Agent Commons Collaborative Research
Familial restrictive cardiomyopathy
rareAn instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0016340 Orphanet:217635
- Also known as
- hereditary restrictive cardiomyopathy
Subtypes
Disease Rare Not rare Subtypes
- Atrial standstill MONDO:0015281 2
- Glycogen storage disease II MONDO:0009290 GAA 2
- Idiopathic hypereosinophilic syndrome MONDO:0011895 PDGFRA 1
- ATTRV122I amyloidosis MONDO:0019441
- Gaucher disease type I MONDO:0009265 GBA1
- Cardiomyopathy, familial restrictive, 1 MONDO:0007270 TNNI3
- Cardiomyopathy, familial restrictive, 2 MONDO:0012306
- Cardiomyopathy, familial restrictive, 3 MONDO:0012900
- Cardiomyopathy, familial restrictive, 6 MONDO:0030330
- Dilated cardiomyopathy 1KK MONDO:0014100 MYPN
- Hypertrophic cardiomyopathy 26 MONDO:0014883 FLNC
Projects
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