Abnormal atrioventricular conduction
Symptom Information:
| Symptom ID: | HPO:0005150 | ||
| Synonyms: |
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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) Abnormal atrioventricular conduction(HPO:0005150) MedDRA: |
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| Database Frequency: | 16 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Atrial fibrillation, familial, 10 | (OMIM:614022) |
| Atrial septal defect - atrioventricular conduction defects syndrome | (Orphanet:1479) |
| Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
| Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
| CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
| CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
| Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
| Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |
| Congenital heart block | (Orphanet:60041) |
| Familial atrial fibrillation | (Orphanet:334) |
| Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
| Familial sick sinus syndrome | (Orphanet:166282) |
| Histiocytoid cardiomyopathy | (Orphanet:137675) |
| Idiopathic neonatal atrial flutter | (Orphanet:45452) |
| Sinoatrial node dysfunction and deafness | (Orphanet:324321) |
| Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |