Atrioventricular block
Symptom Information:
Symptom ID: | HPO:0001678 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Abnormal atrioventricular conduction(HPO:0005150) Atrioventricular block(HPO:0001678) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Atrioventricular block(HPO:0001678) Congenital, familial and genetic disorders(MedDRA:10010331) Cardiac and vascular disorders congenital(MedDRA:10007510) Cardiac disorders congenital NEC(MedDRA:10007542) Atrioventricular block(HPO:0001678) Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Atrioventricular block(HPO:0001678) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Cardiac conduction disorders(MedDRA:10000032) Atrioventricular block(HPO:0001678) |
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Database Frequency: | 59 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AA amyloidosis | (Orphanet:85445) |
Arrhythmogenic right ventricular dysplasia, familial, 13 | (OMIM:615616) |
Arrhythmogenic right ventricular dysplasia, familial, 3 | (OMIM:602086) |
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) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Cardiomyopathy, dilated, 1E | (OMIM:601154) |
Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
Cardiomyopathy, familial hypertrophic, 11 | (OMIM:612098) |
Cardiomyopathy, familial hypertrophic, 21 | (OMIM:614676) |
Cardiomyopathy, familial hypertrophic, 6 | (OMIM:600858) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Cardiomyopathy, familial restrictive, 3 | (OMIM:612422) |
Cardiomyopathy-cataract-hip spine disease | (Orphanet:1345) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Congenital heart block | (Orphanet:60041) |
Desminopathy | (Orphanet:98909) |
Fabry disease | (Orphanet:324) |
Familial atrial fibrillation | (Orphanet:334) |
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | (Orphanet:436242) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
Familial long QT syndrome | (Orphanet:768) |
Familial progressive cardiac conduction defect | (Orphanet:871) |
Familial sick sinus syndrome | (Orphanet:166282) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Hemochromatosis, type 1 | (OMIM:235200) |
Holt-Oram syndrome | (Orphanet:392) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Incessant infant ventricular tachycardia | (Orphanet:45453) |
Kearns-Sayre syndrome | (Orphanet:480) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Left ventricular noncompaction | (Orphanet:54260) |
Left ventricular noncompaction 8 | (OMIM:615373) |
Long QT syndrome 10 | (OMIM:611819) |
Long QT syndrome 3 | (OMIM:603830) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK | (OMIM:609438) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II | (OMIM:140400) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Romano-Ward syndrome | (Orphanet:101016) |
Sick sinus syndrome 1, autosomal recessive | (OMIM:608567) |
Sinus node disease and myopia | (OMIM:182190) |
Steinert myotonic dystrophy | (Orphanet:273) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Timothy syndrome | (Orphanet:65283) |
Uhl anomaly | (Orphanet:3403) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED | (OMIM:310300) |