Network variation - Cytoskeleton in neurons |
ENTRY | nt06541 |
Name | Cytoskeleton in neurons |
Category | Pathway view; Cellular process |
Disease | H00266 Hereditary spastic paraplegia H00058 Amyotrophic lateral sclerosis H00268 Lissencephaly H00264 Charcot-Marie-Tooth disease H00768 Autosomal recessive intellectual developmental disorder H00773 Autosomal dominant intellectual developmental disorder H01881 Complex cortical dysplasia with other brain malformations H02022 Griscelli syndrome |
Display | drug-target relation disease type |
Disease name | Disease category | ||
HH16 | H00255 | Hypogonadotropic hypogonadism | Endocrine and metabolic disease |
MRMV4 | H01287 | Congenital mirror movements | Nervous system disease |
CFNS | H00458 | Syndromic craniosynostoses | Congenital malformation |
DWOPNED | H02688 | Dworschak-Punetha neurodevelopmental syndrome | Congenital malformation |
FXS/POF1/FXTAS | H00465 | Fragile X syndrome | Chromosomal abnormality |
H00627 | Premature ovarian failure | Reproductive system disease | |
H01731 | Fragile X tremor/ataxia syndrome | Chromosomal abnormality | |
MRMV1/HGPPS2 | H01287 | Congenital mirror movements | Nervous system disease |
H02450 | Horizontal gaze palsy with progressive scoliosis | Nervous system disease | |
PVNH9/DFNA83 | H00270 | Periventricular nodular heterotopia | Congenital malformation |
H00604 | Deafness, autosomal dominant | Nervous system disease | |
LISX1 | H00268 | Lissencephaly | Congenital malformation |
ALSPDC/PSNP1 | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
H00077 | Progressive supranuclear palsy | Neurodegenerative disease | |
FAP1 | H01025 | Familial adenomatous polyposis | Neoplasm |
MRT74/CDCBM10 | H00768 | Autosomal recessive intellectual developmental disorder | Mental and behavioural disorder |
H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation | |
LIS9 | H00268 | Lissencephaly | Congenital malformation |
HSAN6/EBS3 | H00265 | Hereditary sensory and autonomic neuropathy | Nervous system disease |
H00584 | Epidermolysis bullosa simplex | Congenital malformation | |
MRD44 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRD63 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MCPH17 | H00269 | Primary microcephaly | Congenital malformation |
SMALED2 | H00455 | Spinal muscular atrophy | Neurodegenerative disease |
NEDBA | H02470 | Neurodevelopmental disorder with structural brain abnormalities | Congenital malformation |
CMT2O/SMALED1/CDCBM13 | H00264 | Charcot-Marie-Tooth disease | Neurodegenerative disease |
H00455 | Spinal muscular atrophy | Neurodegenerative disease | |
H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation | |
SRTD3 | H02157 | Short-rib thoracic dysplasia | Congenital malformation |
NEDMIBA | H02461 | Neurodevelopmental disorder with microcephaly | Congenital malformation |
ALS1/HMND14/PS | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
H00856 | Distal hereditary motor neuropathies | Nervous system disease | |
H00879 | Perry syndrome | Neurodegenerative disease | |
LIS4/MHAC | H00268 | Lissencephaly | Congenital malformation |
H01870 | Microhydranencephaly | Congenital malformation | |
LIS1/MDS | H00268 | Lissencephaly | Congenital malformation |
CDCBM3 | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
DEE68 | H00606 | Early infantile epileptic encephalopathy | Nervous system disease |
SPG10/NEIMY | H00266 | Hereditary spastic paraplegia | Nervous system disease |
H02819 | Neonatal intractable myoclonus | Nervous system disease | |
ALS25 | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
CDCBM2 | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
SPOAN | H02114 | Spastic paraplegia, optic atrophy, and neuropathy | Nervous system disease |
RP89 | H00527 | Retinitis pigmentosa | Nervous system disease |
HSAN2C/SPG30/MRD9 | H00265 | Hereditary sensory and autonomic neuropathy | Nervous system disease |
H00266 | Hereditary spastic paraplegia | Nervous system disease | |
H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder | |
CMT2A1 | H00264 | Charcot-Marie-Tooth disease | Neurodegenerative disease |
SPAX2 | H01351 | Spastic ataxia | Neurodegenerative disease |
CFEOM1/3B | H00838 | Congenital fibrosis of the extraocular muscles | Nervous system disease |
CDAIIIA | H00917 | Congenital dyserythropoietic anemia | Hematologic disease |
BRDCS2 | H02663 | Braddock-Carey syndrome | Congenital malformation |
SPG4 | H00266 | Hereditary spastic paraplegia | Nervous system disease |
LIS6 | H00268 | Lissencephaly | Congenital malformation |
LIS3 | H00268 | Lissencephaly | Congenital malformation |
KTCN | H00789 | Keratoconus | Nervous system disease |
ALS22 | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
MACTHC2 | H01740 | Macrothrombocytopenia | Hematologic disease |
CDCBM6/CSCSC1 | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
H01579 | Congenital symmetric circumferential skin creases | Congenital malformation | |
MACTHC1 | H01740 | Macrothrombocytopenia | Hematologic disease |
CDCBM5 | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
CDCBM7 | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
CDCBM1/CFEOM3A | H01881 | Complex cortical dysplasia with other brain malformations | Congenital malformation |
H00838 | Congenital fibrosis of the extraocular muscles | Nervous system disease | |
HLD6/DYT4 | H00679 | Hypomyelinating leukodystrophy | Inherited metabolic disorder |
H00831 | Primary dystonia | Nervous system disease | |
LCAEOD | H00837 | Leber congenital amaurosis | Nervous system disease |
FPVEPD | H02594 | Congenital facial palsy with ptosis and velopharyngeal dysfunction | Nervous system disease |
OOMD2 | H01897 | Oocyte/zygote/embryo maturation arrest | Reproductive system disease |
BNS | H02716 | Becker nevus syndrome | Congenital malformation |
BRWS1/DDS1 | H02023 | Baraitser-Winter syndrome | Congenital malformation |
H01255 | Juvenile-onset dystonia | Congenital malformation | |
DFNA20/26/BRWS2 | H00604 | Deafness, autosomal dominant | Nervous system disease |
H02023 | Baraitser-Winter syndrome | Congenital malformation | |
ALS18 | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
EHT | H01633 | High blood pressure | Cardiovascular disease |
CPSQ3 | H01097 | Spastic quadriplegic cerebral palsy | Nervous system disease |
SPG91/DEE5/HMND11 | H00266 | Hereditary spastic paraplegia | Nervous system disease |
H00606 | Early infantile epileptic encephalopathy | Nervous system disease | |
H00856 | Distal hereditary motor neuropathies | Nervous system disease | |
DDISBA | H02685 | Developmental delay with neuropsychiatric disorders | Congenital malformation |
CMND | H01810 | Congenital myopathy | Nervous system disease |
MATINS/DFNA17 | H00233 | MYH9-related disease | Cardiovascular disease |
H00604 | Deafness, autosomal dominant | Nervous system disease | |
PFIC10/DIAR2/MVID1 | H00624 | Progressive familial intrahepatic cholestasis | Inherited metabolic disorder |
H01174 | Congenital diarrhea | Digestive system disease | |
MRT63 | H00768 | Autosomal recessive intellectual developmental disorder | Mental and behavioural disorder |
MRD53 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRD54 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
NDAGSCW | H02470 | Neurodevelopmental disorder with structural brain abnormalities | Congenital malformation |
MRD67 | H00773 | Autosomal dominant intellectual developmental disorder | Mental and behavioural disorder |
MRT76 | H00768 | Autosomal recessive intellectual developmental disorder | Mental and behavioural disorder |
GS1 | H02022 | Griscelli syndrome | Primary immunodeficiency |
GS3 | H02022 | Griscelli syndrome | Primary immunodeficiency |
GS2 | H02022 | Griscelli syndrome | Primary immunodeficiency |
DFNA22/DFNB37 | H00604 | Deafness, autosomal dominant | Nervous system disease |
H00605 | Deafness, autosomal recessive | Nervous system disease | |
OPDM2 | H02513 | Oculopharyngodistal myopathy | Musculoskeletal disease |
CMT1F/2E/DIG | H00264 | Charcot-Marie-Tooth disease | Neurodegenerative disease |
ALS1 | H00058 | Amyotrophic lateral sclerosis (ALS) | Neurodegenerative disease |
RP7/VMD3/CACD2/MDPT1 | H00527 | Retinitis pigmentosa | Nervous system disease |
H00814 | Vitelliform macular dystrophy | Nervous system disease | |
H01768 | Central areolar choroidal dystrophy | Nervous system disease | |
H01890 | Pattern dystrophies of the retinal pigment epithelium | Nervous system disease | |
CMT2CC | H00264 | Charcot-Marie-Tooth disease | Neurodegenerative disease |
CMT2R | H00264 | Charcot-Marie-Tooth disease | Neurodegenerative disease |
NEDAUS | H02715 | Neurodevelopmental disorder with defects of ubiquitin-proteasome system | Congenital malformation |
GAN1 | H01259 | Giant axonal neuropathy | Neurodegenerative disease |
PCH3 | H00897 | Pontocerebellar hypoplasia | Congenital malformation |