'en:primary immunodeficiency syndrome due to p14 deficiency'
(id=9102855 ; fe=en:primary immunodeficiency syndrome due to p14 deficiency ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=14604 creation date=2017-10-29 touchdate=2025-07-25 19:44:27.000)

≈ 687 relations sortantes en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:congenital hereditary facial paralysis with variable hearing loss syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital hereditary facial paralysis with variable hearing loss syndrome | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:manouvrier syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:spinal muscular atrophy with respiratory distress 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:succinic semialdehyde dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 43 / 1 -> en:tryptophanuria with dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tryptophanuria with dwarfism | rel=r_associated | relid=0 | w=43 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:congenital adrenal hyperplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:faciocardiomelic dysplasia, lethal n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:faciocardiomelic dysplasia, lethal | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:glycine dehydrogenase (decarboxylating) deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:mental retardation smith fineman myers type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mental retardation smith fineman myers type | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:odontohypophosphatasia (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:oliver-mcfarlane syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oliver-mcfarlane syndrome | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 42 / 0.977 -> en:type ii mucolipidosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:type ii mucolipidosis | rel=r_associated | relid=0 | w=42 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 41 / 0.953 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=41 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 41 / 0.953 -> en:netherton syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=41 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 41 / 0.953 -> en:sitosterolemia with xanthomatosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=41 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 40 / 0.93 -> en:beta-aminoisobutyricaciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=40 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 40 / 0.93 -> en:lipoid proteinosis of urbach and wiethe n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=40 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 40 / 0.93 -> en:pyruvate carboxylase deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pyruvate carboxylase deficiency disease | rel=r_associated | relid=0 | w=40 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 40 / 0.93 -> en:smith-mccort dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=40 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 39 / 0.907 -> en:lubani al saleh teebi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lubani al saleh teebi syndrome | rel=r_associated | relid=0 | w=39 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 39 / 0.907 -> en:prickle1-related progressive myoclonus epilepsy with ataxia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=39 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 39 / 0.907 -> en:x-linked mendelian susceptibility to mycobacterial disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:x-linked mendelian susceptibility to mycobacterial disease | rel=r_associated | relid=0 | w=39 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:congenital dyserythropoietic anemia, type ii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:congenital pancreatic enterokinase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:cortisol 11-beta-ketoreductase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cortisol 11-beta-ketoreductase deficiency | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:diaphanospondylodysostosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:hall riggs syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:isolated hypoplasia of the right ventricle n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:popliteal pterygium syndrome, lethal type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:popliteal pterygium syndrome, lethal type | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 38 / 0.884 -> en:spinocerebellar ataxia, autosomal recessive 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=38 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:2p21 microdeletion syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:2p21 microdeletion syndrome | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:baller-gerold syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:brachymetapody-anodontia-hypotrichosis-albinoidism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brachymetapody-anodontia-hypotrichosis-albinoidism | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:mandibuloacral dysplasia with type a lipodystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:metatropic dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:metatropic dwarfism | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:pancreas agenesis, dorsal n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pancreas agenesis, dorsal | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:pseudohypoaldosteronism, type 1, recessive form n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:pyle metaphyseal dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:rachitic dwarf n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:rachitic dwarf | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 37 / 0.86 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=37 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 36 / 0.837 -> en:birth length less than 3rd percentile n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:birth length less than 3rd percentile | rel=r_associated | relid=0 | w=36 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 36 / 0.837 -> en:chondrodysplasia punctata syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=36 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 36 / 0.837 -> en:deficiency of glucosyltransferase 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=36 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 36 / 0.837 -> en:juberg-marsidi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:juberg-marsidi syndrome | rel=r_associated | relid=0 | w=36 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 36 / 0.837 -> en:spondyloepimetaphyseal dysplasia, shohat type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepimetaphyseal dysplasia, shohat type | rel=r_associated | relid=0 | w=36 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:3-hydroxyacyl-coa dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:absent thumb with short stature and immunodeficiency syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:absent thumb with short stature and immunodeficiency syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:al awadi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:albinotic fundus n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:alpha 1-antitrypsin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alpha 1-antitrypsin deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:antley-bixler syndrome, autosomal dominant n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:aplasia cutis with myopia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aplasia cutis with myopia syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:ataxia with vitamin e deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:autosomal recessive spastic paraplegia type 11 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:autosomal recessive spastic paraplegia type 39 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:brain dopamine-serotonin vesicular transport disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brain dopamine-serotonin vesicular transport disease | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:cataract and cardiomyopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cataract and cardiomyopathy | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:chromosome 18 syndromes and antibody deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chromosome 18 syndromes and antibody deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:cog5 congenital disorder of glycosylation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cog5 congenital disorder of glycosylation | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:combined malonic and methylmalonic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:congenital disorder of glycosylation type 1h n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:congenital dyserythropoietic anemia, type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:congenital pontocerebellar hypoplasia type 7 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital pontocerebellar hypoplasia type 7 | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:cranioosteoarthropathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cranioosteoarthropathy | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:deafness, progressive, with stapes fixation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:deficiency of fructokinase n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:deficiency of prolidase n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deficiency of prolidase | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dwarfism | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:dyssegmental dysplasia with glaucoma syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dyssegmental dysplasia with glaucoma syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:dystonia 16 (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dystonia 16 (disorder) | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:factor xi deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:factor xi deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:familial c3b inhibitor deficiency syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:feigenbaum bergeron richardson syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:feigenbaum bergeron richardson syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:heart defects limb shortening n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:hernandez aguirre-negrete syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hernandez aguirre-negrete syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:hnsha due to glutathione reductase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:homocystinuria without methylmalonic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:homocystinuria without methylmalonic aciduria | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:hyperphosphatasia with mental retardation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:hyperprolinemia type 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:isovaleryl-coa dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:isovaleryl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:late-onset junctional epidermolysis bullosa n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:lelis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lelis syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:lymphedema, cardiac septal defects, and characteristic facies n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lymphedema, cardiac septal defects, and characteristic facies | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:mcpherson clemens syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mcpherson clemens syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:mucopolysaccharidosis iii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mucopolysaccharidosis iii | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:myopathy, early-onset, with fatal cardiomyopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:neurodegeneration due to cerebral folate transport deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:o/e - short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:o/e - short stature | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:oculocutaneous albinism type 5 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculocutaneous albinism type 5 | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:palmoplantar keratoderma nagashima type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:palmoplantar keratoderma nagashima type | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:pancreatic triacylglycerol lipase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:pentosuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pentosuria | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:progressive cavitating leukoencephalopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:progressive cavitating leukoencephalopathy | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:rapadilino syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:renal dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:renal dwarfism | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:robinow-like syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:schaap taylor baraitser syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:short stature syndrome, brussels type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature syndrome, brussels type | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:sulfite oxidase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:teebi naguib al awadi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:teebi naguib al awadi syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:triple x syndrome, epilepsy, and hypogammaglobulinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:triple x syndrome, epilepsy, and hypogammaglobulinemia | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:uv-sensitive syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:warsaw breakage syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:winship viljoen leary syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:winship viljoen leary syndrome | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 35 / 0.814 -> en:xeroderma pigmentosum n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=35 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:achalasia microcephaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:achalasia microcephaly | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:ackerman syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ackerman syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acrodermatitis enteropathica n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acrofacial dysostosis kennedy teebi type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrofacial dysostosis kennedy teebi type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acromesomelic dysplasia, maroteaux type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acromesomelic dysplasia, maroteaux type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acromicric dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:acrorenal mandibular syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:adducted thumbs and arthrogryposis syndrome christian type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:adenylosuccinate lyase deficiency (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:alpha-methylacyl-coa racemase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:aminomethyltransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:aplasia cutis congenita intestinal lymphangiectasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aplasia cutis congenita intestinal lymphangiectasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:aspartylglucosaminuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aspartylglucosaminuria | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:atkin syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:atkin syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:atrophoderma vermiculatum n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal recessive asexual dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:bamforth syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:behrens baumann dust syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:bilateral microtia with deafness and cleft palate syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bilateral microtia with deafness and cleft palate syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:blepharophimosis with ptosis, syndactyly, and short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:blepharophimosis with ptosis, syndactyly, and short stature | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:bothnia retinal dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:brachymorphism-onychodysplasia-dysphalangism syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brachymorphism-onychodysplasia-dysphalangism syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:brown-vialetto-van laere syndrome 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brown-vialetto-van laere syndrome 1 | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:camptodactyly syndrome, guadalajara type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:camptodactyly syndrome, guadalajara type i | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:cantalamessa baldini ambrosi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cantalamessa baldini ambrosi syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:cdags syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cdags syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:cenani-lenz syndactyly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cenani-lenz syndactyly | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:cervical hypertrichosis and peripheral neuropathy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:combined d-2- and l-2-hydroxyglutaric aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:combined d-2- and l-2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:congenital cataract with ataxia and deafness syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:congenital plasminogen activator inhibitor deficiency type 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:congenital pontocerebellar hypoplasia type 8 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital pontocerebellar hypoplasia type 8 | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:corneal cerebellar syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:corneal cerebellar syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:corneal dystrophy and perceptive deafness n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:corneal dystrophy and perceptive deafness | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:deafness and myopia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:diastrophic dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:diastrophic dysplasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:dwarfism, alopecia, pseudoanodontia, cutis laxa n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dwarfism, alopecia, pseudoanodontia, cutis laxa | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:ectodermal dysplasia with blindness syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:ectodermal dysplasia, ectrodactyly, and macular dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ectodermal dysplasia, ectrodactyly, and macular dystrophy | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:ectodermal dysplasia/ skin fragility syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:fructose-1,6-diphosphatase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fructose-1,6-diphosphatase deficiency | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:gingival fibromatosis with facial dysmorphism syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gingival fibromatosis with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:gracile syndrome (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hepatic lipase deficiency (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hepatic lipase deficiency (disorder) | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hmn (hereditary motor neuropathy) proximal type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hmn (hereditary motor neuropathy) proximal type i | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hypomagnesemia 1, intestinal n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:hypothyroid dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypothyroid dwarfism | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:idiopathic short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:idiopathic short stature | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:immunodeficiency associated with 18p syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:immunodeficiency associated with 18p syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:infantile hypophosphatasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:intellectual disability with cataract and kyphosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:intellectual disability with cataract and kyphosis syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:jeune thoracic dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:jeune thoracic dystrophy | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:kaufman-mckusick syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:krasnow qazi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:krasnow qazi syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:lecithin acyltransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:lethal larsen-like syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:lissencephaly type 3 metacarpal bone dysplasia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lissencephaly type 3 metacarpal bone dysplasia syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:lowry wood syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lowry wood syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:malignant hyperthermia with arthrogryposis and torticollis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:malignant hyperthermia with arthrogryposis and torticollis syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:mannosidase deficiency diseases n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mannosidase deficiency diseases | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:maple syrup urine disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:marden walker like syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:marden walker like syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:microcephalic primordial dwarfism toriello type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:microcephaly albinism digital anomalies syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:moderate steroid 21-hydroxylase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:mucopolysaccharidosis iv n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mucopolysaccharidosis iv | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:nathalie syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:neutral lipid storage disease with myopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:nutritional stunting n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nutritional stunting | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:oculotrichodysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculotrichodysplasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:orofaciodigital syndrome 5 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:orofaciodigital syndrome 5 | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:parkinsonism-dystonia, infantile n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:parkinsonism-dystonia, infantile | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:qazi markouizos syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:qazi markouizos syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:retinitis punctata albescens (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:sparse hair with short stature and skin anomaly syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sparse hair with short stature and skin anomaly syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:spondyloenchondrodysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:spondyloepimetaphyseal dysplasia, irapa type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepimetaphyseal dysplasia, irapa type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:spondyloepimetaphyseal dysplasia, pakistani type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepimetaphyseal dysplasia, pakistani type | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:verloes bourguignon syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:wellesley carman french syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 34 / 0.791 -> en:wolman disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:wolman disease | rel=r_associated | relid=0 | w=34 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:3-methylglutaconic aciduria type 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:acrocephalopolydactylous dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrocephalopolydactylous dysplasia | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:acrocephalopolysyndactyly type iv n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrocephalopolysyndactyly type iv | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:anemia, hypochromic microcytic, with iron overload n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:asymmetric short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:asymmetric short stature | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:bardet-biedl syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:bosley-salih-alorainy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bosley-salih-alorainy syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:camptodactyly syndrome guadalajara type 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:camptodactyly syndrome guadalajara type 2 | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:congenital bowing of long bone n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:congenital disorder of glycosylation type 1k n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type 1k | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:congenital intrauterine infection-like syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital intrauterine infection-like syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:cystathionine beta-synthase deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:cystinosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cystinosis | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:de sanctis-cacchione syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:donnai-barrow syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:ear, patella, short stature syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:familial aplasia of the vermis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial aplasia of the vermis | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:fatty acid hydroxylase-associated neurodegeneration n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:fronto-facio-nasal dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:gaze palsy, familial horizontal, with progressive scoliosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:geroderma osteodysplastica n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:glutamate formiminotransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:growth retardation, alopecia, pseudoanodontia and optic atrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:hereditary factor x deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:hmg coa lyase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hmg coa lyase deficiency | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:hypertryptophanemia, familial n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypertryptophanemia, familial | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:immunodeficiency syndrome, variable n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:immunodeficiency syndrome, variable | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:interleukin-1 receptor-associated kinase 4 deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:kapur toriello syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kapur toriello syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:majeed syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:miller-mckusick-malvaux-syndrome (3m syndrome) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:mitochondrial dna depletion syndrome 2 (myopathic type) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:moyamoya disease with early onset achalasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:multiple mitochondrial dysfunctions syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:multiple mitochondrial dysfunctions syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:muscle amp deaminase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:myhre syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:myopathy with exercise intolerance, swedish type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:nivelon nivelon mabille syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nivelon nivelon mabille syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:north american indian childhood cirrhosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:oculopalatocerebral syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculopalatocerebral syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:omphalocele cleft palate syndrome lethal n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:omphalocele cleft palate syndrome lethal | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:otoonychoperoneal syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:pelizaeus merzbacher like disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:pontocerebellar hypoplasia type 6 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pontocerebellar hypoplasia type 6 | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:renal dysplasia - limb defects syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:saito kuba tsuruta syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:santos mateus leal syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:santos mateus leal syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:severe steroid 21-hydroxylase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:siegler brewer carey syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:siegler brewer carey syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:spastic ataxia, charlevoix-saguenay type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:spastic paraplegia 15, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:spondyloepimetaphyseal dysplasia, aggrecan type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepimetaphyseal dysplasia, aggrecan type | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:spondyloepimetaphyseal dysplasia, matrilin-3 related n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepimetaphyseal dysplasia, matrilin-3 related | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:trichohepatoenteric syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:tungland bellman syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:woods black norbury syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:woods black norbury syndrome | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 32 / 0.744 -> en:xanthinuria, type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=32 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:3-@methylglutaconic aciduria, type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:3-@methylglutaconic aciduria, type i | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:5-oxoprolinase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:adult-onset autosomal recessive sideroblastic anemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adult-onset autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:anophthalmia plus syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:anophthalmia plus syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:argininosuccinic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:autosomal recessive ichthyosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:bifid nose with or without anorectal and renal anomalies n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bifid nose with or without anorectal and renal anomalies | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:bixler christian gorlin syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bixler christian gorlin syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:catel manzke syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:catel manzke syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:cerebellar ataxia, cayman type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:childhood hypophosphatasia (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:codas syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:codas syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:cog4 congenital disorder of glycosylation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cog4 congenital disorder of glycosylation | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital cataracts, facial dysmorphism, and neuropathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital disorder of glycosylation type 1l n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type 1l | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital disorder of glycosylation, type id n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation, type id | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital disorder of glycosylation, type im n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation, type im | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital pontocerebellar hypoplasia type 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital pontocerebellar hypoplasia type 3 | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:craniodiaphyseal dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:cutis laxa, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:cytochrome-c oxidase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:deafness enamel hypoplasia nail defects n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deafness enamel hypoplasia nail defects | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:ehlers-danlos syndrome, arthrochalasia type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:familial median cleft of upper and lower lip n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:giacci familial neurogenic acroosteolysis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:glutamate-cysteine ligase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hadziselimovic syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hadziselimovic syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary adrenal unresponsiveness to corticotropin n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary sensory and autonomic neuropathy with deafness and global delay n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary sensory and autonomic neuropathy with deafness and global delay | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:histidinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:histidinemia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hyper-immunoglobulin e syndrome, autosomal dominant n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyper-immunoglobulin e syndrome, autosomal dominant | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hyperammonemia, type iii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyperammonemia, type iii | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hyperprolinemia type 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:hypomagnesemia 5, renal, with ocular involvement n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypomagnesemia 5, renal, with ocular involvement | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:kallman syndrome with heart disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:lethal congenital contracture syndrome 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:lethal congenital erythroderma n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal congenital erythroderma | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:lethal recessive chondrodysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal recessive chondrodysplasia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:leukoencephalopathy, cystic, without megalencephaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:leukoencephalopathy, cystic, without megalencephaly | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:leukotriene c4 synthase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:martsolf syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:martsolf syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:microcephaly cervical spine fusion anomalies n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:morm syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:morm syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:multiple sulfatase deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:najjar syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:neurodegeneration with brain iron accumulation 4 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:neuronal ceroid lipofuscinosis due to cathepsin d deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neuronal ceroid lipofuscinosis due to cathepsin d deficiency | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:niemann-pick diseases n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:niemann-pick diseases | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:oculocerebral hypopigmentation syndrome type preus n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:parkinson disease 14, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:parkinson disease 14, autosomal recessive | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:pelviscapular dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:prader-willi habitus, osteopenia, and camptodactyly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:richards-rundle syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:short stature associated with bone marrow transplant n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature associated with bone marrow transplant | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia with epilepsy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:spondylometaphyseal dysplasia, algerian type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondylometaphyseal dysplasia, algerian type | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:temtamy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:temtamy syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:xanthomatosis, cerebrotendinous n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:xanthomatosis, cerebrotendinous | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 31 / 0.721 -> en:zellweger syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:3-methylglutaconic aciduria type iv n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:achondrogenesis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:acrocephalopolysyndactyly type 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrocephalopolysyndactyly type 2 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:acrofrontofacionasal dysostosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrofrontofacionasal dysostosis syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:adams oliver syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adams oliver syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:al gazali hirschsprung syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:al gazali hirschsprung syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:aldolase a deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aldolase a deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:alkaptonuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:alopecia contractures dwarfism mental retardation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alopecia contractures dwarfism mental retardation | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:autosomal recessive sideroblastic anemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:becker generalized myotonia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:bloom syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:brody myopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brody myopathy | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:charcot-marie-tooth disease, type 2b2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:charcot-marie-tooth disease, type 2b2 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:chylomicron retention disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:combined immunodeficiency due to crac (calcium release activated calcium) channel dysfunction n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:combined immunodeficiency due to crac (calcium release activated calcium) channel dysfunction | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital alpha-2-antiplasmin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital amegakaryocytic thrombocytopenia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital bile acid synthesis defect type 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital bile acid synthesis defect type 3 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital disorder of glycosylation type 1a n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type 1a | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital disorder of glycosylation type 2e n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital disorder of glycosylation, type 2g n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation, type 2g | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:congenital transferrin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:craniosynostosis and intracranial calcification syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:craniosynostosis and intracranial calcification syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:crisponi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:deafness, sensorineural, and male infertility n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:diarrhea 4, malabsorptive, congenital n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:diarrhea 4, malabsorptive, congenital | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:dolichocephalic dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dolichocephalic dwarfism | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:duane anomaly, myopathy, scoliosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:duane anomaly, myopathy, scoliosis syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:ectopia lentis, chorioretinal dystrophy, myopia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:epidermodysplasia verruciformis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:epidermodysplasia verruciformis | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:epiphyseal dysplasia, multiple, 4 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:factor v and factor viii, combined deficiency of n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:familial acantholysis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:fatal infantile lactic acidosis with methylmalonic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:gemss syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gemss syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:halal setton wang syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:halal setton wang syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary factor xii deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary factor xii deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary methemoglobinemia, enzymatic type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hypokalemia, familial n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hypomandibular faciocranial dysostosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hypomyelination and congenital cataract n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hypophosphatemic rickets with hypercalciuria, hereditary n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:hypospadias-mental retardation syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:insulin growth factor i resistance n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:insulin growth factor i resistance | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:jankovic rivera syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:lethal congenital contracture syndrome 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:lethal congenital contracture syndrome type 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:lipodystrophy, intellectual disability, deafness syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lipodystrophy, intellectual disability, deafness syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:lipoprotein glomerulopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:macdermot winter syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:megalencephalic leukoencephalopathy with subcortical cysts n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:mevalonic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mevalonic aciduria | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:microcephaly-capillary malformation syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:microcephaly, amish type (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:mucopolysaccharidosis vi n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mucopolysaccharidosis vi | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:multiple congenital anomalies syndrome with cloverleaf skull n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:multiple congenital anomalies syndrome with cloverleaf skull | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:naxos disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:naxos disease | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:neurodegeneration due to 3-hydroxyisobutyryl coenzyme a hydrolase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neurodegeneration due to 3-hydroxyisobutyryl coenzyme a hydrolase deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:northern epilepsy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:oculocutaneous albinism type 7 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculocutaneous albinism type 7 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:peters-plus syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:pontocerebellar hypoplasia type 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pontocerebellar hypoplasia type 1 | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:primary lateral sclerosis juvenile n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:primary lateral sclerosis juvenile | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:propionic acidemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:pseudovaginal perineoscrotal hypospadias n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pseudovaginal perineoscrotal hypospadias | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:scott bryant graham syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:scott bryant graham syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:spondylocarpotarsal synostosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:spondyloepiphyseal dysplasia reardon type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia reardon type | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:sudden infant death with dysgenesis of the testes syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:ter haar syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ter haar syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:thomas syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:transcobalamin ii deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:type i mucolipidosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:type i mucolipidosis | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 30 / 0.698 -> en:valinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:valinemia | rel=r_associated | relid=0 | w=30 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:5' 10' methylenetetrahydrofolate reductase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:adenine phosphoribosyltransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:amaurosis hypertrichosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:amaurosis hypertrichosis syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:arthrogryposis multiplex congenita whistling face n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:arthrogryposis multiplex congenita whistling face | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:autosomal recessive idiopathic familial dystonia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:autosomal recessive ocular albinism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:autosomal recessive scid n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:bietti crystalline corneoretinal dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:bowen-conradi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:brittle cornea syndrome 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brittle cornea syndrome 1 | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:carbamoyl-phosphate synthetase i deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:cardiomyopathy dilated with woolly hair and keratoderma n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cardiomyopathy dilated with woolly hair and keratoderma | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:cleft palate with stapes fixation and oligodontia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cleft palate with stapes fixation and oligodontia syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:congenital analbuminemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:crigler najjar syndrome, type 1 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:crigler najjar syndrome, type 1 | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:cutaneous photosensitivity and lethal colitis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:dermatoosteolysis kirghizian type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dermatoosteolysis kirghizian type | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:disproportionate short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:disproportionate short stature | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:ehlers-danlos syndrome, progeroid form n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome, progeroid form | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:eiken skeletal dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:eiken skeletal dysplasia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:ellis yale winter syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ellis yale winter syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:ethanolaminosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:fuhrmann syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fuhrmann syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:galloway mowat syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:galloway mowat syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:gamma-glutamyltransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:geleophysic dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:geleophysic dysplasia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:glucocorticoid deficiency with achalasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glucocorticoid deficiency with achalasia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type ii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glycogen storage disease type ii | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type x n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:hemolytic anemia due to pyruvate kinase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:hereditary sensory and autonomic neuropathy with spastic paraplegia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary sensory and autonomic neuropathy with spastic paraplegia | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:hnsha due to glucose phosphate isomerase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:infantile globoid cell leukodystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:jervell-lange nielsen syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:jervell-lange nielsen syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:knobloch syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:lathosterolosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lathosterolosis | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:laurence-moon syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:medium-chain acyl-coenzyme a dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:medium-chain acyl-coenzyme a dehydrogenase deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:microphthalmia, syndromic 10 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microphthalmia, syndromic 10 | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:mucopolysaccharidosis vii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mucopolysaccharidosis vii | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:nonaka myopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:oculocutaneous albinism type 4 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:papillon-lefevre disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:papillon-lefevre disease | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:pituitary dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pituitary dwarfism | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:primary hyperoxaluria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:proportionate short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:proportionate short stature | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:renal tubulopathy with encephalopathy and liver failure syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:rna polymerase iii-related leukodystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:senile dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:senile dwarfism | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:sesame syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sesame syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:short stature, pituitary and cerebellar defect and small sella turcica syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:spondyloenchondrodysplasia with immune dysregulation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:tel hashomer camptodactyly syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tel hashomer camptodactyly syndrome | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:tetra-amelia autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 29 / 0.674 -> en:tyrosine transaminase deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tyrosine transaminase deficiency disease | rel=r_associated | relid=0 | w=29 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:acrofacial dysostosis rodriguez type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrofacial dysostosis rodriguez type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta - recessive - rough n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:arginine:glycine amidinotransferase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:arterial tortuosity syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:asexual dwarfism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:asexual dwarfism | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:ateliotic dwarfism without insulinopenia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:autoimmune lymphoproliferative syndrome with recurrent viral infection n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autoimmune lymphoproliferative syndrome with recurrent viral infection | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:bartter syndrome, type 4a n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bartter syndrome, type 4a | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:brachydactyly syndrome type b n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:charcot-marie-tooth disease type 4 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:childhood myocerebrohepatopathy spectrum n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:chitty hall baraitser syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:chromosome 22 abnormalities with hypogammaglobulinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chromosome 22 abnormalities with hypogammaglobulinemia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:classical phenylketonuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:cohen syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:congenital disorder of glycosylation type ig n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:congenital hypoplasia of ulna and intellectual disability syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital hypoplasia of ulna and intellectual disability syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:congenital malformation syndromes associated with short stature n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital malformation syndromes associated with short stature | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:corpus callosum agenesis neuronopathy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:corpus callosum, agenesis of, with facial anomalies and robin sequence n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:crome syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:crome syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:cryptophthalmos syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:deletion of x-chromosome and hypogammaglobulinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deletion of x-chromosome and hypogammaglobulinemia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:dicarboxylicaminoaciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:digitorenocerebral syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:digitorenocerebral syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:dihydrouracil dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:donohue syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:ehlers-danlos syndrome type 6 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome type 6 | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:encephalopathy due to sulfite oxidase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:epidermolysis bullosa simplex with pyloric atresia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:fryns macrocephaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:generalized peeling skin syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:gluthathione synthetase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gluthathione synthetase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease type i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:goldberg-shprintzen megacolon syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:goldberg-shprintzen megacolon syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:gurrieri sammito bellussi syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:haspeslagh fryns muelenaere syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:hereditary fructose intolerance syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary fructose intolerance syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:hereditary palmoplantar keratoderma gamborg nielsen type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:hernandez fragoso syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hernandez fragoso syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:hydrolethalus syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hydrolethalus syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:infantile dwarf n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:infantile dwarf | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:iron-refractory iron deficiency anemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:iron-refractory iron deficiency anemia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:jaundice, chronic idiopathic n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:jaundice, chronic idiopathic | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:leukodystrophy, dysmyelinating, with oligodontia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:leukodystrophy, dysmyelinating, with oligodontia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:lissencephaly syndrome, norman-roberts type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:marles greenberg persaud syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:mauriac syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mauriac syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:methylcrotonyl-coa carboxylase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:methylmalonyl-coenzyme a mutase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:mucopolysaccharidosis i n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:multiple epiphyseal dysplasia al-gazali type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:multiple epiphyseal dysplasia al-gazali type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:nijmegen breakage syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:nijmegen breakage syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:obesity due to prohormone convertase i deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:obesity due to prohormone convertase i deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:oculocutaneous albinism type 6 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:peeling skin syndrome, acral type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:pseudocholinesterase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:pseudotrisomy 13 syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:pyknoachondrogenesis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pyknoachondrogenesis | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:rud syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:rud syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:sarcosinemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:short stature co-occurrent and due to endocrine disorder n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature co-occurrent and due to endocrine disorder | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:spondylo-ocular syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:spondyloepiphyseal dysplasia tarda kohn type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:tay-sachs disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:teebi kaurah syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:teebi kaurah syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:viljoen kallis voges syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:viljoen kallis voges syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 28 / 0.651 -> en:zunich neuroectodermal syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=28 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:3-methylglutaconic aciduria type 5 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:absent corpus callosum cataract immunodeficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:absent corpus callosum cataract immunodeficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:acrocapitofemoral dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrocapitofemoral dysplasia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:al gazali aziz salem syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:al gazali aziz salem syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:alpha-fetoprotein deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:alport syndrome, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alport syndrome, autosomal recessive | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:amish infantile epilepsy syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:amish infantile epilepsy syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:ataxia telangiectasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ataxia telangiectasia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal recessive distal osteolysis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal recessive muscular dystrophy with limb girdle distribution n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:beemer ertbruggen syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:beemer ertbruggen syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:biemond syndrome type 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:biemond syndrome type 2 | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:biotinidase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:braddock syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:brain calcification rajab type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:campomelia cumming type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:campomelia cumming type | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:cerebrofaciothoracic dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cerebrofaciothoracic dysplasia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, type 2h n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:charcot-marie-tooth disease, type 2h | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:chorea acanthocytosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chorea acanthocytosis syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:chronic atrial and intestinal dysrhythmia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:chronic atrial and intestinal dysrhythmia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:cleft palate with short stature and vertebral anomaly syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cleft palate with short stature and vertebral anomaly syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:congenital disorder of glycosylation, type iih n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation, type iih | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:congenital leptin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:congenital sucrase-isomaltase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:deiodinase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:deiodinase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:desmosterolosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:dyskeratosis congenita, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:ehlers-danlos syndrome, cardiac valvular form n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome, cardiac valvular form | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:enterokinase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:familial hypoaldosteronism n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:fountain syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:haim-munk syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:haim-munk syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:hair defect with photosensitivity and mental retardation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hair defect with photosensitivity and mental retardation | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:hepatolenticular degeneration n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> 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:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:hnsha due to glutathione synthetase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:hypogonadism-cataract syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypogonadism-cataract syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:hypotonia-cystinuria syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hypotonia-cystinuria syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:insulin-dependent diabetes mellitus secretory diarrhea syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:isaacs syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:kaufman oculocerebrofacial syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:kuskokwim disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:methylene thf reductase deficiency and homocystinuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:multicentric osteolysis nodulosis arthropathy spectrum n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:muscle-eye-brain disease, congenital muscular dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:orofaciodigital syndrome 9 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:orotic aciduria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:pacman dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pacman dysplasia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:pontocerebellar hypoplasia type 2 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:porphobilinogen synthase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:presentey anomaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:prolonged electroretinal response suppression n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:reardon hall slaney syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:severe early childhood onset retinal dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:short stature due to primary acid labile subunit deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature due to primary acid labile subunit deficiency | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:sinus histiocytosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sinus histiocytosis | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:spondyloepiphyseal dysplasia tarda, toledo type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:thanatophoric dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:tyrosinemia, type iii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:vacterl syndrome with hydrocephalus n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:vacterl syndrome with hydrocephalus | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:visceral myopathy familial external ophthalmoplegia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:visceral myopathy familial external ophthalmoplegia | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 27 / 0.628 -> en:waardenburg anophthalmia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=27 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:12q14 microdeletion syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:acid phosphatase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:acrocallosal syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:acrootoocular syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:acrootoocular syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:adrenal gland hyperplasia ii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:allanson pantzar mcleod syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:alpha, alpha-trehalase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:alstrom syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:aminoacylase 1 deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder) n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:autoinflammation, lipodystrophy and dermatosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:autosomal recessive primary microcephaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:basal ganglia disease, biotin-responsive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:behr syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:behr syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:burn-mckeown syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:burn-mckeown syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:cahmr syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cahmr syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:cerebellar ataxia ectodermal dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:citrin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:combined saposin deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:combined saposin deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:congenital disorder of glycosylation type ic n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:cooper jabs syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:craniofacial dyssynostosis syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:craniofacial dyssynostosis syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:craniofacial ulnar renal syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:diaphragmatic defect, limb deficiency, skull defect syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:diaphragmatic defect, limb deficiency, skull defect syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:dimethylglycine dehydrogenase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dimethylglycine dehydrogenase deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:dk phocomelia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:dk phocomelia syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:ehlers-danlos syndrome, musculocontractural type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ehlers-danlos syndrome, musculocontractural type | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:familial renal iminoglycinuria n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:fibular hypoplasia and complex brachydactyly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:fine-lubinsky syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fine-lubinsky syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:fucosidase deficiency disease n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:fucosidase deficiency disease | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:hemochromatosis, type 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hemochromatosis, type 3 | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:hereditary arterial and articular multiple calcification syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:hereditary spastic paralysis, infantile onset ascending n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:hyperargininemia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hyperargininemia | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:intestinal epithelial dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:isolated hyperchlorhidrosis n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:kaplan plauchu fitch syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:kaplan plauchu fitch syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:lactase deficiency, congenital n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:laron syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:laron syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:laryngoonychocutaneous syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:laryngoonychocutaneous syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:macular coloboma, cleft palate, hallux valgus syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:macular coloboma, cleft palate, hallux valgus syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:macular corneal dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:olivopontocerebellar hypoplasia, fetal-onset n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:olivopontocerebellar hypoplasia, fetal-onset | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:persistent mullerian duct syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:phenylketonuria ii n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:polyglucosan body disease, adult form n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:polyglucosan body disease, adult form | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:purine-nucleoside phosphorylase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:retinal cone dystrophy 3b n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:retinal cone dystrophy 3b | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:say barber miller syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:say barber miller syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:short stature due to radiation therapy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature due to radiation therapy | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:sonoda syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:split-hand/foot malformation 3 n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia, omani type n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:taurodontia with absent teeth and sparse hair syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:taurodontia with absent teeth and sparse hair syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:urocanase deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:volcke soekarman syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:volcke soekarman syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:walker-warburg congenital muscular dystrophy n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:walker-warburg congenital muscular dystrophy | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:wiedemann-rautenstrauch syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:wiedemann-rautenstrauch syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:zellweger-like syndrome without peroxisomal anomaly n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> en:zlotogora-ogur syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:zlotogora-ogur syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 26 / 0.605 -> syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 25 / 0.581 -> en:primary n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:primary | rel=r_associated | relid=0 | w=25 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:larsen-like osseous dysplasia, short stature syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:larsen-like osseous dysplasia, short stature syndrome | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:neutrophil immunodeficiency syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:neutrophil immunodeficiency syndrome | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:ras-associated autoimmune leukoproliferative disorder n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:ras-associated autoimmune leukoproliferative disorder | rel=r_associated | relid=0 | w=20 en:primary immunodeficiency syndrome due to p14 deficiency -- r_associated #0: 20 / 0.465 -> en:short stature of childhood n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:short stature of childhood | rel=r_associated | relid=0 | w=20

≈ 703 relations entrantes en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 42 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ectodermal dysplasia with blindness syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=42 en:craniofacial ulnar renal syndrome --- r_associated #0: 41 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:craniofacial ulnar renal syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=41 en:hall riggs syndrome --- r_associated #0: 41 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hall riggs syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=41 en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 41 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=41 en:neutrophil immunodeficiency syndrome --- r_associated #0: 41 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neutrophil immunodeficiency syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=41 en:familial median cleft of upper and lower lip --- r_associated #0: 39 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial median cleft of upper and lower lip | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=39 en:bestrophinopathy, autosomal recessive --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bestrophinopathy, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:deafness and myopia syndrome --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deafness and myopia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:kallman syndrome with heart disease --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kallman syndrome with heart disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:manouvrier syndrome --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:manouvrier syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 35 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=35 en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:congenital disorder of glycosylation type 1h --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type 1h | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:fountain syndrome --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fountain syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:larsen-like osseous dysplasia, short stature syndrome --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:larsen-like osseous dysplasia, short stature syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:late-onset junctional epidermolysis bullosa --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:late-onset junctional epidermolysis bullosa | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:oculocutaneous albinism type 6 --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculocutaneous albinism type 6 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:pelviscapular dysplasia --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pelviscapular dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 34 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=34 en:acrorenal mandibular syndrome --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrorenal mandibular syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:braddock syndrome --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:braddock syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:congenital analbuminemia --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital analbuminemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:cooper jabs syndrome --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cooper jabs syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:hypomandibular faciocranial dysostosis --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypomandibular faciocranial dysostosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:najjar syndrome --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:najjar syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:ras-associated autoimmune leukoproliferative disorder --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ras-associated autoimmune leukoproliferative disorder | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:renal dysplasia - limb defects syndrome --- r_associated #0: 32 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:renal dysplasia - limb defects syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=32 en:bamforth syndrome --- r_associated #0: 31 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bamforth syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=31 en:congenital disorder of glycosylation type 2e --- r_associated #0: 31 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type 2e | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=31 en:congenital disorder of glycosylation, type if --- r_associated #0: 31 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation, type if | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=31 en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 31 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=31 en:12q14 microdeletion syndrome --- r_associated #0: 30 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:12q14 microdeletion syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=30 en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 30 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=30 en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 30 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=30 en:robinow-like syndrome --- r_associated #0: 30 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:robinow-like syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=30 en:short stature syndrome, brussels type --- r_associated #0: 30 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature syndrome, brussels type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=30 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 29 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=29 en:generalized peeling skin syndrome --- r_associated #0: 29 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:generalized peeling skin syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=29 en:lethal larsen-like syndrome --- r_associated #0: 29 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal larsen-like syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=29 en:moyamoya disease with early onset achalasia --- r_associated #0: 29 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:moyamoya disease with early onset achalasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=29 en:split-hand/foot malformation 3 --- r_associated #0: 29 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:split-hand/foot malformation 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=29 en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:congenital disorder of glycosylation type id --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type id | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:insulin growth factor i deficiency --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:insulin growth factor i deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephaly albinism digital anomalies syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:pili torti onychodysplasia syndrome --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pili torti onychodysplasia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 28 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=28 en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 27 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=27 en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 27 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=27 en:congenital disorder of glycosylation type ie --- r_associated #0: 27 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type ie | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=27 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 27 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=27 en:diaphanospondylodysostosis --- r_associated #0: 27 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:diaphanospondylodysostosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=27 en:anauxetic dysplasia --- r_associated #0: 26 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:anauxetic dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=26 en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 26 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=26 en:brain calcification rajab type --- r_associated #0: 26 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brain calcification rajab type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=26 en:heart defects limb shortening --- r_associated #0: 26 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:heart defects limb shortening | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=26 en:short stature of childhood --- r_associated #0: 26 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature of childhood | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=26 en:2p21 microdeletion syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:2p21 microdeletion syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:3-@methylglutaconic aciduria, type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:3-@methylglutaconic aciduria, type i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:3-methylglutaconic aciduria type 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:3-methylglutaconic aciduria type 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:3-methylglutaconic aciduria type 5 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:3-methylglutaconic aciduria type 5 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:3-methylglutaconic aciduria type iv --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:3-methylglutaconic aciduria type iv | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:5-oxoprolinase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:5-oxoprolinase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:absent corpus callosum cataract immunodeficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:absent corpus callosum cataract immunodeficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:absent thumb with short stature and immunodeficiency syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:absent thumb with short stature and immunodeficiency syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:achalasia microcephaly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:achalasia microcephaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:achondrogenesis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:achondrogenesis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acid phosphatase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acid phosphatase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ackerman syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ackerman syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrocallosal syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrocallosal syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrocapitofemoral dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrocapitofemoral dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrocephalopolydactylous dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrocephalopolydactylous dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrocephalopolysyndactyly type 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrocephalopolysyndactyly type 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrocephalopolysyndactyly type iv --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrocephalopolysyndactyly type iv | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrodermatitis enteropathica --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrodermatitis enteropathica | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrofacial dysostosis kennedy teebi type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrofacial dysostosis kennedy teebi type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrofacial dysostosis rodriguez type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrofacial dysostosis rodriguez type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrofrontofacionasal dysostosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrofrontofacionasal dysostosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acromesomelic dysplasia, maroteaux type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acromesomelic dysplasia, maroteaux type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acromicric dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acromicric dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:acrootoocular syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:acrootoocular syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:adams oliver syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adams oliver syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adenine phosphoribosyltransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:adrenal gland hyperplasia ii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adrenal gland hyperplasia ii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:adult-onset autosomal recessive sideroblastic anemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:adult-onset autosomal recessive sideroblastic anemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:al awadi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:al awadi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:al gazali aziz salem syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:al gazali aziz salem syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:al gazali hirschsprung syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:al gazali hirschsprung syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:albinotic fundus --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:albinotic fundus | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aldolase a deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aldolase a deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alkaptonuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alkaptonuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:allanson pantzar mcleod syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:allanson pantzar mcleod syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alopecia contractures dwarfism mental retardation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alopecia contractures dwarfism mental retardation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alpha 1-antitrypsin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alpha 1-antitrypsin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alpha, alpha-trehalase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alpha, alpha-trehalase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alpha-fetoprotein deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alpha-fetoprotein deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alport syndrome, autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alport syndrome, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:alstrom syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:alstrom syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:amaurosis hypertrichosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:amaurosis hypertrichosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:amelogenesis imperfecta - recessive - rough | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aminoacylase 1 deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aminoacylase 1 deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aminomethyltransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aminomethyltransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:amish infantile epilepsy syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:amish infantile epilepsy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia plus syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:anophthalmia plus syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:antley-bixler syndrome, autosomal dominant | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aplasia cutis congenita intestinal lymphangiectasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aplasia cutis congenita intestinal lymphangiectasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aplasia cutis with myopia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aplasia cutis with myopia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:arginine:glycine amidinotransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:argininosuccinic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:argininosuccinic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:arterial tortuosity syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:arterial tortuosity syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:arthrogryposis multiplex congenita whistling face --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:arthrogryposis multiplex congenita whistling face | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:asexual dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:asexual dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:aspartylglucosaminuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:aspartylglucosaminuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:asymmetric short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:asymmetric short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ataxia telangiectasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ataxia telangiectasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ataxia with vitamin e deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ataxia with vitamin e deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ateliotic dwarfism without insulinopenia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ateliotic dwarfism without insulinopenia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:atkin syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:atkin syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:atrophoderma vermiculatum --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:atrophoderma vermiculatum | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autoimmune lymphoproliferative syndrome with recurrent viral infection --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autoimmune lymphoproliferative syndrome with recurrent viral infection | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive asexual dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive asexual dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive distal osteolysis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive ichthyosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive ichthyosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive idiopathic familial dystonia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive ocular albinism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive ocular albinism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive primary microcephaly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive primary microcephaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive scid --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive scid | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive sideroblastic anemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive sideroblastic anemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:baller-gerold syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:baller-gerold syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bardet-biedl syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bardet-biedl syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bartter syndrome, type 4a --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bartter syndrome, type 4a | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:basal ganglia disease, biotin-responsive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:basal ganglia disease, biotin-responsive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:becker generalized myotonia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:becker generalized myotonia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:beemer ertbruggen syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:beemer ertbruggen syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:behr syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:behr syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:behrens baumann dust syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:behrens baumann dust syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:beta-aminoisobutyricaciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:beta-aminoisobutyricaciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:biemond syndrome type 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:biemond syndrome type 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bietti crystalline corneoretinal dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bifid nose with or without anorectal and renal anomalies --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bifid nose with or without anorectal and renal anomalies | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bilateral microtia with deafness and cleft palate syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bilateral microtia with deafness and cleft palate syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:biotinidase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:biotinidase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:birth length less than 3rd percentile --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:birth length less than 3rd percentile | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bixler christian gorlin syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bixler christian gorlin syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:blepharophimosis with ptosis, syndactyly, and short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:blepharophimosis with ptosis, syndactyly, and short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bloom syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bloom syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bosley-salih-alorainy syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bosley-salih-alorainy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bothnia retinal dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bothnia retinal dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:bowen-conradi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:bowen-conradi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brachydactyly syndrome type b --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brachydactyly syndrome type b | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brachymetapody-anodontia-hypotrichosis-albinoidism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brachymetapody-anodontia-hypotrichosis-albinoidism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brachymorphism-onychodysplasia-dysphalangism syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brachymorphism-onychodysplasia-dysphalangism syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brain dopamine-serotonin vesicular transport disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brain dopamine-serotonin vesicular transport disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brittle cornea syndrome 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brittle cornea syndrome 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brody myopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brody myopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:brown-vialetto-van laere syndrome 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:brown-vialetto-van laere syndrome 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:burn-mckeown syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:burn-mckeown syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cahmr syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cahmr syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:campomelia cumming type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:campomelia cumming type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:camptodactyly syndrome guadalajara type 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:camptodactyly syndrome guadalajara type 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:camptodactyly syndrome, guadalajara type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:camptodactyly syndrome, guadalajara type i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cantalamessa baldini ambrosi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cantalamessa baldini ambrosi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cardiomyopathy dilated with woolly hair and keratoderma --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cardiomyopathy dilated with woolly hair and keratoderma | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cataract and cardiomyopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cataract and cardiomyopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:catel manzke syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:catel manzke syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cdags syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cdags syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cenani-lenz syndactyly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cenani-lenz syndactyly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, cayman type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cerebellar ataxia, cayman type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cerebrofaciothoracic dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cerebrofaciothoracic dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease type 4 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:charcot-marie-tooth disease type 4 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, type 2b2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:charcot-marie-tooth disease, type 2b2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, type 2h --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:charcot-marie-tooth disease, type 2h | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:childhood hypophosphatasia (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:childhood hypophosphatasia (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:childhood myocerebrohepatopathy spectrum | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chitty hall baraitser syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chitty hall baraitser syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chondrodysplasia punctata syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chondrodysplasia punctata syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chorea acanthocytosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chorea acanthocytosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chromosome 18 syndromes and antibody deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chromosome 18 syndromes and antibody deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chromosome 22 abnormalities with hypogammaglobulinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chromosome 22 abnormalities with hypogammaglobulinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chronic atrial and intestinal dysrhythmia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chronic atrial and intestinal dysrhythmia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:chylomicron retention disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:chylomicron retention disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:citrin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:citrin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:classical phenylketonuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:classical phenylketonuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cleft palate with short stature and vertebral anomaly syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cleft palate with short stature and vertebral anomaly syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cleft palate with stapes fixation and oligodontia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cleft palate with stapes fixation and oligodontia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:codas syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:codas syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cog4 congenital disorder of glycosylation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cog4 congenital disorder of glycosylation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cog5 congenital disorder of glycosylation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cog5 congenital disorder of glycosylation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cohen syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cohen syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:combined d-2- and l-2-hydroxyglutaric aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:combined d-2- and l-2-hydroxyglutaric aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:combined immunodeficiency due to crac (calcium release activated calcium) channel dysfunction --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:combined immunodeficiency due to crac (calcium release activated calcium) channel dysfunction | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:combined malonic and methylmalonic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:combined malonic and methylmalonic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:combined saposin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:combined saposin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital adrenal hyperplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital adrenal hyperplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital bile acid synthesis defect type 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital bile acid synthesis defect type 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital bowing of long bone --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital bowing of long bone | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type 1a --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type 1a | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type 1k --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type 1k | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type 1l --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type 1l | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type ic --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type ic | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type ig --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation type ig | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation, type 2g --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation, type 2g | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation, type id --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation, type id | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation, type iih --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation, type iih | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation, type im --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital disorder of glycosylation, type im | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital dyserythropoietic anemia, type i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital dyserythropoietic anemia, type ii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital hereditary facial paralysis with variable hearing loss syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital hereditary facial paralysis with variable hearing loss syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital hypoplasia of ulna and intellectual disability syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital hypoplasia of ulna and intellectual disability syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital intrauterine infection-like syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital intrauterine infection-like syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital leptin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital leptin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital malformation syndromes associated with short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital malformation syndromes associated with short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital pancreatic enterokinase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital pancreatic enterokinase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital pontocerebellar hypoplasia type 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital pontocerebellar hypoplasia type 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital pontocerebellar hypoplasia type 7 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital pontocerebellar hypoplasia type 7 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital pontocerebellar hypoplasia type 8 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital pontocerebellar hypoplasia type 8 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital sucrase-isomaltase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital sucrase-isomaltase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:congenital transferrin deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:congenital transferrin deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:corneal cerebellar syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:corneal cerebellar syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:corneal dystrophy and perceptive deafness --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:corneal dystrophy and perceptive deafness | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:corpus callosum agenesis neuronopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:corpus callosum agenesis neuronopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:corpus callosum, agenesis of, with facial anomalies and robin sequence --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cortisol 11-beta-ketoreductase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cortisol 11-beta-ketoreductase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:craniodiaphyseal dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:craniodiaphyseal dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:craniofacial dyssynostosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:craniofacial dyssynostosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cranioosteoarthropathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cranioosteoarthropathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:craniosynostosis and intracranial calcification syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:craniosynostosis and intracranial calcification syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:crigler najjar syndrome, type 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:crigler najjar syndrome, type 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:crisponi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:crisponi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:crome syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:crome syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cryptophthalmos syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cutis laxa, autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cutis laxa, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cystathionine beta-synthase deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cystathionine beta-synthase deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cystinosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cystinosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:cytochrome-c oxidase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:cytochrome-c oxidase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:de sanctis-cacchione syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deafness enamel hypoplasia nail defects --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deafness enamel hypoplasia nail defects | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deafness, progressive, with stapes fixation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deafness, progressive, with stapes fixation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deafness, sensorineural, and male infertility --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deafness, sensorineural, and male infertility | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deficiency of fructokinase --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deficiency of fructokinase | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deficiency of glucosyltransferase 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deficiency of glucosyltransferase 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deficiency of prolidase --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deficiency of prolidase | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deiodinase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deiodinase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:deletion of x-chromosome and hypogammaglobulinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:deletion of x-chromosome and hypogammaglobulinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dermatoosteolysis kirghizian type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dermatoosteolysis kirghizian type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:desmosterolosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:desmosterolosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:diaphragmatic defect, limb deficiency, skull defect syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:diaphragmatic defect, limb deficiency, skull defect syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:diarrhea 4, malabsorptive, congenital --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:diarrhea 4, malabsorptive, congenital | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:diastrophic dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:diastrophic dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dicarboxylicaminoaciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dicarboxylicaminoaciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:digitorenocerebral syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:digitorenocerebral syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dihydrouracil dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dimethylglycine dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dimethylglycine dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:disproportionate short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:disproportionate short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dk phocomelia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dk phocomelia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dolichocephalic dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dolichocephalic dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:donnai-barrow syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:donnai-barrow syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:donohue syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:donohue syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:duane anomaly, myopathy, scoliosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:duane anomaly, myopathy, scoliosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dwarfism, alopecia, pseudoanodontia, cutis laxa --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dwarfism, alopecia, pseudoanodontia, cutis laxa | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dyskeratosis congenita, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dyssegmental dysplasia with glaucoma syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dyssegmental dysplasia with glaucoma syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:dystonia 16 (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:dystonia 16 (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ear, patella, short stature syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ear, patella, short stature syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ectodermal dysplasia, ectrodactyly, and macular dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ectodermal dysplasia, ectrodactyly, and macular dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ectopia lentis, chorioretinal dystrophy, myopia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome type 6 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome type 6 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, cardiac valvular form --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome, cardiac valvular form | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, musculocontractural type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome, musculocontractural type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, progeroid form --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ehlers-danlos syndrome, progeroid form | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:eiken skeletal dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:eiken skeletal dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ellis yale winter syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ellis yale winter syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:enterokinase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:enterokinase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:epidermodysplasia verruciformis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:epidermodysplasia verruciformis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ethanolaminosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ethanolaminosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:faciocardiomelic dysplasia, lethal --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:faciocardiomelic dysplasia, lethal | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:factor v and factor viii, combined deficiency of --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:factor v and factor viii, combined deficiency of | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:factor xi deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:factor xi deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial acantholysis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial acantholysis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial aplasia of the vermis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial aplasia of the vermis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial c3b inhibitor deficiency syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial hypoaldosteronism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial hypoaldosteronism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:familial renal iminoglycinuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:familial renal iminoglycinuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:feigenbaum bergeron richardson syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:feigenbaum bergeron richardson syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fibular hypoplasia and complex brachydactyly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fine-lubinsky syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fine-lubinsky syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fronto-facio-nasal dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fronto-facio-nasal dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fructose-1,6-diphosphatase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fructose-1,6-diphosphatase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fryns macrocephaly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fryns macrocephaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fucosidase deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fucosidase deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:fuhrmann syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:fuhrmann syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:galloway mowat syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:galloway mowat syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gamma-glutamyltransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gamma-glutamyltransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:geleophysic dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:geleophysic dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gemss syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gemss syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:geroderma osteodysplastica --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:geroderma osteodysplastica | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:giacci familial neurogenic acroosteolysis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:giacci familial neurogenic acroosteolysis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gingival fibromatosis with facial dysmorphism syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gingival fibromatosis with facial dysmorphism syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glucocorticoid deficiency with achalasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glucocorticoid deficiency with achalasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glutamate formiminotransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glutamate formiminotransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glutamate-cysteine ligase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glutamate-cysteine ligase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gluthathione synthetase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gluthathione synthetase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glycogen storage disease type i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type ii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glycogen storage disease type ii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type x --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:glycogen storage disease type x | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:goldberg-shprintzen megacolon syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:goldberg-shprintzen megacolon syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gracile syndrome (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gracile syndrome (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:growth retardation, alopecia, pseudoanodontia and optic atrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:gurrieri sammito bellussi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:gurrieri sammito bellussi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hadziselimovic syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hadziselimovic syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:haim-munk syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:haim-munk syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hair defect with photosensitivity and mental retardation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hair defect with photosensitivity and mental retardation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:halal setton wang syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:halal setton wang syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:haspeslagh fryns muelenaere syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hemochromatosis, type 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hemochromatosis, type 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hepatic lipase deficiency (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hepatic lipase deficiency (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hepatolenticular degeneration --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hepatolenticular degeneration | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary factor x deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary factor x deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary factor xii deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary factor xii deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary fructose intolerance syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary fructose intolerance syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary sensory and autonomic neuropathy with deafness and global delay --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary sensory and autonomic neuropathy with deafness and global delay | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary sensory and autonomic neuropathy with spastic paraplegia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary sensory and autonomic neuropathy with spastic paraplegia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hernandez aguirre-negrete syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hernandez aguirre-negrete syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hernandez fragoso syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hernandez fragoso syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:histidinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:histidinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hmg coa lyase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hmg coa lyase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hmn (hereditary motor neuropathy) proximal type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hmn (hereditary motor neuropathy) proximal type i | 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 --> 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 glucose phosphate isomerase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to glutathione reductase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hnsha due to glutathione reductase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hnsha due to glutathione synthetase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:homocystinuria without methylmalonic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:homocystinuria without methylmalonic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hydrolethalus syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hydrolethalus syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyper-immunoglobulin e syndrome, autosomal dominant --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyper-immunoglobulin e syndrome, autosomal dominant | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyperammonemia, type iii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyperammonemia, type iii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyperargininemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyperargininemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyperphosphatasia with mental retardation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyperphosphatasia with mental retardation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyperprolinemia type 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyperprolinemia type 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hyperprolinemia type 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hyperprolinemia type 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypertryptophanemia, familial --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypertryptophanemia, familial | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypogonadism-cataract syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypogonadism-cataract syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypokalemia, familial --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypokalemia, familial | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypomagnesemia 1, intestinal --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypomagnesemia 1, intestinal | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypomagnesemia 5, renal, with ocular involvement --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypomagnesemia 5, renal, with ocular involvement | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypomyelination and congenital cataract --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypomyelination and congenital cataract | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypospadias-mental retardation syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypospadias-mental retardation syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypothyroid dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypothyroid dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hypotonia-cystinuria syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hypotonia-cystinuria syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:idiopathic short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:idiopathic short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:immunodeficiency associated with 18p syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:immunodeficiency associated with 18p syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:immunodeficiency syndrome, variable --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:immunodeficiency syndrome, variable | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:infantile dwarf --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:infantile dwarf | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:infantile globoid cell leukodystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:infantile globoid cell leukodystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:infantile hypophosphatasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:infantile hypophosphatasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:insulin growth factor i resistance --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:insulin growth factor i resistance | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:insulin-dependent diabetes mellitus secretory diarrhea syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:intellectual disability with cataract and kyphosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:intellectual disability with cataract and kyphosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:intestinal epithelial dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:intestinal epithelial dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:iron-refractory iron deficiency anemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:iron-refractory iron deficiency anemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:isaacs syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:isaacs syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:isolated hyperchlorhidrosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:isolated hyperchlorhidrosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:isolated hypoplasia of the right ventricle --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:isolated hypoplasia of the right ventricle | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:isovaleryl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:isovaleryl-coa dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:jankovic rivera syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:jankovic rivera syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:jaundice, chronic idiopathic --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:jaundice, chronic idiopathic | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:jervell-lange nielsen syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:jervell-lange nielsen syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:jeune thoracic dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:jeune thoracic dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:juberg-marsidi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:juberg-marsidi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:kaplan plauchu fitch syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kaplan plauchu fitch syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:kapur toriello syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kapur toriello syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:kaufman oculocerebrofacial syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kaufman oculocerebrofacial syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:kaufman-mckusick syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kaufman-mckusick syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:knobloch syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:knobloch syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:krasnow qazi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:krasnow qazi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:kuskokwim disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:kuskokwim disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lactase deficiency, congenital --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lactase deficiency, congenital | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:laron syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:laron syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:laryngoonychocutaneous syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:laryngoonychocutaneous syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lathosterolosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lathosterolosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:laurence-moon syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:laurence-moon syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lecithin acyltransferase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lecithin acyltransferase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lelis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lelis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lethal congenital contracture syndrome 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal congenital contracture syndrome 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lethal congenital contracture syndrome 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal congenital contracture syndrome 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lethal congenital contracture syndrome type 3 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal congenital contracture syndrome type 3 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lethal congenital erythroderma --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal congenital erythroderma | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lethal recessive chondrodysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lethal recessive chondrodysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:leukodystrophy, dysmyelinating, with oligodontia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:leukodystrophy, dysmyelinating, with oligodontia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy, cystic, without megalencephaly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:leukoencephalopathy, cystic, without megalencephaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:leukotriene c4 synthase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:leukotriene c4 synthase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lipodystrophy, intellectual disability, deafness syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lipodystrophy, intellectual disability, deafness syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lipoid proteinosis of urbach and wiethe | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lipoprotein glomerulopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lipoprotein glomerulopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lissencephaly syndrome, norman-roberts type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lissencephaly type 3 metacarpal bone dysplasia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lissencephaly type 3 metacarpal bone dysplasia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lowry wood syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lowry wood syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lubani al saleh teebi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lubani al saleh teebi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lymphedema, cardiac septal defects, and characteristic facies --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lymphedema, cardiac septal defects, and characteristic facies | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:macdermot winter syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:macdermot winter syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:macular coloboma, cleft palate, hallux valgus syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:macular coloboma, cleft palate, hallux valgus syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:macular corneal dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:macular corneal dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:majeed syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:majeed syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:malignant hyperthermia with arthrogryposis and torticollis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:malignant hyperthermia with arthrogryposis and torticollis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mannosidase deficiency diseases --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mannosidase deficiency diseases | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:maple syrup urine disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:maple syrup urine disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:marden walker like syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:marden walker like syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:marles greenberg persaud syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:marles greenberg persaud syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:martsolf syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:martsolf syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mauriac syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mauriac syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mcpherson clemens syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mcpherson clemens syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:medium-chain acyl-coenzyme a dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:medium-chain acyl-coenzyme a dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mental retardation smith fineman myers type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mental retardation smith fineman myers type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:metatropic dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:metatropic dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mevalonic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mevalonic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microcephalic primordial dwarfism toriello type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephalic primordial dwarfism toriello type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microcephaly cervical spine fusion anomalies --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephaly cervical spine fusion anomalies | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microcephaly, amish type (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephaly, amish type (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microcephaly-capillary malformation syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microcephaly-capillary malformation syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 10 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:microphthalmia, syndromic 10 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:morm syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:morm syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mucopolysaccharidosis i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mucopolysaccharidosis i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mucopolysaccharidosis iii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mucopolysaccharidosis iii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mucopolysaccharidosis iv --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mucopolysaccharidosis iv | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mucopolysaccharidosis vi --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mucopolysaccharidosis vi | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:mucopolysaccharidosis vii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:mucopolysaccharidosis vii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:multiple congenital anomalies syndrome with cloverleaf skull --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:multiple congenital anomalies syndrome with cloverleaf skull | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:multiple epiphyseal dysplasia al-gazali type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:multiple epiphyseal dysplasia al-gazali type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:multiple mitochondrial dysfunctions syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:multiple mitochondrial dysfunctions syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:multiple sulfatase deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:multiple sulfatase deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:muscle amp deaminase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:muscle amp deaminase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:myhre syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:myhre syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:myopathy with exercise intolerance, swedish type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:myopathy with exercise intolerance, swedish type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nathalie syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nathalie syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:naxos disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:naxos disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:netherton syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:netherton syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:neurodegeneration due to 3-hydroxyisobutyryl coenzyme a hydrolase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neurodegeneration due to 3-hydroxyisobutyryl coenzyme a hydrolase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:neuronal ceroid lipofuscinosis due to cathepsin d deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neuronal ceroid lipofuscinosis due to cathepsin d deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:neutral lipid storage disease with myopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:neutral lipid storage disease with myopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:niemann-pick diseases --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:niemann-pick diseases | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nijmegen breakage syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nijmegen breakage syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nivelon nivelon mabille syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nivelon nivelon mabille syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nonaka myopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nonaka myopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:north american indian childhood cirrhosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:north american indian childhood cirrhosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:northern epilepsy syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:northern epilepsy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:nutritional stunting --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:nutritional stunting | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:o/e - short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:o/e - short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:obesity due to prohormone convertase i deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:obesity due to prohormone convertase i deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculocutaneous albinism type 4 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculocutaneous albinism type 4 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculocutaneous albinism type 5 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculocutaneous albinism type 5 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculocutaneous albinism type 7 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculocutaneous albinism type 7 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculopalatocerebral syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculopalatocerebral syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oculotrichodysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oculotrichodysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:odontohypophosphatasia (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:odontohypophosphatasia (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:oliver-mcfarlane syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:oliver-mcfarlane syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:olivopontocerebellar hypoplasia, fetal-onset --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:olivopontocerebellar hypoplasia, fetal-onset | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:omphalocele cleft palate syndrome lethal --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:omphalocele cleft palate syndrome lethal | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 5 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:orofaciodigital syndrome 5 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 9 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:orofaciodigital syndrome 9 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:orotic aciduria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:orotic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:otoonychoperoneal syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:otoonychoperoneal syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pacman dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pacman dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:palmoplantar keratoderma nagashima type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:palmoplantar keratoderma nagashima type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pancreas agenesis, dorsal --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pancreas agenesis, dorsal | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:papillon-lefevre disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:papillon-lefevre disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:parkinson disease 14, autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:parkinson disease 14, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:parkinsonism-dystonia, infantile --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:parkinsonism-dystonia, infantile | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:peeling skin syndrome, acral type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:peeling skin syndrome, acral type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pelizaeus merzbacher like disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pelizaeus merzbacher like disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pentosuria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pentosuria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:persistent mullerian duct syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:persistent mullerian duct syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:peters-plus syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:peters-plus syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:phenylketonuria ii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:phenylketonuria ii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pituitary dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pituitary dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:polyglucosan body disease, adult form --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:polyglucosan body disease, adult form | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pontocerebellar hypoplasia type 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pontocerebellar hypoplasia type 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pontocerebellar hypoplasia type 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pontocerebellar hypoplasia type 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pontocerebellar hypoplasia type 6 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pontocerebellar hypoplasia type 6 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:popliteal pterygium syndrome, lethal type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:popliteal pterygium syndrome, lethal type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:porphobilinogen synthase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:porphobilinogen synthase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:presentey anomaly --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:presentey anomaly | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:primary hyperoxaluria --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:primary hyperoxaluria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:primary lateral sclerosis juvenile --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:primary lateral sclerosis juvenile | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:progressive cavitating leukoencephalopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:progressive cavitating leukoencephalopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:prolonged electroretinal response suppression | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:propionic acidemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:propionic acidemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:proportionate short stature --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:proportionate short stature | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pseudocholinesterase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pseudocholinesterase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pseudotrisomy 13 syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pseudotrisomy 13 syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pseudovaginal perineoscrotal hypospadias --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pseudovaginal perineoscrotal hypospadias | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:purine-nucleoside phosphorylase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pyknoachondrogenesis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pyknoachondrogenesis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pyle metaphyseal dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pyle metaphyseal dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:pyruvate carboxylase deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:pyruvate carboxylase deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:qazi markouizos syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:qazi markouizos syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:rachitic dwarf --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:rachitic dwarf | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:rapadilino syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:rapadilino syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:reardon hall slaney syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:reardon hall slaney syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:renal dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:renal dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:retinal cone dystrophy 3b --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:retinal cone dystrophy 3b | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:retinitis punctata albescens (disorder) --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:retinitis punctata albescens (disorder) | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:richards-rundle syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:richards-rundle syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:rna polymerase iii-related leukodystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:rna polymerase iii-related leukodystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:rud syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:rud syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:saito kuba tsuruta syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:saito kuba tsuruta syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:santos mateus leal syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:santos mateus leal syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sarcosinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sarcosinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:say barber miller syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:say barber miller syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:schaap taylor baraitser syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:schaap taylor baraitser syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:scott bryant graham syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:scott bryant graham syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:senile dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:senile dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sesame syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sesame syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:severe early childhood onset retinal dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:severe early childhood onset retinal dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:severe steroid 21-hydroxylase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:short stature associated with bone marrow transplant --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature associated with bone marrow transplant | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:short stature co-occurrent and due to endocrine disorder --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature co-occurrent and due to endocrine disorder | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:short stature due to primary acid labile subunit deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature due to primary acid labile subunit deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:short stature due to radiation therapy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature due to radiation therapy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:short stature, pituitary and cerebellar defect and small sella turcica syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:siegler brewer carey syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:siegler brewer carey syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sinus histiocytosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sinus histiocytosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sitosterolemia with xanthomatosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sitosterolemia with xanthomatosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:smith-mccort dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:smith-mccort dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sonoda syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sonoda syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sparse hair with short stature and skin anomaly syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sparse hair with short stature and skin anomaly syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spastic paraplegia 15, autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia with epilepsy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spinocerebellar ataxia with epilepsy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondylo-ocular syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondylo-ocular syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondylocarpotarsal synostosis syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloenchondrodysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloenchondrodysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, aggrecan type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepimetaphyseal dysplasia, aggrecan type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, irapa type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepimetaphyseal dysplasia, irapa type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, matrilin-3 related --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepimetaphyseal dysplasia, matrilin-3 related | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, pakistani type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepimetaphyseal dysplasia, pakistani type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, shohat type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepimetaphyseal dysplasia, shohat type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia reardon type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia reardon type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:spondylometaphyseal dysplasia, algerian type --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:spondylometaphyseal dysplasia, algerian type | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:sulfite oxidase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:sulfite oxidase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:taurodontia with absent teeth and sparse hair syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:taurodontia with absent teeth and sparse hair syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tay-sachs disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tay-sachs disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:teebi kaurah syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:teebi kaurah syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:teebi naguib al awadi syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:teebi naguib al awadi syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tel hashomer camptodactyly syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tel hashomer camptodactyly syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:temtamy syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:temtamy syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:ter haar syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:ter haar syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tetra-amelia autosomal recessive --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tetra-amelia autosomal recessive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:thanatophoric dysplasia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:thanatophoric dysplasia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:thomas syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:thomas syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:transcobalamin ii deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:transcobalamin ii deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:trichohepatoenteric syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:trichohepatoenteric syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:triple x syndrome, epilepsy, and hypogammaglobulinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:triple x syndrome, epilepsy, and hypogammaglobulinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tryptophanuria with dwarfism --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tryptophanuria with dwarfism | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tungland bellman syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tungland bellman syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:type i mucolipidosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:type i mucolipidosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:type ii mucolipidosis --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:type ii mucolipidosis | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tyrosine transaminase deficiency disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tyrosine transaminase deficiency disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:tyrosinemia, type iii --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:tyrosinemia, type iii | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:urocanase deficiency --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:urocanase deficiency | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:uv-sensitive syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:uv-sensitive syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:vacterl syndrome with hydrocephalus --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:vacterl syndrome with hydrocephalus | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:valinemia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:valinemia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:verloes bourguignon syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:verloes bourguignon syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:viljoen kallis voges syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:viljoen kallis voges syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:visceral myopathy familial external ophthalmoplegia --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:visceral myopathy familial external ophthalmoplegia | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:volcke soekarman syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:volcke soekarman syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:waardenburg anophthalmia syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:waardenburg anophthalmia syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:walker-warburg congenital muscular dystrophy --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:walker-warburg congenital muscular dystrophy | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:warsaw breakage syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:warsaw breakage syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:wellesley carman french syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:wellesley carman french syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:wiedemann-rautenstrauch syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:wiedemann-rautenstrauch syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:winship viljoen leary syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:winship viljoen leary syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:wolman disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:wolman disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:woods black norbury syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:woods black norbury syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:x-linked mendelian susceptibility to mycobacterial disease --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:x-linked mendelian susceptibility to mycobacterial disease | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:xanthinuria, type i --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:xanthinuria, type i | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:xanthomatosis, cerebrotendinous --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:xanthomatosis, cerebrotendinous | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:xeroderma pigmentosum --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:xeroderma pigmentosum | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:zellweger syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:zellweger syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:zlotogora-ogur syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:zlotogora-ogur syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:zunich neuroectodermal syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:zunich neuroectodermal syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 ataxie télangiectasie --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=ataxie télangiectasie | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 déficit en cytochrome oxydase --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=déficit en cytochrome oxydase | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 hypophosphatasie foetale --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=hypophosphatasie foetale | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 hypophosphatasie infantile --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=hypophosphatasie infantile | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=maladie des urines à l'odeur de sirop d'érable | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 maladie du sirop d'érable --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=maladie du sirop d'érable | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 mevalonic aciduria --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=mevalonic aciduria | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 nanisme --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=nanisme | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 nanisme diastrophique --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=nanisme diastrophique | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 syndrome de Viljoen-Kallis-Voges --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=syndrome de Viljoen-Kallis-Voges | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 syndrome de microcéphalie-brachydactylie-déficience intellectuelle --- r_associated #0: 10 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=syndrome de microcéphalie-brachydactylie-déficience intellectuelle | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=10 déficit en céto-acide décarboxylase --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=déficit en céto-acide décarboxylase | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5 en:Nijmegen breakage syndrome --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:Nijmegen breakage syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5 hyperoxalurie primitive --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=hyperoxalurie primitive | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5 leucinose --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=leucinose | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5 maladie de Wolman --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=maladie de Wolman | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5 maladie des urines avec odeur de sirop erable --- r_associated #0: 5 --> en:primary immunodeficiency syndrome due to p14 deficiency n1=maladie des urines avec odeur de sirop erable | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=5