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Familial restrictive cardiomyopathy

MONDO:0016340

An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.

Also known as: hereditary restrictive cardiomyopathy

70 clinical trials for this condition and its sub-types, 0 tagged with Familial restrictive cardiomyopathy itself.

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Where it sits in the disease tree

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Part of

↑ Restrictive cardiomyopathy (330) ↑ Familial cardiomyopathy (219)

Sub-types of Familial restrictive cardiomyopathy

Glycogen storage disease II 31 trials · 41 incl. sub-types
2 sub-types
- Glycogen storage disease due to acid maltase deficiency, late-onset 19 trials
- Glycogen storage disease due to acid maltase deficiency, infantile onset 9 trials
Gaucher disease type I 12 trials
ATTRV122I amyloidosis 7 trials
Atrial standstill 1 trial
2 sub-types
- Atrial standstill 1 0 trials
- Atrial standstill 2 0 trials
Idiopathic hypereosinophilic syndrome 1 trial
1 sub-type
- Idiopathic acute eosinophilic pneumonia 0 trials
Cardiomyopathy, familial restrictive, 1 0 trials
Cardiomyopathy, familial restrictive, 2 0 trials
Cardiomyopathy, familial restrictive, 3 0 trials
Cardiomyopathy, familial restrictive, 6 0 trials
Dilated cardiomyopathy 1KK 0 trials

Including sub-types (70) Tagged with Familial restrictive cardiomyopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.