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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:brain disease
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Accession:DOID:936 term browser browse the term
Definition:Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM.
Synonyms:exact_synonym: Encephalon Disease;   brain diseases;   brain disorder;   brain disorders;   central nervous system intracranial disorders;   encephalon diseases;   encephalopathies;   encephalopathy;   intracranial CNS disorder;   intracranial CNS disorders
 narrow_synonym: INFANTILE ENCEPHALOPATHY
 related_synonym: ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4;   IIAE4
 primary_id: MESH:D001927
 alt_id: OMIM:614212;   RDO:0000283;   RDO:0016187
 xref: ICD10CM:G93.40;   ICD10CM:G93.9;   ICD9CM:348.30;   ICD9CM:348.9;   NCI:C26920;   NCI:C96413;   OMIM:PS610551;   OMIM:PS614388
For additional species annotation, visit the Alliance of Genome Resources.


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Term Annotations click to browse term
  disease 16045
    disease of anatomical entity 15292
      nervous system disease 10879
        central nervous system disease 9020
          brain disease 8346
            Acute Febrile Encephalopathy 0
            Athabaskan brainstem dysgenesis syndrome 2
            BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS 1
            Beta-Ureidopropionase Deficiency 1
            Brain Abscess + 1
            Brain Death 5
            Brain Hypoxia + 96
            Brain Injuries + 271
            Brain Neoplasms + 1295
            Central Auditory Diseases + 7
            Chronic Brain Damage + 21
            Colpocephaly 0
            Congenital Cerebral Granulomas 0
            Crome Syndrome 0
            Dermatoleukodystrophy 0
            ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2 1
            ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED 1
            ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8 1
            ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 3
            ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY 1
            ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM 1
            Headache Disorders + 52
            Keratosis Follicularis Dwarfism Cerebral Atrophy 0
            Kuzniecky Andermann Syndrome 0
            Leukoencephalopathies + 455
            Metabolic Brain Diseases + 573
            Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization 1
            Myopathy, Epilepsy, and Progressive Cerebral Atrophy 1
            Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities 2
            Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart 1
            Non-Lissencephalic Cortical Dysplasia 0
            Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis 2
            Progressive Encephalopathy with Amyotrophy and Optic Atrophy 1
            Progressive Encephalopathy, with or without Lipodystrophy 1
            Pseudo-TORCH Syndrome + 3
            Rambaud Galian Syndrome 0
            Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations 1
            Sener Syndrome 0
            Sepsis-Associated Encephalopathy 4
            Spastic Pseudosclerosis 0
            Subdural Effusion 0
            Thyrocerebral-Retinal Syndrome 0
            Wernicke encephalopathy 2
            akinetic mutism 0
            alveolar echinococcosis 3
            amblyopia + 5
            basal ganglia disease + 570
            baylisascariasis 0
            brain compression 1
            brain edema + 32
            central nervous system origin vertigo 0
            cerebellar disease + 448
            cerebral degeneration + 272
            cerebritis 0
            cerebrovascular disease + 831
            complex cortical dysplasia with other brain malformations + 743
            cystic echinococcosis 5
            dementia + 670
            diabetic encephalopathy 8
            disease of mental health + 6016
            encephalitis + 74
            encephalomalacia + 7
            epilepsy + 1528
            hepatic encephalopathy + 34
            heterophyiasis 0
            hydrocephalus + 118
            hypoglycemic coma 0
            hypothalamic disease + 195
            infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly 1
            intracranial hypertension + 4
            intracranial hypotension 0
            lymphocytic choriomeningitis 2
            movement disease + 1158
            neuroschistosomiasis 0
            paragonimiasis 0
            phaeohyphomycosis + 0
            prion disease + 42
            pseudobulbar palsy + 0
            senile degeneration of brain 0
            sparganosis 0
            tertiary neurosyphilis + 0
            thalamic disease + 195
            toxocariasis + 2
            transient global amnesia 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.