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ENTRY	nt06507
Name	TGFB signaling
Category	Pathway view; Signal transduction
Pathway	hsa04350 TGF-beta signaling pathway
Disease	H00800 Loeys-Dietz syndrome H00482 Brachydactyly H00211 Hereditary hemochromatosis H00533 Hereditary hemorrhagic telangiectasia
Display	drug-target relation   disease type

N00063        CED     LDS4     LDS5     LDS1A/2A/AAT5     LDS1B/2BAAT3     CRC     LDS3     LDS6 N00531    HBV N00507    HTLV-1 N01460        GPHYSD2/MFS     GPHYSD3/DASS   N01456        FOP N01459        HTX5     HTX4   N01453        BDA2     BDA1C/BDA2/AMD2/SYNS2/SYM1B     SYNS4     JPS/HMPS     BDA1D/BDA2/AMD3 N01428        BDB2/SYNS1/SYM1A/TCC     STHAG9   N01458        HFE2B N01461        HFE2A     HFE1     HFE3   N01426        HHT5     PPH1     HHT2     PPH2     JPHT/JPS/MYHRS N01462        HHT1   N01455        ODG2   N01454        PMDS1     PMDS2   N01457        MSLHP

CED	H00434	Camurati-Engelmann disease
LDS4	H00800	Loeys-Dietz syndrome
LDS5	H00800	Loeys-Dietz syndrome
LDS1A	H00800	Loeys-Dietz syndrome
2A	H00801	Familial thoracic aortic aneurysm and dissection
LDS1B	H00800	Loeys-Dietz syndrome
2BAAT3	H00801	Familial thoracic aortic aneurysm and dissection
CRC	H00020	Colorectal cancer
LDS3	H00800	Loeys-Dietz syndrome
LDS6	H00800	Loeys-Dietz syndrome
HBV	H00048	Hepatocellular carcinoma
HTLV-1	H00009	Adult T-cell leukemia
GPHYSD2	H00900	Geleophysic dysplasia
MFS	H00653	Marfan syndrome
GPHYSD3	H00900	Geleophysic dysplasia
DASS	H00625	Tooth agenesis
FOP	H00430	Fibrodysplasia ossificans progressiva
HTX5	H00632	Heterotaxy
HTX4	H00632	Heterotaxy
BDA2	H00482	Brachydactyly
BDA1C	H00482	Brachydactyly
AMD2	H00484	Multiple synostosis syndrome
SYNS2	H00851	Proximal symphalangism
SYNS4	H00484	Multiple synostosis syndrome
JPS	H01023	Juvenile polyposis syndrome
HMPS	H01024	Hereditary mixed polyposis syndrome
BDA1D	H00482	Brachydactyly
BDB2	H00482	Brachydactyly
SYNS1	H00484	Multiple synostosis syndrome
SYM1A	H00851	Proximal symphalangism
TCC	H00778	Tarsal-carpal coalition syndrome
STHAG9	H00625	Tooth agenesis
HFE2B	H00211	Hemochromatosis
HFE2A	H00211	Hemochromatosis
HFE1	H00211	Hemochromatosis
HFE3	H00211	Hemochromatosis
HHT5	H00533	Hereditary hemorrhagic telangiectasia
PPH1	H01619	Primary pulmonary hypertension
HHT2	H00533	Hereditary hemorrhagic telangiectasia
PPH2	H01619	Primary pulmonary hypertension
JPHT	H00533	Hereditary hemorrhagic telangiectasia
MYHRS	H02102	Myhre syndrome
HHT1	H00533	Hereditary hemorrhagic telangiectasia
ODG2	H00599	Ovarian dysgenesis
PMDS1	H00609	Persistent Mullerian duct syndrome
PMDS2	H00609	Persistent Mullerian duct syndrome
MSLHP	H02452	Muscle hypertrophy