'en:chromosomal alterations of group g and y'
(id=7114533 ; fe=en:chromosomal alterations of group g and y ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=5889 creation date=2017-06-25 touchdate=2025-07-24 22:30:29.000)

≈ 95 relations sortantes en:chromosomal alterations of group g and y -- r_associated #0: 30 / 1 -> en:balanced rearrangement and structural marker n1=en:chromosomal alterations of group g and y | n2=en:balanced rearrangement and structural marker | rel=r_associated | relid=0 | w=30 en:chromosomal alterations of group g and y -- r_associated #0: 30 / 1 -> en:isochromosome n1=en:chromosomal alterations of group g and y | n2=en:isochromosome | rel=r_associated | relid=0 | w=30 en:chromosomal alterations of group g and y -- r_associated #0: 30 / 1 -> en:prader-willi syndrome n1=en:chromosomal alterations of group g and y | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=30 en:chromosomal alterations of group g and y -- r_associated #0: 29 / 0.967 -> en:digeorge syndrome n1=en:chromosomal alterations of group g and y | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=29 en:chromosomal alterations of group g and y -- r_associated #0: 29 / 0.967 -> en:down syndrome n1=en:chromosomal alterations of group g and y | n2=en:down syndrome | rel=r_associated | relid=0 | w=29 en:chromosomal alterations of group g and y -- r_associated #0: 29 / 0.967 -> en:fetus with chromosomal abnormality n1=en:chromosomal alterations of group g and y | n2=en:fetus with chromosomal abnormality | rel=r_associated | relid=0 | w=29 en:chromosomal alterations of group g and y -- r_associated #0: 29 / 0.967 -> en:fragile x syndrome n1=en:chromosomal alterations of group g and y | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=29 en:chromosomal alterations of group g and y -- r_associated #0: 28 / 0.933 -> en:beckwith-wiedemann syndrome n1=en:chromosomal alterations of group g and y | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=28 en:chromosomal alterations of group g and y -- r_associated #0: 28 / 0.933 -> en:meretoja syndrome n1=en:chromosomal alterations of group g and y | n2=en:meretoja syndrome | rel=r_associated | relid=0 | w=28 en:chromosomal alterations of group g and y -- r_associated #0: 28 / 0.933 -> en:sotos syndrome n1=en:chromosomal alterations of group g and y | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=28 en:chromosomal alterations of group g and y -- r_associated #0: 27 / 0.9 -> en:smith-magenis syndrome n1=en:chromosomal alterations of group g and y | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=27 en:chromosomal alterations of group g and y -- r_associated #0: 25 / 0.833 -> en:angelman syndrome n1=en:chromosomal alterations of group g and y | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=25 en:chromosomal alterations of group g and y -- r_associated #0: 25 / 0.833 -> en:klinefelter syndrome n1=en:chromosomal alterations of group g and y | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=25 en:chromosomal alterations of group g and y -- r_associated #0: 25 / 0.833 -> en:wolf-hirschhorn syndrome n1=en:chromosomal alterations of group g and y | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=25 en:chromosomal alterations of group g and y -- r_associated #0: 24 / 0.8 -> en:lesion n1=en:chromosomal alterations of group g and y | n2=en:lesion | rel=r_associated | relid=0 | w=24 en:chromosomal alterations of group g and y -- r_associated #0: 23 / 0.767 -> en:melnick-fraser syndrome n1=en:chromosomal alterations of group g and y | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=23 en:chromosomal alterations of group g and y -- r_associated #0: 22 / 0.733 -> en:congenital n1=en:chromosomal alterations of group g and y | n2=en:congenital | rel=r_associated | relid=0 | w=22 en:chromosomal alterations of group g and y -- r_associated #0: 21 / 0.7 -> en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg n1=en:chromosomal alterations of group g and y | n2=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | rel=r_associated | relid=0 | w=21 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> congénital n1=en:chromosomal alterations of group g and y | n2=congénital | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> congenital n1=en:chromosomal alterations of group g and y | n2=congenital | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> congénitale n1=en:chromosomal alterations of group g and y | n2=congénitale | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> contractures congénitales et arachnodactylie n1=en:chromosomal alterations of group g and y | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:22q11 deletion syndrome n1=en:chromosomal alterations of group g and y | n2=en:22q11 deletion syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:absence of sex chromosome n1=en:chromosomal alterations of group g and y | n2=en:absence of sex chromosome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Angelman syndrome n1=en:chromosomal alterations of group g and y | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:anomaly of chromosome pair n1=en:chromosomal alterations of group g and y | n2=en:anomaly of chromosome pair | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:autosomal deletion syndromes n1=en:chromosomal alterations of group g and y | n2=en:autosomal deletion syndromes | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:balanced autosomal translocation in normal individual n1=en:chromosomal alterations of group g and y | n2=en:balanced autosomal translocation in normal individual | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:cerebral gigantism n1=en:chromosomal alterations of group g and y | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chimera disorder n1=en:chromosomal alterations of group g and y | n2=en:chimera disorder | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosomal abnormality in fetus affecting management of mother n1=en:chromosomal alterations of group g and y | n2=en:chromosomal abnormality in fetus affecting management of mother | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication n1=en:chromosomal alterations of group g and y | n2=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition n1=en:chromosomal alterations of group g and y | n2=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosomal inversion n1=en:chromosomal alterations of group g and y | n2=en:chromosomal inversion | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosomal translocation n1=en:chromosomal alterations of group g and y | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:chromosome replaced with ring or dicentric n1=en:chromosomal alterations of group g and y | n2=en:chromosome replaced with ring or dicentric | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:complete trisomy 13 syndrome n1=en:chromosomal alterations of group g and y | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:complete trisomy 18 syndrome n1=en:chromosomal alterations of group g and y | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:cri du chat syndrome n1=en:chromosomal alterations of group g and y | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Down syndrome n1=en:chromosomal alterations of group g and y | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:duplication seen only at prometaphase n1=en:chromosomal alterations of group g and y | n2=en:duplication seen only at prometaphase | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:duplication with other complex rearrangement n1=en:chromosomal alterations of group g and y | n2=en:duplication with other complex rearrangement | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:emanuel syndrome n1=en:chromosomal alterations of group g and y | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:extra unidentified structurally abnormal chromosome (disorder) n1=en:chromosomal alterations of group g and y | n2=en:extra unidentified structurally abnormal chromosome (disorder) | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:fragile X syndrome n1=en:chromosomal alterations of group g and y | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:group chromosomal alteration n1=en:chromosomal alterations of group g and y | n2=en:group chromosomal alteration | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:holoprosencephaly n1=en:chromosomal alterations of group g and y | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:jacobsen syndrome n1=en:chromosomal alterations of group g and y | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Klinefelter syndrome n1=en:chromosomal alterations of group g and y | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Martin-Bell's syndrome n1=en:chromosomal alterations of group g and y | n2=en:Martin-Bell's syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:mosaic variegated aneuploidy syndrome n1=en:chromosomal alterations of group g and y | n2=en:mosaic variegated aneuploidy syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:other conditions due to autosomal anomalies n1=en:chromosomal alterations of group g and y | n2=en:other conditions due to autosomal anomalies | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:other conditions due to chromosome anomalies n1=en:chromosomal alterations of group g and y | n2=en:other conditions due to chromosome anomalies | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:polyploidy n1=en:chromosomal alterations of group g and y | n2=en:polyploidy | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Prader-Willi syndrome n1=en:chromosomal alterations of group g and y | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:pseudotrisomy 18 n1=en:chromosomal alterations of group g and y | n2=en:pseudotrisomy 18 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:russell-silver syndrome n1=en:chromosomal alterations of group g and y | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:sex chromosome aberrations n1=en:chromosomal alterations of group g and y | n2=en:sex chromosome aberrations | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:sex chromosome disorders n1=en:chromosomal alterations of group g and y | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Soto's syndrome n1=en:chromosomal alterations of group g and y | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:sotos' syndrome n1=en:chromosomal alterations of group g and y | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Sotos' syndrome n1=en:chromosomal alterations of group g and y | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:supernumerary circular chromosome n1=en:chromosomal alterations of group g and y | n2=en:supernumerary circular chromosome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:triploidy, diploidy, mixoploidy syndrome n1=en:chromosomal alterations of group g and y | n2=en:triploidy, diploidy, mixoploidy syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:unbalanced translocation and insertion n1=en:chromosomal alterations of group g and y | n2=en:unbalanced translocation and insertion | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:unbalanced translocation of chromosome n1=en:chromosomal alterations of group g and y | n2=en:unbalanced translocation of chromosome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:Williams syndrome n1=en:chromosomal alterations of group g and y | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:williams syndrome n1=en:chromosomal alterations of group g and y | n2=en:williams syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome n1=en:chromosomal alterations of group g and y | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> gigantisme cérébral n1=en:chromosomal alterations of group g and y | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> holoprosencéphalie n1=en:chromosomal alterations of group g and y | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> holoprosencéphalie de type 2 n1=en:chromosomal alterations of group g and y | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> holoprosencéphalie de type 3 n1=en:chromosomal alterations of group g and y | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> holoprosencéphalie de type 4 n1=en:chromosomal alterations of group g and y | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> holoprosencéphalie familiale alobaire de type 1 n1=en:chromosomal alterations of group g and y | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> inversion chromosomique n1=en:chromosomal alterations of group g and y | n2=inversion chromosomique | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> isochromosome n1=en:chromosomal alterations of group g and y | n2=isochromosome | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> maladie du cri du chat n1=en:chromosomal alterations of group g and y | n2=maladie du cri du chat | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> microdélétion 5q35 n1=en:chromosomal alterations of group g and y | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> nystagmus congénital isolé n1=en:chromosomal alterations of group g and y | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> polyploïdie n1=en:chromosomal alterations of group g and y | n2=polyploïdie | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> Silver-Russell (syndrome de) n1=en:chromosomal alterations of group g and y | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> Sotos (syndrome de) n1=en:chromosomal alterations of group g and y | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome d'Angelman n1=en:chromosomal alterations of group g and y | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> Syndrome d'Angelman n1=en:chromosomal alterations of group g and y | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome d'angelman n1=en:chromosomal alterations of group g and y | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de fragilité du chromosome X n1=en:chromosomal alterations of group g and y | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de Jacobsen n1=en:chromosomal alterations of group g and y | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de Martin-Bell n1=en:chromosomal alterations of group g and y | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de silver-russell n1=en:chromosomal alterations of group g and y | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de Silver-Russell n1=en:chromosomal alterations of group g and y | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de soto n1=en:chromosomal alterations of group g and y | n2=syndrome de soto | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de Sotos n1=en:chromosomal alterations of group g and y | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> syndrome de sotos n1=en:chromosomal alterations of group g and y | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20 en:chromosomal alterations of group g and y -- r_associated #0: 20 / 0.667 -> trisomie n1=en:chromosomal alterations of group g and y | n2=trisomie | rel=r_associated | relid=0 | w=20

≈ 179 relations entrantes en:sotos syndrome --- r_associated #0: 202 --> en:chromosomal alterations of group g and y n1=en:sotos syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=202 gigantisme cérébral --- r_associated #0: 201 --> en:chromosomal alterations of group g and y n1=gigantisme cérébral | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=201 syndrome de soto --- r_associated #0: 200 --> en:chromosomal alterations of group g and y n1=syndrome de soto | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=200 syndrome de Sotos --- r_associated #0: 195 --> en:chromosomal alterations of group g and y n1=syndrome de Sotos | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=195 en:sotos' syndrome --- r_associated #0: 190 --> en:chromosomal alterations of group g and y n1=en:sotos' syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=190 en:angelman syndrome --- r_associated #0: 134 --> en:chromosomal alterations of group g and y n1=en:angelman syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=134 syndrome d'Angelman --- r_associated #0: 130 --> en:chromosomal alterations of group g and y n1=syndrome d'Angelman | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=130 holoprosencéphalie --- r_associated #0: 105 --> en:chromosomal alterations of group g and y n1=holoprosencéphalie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=105 en:holoprosencephaly --- r_associated #0: 104 --> en:chromosomal alterations of group g and y n1=en:holoprosencephaly | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=104 en:Angelman syndrome --- r_associated #0: 90 --> en:chromosomal alterations of group g and y n1=en:Angelman syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=90 en:jacobsen syndrome --- r_associated #0: 90 --> en:chromosomal alterations of group g and y n1=en:jacobsen syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=90 syndrome de Jacobsen --- r_associated #0: 87 --> en:chromosomal alterations of group g and y n1=syndrome de Jacobsen | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=87 en:fragile x syndrome --- r_associated #0: 74 --> en:chromosomal alterations of group g and y n1=en:fragile x syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=74 en:fragile X syndrome --- r_associated #0: 70 --> en:chromosomal alterations of group g and y n1=en:fragile X syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=70 en:russell-silver syndrome --- r_associated #0: 67 --> en:chromosomal alterations of group g and y n1=en:russell-silver syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=67 Syndrome d'Angelman --- r_associated #0: 65 --> en:chromosomal alterations of group g and y n1=Syndrome d'Angelman | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=65 syndrome de fragilité du chromosome X --- r_associated #0: 65 --> en:chromosomal alterations of group g and y n1=syndrome de fragilité du chromosome X | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=65 syndrome de Silver-Russell --- r_associated #0: 63 --> en:chromosomal alterations of group g and y n1=syndrome de Silver-Russell | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=63 en:Klinefelter syndrome --- r_associated #0: 60 --> en:chromosomal alterations of group g and y n1=en:Klinefelter syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=60 en:Sotos' syndrome --- r_associated #0: 60 --> en:chromosomal alterations of group g and y n1=en:Sotos' syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=60 en:klinefelter syndrome --- r_associated #0: 56 --> en:chromosomal alterations of group g and y n1=en:klinefelter syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=56 syndrome d'angelman --- r_associated #0: 56 --> en:chromosomal alterations of group g and y n1=syndrome d'angelman | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=56 syndrome de silver-russell --- r_associated #0: 52 --> en:chromosomal alterations of group g and y n1=syndrome de silver-russell | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=52 congénital --- r_associated #0: 51 --> en:chromosomal alterations of group g and y n1=congénital | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=51 congénitale --- r_associated #0: 51 --> en:chromosomal alterations of group g and y n1=congénitale | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=51 en:congenital --- r_associated #0: 51 --> en:chromosomal alterations of group g and y n1=en:congenital | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=51 syndrome de sotos --- r_associated #0: 48 --> en:chromosomal alterations of group g and y n1=syndrome de sotos | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=48 en:prader-willi syndrome --- r_associated #0: 47 --> en:chromosomal alterations of group g and y n1=en:prader-willi syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=47 congenital --- r_associated #0: 46 --> en:chromosomal alterations of group g and y n1=congenital | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=46 en:Prader-Willi syndrome --- r_associated #0: 45 --> en:chromosomal alterations of group g and y n1=en:Prader-Willi syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=45 holoprosencéphalie de type 2 --- r_associated #0: 45 --> en:chromosomal alterations of group g and y n1=holoprosencéphalie de type 2 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=45 Silver-Russell (syndrome de) --- r_associated #0: 44 --> en:chromosomal alterations of group g and y n1=Silver-Russell (syndrome de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=44 Sotos (syndrome de) --- r_associated #0: 41 --> en:chromosomal alterations of group g and y n1=Sotos (syndrome de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=41 en:Soto's syndrome --- r_associated #0: 40 --> en:chromosomal alterations of group g and y n1=en:Soto's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=40 en:other conditions due to chromosome anomalies --- r_associated #0: 40 --> en:chromosomal alterations of group g and y n1=en:other conditions due to chromosome anomalies | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=40 holoprosencéphalie familiale alobaire de type 1 --- r_associated #0: 40 --> en:chromosomal alterations of group g and y n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=40 en:balanced rearrangement and structural marker --- r_associated #0: 39 --> en:chromosomal alterations of group g and y n1=en:balanced rearrangement and structural marker | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=39 en:cerebral gigantism --- r_associated #0: 39 --> en:chromosomal alterations of group g and y n1=en:cerebral gigantism | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=39 holoprosencéphalie de type 4 --- r_associated #0: 37 --> en:chromosomal alterations of group g and y n1=holoprosencéphalie de type 4 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=37 en:absence of sex chromosome --- r_associated #0: 36 --> en:chromosomal alterations of group g and y n1=en:absence of sex chromosome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=36 en:wolf-hirschhorn syndrome --- r_associated #0: 36 --> en:chromosomal alterations of group g and y n1=en:wolf-hirschhorn syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=36 isochromosome --- r_associated #0: 36 --> en:chromosomal alterations of group g and y n1=isochromosome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=36 nystagmus congénital isolé --- r_associated #0: 36 --> en:chromosomal alterations of group g and y n1=nystagmus congénital isolé | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=36 en:Down syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:Down syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:autosomal deletion syndromes --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:autosomal deletion syndromes | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:complete trisomy 13 syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:complete trisomy 13 syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:down syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:down syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:meretoja syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:meretoja syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:sex chromosome aberrations --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:sex chromosome aberrations | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:triploidy, diploidy, mixoploidy syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:triploidy, diploidy, mixoploidy syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:unbalanced translocation of chromosome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:unbalanced translocation of chromosome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 trisomie --- r_associated #0: 35 --> en:chromosomal alterations of group g and y n1=trisomie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=35 en:chromosome replaced with ring or dicentric --- r_associated #0: 34 --> en:chromosomal alterations of group g and y n1=en:chromosome replaced with ring or dicentric | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=34 en:polyploidy --- r_associated #0: 34 --> en:chromosomal alterations of group g and y n1=en:polyploidy | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=34 en:trisomy --- r_associated #0: 34 --> en:chromosomal alterations of group g and y n1=en:trisomy | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=34 polyploïdie --- r_associated #0: 34 --> en:chromosomal alterations of group g and y n1=polyploïdie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=34 en:Williams syndrome --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:Williams syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:anomaly of chromosome pair --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:anomaly of chromosome pair | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:chromosomal translocation --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:chromosomal translocation | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:duplication with other complex rearrangement --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:duplication with other complex rearrangement | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:isochromosome --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:isochromosome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:lesion --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:lesion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:mosaic variegated aneuploidy syndrome --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:mosaic variegated aneuploidy syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:williams syndrome --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=en:williams syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 holoprosencéphalie de type 3 --- r_associated #0: 32 --> en:chromosomal alterations of group g and y n1=holoprosencéphalie de type 3 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32 en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:complete trisomy 18 syndrome --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:complete trisomy 18 syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:melnick-fraser syndrome --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:melnick-fraser syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:other conditions due to autosomal anomalies --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:other conditions due to autosomal anomalies | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:smith-magenis syndrome --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:smith-magenis syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:supernumerary circular chromosome --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=en:supernumerary circular chromosome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 inversion chromosomique --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=inversion chromosomique | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 syndrome de Martin-Bell --- r_associated #0: 31 --> en:chromosomal alterations of group g and y n1=syndrome de Martin-Bell | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=31 en:beckwith-wiedemann syndrome --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:beckwith-wiedemann syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 en:chimera disorder --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:chimera disorder | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 en:cri du chat syndrome --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:cri du chat syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 en:group chromosomal alteration --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:group chromosomal alteration | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 en:pseudotrisomy 18 --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:pseudotrisomy 18 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 en:unbalanced translocation and insertion --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=en:unbalanced translocation and insertion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 maladie du cri du chat --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=maladie du cri du chat | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 triskélion --- r_associated #0: 30 --> en:chromosomal alterations of group g and y n1=triskélion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=30 contractures congénitales et arachnodactylie --- r_associated #0: 29 --> en:chromosomal alterations of group g and y n1=contractures congénitales et arachnodactylie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=29 en:Martin-Bell's syndrome --- r_associated #0: 29 --> en:chromosomal alterations of group g and y n1=en:Martin-Bell's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=29 en:extra unidentified structurally abnormal chromosome (disorder) --- r_associated #0: 29 --> en:chromosomal alterations of group g and y n1=en:extra unidentified structurally abnormal chromosome (disorder) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=29 en:fetus with chromosomal abnormality --- r_associated #0: 29 --> en:chromosomal alterations of group g and y n1=en:fetus with chromosomal abnormality | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=29 en:22q11 deletion syndrome --- r_associated #0: 28 --> en:chromosomal alterations of group g and y n1=en:22q11 deletion syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=28 en:chromosomal abnormality in fetus affecting management of mother --- r_associated #0: 28 --> en:chromosomal alterations of group g and y n1=en:chromosomal abnormality in fetus affecting management of mother | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=28 en:chromosomal inversion --- r_associated #0: 28 --> en:chromosomal alterations of group g and y n1=en:chromosomal inversion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=28 en:duplication seen only at prometaphase --- r_associated #0: 28 --> en:chromosomal alterations of group g and y n1=en:duplication seen only at prometaphase | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=28 TPN ou NADP --- r_associated #0: 27 --> en:chromosomal alterations of group g and y n1=TPN ou NADP | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=27 en:digeorge syndrome --- r_associated #0: 27 --> en:chromosomal alterations of group g and y n1=en:digeorge syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=27 en:sex chromosome disorders --- r_associated #0: 27 --> en:chromosomal alterations of group g and y n1=en:sex chromosome disorders | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=27 en:balanced autosomal translocation in normal individual --- r_associated #0: 26 --> en:chromosomal alterations of group g and y n1=en:balanced autosomal translocation in normal individual | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=26 en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition --- r_associated #0: 26 --> en:chromosomal alterations of group g and y n1=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=26 en:emanuel syndrome --- r_associated #0: 26 --> en:chromosomal alterations of group g and y n1=en:emanuel syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=26 microdélétion 5q35 --- r_associated #0: 26 --> en:chromosomal alterations of group g and y n1=microdélétion 5q35 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=26 Hölmgren (triade de) --- r_associated #0: 25 --> en:chromosomal alterations of group g and y n1=Hölmgren (triade de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=25 Jacobsen (syndrome de) --- r_associated #0: 25 --> en:chromosomal alterations of group g and y n1=Jacobsen (syndrome de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=25 en:micronuclei, chromosome-defective --- r_associated #0: 25 --> en:chromosomal alterations of group g and y n1=en:micronuclei, chromosome-defective | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=25 syndrome de Williams --- r_associated #0: 24 --> en:chromosomal alterations of group g and y n1=syndrome de Williams | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=24 en:nystagmus --- r_associated #0: 23 --> en:chromosomal alterations of group g and y n1=en:nystagmus | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=23 en:chromosome inversion --- r_associated #0: 22 --> en:chromosomal alterations of group g and y n1=en:chromosome inversion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=22 en:Angelman's syndrome --- r_associated #0: 21 --> en:chromosomal alterations of group g and y n1=en:Angelman's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=21 syndrome de Prader-Willi --- r_associated #0: 21 --> en:chromosomal alterations of group g and y n1=syndrome de Prader-Willi | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=21 trisomie 21 --- r_associated #0: 16 --> en:chromosomal alterations of group g and y n1=trisomie 21 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=16 Giessen (test de) --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=Giessen (test de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triple arthrodèse --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triple arthrodèse | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triple opération à la française --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triple opération à la française | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triploïdie --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triploïdie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triptans --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triptans | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triquétrum --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triquétrum | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 triradialis sulcus de Turner --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=triradialis sulcus de Turner | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 tris --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=tris | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 trismus --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=trismus | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:chromosomal alterations of group g and y n1=trisomie du bras court du chromosome 3 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=15 mongolisme --- r_associated #0: 11 --> en:chromosomal alterations of group g and y n1=mongolisme | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=11 Angelman (syndrome d') --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Angelman (syndrome d') | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 CONGÉNITALE --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=CONGÉNITALE | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 HLP3 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=HLP3 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 HPE3 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=HPE3 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 HPE4 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=HPE4 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 Inversion chromosomique --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Inversion chromosomique | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Martin-Bell (syndrome de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 Syndrome de Prader-Willi --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Syndrome de Prader-Willi | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 Syndrome de Sotos --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Syndrome de Sotos | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 Trisomie --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=Trisomie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:5p minus syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:5p minus syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:5q microdeletion --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:5q microdeletion | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Down's --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Down's | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Down's syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Down's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Lejeune's syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Lejeune's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:PWS --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:PWS | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Smith-Magenis syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Sotos's syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Sotos's syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:WBS --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:WBS | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Williams' syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Williams' syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:Williams-Beuren syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:cat cry disease --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:cat cry disease | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:cat cry syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:cat cry syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:chromosome 5p deletion syndrome --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:chromosome 5p deletion syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:contractural arachnodactyly --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:contractural arachnodactyly | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:trisomy 21 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:trisomy 21 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:type 1 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:type 1 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:type 2 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:type 2 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:type 3 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:type 3 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 en:type 4 --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=en:type 4 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holocentromère --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holocentromère | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holocentromérique --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holocentromérique | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holocrine --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holocrine | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holodiastolique --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holodiastolique | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holoenzyme --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holoenzyme | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 hologamie --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=hologamie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 hologynique --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=hologynique | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holomérocrine --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holomérocrine | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holophrase --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holophrase | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 holoproencéphalie --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=holoproencéphalie | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 inversion (zone d') --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=inversion (zone d') | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 nystagmus --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=nystagmus | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 nystagmus héréditaire vertical --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=nystagmus héréditaire vertical | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 nystagmus lié au sexe --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=nystagmus lié au sexe | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 nystagmus myoclonies --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=nystagmus myoclonies | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 souche de référence --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=souche de référence | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 souche transduite --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=souche transduite | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=triphosphopyridine-nucléotide | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 trisomie 9p --- r_associated #0: 10 --> en:chromosomal alterations of group g and y n1=trisomie 9p | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=10 trisomie 13 --- r_associated #0: 6 --> en:chromosomal alterations of group g and y n1=trisomie 13 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=6 trisomie 18 --- r_associated #0: 6 --> en:chromosomal alterations of group g and y n1=trisomie 18 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=6 Maladie du cri du chat --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=Maladie du cri du chat | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 Williams (syndrome de) --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=Williams (syndrome de) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 cri du chat (maladie du) --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=cri du chat (maladie du) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 en:cat's cry syndrome --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=en:cat's cry syndrome | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 isobare (solution) --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=isobare (solution) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 nystagmus (zone de moindre) --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=nystagmus (zone de moindre) | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 triplet (CGG) n --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=triplet (CGG) n | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 trisomie 17p11.2 --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=trisomie 17p11.2 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5 trisomie 8 --- r_associated #0: 5 --> en:chromosomal alterations of group g and y n1=trisomie 8 | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=5