Cardiomyopathy, and Vertigo

Diseases related with Cardiomyopathy and Vertigo

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


Top matches:

Medium match ATRIAL FIBRILLATION, FAMILIAL, 6; ATFB6


Atrial fibrillation (AF) is the most common sustained cardiac rhythm disturbance, affecting more than 2 million Americans, with an overall prevalence of 0.89%. The prevalence increases rapidly with age, to 2.3% between the ages of 40 and 60 years, and to 5.9% over the age of 65. The most dreaded complication is thromboembolic stroke (Brugada et al., 1997).For a discussion of genetic heterogeneity of atrial fibrillation, see {608583}.

Related symptoms:

  • Hypertension
  • Cardiomyopathy
  • Stroke
  • Vertigo
  • Tachycardia


SOURCES: OMIM MESH MENDELIAN

More info about ATRIAL FIBRILLATION, FAMILIAL, 6; ATFB6

Medium match CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10


CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10 Is also known as cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2

Related symptoms:

  • Cardiomyopathy
  • Dyspnea
  • Hypertrophic cardiomyopathy
  • Vertigo
  • Tachycardia


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10

Medium match FAMILIAL ATRIAL FIBRILLATION


Familial atrial fibrillation is a rare, genetically heterogenous cardiac disease characterized by erratic activation of the atria with an irregular ventricular response, in various members of a single family. It may be asymptomatic or associated with palpitations, dyspnea and light-headedness. Concomitant rhythm disorders and cardiomyopathies are frequently reported.

FAMILIAL ATRIAL FIBRILLATION Is also known as atrial fibrillation, autosomal dominant

Related symptoms:

  • Pain
  • Respiratory distress
  • Arrhythmia
  • Stroke
  • Dilated cardiomyopathy


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about FAMILIAL ATRIAL FIBRILLATION

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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 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 GLYCOGEN STORAGE DISEASE WITH SEVERE CARDIOMYOPATHY DUE TO GLYCOGENIN DEFICIENCY


Glycogen storage disease type 15 is an extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal muscle.

GLYCOGEN STORAGE DISEASE WITH SEVERE CARDIOMYOPATHY DUE TO GLYCOGENIN DEFICIENCY Is also known as gyg1 deficiency|glycogen storage disease type xv|glycogenosis with severe cardiomyopathy due to glycogenin deficiency|glycogenin deficiency|gsd type 15|glycogen storage disease type 15|glycogenosis type 15|glycogenosis type xv|gsd xv|gsd type xv|gsd with

Related symptoms:

  • Muscle weakness
  • Peripheral neuropathy
  • Respiratory distress
  • Cardiomyopathy
  • Myopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about GLYCOGEN STORAGE DISEASE WITH SEVERE CARDIOMYOPATHY DUE TO GLYCOGENIN DEFICIENCY

Medium match ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY TYPE 1


Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 1 is a very rare and severe type of NAGA deficiency (see this term) characterized by infantile neuroaxonal dystrophy.

ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY TYPE 1 Is also known as schindler disease type 1|naga deficiency type 1

Related symptoms:

  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Nystagmus
  • Strabismus


SOURCES: ORPHANET MENDELIAN

More info about ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY TYPE 1

Medium match CYCLIC VOMITING SYNDROME; CVS


Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM MENDELIAN

More info about CYCLIC VOMITING SYNDROME; CVS

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 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

Top 5 symptoms//phenotypes associated to Cardiomyopathy and Vertigo

Symptoms // Phenotype % cases
Tachycardia Common - Between 50% and 80% cases
Palpitations Common - Between 50% and 80% cases
Arrhythmia Uncommon - Between 30% and 50% cases
Muscle weakness Uncommon - Between 30% and 50% cases
Sudden cardiac death Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Cardiomyopathy and Vertigo. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Congestive heart failure Hypertrophic cardiomyopathy Fatigue Syncope Respiratory distress Hearing impairment T-wave inversion Seizures Peripheral neuropathy Pain Ventricular fibrillation Myopathy Ventricular tachycardia Chest pain Dyspnea Atrial fibrillation Stroke Diabetes mellitus

Rare Symptoms - Less than 30% cases


Exertional dyspnea Retinopathy Right bundle branch block Ventricular arrhythmia Hyperkeratosis Hyperhidrosis Hypertension Bundle branch block Global developmental delay Strabismus Muscular hypotonia Hepatomegaly Optic atrophy Autism Ataxia Intellectual disability Alopecia Aplasia/Hypoplasia of the cerebellum ST segment elevation Supraventricular tachycardia Abnormal heart morphology Paroxysmal atrial fibrillation Atrial flutter Cardiomegaly Atrioventricular block Dilated cardiomyopathy Left ventricular septal hypertrophy Ventricular extrasystoles Prolonged QRS complex Cardiac arrest Thromboembolic stroke Growth delay Glomerulopathy Lethargy Nausea and vomiting Nausea Migraine Anorexia Pallor Abnormal autonomic nervous system physiology Exercise intolerance Abnormality of mitochondrial metabolism Telangiectasia of the skin Gastrointestinal dysmotility Splenomegaly Attention deficit hyperactivity disorder Abdominal pain Abnormality of brainstem morphology Photophobia Cognitive impairment Headache Behavioral abnormality Progressive sensorineural hearing impairment Generalized hypotonia Diarrhea Microcephaly Left bundle branch block Vomiting Retinal atrophy Fever Motor delay Abnormality of lipid metabolism External ophthalmoplegia Osteoporosis Abnormal retinal morphology Abnormality of the kidney Ptosis Visual impairment Dysarthria Renal insufficiency Constipation Myalgia Proteinuria Ophthalmoplegia Generalized amyotrophy Malabsorption Unsteady gait Retinal degeneration Constriction of peripheral visual field Ragged-red muscle fibers Pigmentary retinopathy Bilateral sensorineural hearing impairment Type II diabetes mellitus Cataract Abnormality of the hypothalamus-pituitary axis Macular dystrophy Hyperpigmentation of the skin Pancytopenia Hypogonadism Arthralgia Cirrhosis Hepatic steatosis Ascites Limitation of joint mobility Cholestasis Gynecomastia Chondrocalcinosis Joint dislocation Impotence Arthropathy Hepatocellular carcinoma Exocrine pancreatic insufficiency Increased serum ferritin Vestibular dysfunction Hyperglycemia Sensorineural hearing impairment Abdominal wall muscle weakness Hemiplegia/hemiparesis Long eyelashes Palmoplantar keratoderma Sepsis Ectodermal dysplasia Abnormal blistering of the skin Cyanosis Epidermal acanthosis Sparse scalp hair Sparse and thin eyebrow Nail dystrophy Acanthosis nigricans Brittle hair Akinesia Fragile skin Curly hair Alopecia of scalp Woolly hair Cleft upper lip Erythema Reduced ejection fraction Anxiety Sick sinus syndrome Left ventricular hypertrophy Asymmetric septal hypertrophy Abnormal atrioventricular conduction Permanent atrial fibrillation Abnormal electrophysiology of sinoatrial node origin AV nodal tachycardia Hypotension Respiratory failure Muscle fibrillation Wolff-Parkinson-White syndrome Shortened PR interval Ventricular preexcitation Paroxysmal supraventricular tachycardia Ventricular preexcitation with multiple accessory pathways Dilatation Clubbing of fingers Onycholysis Cerebral visual impairment Intellectual disability, severe Neck flexor weakness Abnormal levels of creatine kinase in blood Cardiomyocyte hypertrophy Increased mitochondrial number Decreased muscle glycogen content Nystagmus Spasticity Myoclonus Upper limb muscle weakness Developmental regression Abnormal pyramidal sign Paresthesia Sensory neuropathy Abnormality of extrapyramidal motor function Telangiectasia Lymphedema Shoulder girdle muscle weakness Myoglobinuria Hypergranulosis Ventricular flutter Right ventricular cardiomyopathy Abnormality of hair texture Acantholysis Abnormal T-wave Right ventricular dilatation Paroxysmal ventricular tachycardia Abnormal right ventricle morphology Abnormal morphology of right ventricular trabeculae Abnormal EKG Hypothyroidism Peripheral axonal neuropathy Ventricular hypertrophy Foot dorsiflexor weakness Scapular winging EMG: myopathic abnormalities Decreased muscle mass Abnormal chorioretinal morphology



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Ventricular septal defect and Intestinal malrotation, related diseases and genetic alterations Dysarthria and Craniosynostosis, related diseases and genetic alterations Intellectual disability, severe and Primary amenorrhea, related diseases and genetic alterations Low-set ears and Attention deficit hyperactivity disorder, related diseases and genetic alterations Immunodeficiency and Hepatocellular carcinoma, related diseases and genetic alterations Skeletal muscle atrophy and High myopia, related diseases and genetic alterations

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