Congestive heart failure, and Stroke

Diseases related with Congestive heart failure and Stroke

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Stroke that can help you solving undiagnosed cases.


Top matches:

Medium match CARDIOMYOPATHY, DILATED, 1E; CMD1E


CARDIOMYOPATHY, DILATED, 1E; CMD1E Is also known as cdcd2|cardiomyopathy, dilated, with conduction defect 2|cardiomyopathy, dilated, with conduction disorder and arrhythmia

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia
  • Dyspnea
  • Stroke


SOURCES: MESH OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1E; CMD1E

Medium match AORTIC ANEURYSM, FAMILIAL THORACIC 4; AAT4


AORTIC ANEURYSM, FAMILIAL THORACIC 4; AAT4 Is also known as faa4|aortic aneurysm/aortic dissection and patent ductus arteriosus

Related symptoms:

  • Congestive heart failure
  • Dilatation
  • Patent ductus arteriosus
  • Stroke
  • Aortic regurgitation


SOURCES: MESH OMIM MENDELIAN

More info about AORTIC ANEURYSM, FAMILIAL THORACIC 4; AAT4

Medium match ATRIAL STANDSTILL 2; ATRST2


Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005).

ATRIAL STANDSTILL 2; ATRST2 Is also known as cardiomyopathy, atrial dilated, with atrial standstill|atrial dilation and standstill

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dyspnea
  • Scarring
  • Stroke


SOURCES: OMIM MENDELIAN

More info about ATRIAL STANDSTILL 2; ATRST2

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Other less relevant matches:

Medium match WOLFF-PARKINSON-WHITE SYNDROME


A group of conditions in which HEART VENTRICLE activation by the atrial impulse is faster than the normal impulse conduction from the SINOATRIAL NODE. In these pre-excitation syndromes, atrial impulses often bypass the ATRIOVENTRICULAR NODE delay and travel via ACCESSORY CONDUCTING PATHWAYS connecting the atrium directly to the BUNDLE OF HIS.

WOLFF-PARKINSON-WHITE SYNDROME Is also known as wpw syndrome

Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia


SOURCES: OMIM ORPHANET MENDELIAN

More info about WOLFF-PARKINSON-WHITE SYNDROME

Medium match CARDIOMYOPATHY, DILATED, 1S; CMD1S


Related symptoms:

  • Muscle weakness
  • Ventriculomegaly
  • Cardiomyopathy
  • Myopathy
  • Congestive heart failure


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1S; CMD1S

Medium match FAMILIAL ISOLATED DILATED CARDIOMYOPATHY


Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia.

FAMILIAL ISOLATED DILATED CARDIOMYOPATHY Is also known as cardiomyopathy, familial dilated|cardiomyopathy, familial dilated, 1|cmpd1|familial or idiopathic dilated cardiomyopathy|fdc

Related symptoms:

  • Sensorineural hearing impairment
  • Feeding difficulties
  • Fatigue
  • Ventriculomegaly
  • Cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL ISOLATED DILATED CARDIOMYOPATHY

Medium match CEREBRAL CAVERNOUS MALFORMATIONS; CCM


Cerebral cavernous angiomas are relatively rare vascular malformations that may involve any part of the central nervous system. Cerebral cavernous angiomas are to be distinguished from cerebral arteriovenous malformations ({106070}, {108010}). CCMs are venous and not demonstrable by arteriography; hence they are referred to as angiographically silent.Capillary hemangiomas (OMIM ) are classified as distinct from vascular malformations in that hemangiomas are benign, highly proliferative lesions involving aberrant localized growth of capillary endothelium. Hemangiomas develop shortly after birth. In contrast, vascular malformations are present from birth, tend to grow with the individual, do not regress, and show normal rates of endothelial cell turnover (Mulliken and Young, 1988). Genetic Heterogeneity of CCMCCM2 (OMIM ) is caused by mutation in the CCM2/malcavernin gene (OMIM ), and CCM3 (OMIM ) is caused by mutation in the PDCD10 gene (OMIM ).Evidence suggests that a 2-hit mechanism involving biallelic germline and somatic mutations is responsible for CCM1 pathogenesis, see PATHOGENESIS and MOLECULAR GENETICS sections.

CEREBRAL CAVERNOUS MALFORMATIONS; CCM Is also known as cam|cerebral capillary malformations|cavernous angiomatous malformations|cavernous angioma, familial

Related symptoms:

  • Seizures
  • Muscle weakness
  • Hepatomegaly
  • Congestive heart failure
  • Headache


SOURCES: ORPHANET OMIM MENDELIAN

More info about CEREBRAL CAVERNOUS MALFORMATIONS; CCM

Medium match FAMILIAL ATRIAL MYXOMA


Familial atrial myxoma is a rare, genetic cardiac tumor characterized by the presence of a primary, benign, gelatinous mass located in the atria and composed of primitive connective tissue cells and stroma (resembling mesenchyme) in several members of a family. Clinical presentation depends on the size, mobility and location of tumor, ranging from nonspecific and/or constitutional symptoms to sudden cardiac death, and includes dyspnea, hemoptisis, syncope, fatigue, fever, cutaneous rash, increases in venous pressure and/or peripheral edema.

FAMILIAL ATRIAL MYXOMA Is also known as atrial myxoma, familial

Related symptoms:

  • Seizures
  • Cognitive impairment
  • Fever
  • Atrial septal defect
  • Congestive heart failure


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about FAMILIAL ATRIAL MYXOMA

Medium match HEREDITARY HEMORRHAGIC TELANGIECTASIA


Rendu-Osler-Weber disease, also called hereditary hemorrhagic telangiectasia (HHT), is a disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.

HEREDITARY HEMORRHAGIC TELANGIECTASIA Is also known as hht|rendu-osler disease|rendu-osler-weber disease

Related symptoms:

  • Seizures
  • Congestive heart failure
  • Cirrhosis
  • Hepatic failure
  • Hematuria


SOURCES: ORPHANET MENDELIAN

More info about HEREDITARY HEMORRHAGIC TELANGIECTASIA

Medium match MOYAMOYA ANGIOPATHY-SHORT STATURE-FACIAL DYSMORPHISM-HYPERGONADOTROPIC HYPOGONADISM SYNDROME


Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism.

MOYAMOYA ANGIOPATHY-SHORT STATURE-FACIAL DYSMORPHISM-HYPERGONADOTROPIC HYPOGONADISM SYNDROME Is also known as syndromic moyamoya disease|moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism|chromosome xq28 deletion syndrome, 3.4-kb

Related symptoms:

  • Seizures
  • Global developmental delay
  • Short stature
  • Hypertelorism
  • Abnormal facial shape


SOURCES: ORPHANET OMIM MENDELIAN

More info about MOYAMOYA ANGIOPATHY-SHORT STATURE-FACIAL DYSMORPHISM-HYPERGONADOTROPIC HYPOGONADISM SYNDROME

Top 5 symptoms//phenotypes associated to Congestive heart failure and Stroke

Symptoms // Phenotype % cases
Cardiomyopathy Common - Between 50% and 80% cases
Syncope Uncommon - Between 30% and 50% cases
Cerebral hemorrhage Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
Palpitations Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Stroke. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Dilatation Dilated cardiomyopathy Dyspnea Atrial fibrillation Abnormal left ventricle morphology Ventricular arrhythmia Arrhythmia

Rare Symptoms - Less than 30% cases


Thromboembolism Headache Pulmonary embolism Tachycardia Muscle weakness Hypertrophic cardiomyopathy Subarachnoid hemorrhage Chest pain Cardiomegaly Coronary artery atherosclerosis Ventriculomegaly Myopathy Pulmonary arterial hypertension Migraine Tricuspid regurgitation Bicuspid aortic valve Ischemic stroke Left bundle branch block Supraventricular tachycardia Atrial flutter Cavernous hemangioma Reduced systolic function Atrioventricular block Atrial arrhythmia Atrial standstill Bradycardia Sudden cardiac death Gastrointestinal hemorrhage Epistaxis Endocarditis Hematuria Nephrolithiasis Hepatic failure Cirrhosis Pulmonic valve myxoma Cardiac myxoma Bacterial endocarditis Amblyopia Increased inflammatory response Orthopnea Hepatic vascular malformations Pulmonary edema Mitral valve prolapse Behavioral abnormality Confusion Atrial septal defect Abnormality of skin pigmentation Coma Fever Cognitive impairment Cholestasis Retinal vascular malformation Neoplasm of the skin Easy fatigability Heart murmur Exertional dyspnea Dilatation of the cerebral artery Growth hormone excess Jaundice Edema of the lower limbs Ascites Intestinal polyposis Venous thrombosis Growth hormone deficiency Low-set ears Hypertension Long philtrum Hypogonadism Retrognathia Deeply set eye Wide nose Small hand Decreased testicular size Cataract Short phalanx of finger Hypergonadotropic hypogonadism Azoospermia Premature graying of hair Stroke-like episode Congenital ptosis Broad finger Abnormality of the nares Abnormal hand morphology Ptosis Abnormal facial shape Cholelithiasis Varicocele Portal hypertension Microcytic anemia Telangiectasia of the skin Hemoptysis Transient ischemic attack Arteriovenous malformation Abnormality of the cerebral vasculature Esophageal varix Visceral angiomatosis Hypertelorism Conjunctival telangiectasia Cholecystitis Spontaneous hematomas Abnormality of cardiovascular system physiology Peripheral arteriovenous fistula Mucosal telangiectasiae Retinal telangiectasia Global developmental delay Short stature Retrobulbar optic neuritis Impaired myocardial contractility Venous malformation Cardiac arrest Atrial cardiomyopathy Pain Respiratory distress Abnormal heart morphology Anxiety Vertigo Hypotension Ventricular fibrillation Dilatation of the ventricular cavity Muscle fibrillation Wolff-Parkinson-White syndrome Paroxysmal atrial fibrillation Prolonged QRS complex Shortened PR interval Ventricular preexcitation Paroxysmal supraventricular tachycardia Hyperpepsinogenemia I Tetraplegia Proximal muscle weakness Aortic regurgitation Right bundle branch block Heart block Ventricular extrasystoles ST segment elevation Third degree atrioventricular block Premature atrial contractions Patent ductus arteriosus Aortic aneurysm Scarring Abnormality of the vasculature Aortic dissection Left ventricular failure Thoracic aortic aneurysm Ascending aortic dissection Cystic medial necrosis Abnormal iris pigmentation Aortic stiffness Ventricular preexcitation with multiple accessory pathways Pulmonic stenosis Neuritis Paralysis Palmoplantar hyperkeratosis Congenital sensorineural hearing impairment Lipoatrophy Severe sensorineural hearing impairment Abnormality of neutrophils Diffuse palmoplantar hyperkeratosis Hepatomegaly Lower limb muscle weakness EMG abnormality Abnormality of the skin Focal-onset seizure Cerebral calcification Telangiectasia Hemangioma Intracranial hemorrhage Abnormality of the musculature Capillary hemangioma Tachypnea Palmoplantar keratoderma Coarctation of aorta Aortic arch aneurysm Ventricular hypertrophy Shock Pulmonary artery stenosis Left ventricular noncompaction T-wave inversion First degree atrioventricular block Cardiogenic shock Left ventricular noncompaction cardiomyopathy Cough Pulmonary artery hypoplasia ST segment depression Ebstein anomaly of the tricuspid valve Sensorineural hearing impairment Feeding difficulties Fatigue Edema Elevated serum creatine phosphokinase Moyamoya phenomenon



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