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ENTRY	nt06511
Name	NOTCH signaling
Category	Pathway view; Signal transduction
Pathway	hsa04330 Notch signaling pathway
Display	drug-target relation   disease type

N00086        SCDO1     AOS6     TOF/ALGS1     AOVD1/AOS5     HJCYS/ALGS2     IFM2/CADASIL/LMS     AOS3 N00380    HPV N00381    HPV N00382    HPV   N01478        NISBD1     ACNINV1     ACNINV2     ACNINV3   N01479        LVNC7   N01480        SCDO4     SCDO3 N01481        SCDO5     SCDO2     SCDO6

		Disease name	Disease category
SCDO1	H00517	Spondylocostal dysostosis	Congenital malformation
AOS6	H01413	Adams-Oliver syndrome	Congenital malformation
TOF/ALGS1	H00549	Tetralogy of Fallot	Congenital malformation
	H00551	Alagille syndrome	Congenital malformation
AOVD1/AOS5	H00554	Aortic valve disease	Congenital malformation
	H01413	Adams-Oliver syndrome	Congenital malformation
HJCYS/ALGS2	H00623	Hajdu-Cheney syndrome	Musculoskeletal disease
	H00551	Alagille syndrome	Congenital malformation
IFM2/CADASIL/LMS	H01910	Infantile myofibromatosis	Neoplasm
	H00536	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)	Congenital malformation
	H01893	Lateral meningocele syndrome	Congenital malformation
AOS3	H01413	Adams-Oliver syndrome	Congenital malformation
HPV	H00030	Cervical cancer	Cancer
NISBD1	H02467	Neonatal inflammatory skin and bowel disease	Immune system disease
ACNINV1	H00681	Acne inversa	Skin disease
ACNINV2	H00681	Acne inversa	Skin disease
ACNINV3	H00681	Acne inversa	Skin disease
LVNC7	H01216	Left ventricular noncompaction	Cardiovascular disease
SCDO4	H00517	Spondylocostal dysostosis	Congenital malformation
SCDO3	H00517	Spondylocostal dysostosis	Congenital malformation
SCDO5	H00517	Spondylocostal dysostosis	Congenital malformation
SCDO2	H00517	Spondylocostal dysostosis	Congenital malformation
SCDO6	H00517	Spondylocostal dysostosis	Congenital malformation