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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:nervous system disease
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Accession:DOID:863 term browser browse the term
Definition:Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle.
Synonyms:exact_synonym: Nervous System Disorder;   Nervous System Disorders;   Neurologic Disorder;   Neurologic Disorders;   Neurological Disorder;   Neurological Disorders;   nervous system diseases
 primary_id: MESH:D009422;   RDO:0001228
 xref: ICD9CM:349.9;   NCI:C26835
 subset: RGD_JBrowse_slim
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18836
    disease of anatomical entity 17322
      nervous system disease 13416
        Chronobiology Disorders + 57
        Congenital Cataracts, Facial Dysmorphism, and Neuropathy 1
        Gerstmann syndrome 0
        Infantile Multisystem Neurologic Disease with Osseous Fragility 0
        NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1
        Nerve Injuries + 38
        Nervous System Malformations + 1195
        Nervous System Neoplasms + 1896
        Nervous System Trauma + 531
        Neurocutaneous Syndromes + 168
        Neurologic Manifestations + 4764
        Norrie disease 5
        Polyglucosan Body Disease, Adult Form 1
        Roy Maroteaux Kremp Syndrome 0
        Tang Hsi Ryu Syndrome 0
        alpha-methylacyl-CoA racemase deficiency 3
        autoimmune disease of the nervous system + 367
        autonomic nervous system disease + 64
        central nervous system disease + 11456
        congenital nervous system abnormality + 588
        diplegia of upper limb 0
        herpes zoster + 4
        intestinal pseudo-obstruction + 27
        neurodegenerative disease + 3539
        neurogenic arthrogryposis multiplex congenita + 3
        peripheral nervous system disease + 2676
        sensory system disease + 5717
        toxic encephalopathy + 172
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.