spastic paraplegia type 39 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:biotinidase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:braddock syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:brain calcification rajab type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:chronic non-spherocytic hemolytic anemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:chronic non-spherocytic hemolytic anemia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1h n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 2e n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:craniofacial ulnar renal syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:deafness and myopia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:drug-induced enzyme deficiency anemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:drug-induced enzyme deficiency anemia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Dubin-Sprinz disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:familial median cleft of upper and lower lip n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:fountain syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:glucose-6-phosphate dehydrogenase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:glutathione synthetase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:haemolysis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:haemolysis | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hemolysis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hemolysis | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hereditary factor xii deficiency disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:histidinaemia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hnsha due to hexokinase deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to hexokinase deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:I-cell disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:kallman syndrome with heart disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Leroy's i-cell disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Leroy's i-cell disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:lethal hemolytic anemia and genital anomaly syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lethal hemolytic anemia and genital anomaly syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:leucinosis n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:leucinosis | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:manouvrier syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:moyamoya disease with early onset achalasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:mucopolysaccharidosis i n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:najjar syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Niemann-Pick disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:oculocutaneous albinism type 6 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:type a 14 n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:type a 14 | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:tyrosinemia type II n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:tyrosinemia type II | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Wolman's disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:wolman's disease n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:wolman's disease | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> en:zellweger-like syndrome without peroxisomal anomaly n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> fucosidose n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=fucosidose | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hématolyse n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hématolyse | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hémolyse n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hémolyse | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> histidinémie n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=histidinémie | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> histiocytose sinusale hémophagocytaire n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> intolérance au fructose n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> leucinose n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=leucinose | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de Niemann-Pick n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> Maladie de Tay-Sachs n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=Maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> Maladie de Wolman n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de Wolman n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie de wolman n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie de wolman | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> mucolipidose II n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=mucolipidose II | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> mucolipidose type II n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> mucolipidose type ii n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> oxalose n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=oxalose | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> oxalose primitive n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=oxalose primitive | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> oxaloses n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=oxaloses | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> rétention des chylomicrons (maladie de la) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> stomatocytose héréditaire n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=stomatocytose héréditaire | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> syndrome de synostose spondylo-carpo-tarsale n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> syndrome de Zellweger n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=syndrome de Zellweger | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> Wolman (maladie de) n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20 en:hnsha due to diphosphoglycerate mutase deficiency -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20

≈ 582 relations entrantes en:maple syrup urine disease --- r_associated #0: 697 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:maple syrup urine disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=697 leucinose --- r_associated #0: 598.82 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=leucinose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=598.82 maladie du sirop d'érable --- r_associated #0: 594.46 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie du sirop d'érable | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=594.46 en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:branched-chain ketoaciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=520 en:classical maple syrup urine disease --- r_associated #0: 280 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:classical maple syrup urine disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=280 en:thiamin-responsive maple syrup urine disease --- r_associated #0: 280 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:thiamin-responsive maple syrup urine disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=280 déficit en céto-acide décarboxylase --- r_associated #0: 275 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en céto-acide décarboxylase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=275 maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 275 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie des urines à l'odeur de sirop d'érable | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=275 maladie des urines avec odeur de sirop erable --- r_associated #0: 270 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie des urines avec odeur de sirop erable | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=270 hypophosphatasie infantile --- r_associated #0: 217 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hypophosphatasie infantile | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=217 en:infantile hypophosphatasia --- r_associated #0: 215 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:infantile hypophosphatasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=215 hypophosphatasie foetale --- r_associated #0: 213 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hypophosphatasie foetale | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=213 en:pyruvate carboxylase deficiency --- r_associated #0: 180 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pyruvate carboxylase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=180 en:walker-warburg syndrome --- r_associated #0: 180 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:walker-warburg syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=180 syndrome de Walker-Warburg --- r_associated #0: 178 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Walker-Warburg | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=178 déficit en pyruvate carboxylase --- r_associated #0: 177 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en pyruvate carboxylase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=177 en:xeroderma pigmentosum --- r_associated #0: 175 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:xeroderma pigmentosum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=175 en:zellweger syndrome --- r_associated #0: 173 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:zellweger syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=173 xeroderma pigmentosum --- r_associated #0: 173 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xeroderma pigmentosum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=173 en:Zellweger syndrome --- r_associated #0: 170 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Zellweger syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=170 hyperoxalurie primitive --- r_associated #0: 120 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperoxalurie primitive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=120 en:cytochrome-c oxidase deficiency --- r_associated #0: 114 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cytochrome-c oxidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=114 déficit en cytochrome oxydase --- r_associated #0: 112 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en cytochrome oxydase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=112 en:primary hyperoxaluria --- r_associated #0: 111 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:primary hyperoxaluria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=111 hyperoxalurie primaire --- r_associated #0: 111 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperoxalurie primaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=111 oxalose primitive --- r_associated #0: 111 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=oxalose primitive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=111 oxaloses --- r_associated #0: 111 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=oxaloses | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=111 oxalose --- r_associated #0: 105 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=oxalose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=105 déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en cytochrome-c oxydase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=95 hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperplasie congénitale des surrénales | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=95 en:congenital adrenal hyperplasia --- r_associated #0: 93 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital adrenal hyperplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=93 en:dubin-johnson syndrome --- r_associated #0: 64 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:dubin-johnson syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=64 syndrome de dubin-johnson --- r_associated #0: 60 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de dubin-johnson | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=60 en:mucopolysaccharidosis type i --- r_associated #0: 58 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mucopolysaccharidosis type i | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=58 hémolyse --- r_associated #0: 56 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémolyse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=56 Xeroderma pigmentosum --- r_associated #0: 55 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Xeroderma pigmentosum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=55 en:mucopolysaccharidosis i --- r_associated #0: 55 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mucopolysaccharidosis i | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=55 en:niemann-pick disease --- r_associated #0: 54 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:niemann-pick disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=54 hématolyse --- r_associated #0: 53 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hématolyse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=53 en:tay-sachs disease --- r_associated #0: 52 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tay-sachs disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=52 syndrome de Dubin-Johnson --- r_associated #0: 52 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Dubin-Johnson | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=52 xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthomatose cérébro-tendineuse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=51 xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthomatose cérébrotendineuse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=51 en:Niemann-Pick disease --- r_associated #0: 50 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Niemann-Pick disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=50 en:Tay-Sachs disease --- r_associated #0: 50 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Tay-Sachs disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=50 en:cerebrotendinous xanthomatosis --- r_associated #0: 50 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cerebrotendinous xanthomatosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=50 xérodermite pigmentaire --- r_associated #0: 50 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xérodermite pigmentaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=50 van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 48 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=48 en:hemolysis --- r_associated #0: 47 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hemolysis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=47 sirop d'érable (urine à odeur de) --- r_associated #0: 47 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sirop d'érable (urine à odeur de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=47 en:wolman disease --- r_associated #0: 46 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:wolman disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=46 maladie de Wolman --- r_associated #0: 46 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de Wolman | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=46 acrodermatite entéropathique --- r_associated #0: 45 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=acrodermatite entéropathique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=45 en:Wolman's disease --- r_associated #0: 45 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Wolman's disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=45 intolérance au fructose --- r_associated #0: 45 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=intolérance au fructose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=45 xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 45 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=45 maladie de wolman --- r_associated #0: 44 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de wolman | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=44 en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 43 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=43 en:hereditary factor x deficiency disease --- r_associated #0: 43 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary factor x deficiency disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=43 en:hereditary fructose intolerance --- r_associated #0: 43 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary fructose intolerance | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=43 en:acrodermatitis enteropathica --- r_associated #0: 42 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:acrodermatitis enteropathica | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=42 en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 42 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=42 en:muscle amp deaminase deficiency --- r_associated #0: 42 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:muscle amp deaminase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=42 en:robinow-like syndrome --- r_associated #0: 42 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:robinow-like syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=42 en:drug-induced enzyme deficiency anemia --- r_associated #0: 41 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:drug-induced enzyme deficiency anemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=41 en:factor v and factor viii, combined deficiency of --- r_associated #0: 41 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:factor v and factor viii, combined deficiency of | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=41 en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 41 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=41 stomatocytose héréditaire --- r_associated #0: 41 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=stomatocytose héréditaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=41 Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Walker-Warburg (syndrome de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 en:alpha, alpha-trehalase deficiency --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alpha, alpha-trehalase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 en:haemolysis --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:haemolysis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 en:sonoda syndrome --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sonoda syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 maladie de Niemann-Pick --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de Niemann-Pick | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 maladie de Tay-sachs --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de Tay-sachs | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 maladie de tay-sachs --- r_associated #0: 40 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de tay-sachs | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=40 en:hereditary stomatocytosis --- r_associated #0: 39 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary stomatocytosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=39 en:macular corneal dystrophy --- r_associated #0: 39 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:macular corneal dystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=39 rétention des chylomicrons (maladie de la) --- r_associated #0: 39 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention des chylomicrons (maladie de la) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=39 en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 38 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:5 alpha steroid reductase 2 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=38 en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 38 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=38 en:maple-tree syrup disease --- r_associated #0: 38 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:maple-tree syrup disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=38 en:aminoacylase 1 deficiency --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:aminoacylase 1 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 en:chylomicron retention disease --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:chylomicron retention disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 en:deafness, progressive, with stapes fixation --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deafness, progressive, with stapes fixation | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 en:fountain syndrome --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fountain syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 en:nathalie syndrome --- r_associated #0: 37 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:nathalie syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=37 déficit en prolidase --- r_associated #0: 36 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en prolidase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=36 en:chronic non-spherocytic hemolytic anemia --- r_associated #0: 36 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:chronic non-spherocytic hemolytic anemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=36 en:spinocerebellar ataxia with epilepsy --- r_associated #0: 36 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spinocerebellar ataxia with epilepsy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=36 en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 36 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:syndrome of apparent mineralocorticoid excess | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=36 Wolman (maladie de) --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Wolman (maladie de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:2-hydroxyglutaric aciduria --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:2-hydroxyglutaric aciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:I-cell disease --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:I-cell disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:acrocallosal syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:acrocallosal syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:aminomethyltransferase deficiency --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:aminomethyltransferase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:argininemia --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:argininemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:bestrophinopathy, autosomal recessive --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bestrophinopathy, autosomal recessive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:congenital disorder of glycosylation type 1h --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type 1h | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:congenital disorder of glycosylation type id --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type id | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:craniofacial ulnar renal syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:craniofacial ulnar renal syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:cutis laxa, autosomal recessive --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cutis laxa, autosomal recessive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:enterokinase deficiency --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:enterokinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:ethanolaminosis --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ethanolaminosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:familial median cleft of upper and lower lip --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial median cleft of upper and lower lip | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:familial renal iminoglycinuria --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial renal iminoglycinuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:hereditary factor xii deficiency disease --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary factor xii deficiency disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:i-cell disease --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:i-cell disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:jervell and lange nielsen syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:jervell and lange nielsen syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:lethal hemolytic anemia and genital anomaly syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lethal hemolytic anemia and genital anomaly syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:manouvrier syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:manouvrier syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:n-acetylglutamate synthase deficiency --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:n-acetylglutamate synthase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:naxos disease --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:naxos disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:northern epilepsy syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:northern epilepsy syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:papillon-lefevre syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:papillon-lefevre syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:peeling skin syndrome, acral type --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:peeling skin syndrome, acral type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:persistent mullerian duct syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:persistent mullerian duct syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:prolonged electroretinal response suppression --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:prolonged electroretinal response suppression | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:reardon hall slaney syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:reardon hall slaney syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 en:spondylo-ocular syndrome --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondylo-ocular syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 mucolipidose type II --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mucolipidose type II | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 mucolipidose type ii --- r_associated #0: 35 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mucolipidose type ii | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35 dysplasie craniodiaphysaire --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=dysplasie craniodiaphysaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive distal osteolysis syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:autosomal recessive scid --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive scid | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:biotinidase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:biotinidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:brain calcification rajab type --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:brain calcification rajab type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:congenital disorder of glycosylation type ie --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type ie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:congenital leptin deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital leptin deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:crisponi syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:crisponi syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:cystathionine beta-synthase deficiency disease --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cystathionine beta-synthase deficiency disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:deafness, sensorineural, and male infertility --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deafness, sensorineural, and male infertility | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:diaphanospondylodysostosis --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:diaphanospondylodysostosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:fronto-facio-nasal dysplasia --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fronto-facio-nasal dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:glutamate formiminotransferase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glutamate formiminotransferase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:glycogen storage disease type x --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glycogen storage disease type x | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:gurrieri sammito bellussi syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:gurrieri sammito bellussi syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:hnsha due to nadh diaphorase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to nadh diaphorase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:hnsha due to phosphofructokinase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to phosphofructokinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:hyperphosphatasia with mental retardation --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hyperphosphatasia with mental retardation | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:hypomagnesemia 1, intestinal --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypomagnesemia 1, intestinal | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:lethal congenital contracture syndrome type 3 --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lethal congenital contracture syndrome type 3 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:leukotriene c4 synthase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:leukotriene c4 synthase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:mannosidosis --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mannosidosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:microcephaly albinism digital anomalies syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:morquio syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:morquio syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:moyamoya disease with early onset achalasia --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:moyamoya disease with early onset achalasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:oculocutaneous albinism type 6 --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:oculocutaneous albinism type 6 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:prolidase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:prolidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:purine-nucleoside phosphorylase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:sanfilippo syndrome --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sanfilippo syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:urocanase deficiency --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:urocanase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:valinemia --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:valinemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 en:werdnig-hoffmann disease --- r_associated #0: 34 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:werdnig-hoffmann disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=34 histiocytose sinusale hémophagocytaire --- r_associated #0: 33 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histiocytose sinusale hémophagocytaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=33 en:21-hydroxylase deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:21-hydroxylase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:acrorenal mandibular syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:acrorenal mandibular syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:alpha-1 antitrypsin deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alpha-1 antitrypsin deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:amelogenesis imperfecta - recessive - rough | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:anemia due to pentose phosphate pathway defect --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:anemia due to pentose phosphate pathway defect | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:ataxia with vitamin e deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ataxia with vitamin e deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive idiopathic familial dystonia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:bowen-conradi syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bowen-conradi syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:craniodiaphyseal dysplasia --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:craniodiaphyseal dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:erythropenia --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:erythropenia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:fryns macrocephaly --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fryns macrocephaly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:gracile syndrome (disorder) --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:gracile syndrome (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:hypospadias-mental retardation syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypospadias-mental retardation syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:laron syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:laron syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:leucinosis --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:leucinosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lissencephaly syndrome, norman-roberts type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:microcephaly-capillary malformation syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:multiple sulfatase deficiency disease --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:multiple sulfatase deficiency disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:najjar syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:najjar syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:presentey anomaly --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:presentey anomaly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:richards-rundle syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:richards-rundle syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:saito kuba tsuruta syndrome --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:saito kuba tsuruta syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 32 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32 ahhns par déficit en diphosphoglycérate mutase --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=ahhns par déficit en diphosphoglycérate mutase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 déficit en neuraminidase --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en neuraminidase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:3-methylglutaconic aciduria type 5 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:3-methylglutaconic aciduria type 5 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:acid phosphatase deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:acid phosphatase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:behrens baumann dust syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:behrens baumann dust syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bietti crystalline corneoretinal dystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:childhood hypophosphatasia (disorder) --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:childhood hypophosphatasia (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:citrin deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:citrin deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hereditary factor xi deficiency disease --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary factor xi deficiency disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hnsha due to aldolase a deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to aldolase a deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hyperprolinemia type 1 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hyperprolinemia type 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hyperprolinemia type 2 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hyperprolinemia type 2 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hypomandibular faciocranial dysostosis --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypomandibular faciocranial dysostosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hypomyelination and congenital cataract --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypomyelination and congenital cataract | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:hypophosphatasia infantile --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypophosphatasia infantile | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:isaacs syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:isaacs syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:isovaleric acidemia --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:isovaleric acidemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:late-onset junctional epidermolysis bullosa --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:late-onset junctional epidermolysis bullosa | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:lethal congenital contracture syndrome 2 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lethal congenital contracture syndrome 2 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:north american indian childhood cirrhosis --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:north american indian childhood cirrhosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:porphobilinogen synthase deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:porphobilinogen synthase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:rapadilino syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:rapadilino syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:renal dysplasia - limb defects syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:renal dysplasia - limb defects syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:severe steroid 21-hydroxylase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:sitosterolemia with xanthomatosis --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sitosterolemia with xanthomatosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:split-hand/foot malformation 3 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:split-hand/foot malformation 3 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondylocarpotarsal synostosis syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:thyroid dyshormonogenesis 4 --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:thyroid dyshormonogenesis 4 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 en:tungland bellman syndrome --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tungland bellman syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 fucosidose --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=fucosidose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 histidinémie --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidinémie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 mucolipidose II --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mucolipidose II | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 neuro-acanthocytose --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=neuro-acanthocytose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 31 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=31 Maladie de Tay-Sachs --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Maladie de Tay-Sachs | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 déficit congénital en mégacaryocytes --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit congénital en mégacaryocytes | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:al awadi syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:al awadi syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:anauxetic dysplasia --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:anauxetic dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:autosomal recessive ocular albinism --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive ocular albinism | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:bardet-biedl syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bardet-biedl syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:brachydactyly syndrome type b --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:brachydactyly syndrome type b | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:braddock syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:braddock syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:congenital disorder of glycosylation type 2e --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type 2e | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:congenital disorder of glycosylation type ic --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type ic | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:congenital disorder of glycosylation, type if --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation, type if | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:congenital transferrin deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital transferrin deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:desmosterolosis --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:desmosterolosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:dicarboxylicaminoaciduria --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:dicarboxylicaminoaciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:ehlers-danlos syndrome, type vi --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ehlers-danlos syndrome, type vi | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:glutathione synthetase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glutathione synthetase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to decreased adenosine deaminase activity --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to decreased adenosine deaminase activity | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to gamma glutamyl cysteine synthetase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to gamma glutamyl cysteine synthetase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to hexokinase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to hexokinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hnsha due to phosphoglycerate kinase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to phosphoglycerate kinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:hypokalemia, familial --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypokalemia, familial | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:infantile globoid cell leukodystrophy --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:infantile globoid cell leukodystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:isolated hyperchlorhidrosis --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:isolated hyperchlorhidrosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:jankovic rivera syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:jankovic rivera syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:lethal congenital contracture syndrome 1 --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lethal congenital contracture syndrome 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:lethal larsen-like syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:lethal larsen-like syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:maroteaux-lamy syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:maroteaux-lamy syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:microcephaly, amish type (disorder) --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:microcephaly, amish type (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:rna polymerase iii-related leukodystrophy --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:rna polymerase iii-related leukodystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:sulfite oxidase deficiency --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sulfite oxidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:xanthinuria, type i --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:xanthinuria, type i | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 maladie de Tay-Sachs --- r_associated #0: 30 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de Tay-Sachs | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=30 déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:3-methylglutaconic aciduria type 1 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:3-methylglutaconic aciduria type 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:adenosine deaminase superactivity --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:adenosine deaminase superactivity | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:alkaptonuria --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alkaptonuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:antley-bixler syndrome, autosomal dominant | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:aspartylglycosaminuria --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:aspartylglycosaminuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:behr syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:behr syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:cerebellar ataxia, cayman type --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cerebellar ataxia, cayman type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:chitty hall baraitser syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:chitty hall baraitser syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:classical phenylketonuria --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:classical phenylketonuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital analbuminemia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital analbuminemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital disorder of glycosylation type ia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type ia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital dyserythropoietic anemia, type i --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital dyserythropoietic anemia, type i | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:congenital sucrase-isomaltase deficiency --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital sucrase-isomaltase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:deficiency of hexokinase (disorder) --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deficiency of hexokinase (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:donnai-barrow syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:donnai-barrow syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:glucose-6-phosphate dehydrogenase deficiency anemia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:heart defects limb shortening --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:heart defects limb shortening | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:laurence-moon syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:laurence-moon syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:macdermot winter syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:macdermot winter syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:pelviscapular dysplasia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pelviscapular dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:pontocerebellar hypoplasia type 2 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pontocerebellar hypoplasia type 2 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:pseudocholinesterase deficiency --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pseudocholinesterase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:spondyloenchondrodysplasia --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondyloenchondrodysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:type a 14 --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:type a 14 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:warsaw breakage syndrome --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:warsaw breakage syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 en:wolman's disease --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:wolman's disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 syndrome de Laurence-Moon --- r_associated #0: 29 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Laurence-Moon | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=29 adénite sinusale cytophagique --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=adénite sinusale cytophagique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:adenine phosphoribosyltransferase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:albinotic fundus --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:albinotic fundus | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:brown-vialetto-van laere syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:brown-vialetto-van laere syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:congenital bowing of long bone --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital bowing of long bone | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital dyserythropoietic anemia, type ii | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:corpus callosum agenesis neuronopathy --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:corpus callosum agenesis neuronopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:crigler-najjar syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:crigler-najjar syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:deficiency of glucosyltransferase 1 --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deficiency of glucosyltransferase 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:familial hypoaldosteronism --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial hypoaldosteronism | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:fucosidosis --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fucosidosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:hnsha due to nadh-methemoglobin reductase deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to nadh-methemoglobin reductase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:hyperimmunoglobulin e syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hyperimmunoglobulin e syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:kuskokwim disease --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:kuskokwim disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:majeed syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:majeed syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:myopathy with exercise intolerance, swedish type --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:myopathy with exercise intolerance, swedish type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:oculocutaneous albinism type 4 --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:oculocutaneous albinism type 4 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:otoonychoperoneal syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:otoonychoperoneal syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:retinitis punctata albescens (disorder) --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:retinitis punctata albescens (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:sly syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sly syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:thomas syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:thomas syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:transcobalamin ii deficiency --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:transcobalamin ii deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:type ii acrocephalopolysyndactyly --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:type ii acrocephalopolysyndactyly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:tyrosinemia, type iii --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tyrosinemia, type iii | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:waardenburg anophthalmia syndrome --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:waardenburg anophthalmia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 28 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 déficit en biotinidase --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en biotinidase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:3-methylglutaconic aciduria type 3 --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:3-methylglutaconic aciduria type 3 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:5-oxoprolinase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:5-oxoprolinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:Dubin-Sprinz disease --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Dubin-Sprinz disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:allgrove syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:allgrove syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:arginine:glycine amidinotransferase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:atrophoderma vermiculatum --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:atrophoderma vermiculatum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:baller-gerold syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:baller-gerold syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:brody myopathy --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:brody myopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:childhood myocerebrohepatopathy spectrum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:chondrodysplasia punctata syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:chondrodysplasia punctata syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:combined malonic and methylmalonic aciduria --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:combined malonic and methylmalonic aciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:congenital disorder of glycosylation type ig --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital disorder of glycosylation type ig | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital nonspherocytic hemolytic anemia due to inborn error of metabolism | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:congenital pancreatic enterokinase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:congenital pancreatic enterokinase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:cryptophthalmos syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cryptophthalmos syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:cystinosis --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cystinosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:deafness and myopia syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:deafness and myopia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:dyskeratosis congenita, autosomal recessive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:ear, patella, short stature syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ear, patella, short stature syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:generalized peeling skin syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:generalized peeling skin syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:giacci familial neurogenic acroosteolysis --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:giacci familial neurogenic acroosteolysis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:hall riggs syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hall riggs syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:histidinaemia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:histidinaemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:histidinemia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:histidinemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:hmg-coa lyase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hmg-coa lyase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:hnsha due to glutathione reductase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hnsha due to glutathione reductase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:kallman syndrome with heart disease --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:kallman syndrome with heart disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:microcephalic primordial dwarfism toriello type --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:microcephalic primordial dwarfism toriello type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:microcephaly cervical spine fusion anomalies --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:microcephaly cervical spine fusion anomalies | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:morm syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:morm syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:netherton syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:netherton syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:neuraminidase deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neuraminidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:neuroacanthocytosis --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neuroacanthocytosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:neutral lipid storage disease with myopathy --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neutral lipid storage disease with myopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:odontohypophosphatasia (disorder) --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:odontohypophosphatasia (disorder) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:pelizaeus merzbacher like disease --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pelizaeus merzbacher like disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:propionic acidemia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:propionic acidemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:smith-mccort dysplasia --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:smith-mccort dysplasia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spastic paraplegia 15, autosomal recessive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:tyrosinemia type II --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tyrosinemia type II | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 en:verloes bourguignon syndrome --- r_associated #0: 27 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:verloes bourguignon syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=27 Maladie de Wolman --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Maladie de Wolman | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 cétoacidurie à chaînes ramifiées --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=cétoacidurie à chaînes ramifiées | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:3-methylglutaconic aciduria type iv --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:3-methylglutaconic aciduria type iv | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:Leroy's i-cell disease --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Leroy's i-cell disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:alpha-fetoprotein deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alpha-fetoprotein deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:argininosuccinic aciduria --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:argininosuccinic aciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:arterial tortuosity syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:arterial tortuosity syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:ataxia telangiectasia syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ataxia telangiectasia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:ateliotic dwarfism without insulinopenia --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ateliotic dwarfism without insulinopenia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:autosomal recessive primary microcephaly --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive primary microcephaly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:autosomal recessive sideroblastic anemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:bamforth syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bamforth syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:bothnia retinal dystrophy --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:bothnia retinal dystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:charcot-marie-tooth disease type 4 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:cohen syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cohen syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:cooper jabs syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:cooper jabs syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:ectodermal dysplasia with blindness syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:familial acantholysis --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial acantholysis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fibular hypoplasia and complex brachydactyly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:gamma-glutamyltransferase deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:gamma-glutamyltransferase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:geroderma osteodysplastica --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:geroderma osteodysplastica | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:glutamate-cysteine ligase deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:glutamate-cysteine ligase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:insulin growth factor i deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:insulin growth factor i deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:isolated hypoplasia of the right ventricle --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:isolated hypoplasia of the right ventricle | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:knobloch syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:knobloch syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:marles greenberg persaud syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:marles greenberg persaud syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:neonatal progeroid syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:neonatal progeroid syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:nonaka myopathy --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:nonaka myopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:phenylketonuria ii --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:phenylketonuria ii | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:pili torti onychodysplasia syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pili torti onychodysplasia syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:pseudotrisomy 13 syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:sarcosinemia --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:sarcosinemia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:severe early childhood onset retinal dystrophy --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:severe early childhood onset retinal dystrophy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:trichohepatoenteric syndrome --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:trichohepatoenteric syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 en:tyrosinemia type ii --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:tyrosinemia type ii | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 syndrome de Zellweger --- r_associated #0: 26 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Zellweger | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26 déficit en sulfite-oxydase --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit en sulfite-oxydase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:Laurence-Moon's syndrome --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Laurence-Moon's syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:adenosine deaminase overproduction --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:adenosine deaminase overproduction | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:oxalosis --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:oxalosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 xanthique (lithiase) --- r_associated #0: 25 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthique (lithiase) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:Dubin-Johnson's syndrome --- r_associated #0: 24 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Dubin-Johnson's syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=24 en:alstrom syndrome --- r_associated #0: 24 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alstrom syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=24 en:becker generalized myotonia --- r_associated #0: 24 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:becker generalized myotonia | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=24 en:Laron syndrome --- r_associated #0: 23 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Laron syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23 en:Nathalie syndrome --- r_associated #0: 23 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Nathalie syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23 en:allanson pantzar mcleod syndrome --- r_associated #0: 23 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:allanson pantzar mcleod syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23 en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 23 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:familial c3b inhibitor deficiency syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23 maladie de dubin-johnson --- r_associated #0: 23 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de dubin-johnson | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=23 semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 22 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=22 acidurie argininosuccinique --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=acidurie argininosuccinique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 acidémie isovalérique --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=acidémie isovalérique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 acrodermatitis enteropathica --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=acrodermatitis enteropathica | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 alcaptonurie --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=alcaptonurie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 argininémie --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=argininémie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=déficit enzymatique partiel de la surrénale | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 en:zinc-deficiency type --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:zinc-deficiency type | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 idiosyncrasie au fructose --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=idiosyncrasie au fructose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 mannosidose --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mannosidose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mucopolysaccharidose de type 1 | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 mucopolysaccharidose de type I --- r_associated #0: 21 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=mucopolysaccharidose de type I | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=21 Fuchs (syndrome de) --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Fuchs (syndrome de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 His (faisceau de) --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=His (faisceau de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Hyperplasie congénitale des surrénales | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 Intolérance au fructose --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Intolérance au fructose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 Maladie de Niemann-Pick --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Maladie de Niemann-Pick | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Syndrome de Walker-Warburg | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 hémohistioblastique (tissu) --- r_associated #0: 15 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémohistioblastique (tissu) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=15 syndrome de Warburg --- r_associated #0: 11 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Warburg | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=11 Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Dubin-Johnson (syndrome de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Fucosidose --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Fucosidose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Histidinémie --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Histidinémie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Hémolyse --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Hémolyse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Laurence-Moon (syndrome de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Manning (score de) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Manning (score de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Mannosidose --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Mannosidose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Niemann-Pick (maladie de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 alcalose métabolique (classification) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=alcalose métabolique (classification) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 cornée et tyrosinose de type II --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=cornée et tyrosinose de type II | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:HHH syndrome --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:HHH syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:Tay Sachs' disease --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Tay Sachs' disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:alcaptonuria --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:alcaptonuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:homogentisuria --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:homogentisuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:phosphatide thesaurismosis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 en:xanthine lithiasis --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:xanthine lithiasis | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 maladie de niemann-pick --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=maladie de niemann-pick | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 nanisme de type Laron --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=nanisme de type Laron | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 neuraminidase (déficit en) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=neuraminidase (déficit en) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 prolidase (déficit en) --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=prolidase (déficit en) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétention hydrochlorurée sodique --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention hydrochlorurée sodique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétention membraneuse --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention membraneuse | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétention placentaire --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention placentaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétention placentaire du postabortum --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention placentaire du postabortum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétention sudorale --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétention sudorale | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 rétentionniste --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=rétentionniste | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 sirtuine --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sirtuine | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 sisi-test --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sisi-test | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 sismothérapie --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sismothérapie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 syndrome de Nathalie --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Nathalie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 syndrome de zellweger --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de zellweger | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 xanthomatose familiale primitive --- r_associated #0: 10 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthomatose familiale primitive | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=10 Stokvis-Talma (syndrome de) --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Stokvis-Talma (syndrome de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=Tay-Sachs (maladie de) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 en:Sachs' disease --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:Sachs' disease | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 faisceau de His --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=faisceau de His | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 fuchsine --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=fuchsine | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 fucose --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=fucose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 fucosidase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=fucosidase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 fucoside --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=fucoside | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminergie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminergie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminergique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminergique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminolibération --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminolibération | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminolytique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminolytique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminopexie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminopexie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminurie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminurie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histaminémie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histaminémie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidinase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidinase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidine --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidine | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidine-ammoniac-lyase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidine-ammoniac-lyase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidine-décarboxylase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidine-décarboxylase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 histidine-désaminase --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=histidine-désaminase | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperostose vertébrale ankylosante | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hyperoxalurie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperoxalurie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hyperoxalémie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hyperoxalémie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hémojuvéline --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémojuvéline | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hémolymphangiome --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémolymphangiome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hémolysant --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémolysant | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 hémolysat --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=hémolysat | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 semidominance --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=semidominance | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 semiquinone --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=semiquinone | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 syndrome de Fuchs --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=syndrome de Fuchs | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminal --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminal | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminifère --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminifère | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminomateux --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminomateux | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminome --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminome de l'ovaire --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminome de l'ovaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminome du médiastin --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminome du médiastin | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 séminome spermatocytaire --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=séminome spermatocytaire | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 sémiochimique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sémiochimique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 sémiologie extrapyramidale --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=sémiologie extrapyramidale | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthoastrocytome pléomorphe | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthochromie --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthochromie | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthochromie caroténique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthochromie caroténique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthoerythrodermia perstans --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthoerythrodermia perstans | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthogranulome juvénile --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthogranulome juvénile | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthogranulome nécrobiotique | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthogranulome palpébral --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthogranulome palpébral | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthohistiocytome --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthohistiocytome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthoma disseminatum --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthoma disseminatum | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5 xanthomatose --- r_associated #0: 5 --> en:hnsha due to diphosphoglycerate mutase deficiency n1=xanthomatose | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=5