'en:chromosomal translocation'
(id=6891111 ; fe=en:chromosomal translocation ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=10591 creation date=2017-06-25 touchdate=2025-07-20 16:32:40.000) ≈ 220 relations sortantes
- en:chromosomal translocation --
r_associated #0: 42 / 1 ->
en:rearrangement of 3q
n1=en:chromosomal translocation | n2=en:rearrangement of 3q | rel=r_associated | relid=0 | w=42
- en:chromosomal translocation --
r_associated #0: 42 / 1 ->
en:sex chromosome aberrations
n1=en:chromosomal translocation | n2=en:sex chromosome aberrations | rel=r_associated | relid=0 | w=42
- en:chromosomal translocation --
r_associated #0: 41 / 0.976 ->
en:tissue mosaicism
n1=en:chromosomal translocation | n2=en:tissue mosaicism | rel=r_associated | relid=0 | w=41
- en:chromosomal translocation --
r_associated #0: 40 / 0.952 ->
en:complete trisomy 18 syndrome
n1=en:chromosomal translocation | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=40
- en:chromosomal translocation --
r_associated #0: 39 / 0.929 ->
en:emanuel syndrome
n1=en:chromosomal translocation | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=39
- en:chromosomal translocation --
r_associated #0: 38 / 0.905 ->
en:homogeneously staining region
n1=en:chromosomal translocation | n2=en:homogeneously staining region | rel=r_associated | relid=0 | w=38
- en:chromosomal translocation --
r_associated #0: 36 / 0.857 ->
en:balanced autosomal translocation
n1=en:chromosomal translocation | n2=en:balanced autosomal translocation | rel=r_associated | relid=0 | w=36
- en:chromosomal translocation --
r_associated #0: 36 / 0.857 ->
en:chromosome replaced with ring or dicentric
n1=en:chromosomal translocation | n2=en:chromosome replaced with ring or dicentric | rel=r_associated | relid=0 | w=36
- en:chromosomal translocation --
r_associated #0: 36 / 0.857 ->
en:giant rod chromosome
n1=en:chromosomal translocation | n2=en:giant rod chromosome | rel=r_associated | relid=0 | w=36
- en:chromosomal translocation --
r_associated #0: 36 / 0.857 ->
en:meretoja syndrome
n1=en:chromosomal translocation | n2=en:meretoja syndrome | rel=r_associated | relid=0 | w=36
- en:chromosomal translocation --
r_associated #0: 36 / 0.857 ->
en:rearrangement of 6q13
n1=en:chromosomal translocation | n2=en:rearrangement of 6q13 | rel=r_associated | relid=0 | w=36
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:angelman syndrome
n1=en:chromosomal translocation | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:anomaly of chromosome x
n1=en:chromosomal translocation | n2=en:anomaly of chromosome x | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:aspects of radiation effects
n1=en:chromosomal translocation | n2=en:aspects of radiation effects | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:bloom syndrome
n1=en:chromosomal translocation | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition
n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:chromosomal alterations of group b
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group b | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:chromosomal insertion
n1=en:chromosomal translocation | n2=en:chromosomal insertion | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:chromosomal instability
n1=en:chromosomal translocation | n2=en:chromosomal instability | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:cri du chat syndrome
n1=en:chromosomal translocation | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:ddit3 wt allele
n1=en:chromosomal translocation | n2=en:ddit3 wt allele | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:dicentric chromosome
n1=en:chromosomal translocation | n2=en:dicentric chromosome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:gene rearrangement
n1=en:chromosomal translocation | n2=en:gene rearrangement | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:oligosomy
n1=en:chromosomal translocation | n2=en:oligosomy | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:philadelphia chromosome
n1=en:chromosomal translocation | n2=en:philadelphia chromosome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:rearrangement of 21q
n1=en:chromosomal translocation | n2=en:rearrangement of 21q | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:rearrangement of 8q11-13
n1=en:chromosomal translocation | n2=en:rearrangement of 8q11-13 | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:site-directed mutagenesis
n1=en:chromosomal translocation | n2=en:site-directed mutagenesis | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:triploidy, diploidy, mixoploidy syndrome
n1=en:chromosomal translocation | n2=en:triploidy, diploidy, mixoploidy syndrome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:trisomy and partial trisomy of autosome
n1=en:chromosomal translocation | n2=en:trisomy and partial trisomy of autosome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
en:williams syndrome
n1=en:chromosomal translocation | n2=en:williams syndrome | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 35 / 0.833 ->
translocation génétique
n1=en:chromosomal translocation | n2=translocation génétique | rel=r_associated | relid=0 | w=35
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:chimerism
n1=en:chromosomal translocation | n2=en:chimerism | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:chromosomal rearrangement
n1=en:chromosomal translocation | n2=en:chromosomal rearrangement | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:chromosome 9 inversion or duplication
n1=en:chromosomal translocation | n2=en:chromosome 9 inversion or duplication | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:chromosome breakage
n1=en:chromosomal translocation | n2=en:chromosome breakage | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:ddit3 gene
n1=en:chromosomal translocation | n2=en:ddit3 gene | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:digeorge syndrome
n1=en:chromosomal translocation | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:fragile x syndrome
n1=en:chromosomal translocation | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:gelatinous droplike corneal dystrophy
n1=en:chromosomal translocation | n2=en:gelatinous droplike corneal dystrophy | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:genetic aspects
n1=en:chromosomal translocation | n2=en:genetic aspects | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:genomic_region_amplification
n1=en:chromosomal translocation | n2=en:genomic_region_amplification | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:gonadal dysgenesis
n1=en:chromosomal translocation | n2=en:gonadal dysgenesis | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:indel mutation
n1=en:chromosomal translocation | n2=en:indel mutation | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:pseudotrisomy 18
n1=en:chromosomal translocation | n2=en:pseudotrisomy 18 | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:rearrangement of 11q
n1=en:chromosomal translocation | n2=en:rearrangement of 11q | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:rearrangement of 8q21
n1=en:chromosomal translocation | n2=en:rearrangement of 8q21 | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:russell-silver syndrome
n1=en:chromosomal translocation | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:sotos syndrome
n1=en:chromosomal translocation | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:translocation down syndrome
n1=en:chromosomal translocation | n2=en:translocation down syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 34 / 0.81 ->
en:xyy syndrome
n1=en:chromosomal translocation | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=34
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication
n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
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:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:complete trisomy 13 syndrome
n1=en:chromosomal translocation | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:deimmunization
n1=en:chromosomal translocation | n2=en:deimmunization | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:ethics qualifier
n1=en:chromosomal translocation | n2=en:ethics qualifier | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:isochromosome
n1=en:chromosomal translocation | n2=en:isochromosome | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:physiological aspects
n1=en:chromosomal translocation | n2=en:physiological aspects | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:rearrangement of 11q13-21
n1=en:chromosomal translocation | n2=en:rearrangement of 11q13-21 | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:rubinstein-taybi syndrome
n1=en:chromosomal translocation | n2=en:rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:trim24 wt allele
n1=en:chromosomal translocation | n2=en:trim24 wt allele | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:triploidy and polyploidy
n1=en:chromosomal translocation | n2=en:triploidy and polyploidy | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:trisomy
n1=en:chromosomal translocation | n2=en:trisomy | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:turner syndrome
n1=en:chromosomal translocation | n2=en:turner syndrome | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 32 / 0.762 ->
en:wolf-hirschhorn syndrome
n1=en:chromosomal translocation | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=32
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:aberrant chromosome 1
n1=en:chromosomal translocation | n2=en:aberrant chromosome 1 | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:abnormal karyotype
n1=en:chromosomal translocation | n2=en:abnormal karyotype | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:amino acid substitution
n1=en:chromosomal translocation | n2=en:amino acid substitution | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:b lymphoblastic leukemia/lymphoma, not otherwise specified
n1=en:chromosomal translocation | n2=en:b lymphoblastic leukemia/lymphoma, not otherwise specified | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:chromosomal alterations of group a
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group a | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:drug effect
n1=en:chromosomal translocation | n2=en:drug effect | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:klinefelter syndrome
n1=en:chromosomal translocation | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:large-scale state transition
n1=en:chromosomal translocation | n2=en:large-scale state transition | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:polyploidy
n1=en:chromosomal translocation | n2=en:polyploidy | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:prader-willi syndrome
n1=en:chromosomal translocation | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:rearrangement of 2p23
n1=en:chromosomal translocation | n2=en:rearrangement of 2p23 | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 31 / 0.738 ->
en:xxyy syndrome
n1=en:chromosomal translocation | n2=en:xxyy syndrome | rel=r_associated | relid=0 | w=31
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:autosomal translocation
n1=en:chromosomal translocation | n2=en:autosomal translocation | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:balanced chromosomal translocation
n1=en:chromosomal translocation | n2=en:balanced chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg
n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:chromosomal alterations of group d
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group d | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:chromosomal inversion
n1=en:chromosomal translocation | n2=en:chromosomal inversion | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:chromosome disorders, autosomal
n1=en:chromosomal translocation | n2=en:chromosome disorders, autosomal | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:cytogenetic abnormality
n1=en:chromosomal translocation | n2=en:cytogenetic abnormality | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:deletion mutagenesis
n1=en:chromosomal translocation | n2=en:deletion mutagenesis | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:duplication seen only at prometaphase
n1=en:chromosomal translocation | n2=en:duplication seen only at prometaphase | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:extra unidentified structurally abnormal chromosome (disorder)
n1=en:chromosomal translocation | n2=en:extra unidentified structurally abnormal chromosome (disorder) | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:fetus with chromosomal abnormality
n1=en:chromosomal translocation | n2=en:fetus with chromosomal abnormality | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:immunology aspects
n1=en:chromosomal translocation | n2=en:immunology aspects | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:intracellular translocation
n1=en:chromosomal translocation | n2=en:intracellular translocation | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:mosaicism
n1=en:chromosomal translocation | n2=en:mosaicism | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:rearrangement of 17p11-13
n1=en:chromosomal translocation | n2=en:rearrangement of 17p11-13 | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:sequence deletion
n1=en:chromosomal translocation | n2=en:sequence deletion | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
en:suppression, genetic
n1=en:chromosomal translocation | n2=en:suppression, genetic | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 30 / 0.714 ->
translocations chromosomiques
n1=en:chromosomal translocation | n2=translocations chromosomiques | rel=r_associated | relid=0 | w=30
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:balanced rearrangement and structural marker
n1=en:chromosomal translocation | n2=en:balanced rearrangement and structural marker | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:beckwith-wiedemann syndrome
n1=en:chromosomal translocation | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:insertional mutagenesis
n1=en:chromosomal translocation | n2=en:insertional mutagenesis | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:jacobsen syndrome
n1=en:chromosomal translocation | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:linker-scanning mutagenesis
n1=en:chromosomal translocation | n2=en:linker-scanning mutagenesis | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:mosaic variegated aneuploidy syndrome
n1=en:chromosomal translocation | n2=en:mosaic variegated aneuploidy syndrome | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:mutagenesis
n1=en:chromosomal translocation | n2=en:mutagenesis | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:numerical chromosomal abnormality
n1=en:chromosomal translocation | n2=en:numerical chromosomal abnormality | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:other conditions due to autosomal anomalies
n1=en:chromosomal translocation | n2=en:other conditions due to autosomal anomalies | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:rearrangement of 1p11-q11
n1=en:chromosomal translocation | n2=en:rearrangement of 1p11-q11 | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:rearrangement of 6q25
n1=en:chromosomal translocation | n2=en:rearrangement of 6q25 | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:unbalanced translocation and insertion
n1=en:chromosomal translocation | n2=en:unbalanced translocation and insertion | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
n1=en:chromosomal translocation | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 29 / 0.69 ->
translocation chromosomique
n1=en:chromosomal translocation | n2=translocation chromosomique | rel=r_associated | relid=0 | w=29
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:46, xx true hermaphrodite
n1=en:chromosomal translocation | n2=en:46, xx true hermaphrodite | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:absence of sex chromosome
n1=en:chromosomal translocation | n2=en:absence of sex chromosome | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:autosomal deletion syndromes
n1=en:chromosomal translocation | n2=en:autosomal deletion syndromes | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:chromosomal alterations of group f
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group f | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:chromosomal duplication
n1=en:chromosomal translocation | n2=en:chromosomal duplication | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:chromothripsis
n1=en:chromosomal translocation | n2=en:chromothripsis | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:double minutes
n1=en:chromosomal translocation | n2=en:double minutes | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:gene amplification
n1=en:chromosomal translocation | n2=en:gene amplification | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:genetic duplication process
n1=en:chromosomal translocation | n2=en:genetic duplication process | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:group chromosomal alteration
n1=en:chromosomal translocation | n2=en:group chromosomal alteration | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:isodicentric chromosome
n1=en:chromosomal translocation | n2=en:isodicentric chromosome | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:karyotype morphology
n1=en:chromosomal translocation | n2=en:karyotype morphology | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:mutation
n1=en:chromosomal translocation | n2=en:mutation | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:polysomy
n1=en:chromosomal translocation | n2=en:polysomy | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:protein translocation
n1=en:chromosomal translocation | n2=en:protein translocation | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:rearrangement of 1p11-13
n1=en:chromosomal translocation | n2=en:rearrangement of 1p11-13 | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:sex chromosome disorders
n1=en:chromosomal translocation | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:smith-magenis syndrome
n1=en:chromosomal translocation | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:somatic hypermutation, immunoglobulin
n1=en:chromosomal translocation | n2=en:somatic hypermutation, immunoglobulin | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
en:unbalanced translocation of chromosome
n1=en:chromosomal translocation | n2=en:unbalanced translocation of chromosome | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 28 / 0.667 ->
translocation
n1=en:chromosomal translocation | n2=translocation | rel=r_associated | relid=0 | w=28
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:22q11 deletion syndrome
n1=en:chromosomal translocation | n2=en:22q11 deletion syndrome | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:aneuploidy
n1=en:chromosomal translocation | n2=en:aneuploidy | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:balanced autosomal translocation in normal individual
n1=en:chromosomal translocation | n2=en:balanced autosomal translocation in normal individual | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:cellular translocation
n1=en:chromosomal translocation | n2=en:cellular translocation | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:chromosomal abnormality in fetus affecting management of mother
n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus affecting management of mother | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:chromosomal alterations of group c and x
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group c and x | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:chromosomal alterations of group e
n1=en:chromosomal translocation | n2=en:chromosomal alterations of group e | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:chromosomal deletion
n1=en:chromosomal translocation | n2=en:chromosomal deletion | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:chromosomal translocation process
n1=en:chromosomal translocation | n2=en:chromosomal translocation process | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:down syndrome
n1=en:chromosomal translocation | n2=en:down syndrome | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:holoprosencephaly
n1=en:chromosomal translocation | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:melnick-fraser syndrome
n1=en:chromosomal translocation | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:natural vs induced genetic mutation
n1=en:chromosomal translocation | n2=en:natural vs induced genetic mutation | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:other conditions due to chromosome anomalies
n1=en:chromosomal translocation | n2=en:other conditions due to chromosome anomalies | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:sequence inversion
n1=en:chromosomal translocation | n2=en:sequence inversion | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 27 / 0.643 ->
en:trim24 gene
n1=en:chromosomal translocation | n2=en:trim24 gene | rel=r_associated | relid=0 | w=27
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
614 translocations chromosomiques
n1=en:chromosomal translocation | n2=614 translocations chromosomiques | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:alteration of chromosome structure
n1=en:chromosomal translocation | n2=en:alteration of chromosome structure | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:anomaly of chromosome pair
n1=en:chromosomal translocation | n2=en:anomaly of chromosome pair | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:chimera disorder
n1=en:chromosomal translocation | n2=en:chimera disorder | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:chromosome disorder
n1=en:chromosomal translocation | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:chromosomes 1 and 2, monosomy 2q duplication 1p
n1=en:chromosomal translocation | n2=en:chromosomes 1 and 2, monosomy 2q duplication 1p | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:complex karyotype
n1=en:chromosomal translocation | n2=en:complex karyotype | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:derivative chromosome
n1=en:chromosomal translocation | n2=en:derivative chromosome | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:dna repeat expansion
n1=en:chromosomal translocation | n2=en:dna repeat expansion | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:duplication with other complex rearrangement
n1=en:chromosomal translocation | n2=en:duplication with other complex rearrangement | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:genetics
n1=en:chromosomal translocation | n2=en:genetics | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:micronuclei, chromosome-defective
n1=en:chromosomal translocation | n2=en:micronuclei, chromosome-defective | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:nondisjunction, genetic
n1=en:chromosomal translocation | n2=en:nondisjunction, genetic | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:rearrangement of 12q13
n1=en:chromosomal translocation | n2=en:rearrangement of 12q13 | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:supernumerary circular chromosome
n1=en:chromosomal translocation | n2=en:supernumerary circular chromosome | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:translocation
n1=en:chromosomal translocation | n2=en:translocation | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 26 / 0.619 ->
en:uniparental disomy
n1=en:chromosomal translocation | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=26
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
amplification de gènes
n1=en:chromosomal translocation | n2=amplification de gènes | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
anomalie chromosomique
n1=en:chromosomal translocation | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
anomalie cytogénétique
n1=en:chromosomal translocation | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
anormalité des chromosomes
n1=en:chromosomal translocation | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
chimérisme
n1=en:chromosomal translocation | n2=chimérisme | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
délétion chromosomale
n1=en:chromosomal translocation | n2=délétion chromosomale | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
délétion chromosomique
n1=en:chromosomal translocation | n2=délétion chromosomique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
délétion de segment de chromosome
n1=en:chromosomal translocation | n2=délétion de segment de chromosome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
effet d'un médicament
n1=en:chromosomal translocation | n2=effet d'un médicament | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Angelman syndrome
n1=en:chromosomal translocation | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Angelman's syndrome
n1=en:chromosomal translocation | n2=en:Angelman's syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:cerebral gigantism
n1=en:chromosomal translocation | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:chromosomal aberration
n1=en:chromosomal translocation | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:chromosomal abnormality
n1=en:chromosomal translocation | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:chromosome deletion
n1=en:chromosomal translocation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:chromosome inversion
n1=en:chromosomal translocation | n2=en:chromosome inversion | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Down syndrome
n1=en:chromosomal translocation | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:fragile X syndrome
n1=en:chromosomal translocation | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Klinefelter syndrome
n1=en:chromosomal translocation | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:mosaïcism
n1=en:chromosomal translocation | n2=en:mosaïcism | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Prader-Willi syndrome
n1=en:chromosomal translocation | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Soto's syndrome
n1=en:chromosomal translocation | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:sotos' syndrome
n1=en:chromosomal translocation | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Sotos' syndrome
n1=en:chromosomal translocation | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:structural variant:type:pt:^patient:nom
n1=en:chromosomal translocation | n2=en:structural variant:type:pt:^patient:nom | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
en:Williams syndrome
n1=en:chromosomal translocation | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
gigantisme cérébral
n1=en:chromosomal translocation | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
holoprosencéphalie
n1=en:chromosomal translocation | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
holoprosencéphalie de type 2
n1=en:chromosomal translocation | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
holoprosencéphalie de type 3
n1=en:chromosomal translocation | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
holoprosencéphalie de type 4
n1=en:chromosomal translocation | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
holoprosencéphalie familiale alobaire de type 1
n1=en:chromosomal translocation | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
inversion chromosomique
n1=en:chromosomal translocation | n2=inversion chromosomique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
isochromosome
n1=en:chromosomal translocation | n2=isochromosome | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
Jacobsen (syndrome de)
n1=en:chromosomal translocation | n2=Jacobsen (syndrome de) | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
microdélétion 5q35
n1=en:chromosomal translocation | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
mosaïcisme
n1=en:chromosomal translocation | n2=mosaïcisme | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
mutagénèse
n1=en:chromosomal translocation | n2=mutagénèse | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
non disjonction génétique
n1=en:chromosomal translocation | n2=non disjonction génétique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
non-disjonction génétique
n1=en:chromosomal translocation | n2=non-disjonction génétique | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
polyploïdie
n1=en:chromosomal translocation | n2=polyploïdie | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
Silver-Russell (syndrome de)
n1=en:chromosomal translocation | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
Sotos (syndrome de)
n1=en:chromosomal translocation | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome d'Angelman
n1=en:chromosomal translocation | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome d'angelman
n1=en:chromosomal translocation | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
Syndrome d'Angelman
n1=en:chromosomal translocation | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de fragilité du chromosome X
n1=en:chromosomal translocation | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de Jacobsen
n1=en:chromosomal translocation | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de Martin-Bell
n1=en:chromosomal translocation | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de Silver-Russell
n1=en:chromosomal translocation | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de silver-russell
n1=en:chromosomal translocation | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de soto
n1=en:chromosomal translocation | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de Sotos
n1=en:chromosomal translocation | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de sotos
n1=en:chromosomal translocation | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
syndrome de Williams
n1=en:chromosomal translocation | n2=syndrome de Williams | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
trisomie
n1=en:chromosomal translocation | n2=trisomie | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation --
r_associated #0: 20 / 0.476 ->
trouble chromosomique
n1=en:chromosomal translocation | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
| ≈ 319 relations entrantes
- anormalité des chromosomes ---
r_associated #0: 323 -->
en:chromosomal translocation
n1=anormalité des chromosomes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=323
- en:chromosome disorder ---
r_associated #0: 320 -->
en:chromosomal translocation
n1=en:chromosome disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=320
- anomalie chromosomique ---
r_associated #0: 244 -->
en:chromosomal translocation
n1=anomalie chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=244
- trouble chromosomique ---
r_associated #0: 235 -->
en:chromosomal translocation
n1=trouble chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=235
- gigantisme cérébral ---
r_associated #0: 201 -->
en:chromosomal translocation
n1=gigantisme cérébral | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=201
- en:sotos syndrome ---
r_associated #0: 199 -->
en:chromosomal translocation
n1=en:sotos syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=199
- syndrome de Sotos ---
r_associated #0: 195 -->
en:chromosomal translocation
n1=syndrome de Sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=195
- syndrome de soto ---
r_associated #0: 195 -->
en:chromosomal translocation
n1=syndrome de soto | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=195
- en:sotos' syndrome ---
r_associated #0: 190 -->
en:chromosomal translocation
n1=en:sotos' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=190
- en:chromosomal abnormality ---
r_associated #0: 175 -->
en:chromosomal translocation
n1=en:chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=175
- holoprosencéphalie ---
r_associated #0: 101 -->
en:chromosomal translocation
n1=holoprosencéphalie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=101
- chimérisme ---
r_associated #0: 100 -->
en:chromosomal translocation
n1=chimérisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=100
- en:chromosomal deletion ---
r_associated #0: 99 -->
en:chromosomal translocation
n1=en:chromosomal deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=99
- en:holoprosencephaly ---
r_associated #0: 99 -->
en:chromosomal translocation
n1=en:holoprosencephaly | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=99
- délétion chromosomale ---
r_associated #0: 98 -->
en:chromosomal translocation
n1=délétion chromosomale | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=98
- en:chimerism ---
r_associated #0: 98 -->
en:chromosomal translocation
n1=en:chimerism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=98
- délétion de segment de chromosome ---
r_associated #0: 94 -->
en:chromosomal translocation
n1=délétion de segment de chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=94
- en:chromosome deletion ---
r_associated #0: 94 -->
en:chromosomal translocation
n1=en:chromosome deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=94
- délétion chromosomique ---
r_associated #0: 91 -->
en:chromosomal translocation
n1=délétion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=91
- en:jacobsen syndrome ---
r_associated #0: 90 -->
en:chromosomal translocation
n1=en:jacobsen syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=90
- syndrome de Jacobsen ---
r_associated #0: 87 -->
en:chromosomal translocation
n1=syndrome de Jacobsen | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=87
- en:fragile x syndrome ---
r_associated #0: 74 -->
en:chromosomal translocation
n1=en:fragile x syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=74
- en:fragile X syndrome ---
r_associated #0: 70 -->
en:chromosomal translocation
n1=en:fragile X syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=70
- en:Klinefelter syndrome ---
r_associated #0: 67 -->
en:chromosomal translocation
n1=en:Klinefelter syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=67
- syndrome de fragilité du chromosome X ---
r_associated #0: 65 -->
en:chromosomal translocation
n1=syndrome de fragilité du chromosome X | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=65
- en:klinefelter syndrome ---
r_associated #0: 63 -->
en:chromosomal translocation
n1=en:klinefelter syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=63
- anomalie cytogénétique ---
r_associated #0: 60 -->
en:chromosomal translocation
n1=anomalie cytogénétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=60
- en:Sotos' syndrome ---
r_associated #0: 60 -->
en:chromosomal translocation
n1=en:Sotos' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=60
- en:translocation ---
r_associated #0: 56 -->
en:chromosomal translocation
n1=en:translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=56
- translocation ---
r_associated #0: 55 -->
en:chromosomal translocation
n1=translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=55
- syndrome de silver-russell ---
r_associated #0: 54 -->
en:chromosomal translocation
n1=syndrome de silver-russell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=54
- en:down syndrome ---
r_associated #0: 53 -->
en:chromosomal translocation
n1=en:down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=53
- syndrome d'angelman ---
r_associated #0: 53 -->
en:chromosomal translocation
n1=syndrome d'angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=53
- Syndrome d'Angelman ---
r_associated #0: 50 -->
en:chromosomal translocation
n1=Syndrome d'Angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
- en:Down syndrome ---
r_associated #0: 50 -->
en:chromosomal translocation
n1=en:Down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
- mosaïcisme ---
r_associated #0: 50 -->
en:chromosomal translocation
n1=mosaïcisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
- syndrome d'Angelman ---
r_associated #0: 50 -->
en:chromosomal translocation
n1=syndrome d'Angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
- syndrome de Silver-Russell ---
r_associated #0: 50 -->
en:chromosomal translocation
n1=syndrome de Silver-Russell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
- en:prader-willi syndrome ---
r_associated #0: 48 -->
en:chromosomal translocation
n1=en:prader-willi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=48
- en:mosaicism ---
r_associated #0: 47 -->
en:chromosomal translocation
n1=en:mosaicism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=47
- polyploïdie ---
r_associated #0: 47 -->
en:chromosomal translocation
n1=polyploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=47
- en:Prader-Willi syndrome ---
r_associated #0: 45 -->
en:chromosomal translocation
n1=en:Prader-Willi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=45
- en:russell-silver syndrome ---
r_associated #0: 45 -->
en:chromosomal translocation
n1=en:russell-silver syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=45
- effet d'un médicament ---
r_associated #0: 44 -->
en:chromosomal translocation
n1=effet d'un médicament | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=44
- en:polyploidy ---
r_associated #0: 44 -->
en:chromosomal translocation
n1=en:polyploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=44
- en:genetics ---
r_associated #0: 43 -->
en:chromosomal translocation
n1=en:genetics | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=43
- en:drug effect ---
r_associated #0: 42 -->
en:chromosomal translocation
n1=en:drug effect | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=42
- en:other conditions due to autosomal anomalies ---
r_associated #0: 42 -->
en:chromosomal translocation
n1=en:other conditions due to autosomal anomalies | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=42
- en:autosomal deletion syndromes ---
r_associated #0: 41 -->
en:chromosomal translocation
n1=en:autosomal deletion syndromes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
- en:duplication with other complex rearrangement ---
r_associated #0: 41 -->
en:chromosomal translocation
n1=en:duplication with other complex rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
- holoprosencéphalie familiale alobaire de type 1 ---
r_associated #0: 41 -->
en:chromosomal translocation
n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
- syndrome de sotos ---
r_associated #0: 41 -->
en:chromosomal translocation
n1=syndrome de sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
- Silver-Russell (syndrome de) ---
r_associated #0: 40 -->
en:chromosomal translocation
n1=Silver-Russell (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
- en:Angelman syndrome ---
r_associated #0: 40 -->
en:chromosomal translocation
n1=en:Angelman syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
- en:angelman syndrome ---
r_associated #0: 40 -->
en:chromosomal translocation
n1=en:angelman syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
- en:somatic hypermutation, immunoglobulin ---
r_associated #0: 40 -->
en:chromosomal translocation
n1=en:somatic hypermutation, immunoglobulin | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
- en:mosaic variegated aneuploidy syndrome ---
r_associated #0: 39 -->
en:chromosomal translocation
n1=en:mosaic variegated aneuploidy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
- holoprosencéphalie de type 4 ---
r_associated #0: 39 -->
en:chromosomal translocation
n1=holoprosencéphalie de type 4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
- non-disjonction génétique ---
r_associated #0: 39 -->
en:chromosomal translocation
n1=non-disjonction génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
- en:sex chromosome aberrations ---
r_associated #0: 38 -->
en:chromosomal translocation
n1=en:sex chromosome aberrations | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=38
- Sotos (syndrome de) ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=Sotos (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- en:Soto's syndrome ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=en:Soto's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- en:nondisjunction, genetic ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=en:nondisjunction, genetic | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- holoprosencéphalie de type 3 ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=holoprosencéphalie de type 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- non disjonction génétique ---
r_associated #0: 37 -->
en:chromosomal translocation
n1=non disjonction génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
- en:absence of sex chromosome ---
r_associated #0: 36 -->
en:chromosomal translocation
n1=en:absence of sex chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=36
- en:Williams syndrome ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:Williams syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:beckwith-wiedemann syndrome ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:beckwith-wiedemann syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:digeorge syndrome ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:digeorge syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:group chromosomal alteration ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:group chromosomal alteration | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:sex chromosome disorders ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:sex chromosome disorders | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:unbalanced translocation and insertion ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:unbalanced translocation and insertion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:williams syndrome ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:williams syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:wolf-hirschhorn syndrome ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=en:wolf-hirschhorn syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- mutagénèse ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=mutagénèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- translocation chromosomique ---
r_associated #0: 35 -->
en:chromosomal translocation
n1=translocation chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
- en:b lymphoblastic leukemia/lymphoma, not otherwise specified ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:b lymphoblastic leukemia/lymphoma, not otherwise specified | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:cellular translocation ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:cellular translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:chromosomal instability ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:chromosomal instability | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:gene amplification ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:gene amplification | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:mutation ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:numerical chromosomal abnormality ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:numerical chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:polysomy ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=en:polysomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- isochromosome ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=isochromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- trisomie ---
r_associated #0: 34 -->
en:chromosomal translocation
n1=trisomie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
- en:cerebral gigantism ---
r_associated #0: 33 -->
en:chromosomal translocation
n1=en:cerebral gigantism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=33
- en:abnormal karyotype ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:abnormal karyotype | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:balanced rearrangement and structural marker ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:balanced rearrangement and structural marker | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:chromosomal inversion ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:chromosomal inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:chromosomal rearrangement ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:chromosomal rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:chromosomes 1 and 2, monosomy 2q duplication 1p ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:chromosomes 1 and 2, monosomy 2q duplication 1p | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:chromothripsis ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:chromothripsis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:complete trisomy 13 syndrome ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:complete trisomy 13 syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:double minutes ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:double minutes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:emanuel syndrome ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:emanuel syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:meretoja syndrome ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:meretoja syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:mutagenesis ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:rearrangement of 6q13 ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:rearrangement of 6q13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:structural variant:type:pt:^patient:nom ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:structural variant:type:pt:^patient:nom | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:trisomy ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=en:trisomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- mutagenèse ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=mutagenèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- translocation génétique ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=translocation génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- translocations chromosomiques ---
r_associated #0: 32 -->
en:chromosomal translocation
n1=translocations chromosomiques | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
- en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:cri du chat syndrome ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:cri du chat syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:isochromosome ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:isochromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:mosaïcism ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:mosaïcism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:other conditions due to chromosome anomalies ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:other conditions due to chromosome anomalies | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:triploidy, diploidy, mixoploidy syndrome ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:triploidy, diploidy, mixoploidy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- en:unbalanced translocation of chromosome ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=en:unbalanced translocation of chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- holoprosencéphalie de type 2 ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=holoprosencéphalie de type 2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- inversion chromosomique ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=inversion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- syndrome de Martin-Bell ---
r_associated #0: 31 -->
en:chromosomal translocation
n1=syndrome de Martin-Bell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
- TPN ou NADP ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=TPN ou NADP | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- amplification de gènes ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=amplification de gènes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:22q11 deletion syndrome ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:22q11 deletion syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:chromosomal abnormality in fetus affecting management of mother ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:chromosomal abnormality in fetus affecting management of mother | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:deimmunization ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:deimmunization | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:melnick-fraser syndrome ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:melnick-fraser syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:pseudotrisomy 18 ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:pseudotrisomy 18 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:rearrangement of 6q25 ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:rearrangement of 6q25 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:smith-magenis syndrome ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=en:smith-magenis syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- triskélion ---
r_associated #0: 30 -->
en:chromosomal translocation
n1=triskélion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
- en:amino acid substitution ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:amino acid substitution | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:physiological aspects ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:physiological aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:rearrangement of 12q13 ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:rearrangement of 12q13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:rearrangement of 21q ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:rearrangement of 21q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:rearrangement of 2p23 ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:rearrangement of 2p23 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:rearrangement of 3q ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:rearrangement of 3q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- en:trim24 wt allele ---
r_associated #0: 29 -->
en:chromosomal translocation
n1=en:trim24 wt allele | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
- Jacobsen (syndrome de) ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=Jacobsen (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:anomaly of chromosome pair ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:anomaly of chromosome pair | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:autosomal translocation ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:autosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:chromosomal aberration ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:chromosomal aberration | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:ddit3 wt allele ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:ddit3 wt allele | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:extra unidentified structurally abnormal chromosome (disorder) ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:extra unidentified structurally abnormal chromosome (disorder) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:immunology aspects ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:immunology aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:oligosomy ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:oligosomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:supernumerary circular chromosome ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:supernumerary circular chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:tissue mosaicism ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:tissue mosaicism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- microdélétion 5q35 ---
r_associated #0: 28 -->
en:chromosomal translocation
n1=microdélétion 5q35 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
- 614 translocations chromosomiques ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=614 translocations chromosomiques | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:balanced autosomal translocation in normal individual ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:balanced autosomal translocation in normal individual | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:chromosome 9 inversion or duplication ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:chromosome 9 inversion or duplication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:chromosome inversion ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:chromosome inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:chromosome replaced with ring or dicentric ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:chromosome replaced with ring or dicentric | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:duplication seen only at prometaphase ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:duplication seen only at prometaphase | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:genomic_region_amplification ---
r_associated #0: 27 -->
en:chromosomal translocation
n1=en:genomic_region_amplification | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
- en:Angelman's syndrome ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:Angelman's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- en:chimera disorder ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:chimera disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- en:complete trisomy 18 syndrome ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:complete trisomy 18 syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- en:fetus with chromosomal abnormality ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:fetus with chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- en:karyotype morphology ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:karyotype morphology | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- en:rearrangement of 17p11-13 ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=en:rearrangement of 17p11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- syndrome de Williams ---
r_associated #0: 26 -->
en:chromosomal translocation
n1=syndrome de Williams | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
- Hölmgren (triade de) ---
r_associated #0: 25 -->
en:chromosomal translocation
n1=Hölmgren (triade de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=25
- remaniement chromosomique ---
r_associated #0: 24 -->
en:chromosomal translocation
n1=remaniement chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=24
- en:Martin-Bell's syndrome ---
r_associated #0: 23 -->
en:chromosomal translocation
n1=en:Martin-Bell's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=23
- maladie du cri du chat ---
r_associated #0: 22 -->
en:chromosomal translocation
n1=maladie du cri du chat | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=22
- amplification de gène ---
r_associated #0: 21 -->
en:chromosomal translocation
n1=amplification de gène | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
- amplification génique ---
r_associated #0: 21 -->
en:chromosomal translocation
n1=amplification génique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
- syndrome de Prader-Willi ---
r_associated #0: 21 -->
en:chromosomal translocation
n1=syndrome de Prader-Willi | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
- en:46, xx true hermaphrodite ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:46, xx true hermaphrodite | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:aberrant chromosome 1 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:aberrant chromosome 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:alteration of chromosome structure ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:alteration of chromosome structure | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:aneuploidy ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:aneuploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:anomaly of chromosome x ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:anomaly of chromosome x | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:aspects of radiation effects ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:aspects of radiation effects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:balanced autosomal translocation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:balanced autosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:balanced chromosomal translocation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:balanced chromosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:bloom syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:bloom syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group a ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group a | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group b ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group b | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group c and x ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group c and x | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group d ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group d | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group e ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group e | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group f ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal alterations of group f | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal alterations of group g and y ---
r_associated #0: 20 -->
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 duplication ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal duplication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal insertion ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal insertion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosomal translocation process ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosomal translocation process | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosome breakage ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosome breakage | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:chromosome disorders, autosomal ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:chromosome disorders, autosomal | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:complex karyotype ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:complex karyotype | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:cytogenetic abnormality ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:cytogenetic abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:ddit3 gene ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:ddit3 gene | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:deletion mutagenesis ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:deletion mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:derivative chromosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:derivative chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:dicentric chromosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:dicentric chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:dna repeat expansion ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:dna repeat expansion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:ethics qualifier ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:ethics qualifier | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:gelatinous droplike corneal dystrophy ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:gelatinous droplike corneal dystrophy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:gene rearrangement ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:gene rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:genetic aspects ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:genetic aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:genetic duplication process ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:genetic duplication process | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:giant rod chromosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:giant rod chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:gonadal dysgenesis ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:gonadal dysgenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:homogeneously staining region ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:homogeneously staining region | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:indel mutation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:indel mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:insertional mutagenesis ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:insertional mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:intracellular translocation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:intracellular translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:isodicentric chromosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:isodicentric chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:large-scale state transition ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:large-scale state transition | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:linker-scanning mutagenesis ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:linker-scanning mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:micronuclei, chromosome-defective ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:micronuclei, chromosome-defective | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:natural vs induced genetic mutation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:natural vs induced genetic mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:philadelphia chromosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:philadelphia chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:protein translocation ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:protein translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 11q ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 11q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 11q13-21 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 11q13-21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 1p11-13 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 1p11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 1p11-q11 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 1p11-q11 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 8q11-13 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 8q11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rearrangement of 8q21 ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rearrangement of 8q21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:rubinstein-taybi syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:rubinstein-taybi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:sequence deletion ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:sequence deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:sequence inversion ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:sequence inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:site-directed mutagenesis ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:site-directed mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:suppression, genetic ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:suppression, genetic | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:translocation down syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:translocation down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:trim24 gene ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:trim24 gene | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:triploidy and polyploidy ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:triploidy and polyploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:trisomy and partial trisomy of autosome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:trisomy and partial trisomy of autosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:turner syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:turner syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:uniparental disomy ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:uniparental disomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:xxyy syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:xxyy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- en:xyy syndrome ---
r_associated #0: 20 -->
en:chromosomal translocation
n1=en:xyy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
- trisomie 21 ---
r_associated #0: 16 -->
en:chromosomal translocation
n1=trisomie 21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=16
- Child-Pugh (syndrome de) ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=Child-Pugh (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- Giessen (test de) ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=Giessen (test de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- Mutagenèse ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=Mutagenèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triple arthrodèse ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triple arthrodèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triple opération à la française ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triple opération à la française | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triploïdie ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triptans ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triptans | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triquétrum ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triquétrum | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- triradialis sulcus de Turner ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=triradialis sulcus de Turner | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- tris ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=tris | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- trismus ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=trismus | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- trisomie du bras court du chromosome 3 ---
r_associated #0: 15 -->
en:chromosomal translocation
n1=trisomie du bras court du chromosome 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
- mongolisme ---
r_associated #0: 11 -->
en:chromosomal translocation
n1=mongolisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=11
- Amplification génique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Amplification génique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Angelman (syndrome d') ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Angelman (syndrome d') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Anomalie chromosomique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Anomalie chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Délétion chromosomique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Délétion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- HLP3 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=HLP3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- HPE3 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=HPE3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- HPE4 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=HPE4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Inversion chromosomique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Inversion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Martin-Bell (syndrome de) ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Martin-Bell (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Morvan (syndrome de) ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Morvan (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Mutagénèse ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Mutagénèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Syndrome de Prader-Willi ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Syndrome de Prader-Willi | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Syndrome de Sotos ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Syndrome de Sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Translocation chromosomique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Translocation chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- Trisomie ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=Trisomie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- aberration chromosomique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=aberration chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- amplification de triplets nucléotidiques (affections neurologiques liées à l') ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=amplification de triplets nucléotidiques (affections neurologiques liées à l') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- aneuploïdie ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=aneuploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:5p minus syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:5p minus syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:5q microdeletion ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:5q microdeletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Down's ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Down's | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Down's syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Down's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Lejeune's syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Lejeune's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:PWS ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:PWS | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Smith-Magenis syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Smith-Magenis syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Sotos's syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Sotos's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:WBS ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:WBS | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Williams' syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Williams' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:Williams-Beuren syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:Williams-Beuren syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:cat cry disease ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:cat cry disease | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:cat cry syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:cat cry syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:chromosomal disorder ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:chromosomal disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:chromosome 5p deletion syndrome ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:chromosome 5p deletion syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:increase in gene copy number ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:increase in gene copy number | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:mutagenicity ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:mutagenicity | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:trisomy 21 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:trisomy 21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:type 1 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:type 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:type 2 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:type 2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:type 3 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:type 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- en:type 4 ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=en:type 4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holocentromère ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holocentromère | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holocentromérique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holocentromérique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holocrine ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holocrine | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holodiastolique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holodiastolique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holoenzyme ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holoenzyme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- hologamie ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=hologamie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- hologynique ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=hologynique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holomérocrine ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holomérocrine | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holophrase ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holophrase | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- holoproencéphalie ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=holoproencéphalie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- inversion (zone d') ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=inversion (zone d') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- souche de référence ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=souche de référence | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- souche transduite ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=souche transduite | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- triphosphopyridine-nucléotide ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=triphosphopyridine-nucléotide | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- trisomie 9p ---
r_associated #0: 10 -->
en:chromosomal translocation
n1=trisomie 9p | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
- trisomie 13 ---
r_associated #0: 6 -->
en:chromosomal translocation
n1=trisomie 13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=6
- trisomie 18 ---
r_associated #0: 6 -->
en:chromosomal translocation
n1=trisomie 18 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=6
- Chilomastix mesnili ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=Chilomastix mesnili | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- Maladie du cri du chat ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=Maladie du cri du chat | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- Williams (syndrome de) ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=Williams (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- children apperception test ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=children apperception test | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- chimbéré ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=chimbéré | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- chimère homme-animal ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=chimère homme-animal | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- cri du chat (maladie du) ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=cri du chat (maladie du) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- disomie uniparentale ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=disomie uniparentale | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- en:cat's cry syndrome ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=en:cat's cry syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- isobare (solution) ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=isobare (solution) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- syndrome de Child-Pugh ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=syndrome de Child-Pugh | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- translocation de protéines ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=translocation de protéines | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- translocation des protéines ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=translocation des protéines | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- translocation protéique ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=translocation protéique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- triplet (CGG) n ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=triplet (CGG) n | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- trisomie 17p11.2 ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=trisomie 17p11.2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
- trisomie 8 ---
r_associated #0: 5 -->
en:chromosomal translocation
n1=trisomie 8 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
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