KEGG    Network variation - DNA replication
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ENTRYnt06509
NameDNA replication
CategoryPathway view; Replication and repair
Pathwayhsa04110 hsa03030
DiseaseH01889 Meier-Gorlin syndrome
Display drug-target relation   disease type
N01468   
    MGORS1
    MGORS2
    MGORS3
    MGORS5
    MGORS4
    DNFA70
    IMD54
    MGORS8
    MGORS7
 
N01469   
    CILD42
    MGORS6
 
N01470   
    RAPADILINO/RTS2/BGS
    IMAGEI/FILIS
    IMD55
 
N01471   
    IMD80
    VEODS/XLPDR
    PDIL
    PFBMFT6
    CANVAS
    ATLD2
 
N01472   
    MDPL
    SCKL8/PEOA6
    AGS4
    AGS2
    AGS3
    LIG1
 
N01473   
N01474   
    SCKL9
    IBMPFD1/FTDALS6/CMT2Y

MGORS1H01889Meier-Gorlin syndrome
MGORS2H01889Meier-Gorlin syndrome
MGORS3H01889Meier-Gorlin syndrome
MGORS5H01889Meier-Gorlin syndrome
MGORS4H01889Meier-Gorlin syndrome
DNFA70H00604Deafness, autosomal dominant
IMD54H00094Immunodeficiency associated with DNA repair defects
MGORS8H01889Meier-Gorlin syndrome
MGORS7H01889Meier-Gorlin syndrome
CILD42H00564Primary ciliary dyskinesia
MGORS6H01889Meier-Gorlin syndrome
RAPADILINOH00965RAPADILINO syndrome
RTS2H01734Rothmund-Thomson syndrome
BGSH01993Baller-Gerold syndrome
IMAGEIH02369IMAGE-I syndrome
FILISH02370FILS syndrome
IMD55H00093Combined immunodeficiency
IMD80H02525Disorders of innate immunity
VEODSH00658X-linked syndromic intellectual developmental disorder
XLPDRH02484X-linked reticulate pigmentary disorder with systemic manifestations
PDILH02625Primordial dwarfism-immunodeficiency-lipodystrophy syndrome
PFBMFT6H02569Pulmonary fibrosis and/or bone marrow failure, telomere-related
CANVASH02366Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
ATLD2H02014Ataxia-telangiectasia-like syndrome
MDPLH01623MDPL syndrome
SCKL8H00992Seckel syndrome
PEOA6H01118Progressive external ophthalmoplegia
AGS4H00290Aicardi-Goutieres syndrome
AGS2H00290Aicardi-Goutieres syndrome
AGS3H00290Aicardi-Goutieres syndrome
LIG1H00094Immunodeficiency associated with DNA repair defects
SCKL9H00992Seckel syndrome
IBMPFD1H02031Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
FTDALS6H02342Frontotemporal dementia and amyotrophic lateral sclerosis
CMT2YH00264Charcot-Marie-Tooth disease