Network variation - Calcium signaling |
ENTRY | nt06528 |
Name | Calcium signaling |
Category | Pathway view; Signal transduction |
Pathway | hsa04020 Calcium signaling pathway |
Disease | H00720 Long QT syndrome H00728 Brugada syndrome H01019 Catecholaminergic polymorphic ventricular tachycardia H00293 Arrhythmogenic right ventricular cardiomyopathy H00606 Early infantile epileptic encephalopathy H00063 Spinocerebellar ataxia |
Display | drug-target relation disease type |
Disease name | Disease category | ||
HOKPP1 | H00215 | Periodic paralysis | Nervous system disease |
CMYP1B | H01810 | Congenital myopathy | Nervous system disease |
VMCQA | H02320 | Vacuolar myopathy with CASQ1 aggregates | Musculoskeletal disease |
CMYP13 | H01810 | Congenital myopathy | Nervous system disease |
LQT8 | H00720 | Long QT syndrome | Cardiovascular disease |
BRGDA3/NEDHLSS | H00728 | Brugada syndrome | Cardiovascular disease |
H02397 | Neurodevelopmental disorder with movement abnormalities or hypotonia | Congenital malformation | |
CPVT1 | H01019 | Catecholaminergic polymorphic ventricular tachycardia | Cardiovascular disease |
ARVD2 | H00293 | Arrhythmogenic right ventricular cardiomyopathy | Cardiovascular disease |
CPVT5 | H01019 | Catecholaminergic polymorphic ventricular tachycardia | Cardiovascular disease |
CPVT2 | H01019 | Catecholaminergic polymorphic ventricular tachycardia | Cardiovascular disease |
SCA6/FHM1/SHM1 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
H00775 | Hemiplegic migraine | Nervous system disease | |
PASNA | H01603 | Primary aldosteronism | Endocrine and metabolic disease |
DEE69 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
SCA42 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
HALD4/EIG6 | H01603 | Primary aldosteronism | Endocrine and metabolic disease |
H00808 | Idiopathic generalized epilepsies | Nervous system disease | |
NEDSIS | H02397 | Neurodevelopmental disorder with movement abnormalities or hypotonia | Congenital malformation |
DEE42/EA2 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
H00749 | Episodic ataxias | Nervous system disease | |
NEDNEH | H02397 | Neurodevelopmental disorder with movement abnormalities or hypotonia | Congenital malformation |
SANDD | H02636 | Sinoatrial node dysfunction and deafness | Cardiovascular disease |
CSNB2A/CORDX3/AIED | H00787 | Congenital stationary night blindness | Nervous system disease |
H00481 | Cone-rod dystrophy and cone dystrophy | Nervous system disease | |
H00690 | Aland Island eye disease | Nervous system disease | |
DEE46 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
LKS | H01514 | Landau-Kleffner syndrome | Nervous system disease |
DEE27/MRD6 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder | |
DEE101/MRD8/NDHMSR | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder | |
H02705 | Neurodevelopmental disorder with glutamatergic synapse dysfunction | Nervous system disease | |
DFNA41 | H00604 | Deafness, autosomal dominant | Nervous system disease |
TAM1/STRMK | H02258 | Tubular aggregate myopathy | Musculoskeletal disease |
H02259 | Stormorken syndrome | Hematologic disease | |
IMD10 | H00093 | Combined immunodeficiency | Primary immunodeficiency |
TAM2 | H02258 | Tubular aggregate myopathy | Musculoskeletal disease |
IMD9 | H00093 | Combined immunodeficiency | Primary immunodeficiency |
SCA44/SCAR13 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
H01891 | Autosomal recessive spinocerebellar ataxias | Neurodegenerative disease | |
DEE58 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
DEE12 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
SCA29 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
SCA15 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
HCC | H00048 | Hepatocellular carcinoma | Cancer |
Glioma/NSCLC | H00042 | Glioma | Cancer |
H00014 | Non-small cell lung cancer | Cancer | |
DFNB97 | H00605 | Deafness, autosomal recessive | Nervous system disease |
DFNB39 | H00605 | Deafness, autosomal recessive | Nervous system disease |
ANHD | H02281 | Isolated anhidrosis with normal sweat glands | Skin disease |
NDNC3 | H01307 | Nonsyndromic congenital nail disorder | Skin disease |
MLIV | H00144 | Mucolipidosis IV | Inherited metabolic disorder, Lysosomal disease |
BROD | H01129 | Brody myopathy | Nervous system disease |
DAR/AKV | H00715 | Darier disease | Congenital malformation |
H00755 | Acrokeratosis verruciformis | Congenital malformation | |
CMH18 | H00292 | Hypertrophic cardiomyopathy | Cardiovascular disease |
CMD1P | H00294 | Dilated cardiomyopathy | Cardiovascular disease |
DFNA82/DFNB12 | H00604 | Deafness, autosomal dominant | Nervous system disease |
H00605 | Deafness, autosomal recessive | Nervous system disease | |
SCAX1 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
ACCIID | H02641 | Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development | Congenital malformation |
DEE91/IECEE1 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
H02150 | Infantile or early childhood epileptic encephalopathy | Nervous system disease | |
MRD53 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRD54 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRD59 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRT63 | H00768 | Autosomal recessive intellectual developmental disorder | Mental and behavioural disorder |
AAT7/MMIHS1 | H00801 | Familial thoracic aortic aneurysm and dissection | Cardiovascular disease |
H01869 | Megacystis microcolon intestinal hypoperistalsis syndrome | Congenital malformation | |
CMH1 | H00292 | Hypertrophic cardiomyopathy | Cardiovascular disease |
LQT14/CPVT4 | H00720 | Long QT syndrome | Cardiovascular disease |
H01019 | Catecholaminergic polymorphic ventricular tachycardia | Cardiovascular disease | |
LQT15 | H00720 | Long QT syndrome | Cardiovascular disease |
LQT16/CPVT6 | H00720 | Long QT syndrome | Cardiovascular disease |
H01019 | Catecholaminergic polymorphic ventricular tachycardia | Cardiovascular disease | |
SCA14 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |
SCA41 | H00063 | Spinocerebellar ataxia (SCA) | Neurodegenerative disease |