Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypertrophic cardiomyopathy without obstruction |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic obstructive cardiomyopathy |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy secondary to Friedreich's ataxia |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Canine hypertrophic cardiomyopathy |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy secondary to hyperthyroidism |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
[X]Other hypertrophic cardiomyopathy |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy secondary to neuromuscular disorder |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Primary familial hypertrophic cardiomyopathy |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Feline hypertrophic cardiomyopathy |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy associated with another disorder |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy with genetic marker (disorder) |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic mitochondrial cardiomyopathy (disorder) |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Fetal hypertrophic cardiomyopathy (disorder) |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Primary hypertrophic cardiomyopathy (disorder) |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Cardiac septal myectomy (procedure) |
Has focus |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
1 |
A rare disorder characterized by progressive, late onset, autosomal dominant sensorineural hearing loss, QT interval prolongation, and mild cardiac hypertrophy. |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Cardiomyopathy and renal anomaly syndrome (disorder) |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
A rare mitochondrial disease that has a heterogeneous clinical presentation characterized by the association of progressive sensorineural hearing loss with hypertrophic cardiomyopathy and, in the majority of cases, encephalomyopathy symptoms such as ataxia, slurred speech, progressive external ophthalmoparesis (PEO), muscle weakness, myalgia, and exercise intolerance. |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase. |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome is a rare mitochondrial disease due to a defect in coenzyme Q10 biosynthesis that manifests with a broad spectrum of signs and symptoms which may include: neonatal lactic acidosis, global developmental delay, tonus disorder, seizures, reduced spontaneous movements, ventricular hypertrophy, bradycardia, renal tubular dysfunction with massive lactic acid excretion in urine, severe biochemical defect of respiratory chain complexes II/III when assayed together and deficiency of coenzyme Q10 in skeletal muscle. Cerebral and cerebellar atrophy can be seen on magnetic resonance imaging and multiple choroid plexus cysts and symmetrical hyperechoic signal alterations in basal ganglia have been observed on ultrasound. |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy due to glycogen storage disease |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy due to lysosomal disease |
Is a |
False |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophy of septomarginal trabeculation (disorder) |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy due to disorder |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|
Apical hypertrophic cardiomyopathy |
Is a |
True |
Hypertrophic cardiomyopathy |
Inferred relationship |
Some |
|