Atrioventricular block

Symptom Information:

Symptom ID: HPO:0001678
Synonyms:
Atrioventricular nodal disease [HPO:0001678]
Congenital heart block [HPO:0001678]
Heart block [HPO:0001678]
Atrioventricular nodal block [Orphanet:35060]
Heart block [Orphanet:35060]
Atrioventricular block (disorder) [Orphanet:35060]
Heart block (disorder) [Orphanet:35060]
Disorder of heart rhythm [Orphanet:35060]
Nodal block [Orphanet:35060]
Atrioventricular Block [Orphanet:35060]
Heart Block [Orphanet:35060]
Conduction disorder of the heart [Orphanet:35060]
Atrioventricular block [OMIM:Atrioventricular block]
Atrioventricular nodal disease [OMIM:Atrioventricular nodal disease]
Congenital heart block [OMIM:Congenital heart block]
Heart block [OMIM:Heart block]
Cardiac conduction defect/sinoauricular/heart/auriculoventricular/branch block [Orphanet:35060]
Atrioventricular block [Orphanet:35060]
Heart block NOS [Orphanet:35060]
Conduction disorder [Orphanet:35060]
Atrioventricular block [MedDRA:10003671]
Atrioventricular block (NOS) [MedDRA:10003671]
Atrioventricular block incomplete [MedDRA:10003671]
Atrioventricular block NOS [MedDRA:10003671]
Atrioventricular block, other and unspecified [MedDRA:10003671]
Atrioventricular block, unspecified [MedDRA:10003671]
AV block [MedDRA:10003671]
AV block (NOS) [MedDRA:10003671]
Block heart [MedDRA:10003671]
Block incomplete [MedDRA:10003671]
Heart block [MedDRA:10003671]
Heart block atrioventricular [MedDRA:10003671]
Heart block AV [MedDRA:10003671]
Heart block NOS [MedDRA:10003671]
Nodal block [MedDRA:10003671]
Other heart block [MedDRA:10003671]
Heart block (NOS) [MedDRA:10003671]
Conduction disorder [MedDRA:10010276]
Conduction delayed transient [MedDRA:10010276]
Conduction disorder NOS [MedDRA:10010276]
Conduction disorder, unspecified [MedDRA:10010276]
Conduction disorders [MedDRA:10010276]
Defect conduction (NOS) [MedDRA:10010276]
Other specified conduction disorder [MedDRA:10010276]
Other specified conduction disorders [MedDRA:10010276]
Conduction defects [OMIM:Conduction defects]
Conduction defects (in some patients) [OMIM:Conduction defects (in some patients)]
Sinoatrial block [MedDRA:10040736]
Sinoatrial nodal block [Orphanet:35060]
Sinoatrial block (disorder) [Orphanet:35060]
Sinoatrial Block [Orphanet:35060]
Sinoatrial block [OMIM:Sinoatrial block]
Heart block congenital [MedDRA:10019263]
Quality:
Cross references:
HPO:0011675 "Arrhythmia" [Orphanet:35060]
Orphanet:35060 "Cardiac conduction defect/sinoauricular/heart/auriculoventricular/branch block" [Orphanet:35060]
OMIM: "Atrioventricular block" [OMIM:Atrioventricular block]
OMIM: "Atrioventricular nodal disease" [OMIM:Atrioventricular nodal disease]
OMIM: "Congenital heart block" [OMIM:Congenital heart block]
OMIM: "Heart block" [OMIM:Heart block]
OMIM: "Conduction defects" [OMIM:Conduction defects]
OMIM: "Conduction defects (in some patients)" [OMIM:Conduction defects (in some patients)]
OMIM: "Sinoatrial block" [OMIM:Sinoatrial block]
UMLS:C0857153 "Nodal block" [Orphanet:35060]
UMLS:C0004245 "Atrioventricular Block" [Orphanet:35060]
UMLS:C0018794 "Heart Block" [Orphanet:35060]
UMLS:C0264886 "Conduction disorder of the heart" [Orphanet:35060]
UMLS:C0037188 "Sinoatrial Block" [Orphanet:35060]
Is a (Direct Parents):
HPO         Abnormal atrioventricular conduction
MedDRA Cardiac conduction disorders
Orphanet Abnormality of cardiovascular system physiology
MedDRA Cardiac disorders congenital NEC
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)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Atrioventricular block(HPO:0001678)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Atrioventricular block(HPO:0001678)
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)