Primary atrial arrhythmia
Symptom Information:
Symptom ID: | HPO:0001692 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Arrhythmia(HPO:0011675) Tachycardia(HPO:0001649) Supraventricular tachycardia(HPO:0004755) Primary atrial arrhythmia(HPO:0001692) Supraventricular arrhythmia(HPO:0005115) Supraventricular tachycardia(HPO:0004755) Primary atrial arrhythmia(HPO:0001692) MedDRA: |
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Database Frequency: | 16 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATTRV122I amyloidosis | (Orphanet:85451) |
Atrial fibrillation, familial, 10 | (OMIM:614022) |
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Brugada syndrome | (Orphanet:130) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Congenital heart block | (Orphanet:60041) |
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | (Orphanet:436242) |
Familial long QT syndrome | (Orphanet:768) |
Long QT syndrome 1 | (OMIM:192500) |
Long QT syndrome 2 | (OMIM:613688) |
Long QT syndrome 3 | (OMIM:603830) |
Peripartum cardiomyopathy | (Orphanet:563) |
Romano-Ward syndrome | (Orphanet:101016) |
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY | (OMIM:616117) |
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED | (OMIM:310300) |