KEGG    Network variation - Chromosome cohesion and segregation
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ENTRYnt06512
NameChromosome cohesion and segregation
CategoryPathway view; Cellular processes
Pathwayhsa04110
DiseaseH00631 Cornelia de Lange syndrome
H00773 Autosomal dominant intellectual developmental disorder
H00269 Primary microcephaly
Display drug-target relation   disease type
N01482   
    CDLS2/DEE85
    CDLS3
    CDLS4
    MRD47
    HPE13/MKMS
    ATRX/MRXHF1
    CDLS1
    WABS
 
N01483   
    RBS/JHS
    CDLS5
 
N01484   
    MRD21
 
N01485   
    CAID
    NEDLBA
    MRD36
    SCLC/NSCLC
    MRD35
 
N01486   
    RTS1
    FERBON
 
N01497   
    MCPH22
    3KS
    XLID100
    ICF1/FSHD4
    MCPH23
    MCPH21
 
N01498   
    MCPH1
 
N01499   
N01500   
N01501   
    OCNDS

CDLS2H00631Cornelia de Lange syndrome
DEE85H00606Early infantile epileptic encephalopathy
CDLS3H00631Cornelia de Lange syndrome
CDLS4H00631Cornelia de Lange syndrome
MRD47H00773Autosomal dominant intellectual developmental disorder
HPE13H00267Holoprosencephaly
MKMSH02582Mullegama-Klein-Martinez syndrome
ATRXH01752ATR-X syndrome
MRXHF1H02583X-linked intellectual disability-hypotonic facies syndrome
CDLS1H00631Cornelia de Lange syndrome
WABSH00914Warsaw breakage syndrome
RBSH00572Roberts-SC phocomelia syndrome
JHSH02581Juberg-Hayward syndrome
CDLS5H00631Cornelia de Lange syndrome
MRD21H00773Autosomal dominant intellectual developmental disorder
CAIDH02122Chronic atrial and intestinal dysrhythmia
NEDLBAH02470Neurodevelopmental disorder with structural brain abnormalities
MRD36H00773Autosomal dominant intellectual developmental disorder
SCLCH00013Small cell lung cancer
NSCLCH00014Non-small cell lung cancer
MRD35H00773Autosomal dominant intellectual developmental disorder
RTS1H01734Rothmund-Thomson syndrome
FERBONH02584Ferguson-Bonni neurodevelopmental syndrome
MCPH22H00269Primary microcephaly
3KSH02461Neurodevelopmental disorder with microcephaly
XLID100H00480X-linked intellectual developmental disorder
ICF1H02308Immunodeficiency-centromeric instability-facial anomalies syndrome
FSHD4H00591Facioscapulohumeral muscular dystrophy
MCPH23H00269Primary microcephaly
MCPH21H00269Primary microcephaly
MCPH1H00269Primary microcephaly
OCNDSH02460Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies