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ENTRY	nt06502
Name	Nucleotide excision repair
Category	Pathway view; Replication and repair
Pathway	hsa03420
Disease	H00403 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 syndrome	H02560	White-Kernohan syndrome
XPE	H01428	Xeroderma pigmentosum
XPC	H01428	Xeroderma pigmentosum
XPB	H01428	Xeroderma pigmentosum
CS	H00076	Cockayne syndrome
TTD2	H00866	Trichothiodystrophy
XPD	H01428	Xeroderma pigmentosum
TTD1	H00866	Trichothiodystrophy
COFS2	H02570	Cerebro-oculo-facio-skeletal syndrome
TTD3	H00866	Trichothiodystrophy
NEDHIB	H02571	Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
UVSS3	H02131	UV-sensitive syndrome
CSB	H00076	Cockayne syndrome
UVSS1	H02131	UV-sensitive syndrome
COFS1	H02570	Cerebro-oculo-facio-skeletal syndrome
CSA	H00076	Cockayne syndrome
UVSS2	H02131	UV-sensitive syndrome
XPG	H01428	Xeroderma pigmentosum
COFS3	H02570	Cerebro-oculo-facio-skeletal syndrome
XPA	H01428	Xeroderma pigmentosum
PFBMFT	H02569	Pulmonary fibrosis and/or bone marrow failure, telomere-related
XPF	H01428	Xeroderma pigmentosum
FANCQ	H00238	Fanconi anemia
COFS4	H02570	Cerebro-oculo-facio-skeletal syndrome
ATLD	H02014	Ataxia-telangiectasia-like syndrome
XPV	H01428	Xeroderma pigmentosum