KEGG    Network variation - HH signaling
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ENTRYnt06501
NameHH signaling
CategoryPathway view; Signal transduction
Pathwayhsa04340
DiseaseH00039 Basal cell carcinoma
H01835 Neuronal migration disorder
Display drug-target relation   disease type
N00062   
    HPE3/MCOPCB5
    BDA1/ACFD
    BCC
    HPE7/BCNS
    BCNS
    BCC
    EVC/WAD
    EVC/WAD
    BCNS/JBTS32
    JBTS12/ACLS/HLS2
    PAPA8/PPD1
    HPE9
    GCPS/PAPA1/PAPB/PPD4/PHS
 
N01537   
    NNMS
 
N01538   
    HPE11
    DBS

HPE3H00267Holoprosencephaly
MCOPCB5H01027Microphthalmia
BDA1H00482Brachydactyly
ACFDH00675Acrocapitofemoral dysplasia
BCCH00039Basal cell carcinoma
HPE7H00267Holoprosencephaly
BCNSH00895Basal cell nevus syndrome
EVCH00503Ellis-van Creveld syndrome
WADH02158Weyers acrofacial dysostosis
JBTS32H00530Joubert syndrome and related disorders
JBTS12H00530Joubert syndrome and related disorders
ACLSH00263Acrocallosal syndrome
HLS2H01265Hydrolethalus syndrome
PAPA8H01852Postaxial polydactyly
PPD1H02332Preaxial polydactyly
HPE9H00267Holoprosencephaly
GCPSH02161Greig cephalopolysyndactyly syndrome
PAPA1H01852Postaxial polydactyly
PAPBH02332Preaxial polydactyly
PPD4H00502Pallister-Hall syndrome
NNMSH02479Nivelon-Nivelon-Mabille syndrome
HPE11H00267Holoprosencephaly
DBSH00886Donnai-Barrow syndrome