KEGG    Network variation - Nucleotide excision repair
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ENTRYnt06502
NameNucleotide excision repair
CategoryPathway view; Replication and repair
Pathwayhsa03420
DiseaseH00403 Disorders of nucleotide excision repair
Display drug-target relation   disease type
N01425   
    White-Kernohan syndrome
    XPE
    XPC
    XPB/CS/TTD2
    XPD/TTD1/COFS2
    TTD3
 
N01430   
    NEDHIB
    UVSS3
    CSB/UVSS1/COFS1
    CSA/UVSS2
 
N01431   
    XPG/CS/COFS3
    XPA
    PFBMFT
    XPF/CS/FANCQ
    COFS4
    ATLD
    XPV

White-Kernohan syndromeH02560White-Kernohan syndrome
XPEH01428Xeroderma pigmentosum
XPCH01428Xeroderma pigmentosum
XPBH01428Xeroderma pigmentosum
CSH00076Cockayne syndrome
TTD2H00866Trichothiodystrophy
XPDH01428Xeroderma pigmentosum
TTD1H00866Trichothiodystrophy
COFS2H02570Cerebro-oculo-facio-skeletal syndrome
TTD3H00866Trichothiodystrophy
NEDHIBH02571Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
UVSS3H02131UV-sensitive syndrome
CSBH00076Cockayne syndrome
UVSS1H02131UV-sensitive syndrome
COFS1H02570Cerebro-oculo-facio-skeletal syndrome
CSAH00076Cockayne syndrome
UVSS2H02131UV-sensitive syndrome
XPGH01428Xeroderma pigmentosum
COFS3H02570Cerebro-oculo-facio-skeletal syndrome
XPAH01428Xeroderma pigmentosum
PFBMFTH02569Pulmonary fibrosis and/or bone marrow failure, telomere-related
XPFH01428Xeroderma pigmentosum
FANCQH00238Fanconi anemia
COFS4H02570Cerebro-oculo-facio-skeletal syndrome
ATLDH02014Ataxia-telangiectasia-like syndrome
XPVH01428Xeroderma pigmentosum