'en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome'
(id=9103068 ; fe=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1715 creation date=2017-10-29 touchdate=2025-12-29 10:22:30.000)

≈ 74 relations sortantes en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 42 / 1 -> en:hypomandibular faciocranial dysostosis n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=42 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 41 / 0.976 -> en:frontonasal dysplasia sequence n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:frontonasal dysplasia sequence | rel=r_associated | relid=0 | w=41 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 41 / 0.976 -> en:syndrome, omenn's n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:syndrome, omenn's | rel=r_associated | relid=0 | w=41 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 39 / 0.929 -> en:cleft lip sequence n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:cleft lip sequence | rel=r_associated | relid=0 | w=39 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 37 / 0.881 -> en:bifid nose with or without anorectal and renal anomalies n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:bifid nose with or without anorectal and renal anomalies | rel=r_associated | relid=0 | w=37 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:codas syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:codas syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:congenital hereditary facial paralysis with variable hearing loss syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:congenital hereditary facial paralysis with variable hearing loss syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:cranio-orbito-ocular dysraphia syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:cranio-orbito-ocular dysraphia syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:hypospadias-mental retardation syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:microcephaly deafness syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 35 / 0.833 -> en:pashayan syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:pashayan syndrome | rel=r_associated | relid=0 | w=35 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:acromelic frontonasal dysostosis n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:acromelic frontonasal dysostosis | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:agnathia, holoprosencephaly, situs inversus syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:agnathia, holoprosencephaly, situs inversus syndrome | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:blepharophimosis, ptosis, and epicanthus inversus (disorder) n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:chromosome 17, trisomy 17p n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:chromosome 17, trisomy 17p | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:fountain syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:fryns syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:ladda zonana ramer syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:ladda zonana ramer syndrome | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 34 / 0.81 -> en:maxillonasal dysplasia, binder type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:maxillonasal dysplasia, binder type | rel=r_associated | relid=0 | w=34 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:branchio-oto-renal syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:branchio-oto-renal syndrome | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:growth retardation, alopecia, pseudoanodontia and optic atrophy n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:overgrowth, macrocephaly, facial dysmorphism syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:overgrowth, macrocephaly, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:qazi markouizos syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:qazi markouizos syndrome | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:say barber miller syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:say barber miller syndrome | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 32 / 0.762 -> en:severe x-linked intellectual disability gustavson type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:3c syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:3c syndrome | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:arhinia, choanal atresia, and microphthalmia n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:arhinia, choanal atresia, and microphthalmia | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:cerebrooculonasal syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:goldberg-shprintzen megacolon syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:goldberg-shprintzen megacolon syndrome | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 31 / 0.738 -> en:mcpherson clemens syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:mcpherson clemens syndrome | rel=r_associated | relid=0 | w=31 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 30 / 0.714 -> en:deafness-craniofacial syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=30 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 30 / 0.714 -> en:ehlers-danlos syndrome, musculocontractural type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:ehlers-danlos syndrome, musculocontractural type | rel=r_associated | relid=0 | w=30 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 30 / 0.714 -> en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome | rel=r_associated | relid=0 | w=30 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 30 / 0.714 -> en:syndromic x-linked intellectual disability type 11 n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:syndromic x-linked intellectual disability type 11 | rel=r_associated | relid=0 | w=30 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 29 / 0.69 -> en:cayler cardiofacial syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:cayler cardiofacial syndrome | rel=r_associated | relid=0 | w=29 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 29 / 0.69 -> en:haspeslagh fryns muelenaere syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=29 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 29 / 0.69 -> en:kapur toriello syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:kapur toriello syndrome | rel=r_associated | relid=0 | w=29 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 29 / 0.69 -> en:osteosclerosis, developmental delay, craniosynostosis syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:osteosclerosis, developmental delay, craniosynostosis syndrome | rel=r_associated | relid=0 | w=29 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 28 / 0.667 -> en:auriculoocular anomaly and cleft lip syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:auriculoocular anomaly and cleft lip syndrome | rel=r_associated | relid=0 | w=28 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 28 / 0.667 -> en:myopathy, congenital nonprogressive with moebius and robin sequences n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:myopathy, congenital nonprogressive with moebius and robin sequences | rel=r_associated | relid=0 | w=28 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 28 / 0.667 -> en:shprintzen-goldberg syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=28 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 28 / 0.667 -> en:siderius x-linked mental retardation syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:siderius x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 27 / 0.643 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=27 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 27 / 0.643 -> en:membranous cranial ossification, delayed n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:membranous cranial ossification, delayed | rel=r_associated | relid=0 | w=27 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 27 / 0.643 -> en:t-cell negative b-cell positive severe combined immunodeficiency due to jak3 deficiency n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:t-cell negative b-cell positive severe combined immunodeficiency due to jak3 deficiency | rel=r_associated | relid=0 | w=27 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:al gazali aziz salem syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:al gazali aziz salem syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:craniofrontonasal dysplasia n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:grob's syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:grob's syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:hall riggs syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:isotretinoin embryopathy like syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:isotretinoin embryopathy like syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:malignant hyperthermia with arthrogryposis and torticollis syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:malignant hyperthermia with arthrogryposis and torticollis syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:marden walker like syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:marden walker like syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> en:plagiocephaly and x-linked mental retardation n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:plagiocephaly and x-linked mental retardation | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 26 / 0.619 -> syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 25 / 0.595 -> en:severe n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:severe | rel=r_associated | relid=0 | w=25 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 25 / 0.595 -> radiation n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=radiation | rel=r_associated | relid=0 | w=25 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:brachioskeletogenital syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:combined immunodeficiency due to cd3gamma deficiency n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:combined immunodeficiency due to cd3gamma deficiency | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:combined immunodeficiency due to partial rag1 deficiency n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:combined immunodeficiency due to partial rag1 deficiency | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:dysmorphism, pectus carinatum, joint laxity syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:dysmorphism, pectus carinatum, joint laxity syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:ectodermal dysplasia with blindness syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:fara chlupackova syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:fara chlupackova syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:halal syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:hla class 1 deficiency n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hla class 1 deficiency | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:hypertrichosis and acromegaloid facial appearance syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:nablus mask-like facial syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:nablus mask-like facial syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:short stature syndrome, brussels type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:short stature syndrome, brussels type | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:trisomy xq28 syndrome n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:x-linked intellectual disability seemanova type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20 en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome -- r_associated #0: 20 / 0.476 -> en:x-linked intellectual disability stoll type n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20

≈ 77 relations entrantes en:arhinia, choanal atresia, and microphthalmia --- r_associated #0: 40 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:arhinia, choanal atresia, and microphthalmia | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=40 en:fountain syndrome --- r_associated #0: 38 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:fountain syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=38 en:hypertrichosis and acromegaloid facial appearance syndrome --- r_associated #0: 35 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=35 en:dysmorphism, pectus carinatum, joint laxity syndrome --- r_associated #0: 34 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:dysmorphism, pectus carinatum, joint laxity syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=34 en:hypomandibular faciocranial dysostosis --- r_associated #0: 34 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hypomandibular faciocranial dysostosis | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=34 en:hla class 1 deficiency --- r_associated #0: 32 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hla class 1 deficiency | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=32 en:combined immunodeficiency due to partial rag1 deficiency --- r_associated #0: 30 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:combined immunodeficiency due to partial rag1 deficiency | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=30 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 30 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:ectodermal dysplasia with blindness syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=30 en:hall riggs syndrome --- r_associated #0: 30 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hall riggs syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=30 en:brachioskeletogenital syndrome --- r_associated #0: 29 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:brachioskeletogenital syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=29 en:halal syndrome --- r_associated #0: 29 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:halal syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=29 en:trisomy xq28 syndrome --- r_associated #0: 29 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:trisomy xq28 syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=29 en:combined immunodeficiency due to cd3gamma deficiency --- r_associated #0: 28 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:combined immunodeficiency due to cd3gamma deficiency | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=28 en:short stature syndrome, brussels type --- r_associated #0: 28 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:short stature syndrome, brussels type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=28 en:fara chlupackova syndrome --- r_associated #0: 27 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:fara chlupackova syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=27 en:nablus mask-like facial syndrome --- r_associated #0: 27 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:nablus mask-like facial syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability seemanova type --- r_associated #0: 27 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:x-linked intellectual disability seemanova type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability stoll type --- r_associated #0: 27 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:x-linked intellectual disability stoll type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=27 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 26 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=26 en:3c syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:3c syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:acromelic frontonasal dysostosis --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:acromelic frontonasal dysostosis | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:agnathia, holoprosencephaly, situs inversus syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:agnathia, holoprosencephaly, situs inversus syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:al gazali aziz salem syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:al gazali aziz salem syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:auriculoocular anomaly and cleft lip syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:auriculoocular anomaly and cleft lip syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:bifid nose with or without anorectal and renal anomalies --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:bifid nose with or without anorectal and renal anomalies | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:blepharophimosis, ptosis, and epicanthus inversus (disorder) --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:branchio-oto-renal syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:branchio-oto-renal syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:cayler cardiofacial syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:cayler cardiofacial syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:cerebrooculonasal syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:cerebrooculonasal syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 17, trisomy 17p --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:chromosome 17, trisomy 17p | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:cleft lip sequence --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:cleft lip sequence | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:codas syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:codas syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:congenital hereditary facial paralysis with variable hearing loss syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:congenital hereditary facial paralysis with variable hearing loss syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:cranio-orbito-ocular dysraphia syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:cranio-orbito-ocular dysraphia syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:craniofrontonasal dysplasia --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:craniofrontonasal dysplasia | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:deafness-craniofacial syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:deafness-craniofacial syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, musculocontractural type --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:ehlers-danlos syndrome, musculocontractural type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:frontonasal dysplasia sequence --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:frontonasal dysplasia sequence | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:fryns syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:fryns syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:goldberg-shprintzen megacolon syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:goldberg-shprintzen megacolon syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:grob's syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:grob's syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:growth retardation, alopecia, pseudoanodontia and optic atrophy --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:haspeslagh fryns muelenaere syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:hypospadias-mental retardation syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:hypospadias-mental retardation syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:isotretinoin embryopathy like syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:isotretinoin embryopathy like syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:kapur toriello syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:kapur toriello syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:ladda zonana ramer syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:ladda zonana ramer syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:malignant hyperthermia with arthrogryposis and torticollis syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:malignant hyperthermia with arthrogryposis and torticollis syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:marden walker like syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:marden walker like syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:maxillonasal dysplasia, binder type --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:maxillonasal dysplasia, binder type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:mcpherson clemens syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:mcpherson clemens syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:membranous cranial ossification, delayed --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:membranous cranial ossification, delayed | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:microcephaly deafness syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:myopathy, congenital nonprogressive with moebius and robin sequences --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:myopathy, congenital nonprogressive with moebius and robin sequences | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:nephroblastomatosis, fetal ascites, macrosomia and wilms tumor | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:osteosclerosis, developmental delay, craniosynostosis syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:osteosclerosis, developmental delay, craniosynostosis syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:overgrowth, macrocephaly, facial dysmorphism syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:overgrowth, macrocephaly, facial dysmorphism syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:pashayan syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:pashayan syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:plagiocephaly and x-linked mental retardation --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:plagiocephaly and x-linked mental retardation | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:qazi markouizos syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:qazi markouizos syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:say barber miller syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:say barber miller syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:severe x-linked intellectual disability gustavson type --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:severe x-linked intellectual disability gustavson type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:shprintzen-goldberg syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:shprintzen-goldberg syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:siderius x-linked mental retardation syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:siderius x-linked mental retardation syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:syndrome, omenn's --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:syndrome, omenn's | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:syndromic x-linked intellectual disability type 11 --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:syndromic x-linked intellectual disability type 11 | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 en:t-cell negative b-cell positive severe combined immunodeficiency due to jak3 deficiency --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:t-cell negative b-cell positive severe combined immunodeficiency due to jak3 deficiency | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20 dysostose fronto-nasale acromélique --- r_associated #0: 10 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=dysostose fronto-nasale acromélique | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=10 en:Cayler cardiofacial syndrome --- r_associated #0: 10 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:Cayler cardiofacial syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=10 en:Fryns syndrome --- r_associated #0: 10 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=en:Fryns syndrome | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=10 syndrome BOR --- r_associated #0: 10 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=syndrome BOR | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=10 syndrome de bor --- r_associated #0: 10 --> en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome n1=syndrome de bor | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=10