Congestive heart failure, and Vertigo

Diseases related with Congestive heart failure and Vertigo

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


Top matches:

Medium match SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO; SSS3


Sick sinus syndrome may be encountered at any age but is primarily a disease of the elderly and is often secondary to other cardiac disorders when diagnosed in younger individuals. Symptoms are often intermittent and/or nonspecific and include dizziness, syncope, and heart failure. The only effective treatment for symptomatic and irreversible sinus node dysfunction is permanent cardiac pacing, and sick sinus syndrome remains the most common indication for permanent pacemaker implantation (summary by Holm et al., 2011).For a general phenotypic description and a discussion of genetic heterogeneity of sick sinus syndrome, see SSS1 (OMIM ).

Related symptoms:

  • Congestive heart failure
  • Vertigo
  • Syncope
  • Sick sinus syndrome


SOURCES: OMIM MENDELIAN

More info about SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO; SSS3

Medium match SICK SINUS SYNDROME 2; SSS2


SICK SINUS SYNDROME 2; SSS2 Is also known as atrial fibrillation with bradyarrhythmia|sick sinus syndrome 2 with or without cardiac noncompaction and/or ascending aorta dilation|sinus node disease, familial, autosomal dominant|sinus bradycardia syndrome, familial, autosomal dominant

Related symptoms:

  • Intellectual disability
  • Brachydactyly
  • Fatigue
  • Congestive heart failure
  • Abnormality of cardiovascular system morphology


SOURCES: OMIM MESH MENDELIAN

More info about SICK SINUS SYNDROME 2; SSS2

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

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Other less relevant matches:

Medium match NAXOS DISEASE


Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma.

NAXOS DISEASE Is also known as keratosis palmoplantaris with arrhythmogenic cardiomyopathy|palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy|kwwh type i|keratoderma with woolly hair type i|mal de naxos|palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyo

Related symptoms:

  • Fatigue
  • Cardiomyopathy
  • Congestive heart failure
  • Dilatation
  • Arrhythmia


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about NAXOS DISEASE

Medium match PULMONARY HYPERTENSION, PRIMARY, 1; PPH1


Primary pulmonary arterial hypertension is a rare, often fatal, progressive vascular lung disease characterized by increased pulmonary vascular resistance and sustained elevation of mean pulmonary arterial pressure, leading to right ventricular hypertrophy and right heart failure. Pathologic features include a narrowing and thickening of small pulmonary vessels and plexiform lesions. There is pulmonary vascular remodeling of all layers of pulmonary arterial vessels: intimal thickening, smooth muscle cell hypertrophy or hyperplasia, adventitial fibrosis, and occluded vessels by in situ thrombosis (summary by Machado et al., 2009 and Han et al., 2013).Heterozygous mutations in the BMPR2 gene are found in nearly 70% of families with heritable PPH and in 25% of patients with sporadic disease. The disease is more common in women (female:male ratio of 1.7:1). However, the penetrance of PPH1 is incomplete: only about 10 to 20% of individuals with BMPR2 mutations develop the disease during their lifetime, suggesting that development of the disorder is triggered by other genetic or environmental factors. Patients with PPH1 are less likely to respond to acute vasodilater testing and are unlikely to benefit from treatment with calcium channel blockade (summary by Machado et al., 2009 and Han et al., 2013). Genetic Heterogeneity of Primary Pulmonary HypertensionPPH2 (OMIM ) is caused by mutation in the SMAD9 gene (OMIM ) on chromosome 13q13; PPH3 (OMIM ) is caused by mutation in the CAV1 gene (OMIM ) on chromosome 7q31; and PPH4 (OMIM ) is caused by mutation in the KCNK3 gene (OMIM ) on chromosome 2p23.See {265400} for a possible autosomal recessive form of PPH.Primary pulmonary hypertension may also be found in association with hereditary hemorrhagic telangiectasia type 1 (HHT1 ), caused by mutation in the ENG gene (OMIM ), and HHT2 (OMIM ), caused by mutation in the ACVRL1 (ALK1) gene (OMIM ).

PULMONARY HYPERTENSION, PRIMARY, 1; PPH1 Is also known as pulmonary arterial hypertension|pht|pah

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Fatigue
  • Respiratory distress


SOURCES: OMIM ORPHANET MENDELIAN

More info about PULMONARY HYPERTENSION, PRIMARY, 1; PPH1

Medium match SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1


Symptomatic form of hemochromatosis type 1 is a rare, hereditary hemochromatosis characterized by inappropriately regulated intestinal iron absorption which leads to excessive iron storage in various organs and manifests with a wide range of signs and symptoms, including abdominal pain, weakness, lethargy, weight loss, elevated serum aminotransferase levels, increase in skin pigmentation, and/or arthropathy in the metacarpophalangeal joints. Other commonly associated manifestations include hepatomegaly, cirrhosis, liver fibrosis, hepatocellular carcinoma, restrictive cardiomyopathy and/or diabetes mellitus.

SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1 Is also known as symptomatic form of hfe-related hereditary hemochromatosis|symptomatic form of classic hemochromatosis

Related symptoms:

  • Peripheral neuropathy
  • Hepatomegaly
  • Fatigue
  • Cardiomyopathy
  • Congestive heart failure


SOURCES: ORPHANET MENDELIAN

More info about SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1

Medium match JUVENILE POLYPOSIS SYNDROME; JPS


Juvenile polyposis syndrome is an autosomal dominant condition that predisposes gene carriers to various types of tumors. The diagnosis is based on the occurrence of hamartomatous gastrointestinal polyps that turn into malignant lesions in approximately 20% of cases (Handra-Luca et al., 2005).It had been suggested that juvenile polyposis can be caused by mutations in the PTEN gene (OMIM ), the same gene that is mutant in Cowden syndrome-1 (OMIM ). In a comprehensive review of PTEN, Waite and Eng (2002) concluded that juvenile intestinal polyposis is not a so-called PTEN hamartoma-tumor syndrome (PHTS). They suggested that the discovery of the germline PTEN mutation in an individual considered to have JPS should raise a suspicion that the clinical diagnosis is incorrect and that such an individual should be managed medically in the same manner as all patients with PHTS.

JUVENILE POLYPOSIS SYNDROME; JPS Is also known as polyposis, juvenile intestinal|pji|jip|juvenile intestinal polyposis|polyposis, familial, of entire gastrointestinal tract

Related symptoms:

  • Seizures
  • Neoplasm
  • Failure to thrive
  • Pain
  • Cryptorchidism


SOURCES: OMIM MENDELIAN

More info about JUVENILE POLYPOSIS SYNDROME; JPS

Medium match TSH-SECRETING PITUITARY ADENOMA


A rare adenoma of the anterior lobe of the pituitary gland that produces thyrotropin. It is usually associated with goiter and hyperthyroidism.

TSH-SECRETING PITUITARY ADENOMA Is also known as thyrotroph adenoma|pituitary thyrotrophic adenoma|thyroid stimulating hormone-secreting pituitary adenoma|tsh-oma

Related symptoms:

  • Seizures
  • Ptosis
  • Hypertension
  • Tremor
  • Fatigue


SOURCES: ORPHANET MENDELIAN

More info about TSH-SECRETING PITUITARY ADENOMA

Medium match MATERNALLY-INHERITED DIABETES AND DEAFNESS


Maternally inherited diabetes and deafness (MIDD) is a mitochondrial disorder characterized by maternally transmitted diabetes and sensorineural deafness.

MATERNALLY-INHERITED DIABETES AND DEAFNESS Is also known as ballinger-wallace syndrome|diabetes-deafness syndrome, maternally transmitted|mitochondrial diabetes|noninsulin-dependent diabetes mellitus with deafness|niddm with deafness|diabetes mellitus, type ii, with deafness|midd

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Ataxia
  • Sensorineural hearing impairment


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about MATERNALLY-INHERITED DIABETES AND DEAFNESS

Medium match HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA


Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas; see this term).

HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA Is also known as familial pheochromocytoma-paraganglioma

Related symptoms:

  • Tremor
  • Fatigue
  • Congestive heart failure
  • Weight loss
  • Conductive hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA

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

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

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

Uncommon Symptoms - Between 30% and 50% cases


Sudden cardiac death Chest pain Dyspnea Cardiac arrest Respiratory distress Pain Hypotension Seizures Cardiomegaly Cyanosis Arrhythmia

Rare Symptoms - Less than 30% cases


Proteinuria Hepatomegaly Cough Cirrhosis Ascites Epistaxis Clubbing of fingers Ventricular arrhythmia Hemoptysis Telangiectasia Alopecia Osteoporosis Hypogonadism Diabetes mellitus Retinopathy Gynecomastia Impotence Headache Diplopia Hypokalemia Pallor Weight loss Tremor Hyperhidrosis Ptosis Hypertrophic cardiomyopathy Atrioventricular block Tachycardia Stroke Ventricular fibrillation Prolonged QRS complex Ventricular extrasystoles Abnormal heart morphology Ventricular hypertrophy Atrial fibrillation Intellectual disability Sick sinus syndrome Female hypogonadism Elevated urinary epinephrine Central adrenal insufficiency Adrenocorticotropin deficient adrenal insufficiency Paraganglioma of head and neck Increased thyroid-stimulating hormone level Decreased fertility in males Decreased circulating ACTH level Bitemporal hemianopia Recurrent paroxysmal headache Erectile abnormalities Decreased female libido Retinal capillary hemangioma Periodic hypokalemic paresis Abnormality of the pituitary gland Euthyroid hyperthyroxinemia Cranial nerve VI palsy Enlarged pituitary gland Fourth cranial nerve palsy Internal ophthalmoplegia Abnormal visual field test Sudden loss of visual acuity Oculomotor nerve palsy Decreased fertility in females Pericardial effusion Blindness Vomiting Osteopenia Paroxysmal vertigo Nausea and vomiting Delayed puberty Infertility Progressive visual loss Hypogonadotrophic hypogonadism Cranial nerve paralysis Goiter Easy fatigability Positive regitine blocking test Secondary growth hormone deficiency Elevated urinary norepinephrine Hyperthyroidism Growth hormone excess Increased circulating gonadotropin level Prolactin excess Male hypogonadism Adrenocorticotropic hormone deficiency Menstrual irregularities Hemianopia Supraventricular arrhythmia Abnormality of the menstrual cycle Heteronymous hemianopia Elevated urinary dopamine Abnormality of hair density Sensorineural hearing impairment Thyroid crisis Nausea Bundle branch block Vestibular dysfunction Macular dystrophy Abnormal retinal morphology Progressive sensorineural hearing impairment Glomerulopathy Retinal atrophy Pulsatile tinnitus Abnormality of lipid metabolism Left bundle branch block Abnormal chorioretinal morphology Conductive hearing impairment Hematuria Episodic paroxysmal anxiety Dysphonia Hypercalcemia Glomerulosclerosis Cerebral hemorrhage Renal cell carcinoma Aniridia Episodic abdominal pain Vocal cord paralysis Flushing Paraganglioma Adrenal pheochromocytoma Elevated calcitonin Sinus tachycardia Hyperglycemia Aplasia/Hypoplasia of the cerebellum Hearing impairment Myalgia Ataxia Cranial nerve compression Muscle weakness Cataract Visual impairment Dysarthria Extraadrenal pheochromocytoma Optic atrophy Myopathy Renal insufficiency Episodic hyperhidrosis Constipation Hypertension associated with pheochromocytoma Constriction of peripheral visual field Panic attack Hypertensive retinopathy Abnormality of the kidney Ophthalmoplegia Hepatic vascular malformations Unsteady gait Retinal degeneration Pigmentary retinopathy Bilateral sensorineural hearing impairment Type II diabetes mellitus Pancytopenia External ophthalmoplegia Ragged-red muscle fibers Malabsorption Hernia Adenocarcinoma of the colon Reduced ejection fraction Long eyelashes Sparse and thin eyebrow Acanthosis nigricans Ventricular tachycardia Brittle hair Akinesia Right bundle branch block Exertional dyspnea Fragile skin Curly hair Alopecia of scalp Woolly hair Onycholysis Epidermal acanthosis Hypergranulosis T-wave inversion Right ventricular cardiomyopathy Abnormality of hair texture Acantholysis Abnormal T-wave Right ventricular dilatation Paroxysmal ventricular tachycardia Abnormal right ventricle morphology Ventricular flutter Abnormal morphology of right ventricular trabeculae Edema Sparse scalp hair Abnormal blistering of the skin Pulmonary arterial hypertension Atrial flutter Brachydactyly Abnormality of cardiovascular system morphology Mitral valve prolapse Left ventricular hypertrophy Bradycardia Aortic regurgitation Sinus bradycardia Left ventricular noncompaction Anxiety Muscle fibrillation Supraventricular tachycardia Wolff-Parkinson-White syndrome Paroxysmal atrial fibrillation Ectodermal dysplasia Shortened PR interval Ventricular preexcitation Paroxysmal supraventricular tachycardia Ventricular preexcitation with multiple accessory pathways Dilatation Respiratory failure Hyperkeratosis Erythema Dilated cardiomyopathy Nail dystrophy Cleft upper lip Palmoplantar keratoderma Sepsis Recurrent respiratory infections Abnormal lung morphology Duodenal adenocarcinoma Portal hypertension Neoplasm Failure to thrive Cryptorchidism Anemia Macrocephaly Diarrhea Abdominal pain Umbilical hernia Jaundice Carcinoma Gastrointestinal hemorrhage Hypoalbuminemia Clubbing Chondrocalcinosis Colon cancer Hamartoma Polycythemia Hematochezia Intestinal polyposis Rectal prolapse Stomach cancer Hamartomatous polyposis Hematemesis Melena Intussusception Multiple gastric polyps Abnormality of the hypothalamus-pituitary axis Increased serum ferritin Hoarse voice Elevated right atrial pressure Scleroderma Acrocyanosis Capillary hemangioma Right ventricular hypertrophy Edema of the lower limbs Abnormal thrombosis Right ventricular failure Abnormal tricuspid valve morphology Spontaneous, recurrent epistaxis Increased pulmonary vascular resistance Hemangiomatosis Pulmonary capillary hemangiomatosis Arterial intimal fibrosis Exocrine pancreatic insufficiency Pulmonary arterial medial hypertrophy Pulmonary aterial intimal fibrosis Pulmonary artery vasoconstriction Peripheral neuropathy Splenomegaly Arthralgia Hepatic steatosis Limitation of joint mobility Cholestasis Hyperpigmentation of the skin Joint dislocation Arthropathy Hepatocellular carcinoma Arachnoid hemangiomatosis



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