KEGG    Network variation - WNT signaling
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ENTRYnt06505
NameWNT signaling
CategoryPathway view; Signal transduction
Pathwayhsa04310
DiseaseH00485 Robinow syndrome
Display drug-target relation   disease type
N00056   
    BMND16/OI15
    TETAMS1
    Fuhrmann syndrome/AARRS
    STHAG4/OODD/SSPS
    STHAG8/SHFM6
    OMOD2
    NDNC1
    BMND1/VBCH2/OPTA1/OPPG/EVR4
    STHAG7
    ODCRCS
    HCC
    CRC/GC
    CRC/HCC/EC
N00175    KSHV
N01124    Salmonella
N01443   
    FDH
N01442   
    PYL
N01441   
    SOST1/CDD
    SOST2/CLSS
N01440   
    TETAMS2
    NDNC4
    BMND17
 
N01427   
    DRS1
    RRS1/BDB1
    DRS2
    DRS3
N01444    RRS2

BMND16H01593Osteoporosis
OI15H00506Osteogenesis imperfecta
TETAMS1H00636Tetra-amelia syndrome
Fuhrmann syndromeH00846Fuhrmann syndrome
AARRSH00847Al-Awadi/Raas-Rothschild syndrome
STHAG4H00625Tooth agenesis
OODDH00646Odontoonychodermal dysplasia
SSPSH00781Schopf-Schulz-Passarge syndrome
STHAG8H00625Tooth agenesis
SHFM6H00471Split-hand/foot malformation
OMOD2H02154Omodysplasia
NDNC1H01307Nonsyndromic congenital nail disorder
BMND1H01593Osteoporosis
VBCH2H01774Hyperostosis corticalis generalisata
OPTA1H00436Osteopetrosis
OPPGH00451Osteoporosis-pseudoglioma syndrome
EVR4H00589Familial exudative vitreoretinopathy
STHAG7H00625Tooth agenesis
ODCRCSH00857Oligodontia-colorectal cancer syndrome
HCCH00048Hepatocellular carcinoma
CRCH00020Colorectal cancer
GCH00018Gastric cancer
ECH00026Endometrial cancer
KSHVH00041Kaposi sarcoma
SalmonellaH00113Salmonellosis
FDHH00949Focal dermal hypoplasia
PYLH00479Metaphyseal dysplasias
SOST1H00486Sclerosteosis
CDDH02609Craniodiaphyseal dysplasia
SOST2H00486Sclerosteosis
CLSSH00853Cenani-Lenz syndactyly syndrome
TETAMS2H00636Tetra-amelia syndrome
NDNC4H01307Nonsyndromic congenital nail disorder
BMND17H01593Osteoporosis
DRS1H00485Robinow syndrome
RRS1H00485Robinow syndrome
BDB1H00482Brachydactyly
DRS2H00485Robinow syndrome
DRS3H00485Robinow syndrome
RRS2H00485Robinow syndrome