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ENTRY	nt06522
Name	mTOR signaling
Category	Pathway view; Signal transduction
Pathway	hsa04150 mTOR signaling pathway
Disease	H01928 Smith-Kingsmore syndrome
Display	drug-target relation   disease type

N01576        PMSE     PJS N01575        TSC1/LAM/FCDT     AML/SEGA     TSC2/LAM/FCDT     AML/SEGA     MGCPH     SKS/FCDT   N01578        FFEVF1     FFEVF2     FFEVF3   N01584        BHD

PMSE	H01112	Polyhydramnios, megalencephaly, and symptomatic epilepsy
PJS	H00666	Peutz-Jeghers syndrome
TSC1	H00915	Tuberous sclerosis complex
LAM	H00896	Lymphangioleiomyomatosis
FCDT	H01251	Focal cortical dysplasia of Taylor
AML	H01691	Renal angiomyolipoma
SEGA	H01692	Subependymal giant cell astrocytoma
TSC2	H00915	Tuberous sclerosis complex
MGCPH	H02446	Autosomal recessive macrocephaly/megalencephaly syndrome
SKS	H01928	Smith-Kingsmore syndrome
FFEVF1	H02214	Familial focal epilepsy with variable foci
FFEVF2	H02214	Familial focal epilepsy with variable foci
FFEVF3	H02214	Familial focal epilepsy with variable foci
BHD	H00818	Birt-Hogg-Dube syndrome