Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:neurodegenerative disease
go back to main search page
Accession:DOID:1289 term browser browse the term
Definition:Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures.
Synonyms:exact_synonym: Degenerative Diseases, Central Nervous System;   Degenerative Diseases, Spinal Cord;   Degenerative Neurologic Disease;   Degenerative Neurologic Diseases;   Degenerative Neurologic Disorder;   Degenerative Neurologic Disorders;   Nervous System Degenerative Diseases;   Neurodegenerative Diseases;   Neurodegenerative Disorder;   Neurodegenerative Disorders;   Neurologic Degenerative Condition;   Neurologic Degenerative Conditions;   degenerative disease
 narrow_synonym: Neurodegenerative illness progressing to crippling dystonia and death with relentless cerebral atrophy;   PROGRESSIVE NEURODEGENERATIVE DISEASE;   Severe cystic degeneration of the brain
 primary_id: MESH:D019636
 alt_id: RDO:0001411
 xref: ICD10CM:G31.9;   NCI:C27090
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 





Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      nervous system disease 10752
        neurodegenerative disease 3140
          BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS 1
          Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy 1
          Childhood-Onset Neurodegeneration with Brain Atrophy 1
          Childhood-Onset Neurodegeneration with Cerebellar Atrophy 1
          Chronic Traumatic Encephalopathy 0
          FINCA Syndrome 1
          Feigenbaum Bergeron Richardson Syndrome 0
          Huntington's disease-like 2 1
          Idiopathic Basal Ganglia Calcification 1 10
          Idiopathic Basal Ganglia Calcification 6 1
          Idiopathic Basal Ganglia Calcification 7 1
          NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA 1
          NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY 1
          Nervous System Heredodegenerative Disorders + 1896
          Neuronal Intranuclear Inclusion Disease 1
          PEHO syndrome 4
          Paraneoplastic Syndromes, Nervous System + 18
          Pick's disease 10
          Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 0
          Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression 1
          Spastic Pseudosclerosis 0
          Subacute Combined Degeneration 2
          TDP-43 Proteinopathies + 250
          aceruloplasminemia 3
          agenesis of the corpus callosum with peripheral neuropathy 3
          demyelinating disease + 404
          eye degenerative disease + 448
          eyelid degenerative disease + 0
          hereditary ataxia + 218
          motor neuron disease + 363
          multiple system atrophy + 29
          myoclonic cerebellar dyssynergia + 0
          neurodegeneration with brain iron accumulation + 14
          olivopontocerebellar atrophy + 10
          plexopathy 0
          pontocerebellar hypoplasia + 22
          postpoliomyelitis syndrome 0
          primary cerebellar degeneration + 242
          prion disease + 39
          secondary Parkinson disease + 14
          stress-induced childhood-onset neurodegeneration with variable ataxia and seizures 1
          synucleinopathy + 274
          tauopathy + 491
Path 2
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      nervous system disease 10752
        central nervous system disease 8839
          neurodegenerative disease 3140
            BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS 1
            Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy 1
            Childhood-Onset Neurodegeneration with Brain Atrophy 1
            Childhood-Onset Neurodegeneration with Cerebellar Atrophy 1
            Chronic Traumatic Encephalopathy 0
            FINCA Syndrome 1
            Feigenbaum Bergeron Richardson Syndrome 0
            Huntington's disease-like 2 1
            Idiopathic Basal Ganglia Calcification 1 10
            Idiopathic Basal Ganglia Calcification 6 1
            Idiopathic Basal Ganglia Calcification 7 1
            NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA 1
            NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY 1
            Nervous System Heredodegenerative Disorders + 1896
            Neuronal Intranuclear Inclusion Disease 1
            PEHO syndrome 4
            Paraneoplastic Syndromes, Nervous System + 18
            Pick's disease 10
            Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant 0
            Recurrent Metabolic Crises with Variable Encephalomyopathic Features and Neurologic Regression 1
            Spastic Pseudosclerosis 0
            Subacute Combined Degeneration 2
            TDP-43 Proteinopathies + 250
            aceruloplasminemia 3
            agenesis of the corpus callosum with peripheral neuropathy 3
            demyelinating disease + 404
            eye degenerative disease + 448
            eyelid degenerative disease + 0
            hereditary ataxia + 218
            motor neuron disease + 363
            multiple system atrophy + 29
            myoclonic cerebellar dyssynergia + 0
            neurodegeneration with brain iron accumulation + 14
            olivopontocerebellar atrophy + 10
            plexopathy 0
            pontocerebellar hypoplasia + 22
            postpoliomyelitis syndrome 0
            primary cerebellar degeneration + 242
            prion disease + 39
            secondary Parkinson disease + 14
            stress-induced childhood-onset neurodegeneration with variable ataxia and seizures 1
            synucleinopathy + 274
            tauopathy + 491
paths to the root

NHLBI Logo

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