Heredodegenerative Disorders, Nervous System [dědičné degenerativní poruchy nervového systému]

topical
45
Terms

dědičné neurodegenerativní nemoci

 

Degenerative Disease, Nervous System, Hereditary
Degenerative Hereditary Diseases, Nervous System
Degenerative Hereditary Disorders, Nervous System
Hereditary Diseases, Neurodegenerative
Hereditary Neurodegenerative Diseases
Hereditary-Degenerative Disorders, Nervous System
Nervous System Degenerative Hereditary Diseases
Nervous System Diseases, Degenerative, Hereditary
Nervous System Hereditary Degenerative Diseases
Neurodegenerative Diseases, Hereditary

Persistent link   https://www.medvik.cz/link/D020271
Definition

Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.

DUI
D020271 MeSH Browser
CUI
M0328330
History note
2000
Public note
2000

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 3
CO
complications 2
DI
diagnosis 14
DG
diagnostic imaging 1
DH
diet therapy
DT
drug therapy 2
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 11
GE
genetics 14
HI
history 1
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality 1
NU
nursing
PS
parasitology
PA
pathology 3
PP
physiopathology 7
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 1
TH
therapy 4
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 878
C10.574 Neurodegenerative Diseases 641
C10.574.250 Chronic Traumatic Encephalopathy 3
C10.574.500 Heredodegenerative Disorders, Nervous System 45
C10.574.500.024 Alexander Disease 6
C10.574.500.050 Amyloid Neuropathies, Familial 20
C10.574.500.175 Bulbo-Spinal Atrophy, X-Linked 8
C10.574.500.300 Canavan Disease 9
C10.574.500.362 Cockayne Syndrome 4
C10.574.500.393 Dystonia Musculorum Deformans 3
C10.574.500.425 Gerstmann-Straussler-Scheinker Disease 22
C10.574.500.487 Hepatolenticular Degeneration 243
C10.574.500.490 Hereditary Central Nervous System Demyelinating Diseases 11
C10.574.500.493 Hereditary Sensory and Autonomic Neuropathies 26
C10.574.500.495 Hereditary Sensory and Motor Neuropathy 71
C10.574.500.497 Huntington Disease 322
C10.574.500.529 Lafora Disease 1
C10.574.500.545 Myotonia Congenita 17
C10.574.500.547 Myotonic Dystrophy 94
C10.574.500.549 Neurofibromatoses 28
C10.574.500.550 Neuronal Ceroid-Lipofuscinoses 29
C10.574.500.662 Optic Atrophies, Hereditary 5
C10.574.500.700 Pantothenate Kinase-Associated Neurodegeneration 17
C10.574.500.812 Spinal Muscular Atrophies of Childhood 59
C10.574.500.825 Spinocerebellar Degenerations 30
C10.574.500.850 Tourette Syndrome 86
C10.574.500.865 Tuberous Sclerosis 141
C10.574.500.875 Unverricht-Lundborg Syndrome 1
C10.574.562 Motor Neuron Disease 63
C10.574.672 Olivary Degeneration
C10.574.781 Paraneoplastic Syndromes, Nervous System 67
C10.574.827 Postpoliomyelitis Syndrome 26
C10.574.843 Prion Diseases 175
C10.574.910 Subacute Combined Degeneration 1
C10.574.928 Synucleinopathies 28
C10.574.945 Tauopathies 60
C10.574.950 TDP-43 Proteinopathies 13
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.033 Adrenal Hyperplasia, Congenital 225
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 83
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 47
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 61
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 32
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 259
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 328
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 97
C16.320.290 Eye Diseases, Hereditary 57
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 1
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 46
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.400.024 Alexander Disease 6
C16.320.400.050 Amyloid Neuropathies, Familial 20
C16.320.400.100 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.400.150 Canavan Disease 9
C16.320.400.200 Cockayne Syndrome 4
C16.320.400.330 Dystonia Musculorum Deformans 3
C16.320.400.350 Gerstmann-Straussler-Scheinker Disease 22
C16.320.400.361 Hepatolenticular Degeneration 243
C16.320.400.367 Hereditary Central Nervous System Demyelinating Diseases 11
C16.320.400.375 Hereditary Sensory and Motor Neuropathy 71
C16.320.400.415 Hereditary Sensory and Autonomic Neuropathies 26
C16.320.400.430 Huntington Disease 322
C16.320.400.480 Lafora Disease 1
C16.320.400.525 X-Linked Intellectual Disability 17
C16.320.400.540 Myotonia Congenita 17
C16.320.400.542 Myotonic Dystrophy 94
C16.320.400.550 Neuroacanthocytosis 6
C16.320.400.560 Neurofibromatoses 28
C16.320.400.600 Neuronal Ceroid-Lipofuscinoses 29
C16.320.400.630 Optic Atrophies, Hereditary 5
C16.320.400.650 Pantothenate Kinase-Associated Neurodegeneration 17
C16.320.400.765 Spinal Muscular Atrophies of Childhood 59
C16.320.400.780 Spinocerebellar Degenerations 30
C16.320.400.820 Tourette Syndrome 86
C16.320.400.880 Tuberous Sclerosis 141
C16.320.400.940 Unverricht-Lundborg Syndrome 1
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 1
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 5
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 711
C16.320.577 Muscular Dystrophies 140
C16.320.590 Myasthenic Syndromes, Congenital 20
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 143
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 123
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 46
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease Disease MeSH Browser

Cerebrocortical Degeneration of Infancy Disease MeSH Browser

Familial encephalopathy with neuroserpin inclusion bodies Disease MeSH Browser

Fatty Acid Hydroxylase-Associated Neurodegeneration Disease MeSH Browser

Huntington Disease-Like 2 Disease MeSH Browser

Huntington Disease-Like Syndrome Disease MeSH Browser

Lipodystrophy with Congenital Cataracts and Neurodegeneration Disease MeSH Browser

Microphthalmia, Syndromic 10 Disease MeSH Browser

Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers Disease MeSH Browser

Navajo neurohepatopathy Disease MeSH Browser

Neuropathy, Hereditary Sensory, Atypical Disease MeSH Browser

Opticocochleodentate Degeneration Disease MeSH Browser

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Disease MeSH Browser

Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain Disease MeSH Browser

Scapuloperoneal Syndrome, Neurogenic, Kaeser Type Disease MeSH Browser

Spongiform Encephalopathy with Neuropsychiatric Features Disease MeSH Browser

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