Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

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:Hallucinations
go back to main search page
Accession:DOID:9003126 term browser browse the term
Definition:Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS.
Synonyms:exact_synonym: Auditory Hallucination;   Auditory Hallucinations;   Body Sensation Hallucination;   Body Sensation Hallucinations;   Dissociative Hallucination;   Dissociative Hallucinations;   Elementary Hallucination;   Elementary Hallucinations;   Gustatory Hallucination;   Gustatory Hallucinations;   Hallucination;   Hallucination of Body Sensation;   Hallucinations, Formed, of People;   Hallucinations, Internal Body Sensation;   Hallucinations, Visual, Formed;   Hallucinations, Visual, Unformed;   Hypnagogic Hallucination;   Hypnagogic Hallucinations;   Hypnapompic Hallucination;   Hypnapompic Hallucinations;   Kinesthetic Hallucination;   Kinesthetic Hallucinations;   Mood Congruent Hallucination;   Mood Congruent Hallucinations;   Mood Incongruent Hallucination;   Mood Incongruent Hallucinations;   Olfactory Hallucination;   Olfactory Hallucinations;   Organic Hallucination;   Organic Hallucinations;   Reflex Hallucination;   Reflex Hallucinations;   Sensory Hallucination;   Sensory Hallucinations;   Somatic Hallucination;   Somatic Hallucinations;   Tactile Hallucination;   Tactile Hallucinations;   Verbal Auditory Hallucination;   Verbal Auditory Hallucinations;   Visual Hallucination;   Visual Hallucinations
 primary_id: MESH:D006212


show annotations for term's descendants           Sort by:
Hallucinations term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cck cholecystokinin ISO associated with Parkinson Disease;DNA:polymorphism, haplogype:promoter:-45C>T (human) RGD PMID:12777967 RGD:1625802 NCBI chr 8:121,153,499...121,160,194
Ensembl chr 8:121,153,500...121,160,084 		JBrowse link
G Cckar cholecystokinin A receptor ISO associated with Schizophrenia
associated with Parkinson Disease;DNA:polymorphism, haplotype: :779T>C (human)		 RGD PMID:10572328 PMID:12777967 RGD:1358451, RGD:1625802 NCBI chr14:57,292,397...57,300,747
Ensembl chr14:57,292,397...57,300,747 		JBrowse link
G Homer1 homer scaffold protein 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:24126708 NCBI chr 2:24,542,777...24,645,715
Ensembl chr 2:24,543,093...24,644,785 		JBrowse link
G Htr2a 5-hydroxytryptamine receptor 2A ISO CTD Direct Evidence: marker/mechanism CTD PMID:29748632 NCBI chr15:49,950,035...50,022,188
Ensembl chr15:49,950,804...50,020,928 		JBrowse link
G Psen1 presenilin 1 ISO ClinVar Annotator: match by term: Visual hallucination ClinVar PMID:25741868 NCBI chr 6:103,323,052...103,375,088
Ensembl chr 6:103,323,120...103,371,650 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    Pathological Conditions, Signs and Symptoms 13331
      Signs and Symptoms 10807
        Neurologic Manifestations 10039
          Neurobehavioral Manifestations 4594
            Perceptual Disorders 79
              Hallucinations 5
paths to the root