Edema, and Tachycardia

Diseases related with Edema and Tachycardia

In the following list you will find some of the most common rare diseases related to Edema and Tachycardia that can help you solving undiagnosed cases.


Top matches:

Low match BURULI ULCER, SUSCEPTIBILITY TO


Buruli ulcer is an infectious disease prevalent in many tropical and subtropical regions caused by infection with Mycobacterium ulcerans. It is the third most frequent mycobacterial disease in humans worldwide, after tuberculosis (OMIM ) and leprosy (OMIM ). Lesions are most common on exposed parts of the body, especially the limbs. Buruli ulcer derives its name from a county in Uganda, East Africa, north of Kampala, where the disease was found in the late 1950s in hundreds of people living near marshes and riverine areas near the Nile River (Clancey et al., 1961; Barker, 1971). The disease was first described in the medical literature in 1948 in a report on patients in Australia (MacCallum et al., 1948). Patients have also been reported from tropical areas in Latin America and Asia (Stienstra et al., 2006; van der Werf et al., 2005).

BURULI ULCER, SUSCEPTIBILITY TO Is also known as mycobacterium ulcerans, susceptibility to

Related symptoms:

  • Edema


SOURCES: OMIM MENDELIAN

More info about BURULI ULCER, SUSCEPTIBILITY TO

Low match FAMILIAL SHORT QT SYNDROME


Familial short QT syndrome is a newly described cardiologic entity that associates a short QT interval (QT and QTc 300 ms) on the surface electrocardiogram (ECG) with a high risk of syncope or sudden death due to malignant ventricular arrhythmia.

FAMILIAL SHORT QT SYNDROME Is also known as sqts

Related symptoms:

  • Sudden cardiac death
  • Syncope
  • Atrial fibrillation
  • Palpitations
  • Bradycardia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FAMILIAL SHORT QT SYNDROME

Low match CARDIOMYOPATHY, DILATED, 1Y; CMD1Y


Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Edema
  • Atrial septal defect


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1Y; CMD1Y

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Other less relevant matches:

Low match LEFT VENTRICULAR NONCOMPACTION 10; LVNC10


Related symptoms:

  • Hepatomegaly
  • Respiratory distress
  • Congestive heart failure
  • Dyspnea
  • Dilated cardiomyopathy


SOURCES: OMIM MENDELIAN

More info about LEFT VENTRICULAR NONCOMPACTION 10; LVNC10

Low match CARVAJAL SYNDROME


Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome is characterized by woolly hair, palmoplantar keratoderma and dilated cardiomyopathy principally affecting the left ventricle.

CARVAJAL SYNDROME Is also known as keratoderma with woolly hair type ii|palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair|woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome|wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome|

Related symptoms:

  • Cardiomyopathy
  • Edema
  • Congestive heart failure
  • Hyperkeratosis
  • Dilated cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARVAJAL SYNDROME

Low match ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1


Arrhythmogenic right ventricular dysplasia (ARVD) is a clinical and pathologic entity for which the diagnosis rests on electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elements, preferentially involve the right ventricular free wall. It is inherited in an autosomal dominant manner with reduced penetrance and is one of the major genetic causes of juvenile sudden death. When the dysplasia is extensive, it may represent the Uhl anomaly ('parchment right ventricle'). The presenting finding is usually recurrent, sustained ventricular tachycardia with left bundle branch block configuration. Basso et al. (2009) provided a detailed review of ARVD, including diagnosis, pathogenesis, treatment options, and genetics. Genetic Heterogeneity of Familial Arrhythmogenic Right Ventricular DysplasiaOther forms of ARVD include ARVD2 (OMIM ), caused by mutation in the RYR2 gene (OMIM ) on chromosome 1q42-q43; ARVD3 (OMIM ), on chromosome 14q12-q22; ARVD4 (OMIM ), on chromosome 2q32.1-q32.3; ARVD5 (OMIM ), caused by mutation in the TMEM43 gene (OMIM ) on chromosome 3p23; ARVD6 (OMIM ), on chromosome 10p14-p12; ARVD8 (OMIM ), caused by mutation in the DSP gene (OMIM ) on chromosome 6p24; ARVD9 (OMIM ), caused by mutation in the PKP2 gene (OMIM ) on chromosome 12p11; ARVD10 (OMIM ), caused by mutation in the DSG2 (OMIM ) on chromosome 18q12.1; ARVD11 (OMIM ), caused by mutation in the DSC2 gene (OMIM ) on chromosome 18q12.1; ARVD12 (OMIM ), caused by mutation in the JUP gene (OMIM ) on chromosome 17q21; and ARVD13 (OMIM ), caused by mutation in the CTNNA3 gene (OMIM ) on chromosome 10q21.ARVD7 is a former designation for a form of myopathy and ARVD mapped to chromosome 10q22, which was later found to be a form of myofibrillar myopathy (MFM1 ) caused by mutation in the DES gene (OMIM ) on chromosome 2q35.Christensen et al. (2010) screened 65 ARVD probands for mutations in 5 desmosomal genes as well as the TGFB3 gene (OMIM ), and identified 19 different mutations in the desmosomal genes in 12 of the families, including 7 with more than 1 mutation. In 6 families, digenic mutation carriers were identified, with at least 1 of the mutations being absent in the control population. The authors stated that their findings partially supported a gene dosage effect, although phenotypic variation was large.Nitoiu et al. (2014) reviewed desmosome biology in cardiocutaneous syndromes and inherited skin disease, including discussion of the involvement of the DSP, PKP2, DSG2, DSC2, and JUP genes.

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1 Is also known as arvc1|arrhythmogenic right ventricular cardiomyopathy 1

Related symptoms:

  • Fever
  • Cardiomyopathy
  • Edema
  • Myopathy
  • Congestive heart failure


SOURCES: ORPHANET OMIM MENDELIAN

More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1

Low match LEFT VENTRICULAR NONCOMPACTION


Left ventricular noncompaction (LVNC) is a rare cardiomyopathy characterized anatomically by prominent left ventricular trabeculae and deep intratrabecular recesses causing progressive systolic and diastolic dysfunction, conduction abnormalities, and occasionally thromboembolic events.

LEFT VENTRICULAR NONCOMPACTION Is also known as spongy myocardium|lvnc|left ventricular hypertrabeculation|left ventricular noncompaction 1 with or without congenital heart defects

Related symptoms:

  • Abnormal facial shape
  • Ventricular septal defect
  • Respiratory distress
  • Congestive heart failure
  • Patent ductus arteriosus


SOURCES: OMIM ORPHANET MENDELIAN

More info about LEFT VENTRICULAR NONCOMPACTION

Low match ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11


ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 Is also known as arvc11|arrhythmogenic right ventricular cardiomyopathy 11

Related symptoms:

  • Hypertension
  • Cardiomyopathy
  • Dilatation
  • Arrhythmia
  • Hyperkeratosis


SOURCES: MESH OMIM MENDELIAN

More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11

Low match MITOCHONDRIAL HYPERTROPHIC CARDIOMYOPATHY WITH LACTIC ACIDOSIS DUE TO MTO1 DEFICIENCY


Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency is a rare mitochondrial oxidative phosphorylation disorder with complex I and IV deficiency characterized by lactic acidosis, hypotonia, hypertrophic cardiomyopathy and global developmental delay. Other clinical features include feeding difficulties, failure to thrive, seizures, optic atrophy and ataxia.

MITOCHONDRIAL HYPERTROPHIC CARDIOMYOPATHY WITH LACTIC ACIDOSIS DUE TO MTO1 DEFICIENCY Is also known as cardiomyopathy, infantile hypertrophic mitochondrial, and lactic acidosis|coxpd10|combined oxidative phosphorylation defect type 10

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Ataxia


SOURCES: ORPHANET OMIM MENDELIAN

More info about MITOCHONDRIAL HYPERTROPHIC CARDIOMYOPATHY WITH LACTIC ACIDOSIS DUE TO MTO1 DEFICIENCY

Low match MASTOCYTOSIS, CUTANEOUS; MASTC


Mastocytosis, or mast cell disease, is a heterogeneous group of clinical disorders characterized by the abnormal accumulation of mast cells in various tissues, especially in the skin and hematopoietic organs. Mastocytosis usually appears in infancy or early adulthood. In most pediatric cases, the disease is limited to the skin, but it can be associated with systemic symptoms due to the release of mediators from mast cells, even when there is no systemic infiltration. It usually has a good prognosis, with substantial improvement or spontaneous resolution before puberty. In rare cases, the disease may remain active through adolescence as a systemic adult mastocytosis. Cutaneous mastocytosis is characterized by macules, papules, nodules, or diffuse infiltration of the skin, often associated with localized hyperpigmentation. Gentle rubbing of the lesions induces histamine release from mechanically activated mast cells, causing local wheals, erythema, and often pruritus, a phenomenon termed the 'Darier sign.' In contrast to childhood-onset mastocytosis, adult-onset mastocytosis often persists for the lifetime of the patient and is also more likely to be a severe and systemic disease involving numerous organs. In some cases, it is associated with a clonal hematologic non-mast-cell lineage disease, such as a myelodysplastic or myeloproliferative disorder. Adult-onset mastocytosis can also lead to the rare mast cell leukemia, which carries a high risk of mortality (summary by Bodemer et al., 2010 and Kambe et al., 2010).

MASTOCYTOSIS, CUTANEOUS; MASTC Is also known as mastocytosis, maculopapular cutaneous|mastocytosis, diffuse cutaneous|urticaria pigmentosa

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about MASTOCYTOSIS, CUTANEOUS; MASTC

Top 5 symptoms//phenotypes associated to Edema and Tachycardia

Symptoms // Phenotype % cases
Ventricular tachycardia Common - Between 50% and 80% cases
Sudden cardiac death Common - Between 50% and 80% cases
Congestive heart failure Common - Between 50% and 80% cases
Dilated cardiomyopathy Uncommon - Between 30% and 50% cases
Cardiomyopathy Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Edema and Tachycardia. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Arrhythmia Syncope Ventricular arrhythmia Palpitations Dyspnea Cardiac arrest Bundle branch block Atrioventricular block Left bundle branch block Abnormal myocardium morphology Hepatomegaly Left ventricular noncompaction cardiomyopathy Atrial fibrillation Left ventricular noncompaction Respiratory distress Ventricular fibrillation Right bundle branch block

Rare Symptoms - Less than 30% cases


Cardiomegaly Abnormal EKG Right ventricular cardiomyopathy Pulmonary edema Palmoplantar keratoderma Hyperkeratosis Ascites Hypertension Left ventricular hypertrophy Abnormal T-wave Woolly hair Wolff-Parkinson-White syndrome Dilatation Myocarditis T-wave inversion in the right precordial leads Permanent atrial fibrillation Hypertrophic cardiomyopathy Pain Bradycardia T-wave inversion Hepatosplenomegaly Leukemia Myalgia Erythema Skin rash Pruritus Nausea and vomiting Papule Malabsorption Arthralgia Neoplasm Gastroesophageal reflux Decreased activity of mitochondrial respiratory chain Increased serum lactate Infantile muscular hypotonia Pleural effusion Aspiration pneumonia Ketonuria Sinus bradycardia Severe lactic acidosis Hyperalaninemia Ichthyosis Weight loss Anemia Fatigue Diarrhea Splenomegaly Headache Thrombocytopenia Osteoporosis Abdominal pain Lymphadenopathy Shock Nausea Impaired temperature sensation Generalized osteosclerosis Myeloproliferative disorder Hypersplenism Gastrointestinal stroma tumor Immunologic hypersensitivity Asthenia Abnormal eosinophil morphology Flushing Food intolerance Abnormality of the gastric mucosa Mastocytosis Dermatographic urticaria Cutaneous mastocytosis Anaphylactic shock Chronic leukemia Allergy Acute leukemia Cirrhosis Bone marrow hypocellularity Recurrent fractures Asthma Gastrointestinal hemorrhage Hypotension Abnormal blistering of the skin Telangiectasia Bone pain Osteolysis Abnormality of blood and blood-forming tissues Leukopenia Sarcoma Urticaria Lactic acidosis Portal hypertension Loss of consciousness Hypermelanotic macule Metabolic acidosis Right ventricular dilatation Poor speech Myofibrillar myopathy Mildly reduced ejection fraction Fever Myopathy Coronary artery atherosclerosis Elevated erythrocyte sedimentation rate Multiple lipomas ST segment elevation Cardiomyocyte hypertrophy Peripheral edema Dilatation of the ventricular cavity Abnormal right ventricle morphology Abnormality of the left ventricular outflow tract Sinoatrial block Abnormal facial shape Patchy palmoplantar keratoderma Impaired myocardial contractility Patent ductus arteriosus Myocardial infarction Ventricular extrasystoles Paroxysmal atrial fibrillation Shortened QT interval Paroxysmal ventricular tachycardia Atrial septal defect Chest pain Oliguria Congenital bullous ichthyosiform erythroderma Ventricular flutter Reduced number of teeth Skin vesicle Fragile nails Clubbing of fingers Myocardial fibrosis Abnormal atrioventricular conduction Ventricular septal defect Mitral regurgitation Small for gestational age Spasticity Generalized hypotonia Ataxia Growth delay Failure to thrive Muscle weakness Muscular hypotonia Cognitive impairment Seizures Feeding difficulties Motor delay Optic atrophy Dystonia Encephalopathy Acidosis Hypoglycemia Global developmental delay Intellectual disability Hydrops fetalis Abnormal thrombosis Exercise intolerance Hypoplastic left heart Pulmonary embolism Concave nasal ridge Restrictive cardiomyopathy Abnormal left ventricle morphology Right ventricular failure Diffuse palmoplantar hyperkeratosis Biventricular hypertrophy Noncompaction cardiomyopathy Abnormality of the fascia Dehydration Palmoplantar hyperkeratosis Reduced ejection fraction Abnormal echocardiogram Telangiectasia macularis eruptiva perstans



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