Congestive heart failure
Symptom Information:
Symptom ID: | HPO:0001635 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) |