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: panic disorder
Accession: DOID:594
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Definition: An anxiety disorder that is characterized by unexpected and repeated episodes of intense fear accompanied by physical symptoms that may include chest pain, heart palpitations, shortness of breath, dizziness, or abdominal distress. (DO)
Synonyms: exact_synonym: Panic Attack; Panic Attacks; Panic Disorders; panic anxiety syndrome
narrow_synonym: PAND1; PAND2; PAND3; panic disorder 1; panic disorder 2; panic disorder 3; panic disorder with joint laxity; panic disorder without agoraphobia
related_synonym: PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 13q-RELATED; PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 4q-RELATED; PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 9q-RELATED; catechol-o-methyltransferase polymorphism
primary_id: MESH:D016584
alt_id: OMIM:167870 ; OMIM:607853 ; OMIM:609985
xref: EFO:0004262 ; EFO:1001907 ; ICD10CM:F41.0 ; NCI:C34890 ; OMIM:PS167870
For additional species annotation, visit the
Alliance of Genome Resources .
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Adora2a
adenosine A2a receptor
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:12825092
NCBI chrNW_004955455:7,886,720...7,906,214
Ensembl chrNW_004955455:7,895,974...7,906,505
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Adra2a
adrenoceptor alpha 2A
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:14656453
NCBI chrNW_004955485:384,405...387,332
Ensembl chrNW_004955485:385,800...387,240
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Cckbr
cholecystokinin B receptor
ISO
CTD Direct Evidence: marker/mechanism
RGD CTD
PMID:8878350 PMID:15354400
RGD:1358454
NCBI chrNW_004955414:22,001,351...22,011,275
Ensembl chrNW_004955414:22,000,436...22,011,433
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Comt
catechol-O-methyltransferase
ISO
ClinVar Annotator: match by term: CATECHOL-O-METHYLTRANSFERASE POLYMORPHISM
ClinVar
PMID:7304673 PMID:7585135 PMID:8807664 PMID:8886163 PMID:8941353 PMID:9110364 PMID:10395222 PMID:10459407 PMID:11171904 PMID:11381111 PMID:11502905 PMID:11772685 PMID:11925305 PMID:12192614 PMID:12359690 PMID:12402217 PMID:12436243 PMID:12595695 PMID:12611827 PMID:12716966 PMID:12842306 PMID:14966473 PMID:15169701 PMID:15457404 PMID:15457497 PMID:15645182 PMID:15652872 PMID:15821730 PMID:15824744 PMID:15935994 PMID:16043133 PMID:16130008 PMID:16135635 PMID:16275815 PMID:16513880 PMID:16542388 PMID:17504906 PMID:21280081 PMID:25741868 More...
NCBI chrNW_004955442:18,130,282...18,152,153
Ensembl chrNW_004955442:18,130,987...18,137,412
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Crh
corticotropin releasing hormone
ISO
RGD
PMID:14675801
RGD:1358525
NCBI chrNW_004955444:12,989,210...12,991,300
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Htr1a
5-hydroxytryptamine receptor 1A
ISO
RGD
PMID:20817074 PMID:21421022
RGD:5683630 RGD:5683631
NCBI chrNW_004955446:4,913,181...4,917,726
Ensembl chrNW_004955446:4,913,884...4,915,146
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Ins
insulin
ISO
CTD Direct Evidence: marker/mechanism
CTD
PMID:12073167
NCBI chrNW_004955422:13,909,408...13,910,419
Ensembl chrNW_004955422:13,909,407...13,910,419
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Manea
mannosidase endo-alpha
susceptibility
ISO
associated with substance dependence; DNA:SNP:3'utr: (rs1133503) (Human)
RGD
PMID:24473444
RGD:401851911
NCBI chrNW_004955411:21,729,085...21,763,684
Ensembl chrNW_004955411:21,735,550...21,761,750
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Maoa
amine oxidase [flavin-containing] A
ISO
RGD
PMID:15670397
RGD:1600723
NCBI chrNW_004955516:4,494,133...4,576,317
Ensembl chrNW_004955516:4,493,946...4,576,317
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Mbl2
mannose binding lectin 2
susceptibility
ISO
DNA:polymorphism: :
RGD
PMID:24856568
RGD:12910826
NCBI chrNW_004955425:7,704,371...7,708,951
Ensembl chrNW_004955425:7,702,137...7,709,006
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Tph2
tryptophan hydroxylase 2
susceptibility
ISO
DNA:SNP:intron: (rs1386494) (human)
RGD
PMID:17123728
RGD:5686356
NCBI chrNW_004955405:11,877,474...11,981,035
Ensembl chrNW_004955405:11,886,206...11,982,550
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