DiseaseID 18371
室性心动过速
disease
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope and
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Disease: 1Symptom: 12Target: 24Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18371
- Core Entity Id
- 76760
- Source Entity Count
- 1
- Preferred Name
- Tachycardia, Ventricular
- Name Cn
- 室性心动过速
- Name Pinyin
- Shi Xing Xin Dong Guo Su
- Name En
- Tachycardia, Ventricular
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the cardiovascular system
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the cardiovascular system
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope and
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Tachycardia, Ventricular
Role
preferred
Name
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
Role
preferred
Name
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Role
preferred
Name
Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, With Or Without Muscle Weakness
Role
preferred
Name
Catecholaminergic Polymorphic Ventricular Tachycardia
Role
preferred
Name
Familial Ventricular Tachycardia
Role
preferred
Name
Stress-Induced Polymorphic Ventricular Tachycardia
Role
preferred
Name
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
Role
preferred
Name
Bidirectional Tachycardia Induced By Catecholamines
Role
alias
Name
CPVT3
Role
alias
Name
CPVT4
Role
alias
Name
CPVT5
Role
alias
Name
Catecholaminergic Polymorphic Ventricular Tachycardia 1
Role
alias
Name
Catecholaminergic Polymorphic Ventricular Tachycardia 2
Role
alias
Name
Catecholaminergic Polymorphic Ventricular Tachycardia 3
Role
alias
Name
Catecholaminergic Polymorphic Ventricular Tachycardia 4
Role
alias
Name
Catecholaminergic Polymorphic Ventricular Tachycardia 5
Role
alias
Name
Polymorphic Catecholergic Ventricular Tachycardia
Role
alias
Name
Ventricular Tachycardia
Role
alias
Name
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy
Role
alias
Name
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
Role
alias
Name
Ventricular Tachycardia, Familial
Role
alias
Name
Ventricular Tachycardia, Stress-Induced Polymorphic
Role
alias
Name
Vtsip
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0004756
Herb
HBDIS003100HBDIS007831HBDIS014677HBDIS019525HBDIS021819HBDIS029292HBDIS029486
Me Sh
D017180
Omim
192605604772611938614916615441
Umls
C0042514C1631597C3151463C3554047C3809536
Icd10
I47.2
Sym Map
SMDE00334SMDE01128SMDE01484SMDE04800SMDE13796
Do Class
DOID:630DOID:7
Dis Ge Net
C0042514C0340485C1631597C2677794C3151463C3554047C3809536
Orphanet
3286
Umls Sty
T047
Hpo Class
HP:0001626
Me Sh Class
C14C23
Etcm Disease
Catecholaminergic Polymorphic Ventricular Tachycardia
Tcmbank Disease
13614182292309543849372
Itcmdb Generated
ITX-DISEASE-26194EA7EAD9ITX-DISEASE-2DBD63987054ITX-DISEASE-3B7B943AFFE0
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Catecholaminergic Polymorphic Ventricular Tachycardia Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the cardiovascular system
Do Disease Class
disease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the cardiovascular system
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Catecholaminergic Polymorphic Ventricular Tachycardia
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Endocrine diseases
Disease Definition
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder characterized by adrenergically induced ventricular tachycardia (VT) manifesting as syncope andNCI2016_NICHD_1602D:A tachycardia originating in the ventricles of the heart.|NCI2016_FDA_1602D:An abnormally rapid ventricular rhythm with aberrant ventricular excitation, usually in excess of 150 beats per minute.|NCI2016_CTCAE_1602D:A disorder characterized by a dysrhythmia with a heart rate greater than 100 beats per minute that originates distal to the bundle of His.|NCI2016_02D:A disorder characterized by an electrocardiographic finding of three or more consecutive complexes of ventricular origin with a rate greater than a certain threshold (100 or 120 beats per minute are commonly used). The QRS complexes are wide and have an abnormal morphology. (CDISC)|MSH2017_2016_08_12:An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, either as autonomic impulse formation or reentrant impulse conduction. Depending on the etiology, onset of ventricular tachycardia can be paroxysmal (sudden) or nonparoxysmal, its wide QRS complexes can be uniform or polymorphic, and the ventricular beating may be independent of the atrial beating (AV dissociation).
Me Sh Disease Class
Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome