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Ontology Browser

Nervous System Heredodegenerative Disorders (DOID:9001196)
Annotations: Rat: (1901) Mouse: (1919) Human: (2171) Chinchilla: (1764) Bonobo: (1856) Dog: (1877) Squirrel: (1793) Pig: (1881)
Parent Terms Term With Siblings Child Terms
genetic disease +     
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
agenesis of the corpus callosum with peripheral neuropathy  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
Aquaporin 1 Deficiency 
ataxia telangiectasia +   
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
cataract 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy  
Childhood-Onset Neurodegeneration with Brain Atrophy  
Childhood-Onset Neurodegeneration with Cerebellar Atrophy  
chromosomal disease +   
Chronic Traumatic Encephalopathy 
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
demyelinating disease +   
desquamative interstitial pneumonia  
Dwarfism +   
eye degenerative disease +   
eyelid degenerative disease +  
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
Feigenbaum Bergeron Richardson Syndrome 
FINCA Syndrome  
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
hereditary angioedema +   
hereditary ataxia +   
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Huntington's disease-like 2  
hypogonadotropic hypogonadism 5 with or without anosmia +   
Idiopathic Basal Ganglia Calcification 1  
Idiopathic Basal Ganglia Calcification 6  
Idiopathic Basal Ganglia Calcification 7  
Immunodeficiency 38, with Basal Ganglia Calcification  
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Lennox-Gastaut syndrome  
Marfan syndrome +   
monogenic disease +   
motor neuron disease +   
multiple system atrophy +   
myoclonic cerebellar dyssynergia +  
Nervous System Heredodegenerative Disorders +   
Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.
neurodegeneration with brain iron accumulation +   
Neuronal Intranuclear Inclusion Disease  
Nonimmune Chronic Idiopathic Neutropenia, Adult  
olivopontocerebellar atrophy +   
osteochondrodysplasia +   
Paraneoplastic Syndromes, Nervous System +   
Parotidomegaly, Hereditary Bilateral 
PEHO syndrome  
Pick's disease  
platelet-type bleeding disorder 10  
polycystic kidney disease +   
polygenic disease +   
pontocerebellar hypoplasia +   
postpoliomyelitis syndrome 
primary cerebellar degeneration +   
primary hypertrophic osteoarthropathy +   
prion disease +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 
Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression  
Rh deficiency syndrome  
Sacral Agenesis with Vertebral Anomalies  
secondary Parkinson disease +   
Spastic Pseudosclerosis 
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures  
Subacute Combined Degeneration  
synucleinopathy +   
tauopathy +   
TDP-43 Proteinopathies +   
yellow nail syndrome +  
 Wilson disease +   

Exact Synonyms: Degenerative Disease, Nervous System, Hereditary ;   Degenerative Hereditary Disorders, Nervous System ;   Hereditary Neurodegenerative Disease ;   Hereditary Neurodegenerative Diseases ;   Nervous System Degenerative Hereditary Diseases
Primary IDs: MESH:D020271
Alternate IDs: RDO:0002544
Definition Sources: MESH:D020271

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.