Congestive heart failure

Symptom Information:

Symptom ID: HPO:0001635
Synonyms:
Cardiac failure [HPO:0001635]
Cardiac insufficiency [HPO:0001635]
Heart failure [HPO:0001635]
Heart failure [Orphanet:35150]
Circulatory collapse [Orphanet:35120]
Heart failure (disorder) [Orphanet:35150]
Congestive heart failure (disorder) [Orphanet:35150]
Shock (disorder) [Orphanet:35120]
Congestive heart failure [Orphanet:35150]
Shock [Orphanet:35120]
Cardiac failure [OMIM:Cardiac failure]
Congestive heart failure [OMIM:Congestive heart failure]
Heart failure [OMIM:Heart failure]
Heart/cardiac failure [Orphanet:35150]
Collapse/sudden death/cardiac arrest/cardiorespiratory arrest [Orphanet:35120]
Cardiac failure [Orphanet:35150]
Peripheral circulatory failure [Orphanet:35120]
Cardiac failure [MedDRA:10007554]
Cardiac failure (NOS) [MedDRA:10007554]
Cardiac failure aggravated [MedDRA:10007554]
Cardiac failure NOS [MedDRA:10007554]
Cardiac function failed [MedDRA:10007554]
Cardiac function failure [MedDRA:10007554]
Cardiac insufficiency [MedDRA:10007554]
Decompensation cardiac [MedDRA:10007554]
Decompensation myocardial [MedDRA:10007554]
Failure heart [MedDRA:10007554]
Heart failure [MedDRA:10007554]
Heart failure (NOS) [MedDRA:10007554]
Heart failure, unspecified [MedDRA:10007554]
Heart insufficiency [MedDRA:10007554]
Heart insuffiency [MedDRA:10007554]
Insufficiency cardiac [MedDRA:10007554]
Myocardial contraction decreased [MedDRA:10007554]
Myocardial decompensation [MedDRA:10007554]
Heart failure NYHA class I [MedDRA:10007554]
Heart failure NYHA class II [MedDRA:10007554]
Heart failure NYHA class III [MedDRA:10007554]
Heart failure NYHA class IV [MedDRA:10007554]
Decompensated heart failure [MedDRA:10007554]
Recurrent cardiac decompensation [MedDRA:10007554]
Peripheral circulatory failure [MedDRA:10034567]
Collapse circulatory peripheral [MedDRA:10034567]
Collapse peripheral circulatory [MedDRA:10034567]
Collapse peripheral vascular [MedDRA:10034567]
Failure peripheral circulatory [MedDRA:10034567]
Peripheral shutdown [MedDRA:10034567]
Shock [MedDRA:10040560]
Clinically shocked [MedDRA:10040560]
Other shock without mention of trauma [MedDRA:10040560]
Postoperative shock, not elsewhere classified [MedDRA:10040560]
Shock (excl traumatic and specific cause) [MedDRA:10040560]
Shock circulatory [MedDRA:10040560]
Shock during or following labor and delivery [MedDRA:10040560]
Shock during or following labor and delivery, antepartum shock [MedDRA:10040560]
Shock during or following labor and delivery, postpartum shock [MedDRA:10040560]
Shock during or following labor and delivery, unspecified as to episode of care [MedDRA:10040560]
Shock during or following labor and delivery, with delivery, with mention of postpart comp [MedDRA:10040560]
Shock during or following labor and delivery, with delivery, with or w/o mention of antepart cond [MedDRA:10040560]
Shock during or following labor and delivery, with delivery, without mention of antepartum condition [MedDRA:10040560]
Shock during or following labour and delivery [MedDRA:10040560]
Shock following abortion and ectopic and molar pregnancies [MedDRA:10040560]
Shock symptom [MedDRA:10040560]
Shock symptoms [MedDRA:10040560]
Shock vascular [MedDRA:10040560]
Shock without mention of trauma [MedDRA:10040560]
Shock, unspecified [MedDRA:10040560]
Shock-like symptom [MedDRA:10040560]
Surgical shock [MedDRA:10040560]
Refractory shock [MedDRA:10040560]
Circulatory collapse [MedDRA:10009192]
Acute circulatory failure [MedDRA:10009192]
Cardiovascular collapse [MedDRA:10009192]
Circulatory failure [MedDRA:10009192]
Collapse [MedDRA:10009192]
Collapse cardiovascular [MedDRA:10009192]
Collapse circulatory [MedDRA:10009192]
Collapse fleeting [MedDRA:10009192]
Collapse transient [MedDRA:10009192]
Collapse vascular [MedDRA:10009192]
Collapse vasomotor [MedDRA:10009192]
Collapsed [MedDRA:10009192]
Collapsed semi conscious &
shocked [MedDRA:10009192]
Failure circulatory [MedDRA:10009192]
Syncope and collapse [MedDRA:10009192]
Vascular collapse [MedDRA:10009192]
Vasomotor collapse [MedDRA:10009192]
Cardiac failure (secondary to chest deformity) [OMIM:Cardiac failure (secondary to chest deformity)]
Cardiac failure (sudden death has been reported) [OMIM:Cardiac failure (sudden death has been reported)]
Cardiac insufficiency (in some) [OMIM:Cardiac insufficiency (in some)]
Congestive heart failure (Detroit type 107680.0011) [OMIM:Congestive heart failure (Detroit type 107680.0011)]
Congestive heart failure (in a subset of patients) [OMIM:Congestive heart failure (in a subset of patients)]
Congestive heart failure (in some patients) [OMIM:Congestive heart failure (in some patients)]
Heart failure (biventricular in some patients) [OMIM:Heart failure (biventricular in some patients)]
Heart failure (more common in male patients) [OMIM:Heart failure (more common in male patients)]
Shock [OMIM:Shock]
Vascular collapse [OMIM:Vascular collapse]
Heart failures [MedDRA:10019280]
Quality:
Cross references:
Orphanet:35150 "Heart/cardiac failure" [Orphanet:35150]
Orphanet:35120 "Collapse/sudden death/cardiac arrest/cardiorespiratory arrest" [Orphanet:35120]
OMIM: "Cardiac failure" [OMIM:Cardiac failure]
OMIM: "Congestive heart failure" [OMIM:Congestive heart failure]
OMIM: "Heart failure" [OMIM:Heart failure]
OMIM: "Cardiac failure (secondary to chest deformity)" [OMIM:Cardiac failure (secondary to chest deformity)]
OMIM: "Cardiac failure (sudden death has been reported)" [OMIM:Cardiac failure (sudden death has been reported)]
OMIM: "Cardiac insufficiency (in some)" [OMIM:Cardiac insufficiency (in some)]
OMIM: "Congestive heart failure (Detroit type 107680.0011)" [OMIM:Congestive heart failure (Detroit type 107680.0011)]
OMIM: "Congestive heart failure (in a subset of patients)" [OMIM:Congestive heart failure (in a subset of patients)]
OMIM: "Congestive heart failure (in some patients)" [OMIM:Congestive heart failure (in some patients)]
OMIM: "Heart failure (biventricular in some patients)" [OMIM:Heart failure (biventricular in some patients)]
OMIM: "Heart failure (more common in male patients)" [OMIM:Heart failure (more common in male patients)]
OMIM: "Shock" [OMIM:Shock]
OMIM: "Vascular collapse" [OMIM:Vascular collapse]
UMLS:C0018801 "Heart failure" [Orphanet:35150]
UMLS:C0018802 "Congestive heart failure" [Orphanet:35150]
UMLS:C0036974 "Shock" [Orphanet:35120]
Is a (Direct Parents):
HPO         Abnormality of cardiovascular system physiology
Orphanet Abnormality of cardiovascular system physiology
MedDRA Heart failures NEC
MedDRA Cardiac disorders
MedDRA Circulatory collapse and shock
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)
             Congestive heart failure(HPO:0001635)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Congestive heart failure(HPO:0001635)
Vascular disorders(MedDRA:10047065)
    Decreased and nonspecific blood pressure disorders and shock(MedDRA:10011954)
       Circulatory collapse and shock(MedDRA:10009193)
          Congestive heart failure(HPO:0001635)
Database Frequency: 232 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
APOLIPOPROTEIN A-I (OMIM:107680)
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 (OMIM:614473)
ATTRV122I amyloidosis (Orphanet:85451)
Aarskog-Scott syndrome (Orphanet:915)
Aceruloplasminemia (Orphanet:48818)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Adult heart tumor (Orphanet:874)
Alpers syndrome (Orphanet:726)
Alström syndrome (Orphanet:64)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Arrhythmogenic right ventricular dysplasia, familial, 10 (OMIM:610193)
Arrhythmogenic right ventricular dysplasia, familial, 12 (OMIM:611528)
Arrhythmogenic right ventricular dysplasia, familial, 3 (OMIM:602086)
Arrhythmogenic right ventricular dysplasia, familial, 5 (OMIM:604400)
Arrhythmogenic right ventricular dysplasia, familial, 8 (OMIM:607450)
Arrhythmogenic right ventricular dysplasia, familial, 9 (OMIM:609040)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arterial tortuosity syndrome (Orphanet:3342)
Atrial standstill (Orphanet:1344)
Atrial standstill 2 (OMIM:615745)
Atrioventricular canal defect (Orphanet:98722)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Babesiosis (Orphanet:108)
Barth syndrome (Orphanet:111)
Blackfan-Diamond anemia (Orphanet:124)
CANDLE syndrome (Orphanet:325004)
CARDIAC LIPIDOSIS, FAMILIAL (OMIM:212080)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 (OMIM:617047)
CARNEY COMPLEX, TYPE 1 (OMIM:160980)
CEDNIK syndrome (Orphanet:66631)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED (OMIM:302900)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22 (OMIM:616045)
Cardiomyopathy, dilated, 1B (OMIM:600884)
Cardiomyopathy, dilated, 1BB (OMIM:612877)
Cardiomyopathy, dilated, 1C (OMIM:601493)
Cardiomyopathy, dilated, 1CC (OMIM:613122)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, dilated, 1FF (OMIM:613286)
Cardiomyopathy, dilated, 1HH (OMIM:613881)
Cardiomyopathy, dilated, 1I (OMIM:604765)
Cardiomyopathy, dilated, 1II (OMIM:615184)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1L (OMIM:606685)
Cardiomyopathy, dilated, 1M (OMIM:607482)
Cardiomyopathy, dilated, 1O (OMIM:608569)
Cardiomyopathy, dilated, 1P (OMIM:609909)
Cardiomyopathy, dilated, 1Q (OMIM:609915)
Cardiomyopathy, dilated, 1R (OMIM:613424)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy, dilated, 1T (OMIM:613740)
Cardiomyopathy, dilated, 1U (OMIM:613694)
Cardiomyopathy, dilated, 1V (OMIM:613697)
Cardiomyopathy, dilated, 1W (OMIM:611407)
Cardiomyopathy, dilated, 1X (OMIM:611615)
Cardiomyopathy, dilated, 1Y (OMIM:611878)
Cardiomyopathy, dilated, 1Z (OMIM:611879)
Cardiomyopathy, dilated, 2A (OMIM:611880)
Cardiomyopathy, dilated, 2B (OMIM:614672)
Cardiomyopathy, dilated, 3B (OMIM:302045)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Cardiomyopathy, familial hypertrophic, 15 (OMIM:613255)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial hypertrophic, 8 (OMIM:608751)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Carney complex (Orphanet:1359)
Carnitine uptake deficiency (Orphanet:158)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cirrhotic cardiomyopathy (Orphanet:57777)
Cobb syndrome (Orphanet:53721)
Cogan syndrome (Orphanet:1467)
Combined oxidative phosphorylation defect type 17 (Orphanet:369913)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Combined oxidative phosphorylation defect type 9 (Orphanet:319509)
Combined oxidative phosphorylation deficiency type 23 (ORPHA:444013)
Congenital atransferrinemia (Orphanet:1195)
Congenital heart block (Orphanet:60041)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Congenital valvular dysplasia (Orphanet:1864)
Cronkhite-Canada syndrome (Orphanet:2930)
Cutis laxa (Orphanet:209)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dilated cardiomyopathy with ataxia (Orphanet:66634)
Drug-induced autoimmune hemolytic anemia (Orphanet:90037)
Duchenne muscular dystrophy (Orphanet:98896)
Dystrophic epidermolysis bullosa (Orphanet:303)
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY (OMIM:600351)
Early-onset myopathy with fatal cardiomyopathy (Orphanet:289377)
Ebstein malformation (Orphanet:1880)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Endomyocardial fibroelastosis (Orphanet:2022)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erdheim-Chester disease (Orphanet:35687)
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA (OMIM:229310)
Fabry disease (Orphanet:324)
Familial atrial myxoma (Orphanet:615)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial cutaneous collagenoma (Orphanet:53296)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial dyskinesia and facial myokymia (Orphanet:324588)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (Orphanet:439854)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Friedreich ataxia 1 (OMIM:229300)
Friedreich ataxia 2 (OMIM:601992)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
GRAVES DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:275000)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Geleophysic dysplasia (Orphanet:2623)
Generalized arterial calcification of infancy (Orphanet:51608)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Hairy cell leukemia variant (Orphanet:300878)
Hallermann-Streiff syndrome (Orphanet:2108)
Hb Bart's hydrops fetalis (Orphanet:163596)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
His bundle tachycardia (Orphanet:3283)
Histiocytoid cardiomyopathy (Orphanet:137675)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hyaline body myopathy (Orphanet:53698)
Hydrops fetalis (Orphanet:1041)
Hyperkalemic periodic paralysis (Orphanet:682)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic neonatal atrial flutter (Orphanet:45452)
Incontinentia pigmenti (Orphanet:464)
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency (Orphanet:352563)
JMP syndrome (Orphanet:324999)
Kawasaki disease (Orphanet:2331)
Klippel-Trénaunay syndrome (Orphanet:90308)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Left ventricular noncompaction (Orphanet:54260)
Left ventricular noncompaction 1 (OMIM:604169)
Left ventricular noncompaction 10 (OMIM:615396)
Left ventricular noncompaction 2 (OMIM:609470)
Left ventricular noncompaction 8 (OMIM:615373)
Leprechaunism (Orphanet:508)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MELAS (Orphanet:550)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Maternally-inherited Leigh syndrome (Orphanet:255210)
Maternally-inherited diabetes and deafness (Orphanet:225)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Microscopic polyangiitis (Orphanet:727)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency (Orphanet:314637)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Monosomy 18q (Orphanet:1600)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mulibrey nanism (Orphanet:2576)
Multifocal atrial tachycardia (Orphanet:3282)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Nakajo-Nishimura syndrome (Orphanet:2615)
Naxos disease (Orphanet:34217)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Osteogenesis imperfecta type 2 (Orphanet:216804)
PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE (OMIM:260450)
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME (OMIM:171420)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
Papillary fibroelastoma of the heart (Orphanet:208600)
Parkes Weber syndrome (Orphanet:90307)
Patent arterial duct (Orphanet:706)
Pediatric systemic sclerosis (Orphanet:93567)
Peripartum cardiomyopathy (Orphanet:563)
Polyarteritis nodosa (Orphanet:767)
Polymyositis (Orphanet:732)
Primary lipodystrophy (Orphanet:90970)
Proteasome disability syndrome (Orphanet:324977)
Pulmonary arterial hypertension (Orphanet:182090)
Pyruvate carboxylase deficiency (Orphanet:3008)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
REFSUM DISEASE, CLASSIC (OMIM:266500)
Refsum disease (Orphanet:773)
Relapsing polychondritis (Orphanet:728)
Sandhoff disease (Orphanet:796)
Sarcoidosis (Orphanet:797)
Scheie syndrome (Orphanet:93474)
Scleroderma (Orphanet:801)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
Senile systemic amyloidosis (Orphanet:330001)
Sensorineural deafness with dilated cardiomyopathy (Orphanet:217622)
Singleton-Merten dysplasia (Orphanet:85191)
Systemic sclerosis (Orphanet:90291)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Triose phosphate-isomerase deficiency (Orphanet:868)
Tropical endomyocardial fibrosis (Orphanet:75565)
Tuberous sclerosis (Orphanet:805)
Uhl anomaly (Orphanet:3403)
Vici syndrome (Orphanet:1493)
Waldenström macroglobulinemia (Orphanet:33226)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)
Yellow fever (Orphanet:99829)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY (OMIM:616117)
[DEL] COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23 (OMIM:616198)
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL (OMIM:261740)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)