| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Canine dilated cardiomyopathy |
Is a |
False |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Congestive obstructive cardiomyopathy |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Ischemic congestive cardiomyopathy (disorder) |
Is a |
False |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Secondary dilated cardiomyopathy |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Nonischemic congestive cardiomyopathy |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Dilated cardiomyopathy with genetic marker (disorder) |
Is a |
False |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Fetal dilated cardiomyopathy |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Dilated cardiomyopathy 3B (disorder) |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Microcephaly-cardiomyopathy syndrome is characterized by severe intellectual deficit, microcephaly and dilated cardiomyopathy. Hand and foot anomalies have also been reported. The syndrome has been described in three individuals. Transmission is autosomal recessive. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Vici syndrome is a very rare and severe congenital multisystem disorder characterized by the principal features of agenesis of the corpus callosum, cataracts, oculocutaneous hypopigmentation, cardiomyopathy and combined immunodeficiency. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| A rare genetic ectodermal dysplasia syndrome characterised by woolly hair (presenting at birth), palmoplantar keratoderma (developing in the first year of life) and dilated cardiomyopathy with predominant left ventricle involvement (developing in childhood) which can lead to life-threatening heart failure in childhood or adolescence. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| A rare renal disease characterized by hypokalemic metabolic alkalosis secondary to a tubulopathy, hypomagnesemia with hypermagnesuria, severe hypercalciuria and dilated cardiomyopathy. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| A rare triad of dilated cardiomyopathy, premature cataract, and articular disease of the hips and spine characterized by hip joint degeneration, irregular intervertebral discs, and platyspondyly. The ocular abnormalities are often the first symptoms to arise. There have been no further descriptions in the literature since 1985. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| A rare autosomal dominant form of heart-hand syndrome that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Sensorineural deafness with dilated cardiomyopathy is an extremely rare autosomal dominant syndrome described in two families to date and characterized by moderate to severe sensorineural hearing loss manifesting during childhood and associated with late-onset dilated cardiomyopathy that generally progresses to heart failure. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| A rare familial cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Dilated cardiomyopathy caused by anthracycline |
Is a |
False |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Dilated cardiomyopathy due to infiltration |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
| Erythrokeratodermia-cardiomyopathy syndrome is a rare, genetic erythrokeratoderma disorder characterized by generalized cutaneous erythema with fine white scales and pruritus refractory to treatment, progressive dilated cardiomyopathy, palmoplantar keratoderma, sparse or absent eyebrows and eyelashes, sparse scalp hair, nail dystrophy, and dental enamel anomalies. Variable features include failure to thrive, developmental delay, and development of corneal opacities. Histology shows psoriasiform acanthosis, hypogranulosis, and compact orthohyperkeratosis. |
Is a |
True |
Congestive cardiomyopathy (disorder) |
Inferred relationship |
Some |
|
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