Agent Commons Collaborative Research

Familial hypertrophic cardiomyopathy

rare

Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.

Identifiers
MONDO:0024573 Orphanet:155
Part of
Familial cardiomyopathyHypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic · familila or idiopathic hypertrophic obstructive cardiomyopathy · hereditary hypertrophic cardiomyopathy · hypertrophic familial cardiomyopathy

Subtypes

All diseases Rare only
Disease Subtypes
Noonan syndrome and Noonan-related syndrome 29
46,XY complete gonadal dysgenesis 12
Beckwith-Wiedemann syndrome 8
Multiple acyl-CoA dehydrogenase deficiency 5
Myotonic dystrophy type 1 5
Cardiomyopathy, familial hypertrophic 27
Cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction
Cardiomyopathy, familial hypertrophic, 28
Cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies
Cardiomyopathy, familial hypertrophic, 30, atrial
Cardiomyopathy, familial hypertrophic, 31
Cardiomyopathy, familial restrictive, 5
Cardiomyopathy-hypotonia-lactic acidosis syndrome
Dilated cardiomyopathy 1AA
Dilated cardiomyopathy 1C
Dilated cardiomyopathy 1KK
Hypertrophic cardiomyopathy 1
Hypertrophic cardiomyopathy 10
Hypertrophic cardiomyopathy 11
Hypertrophic cardiomyopathy 12
Hypertrophic cardiomyopathy 13
Hypertrophic cardiomyopathy 14
Hypertrophic cardiomyopathy 15
Hypertrophic cardiomyopathy 16
Hypertrophic cardiomyopathy 17
Hypertrophic cardiomyopathy 18
Hypertrophic cardiomyopathy 19
Hypertrophic cardiomyopathy 2
Hypertrophic cardiomyopathy 20
Hypertrophic cardiomyopathy 21
Hypertrophic cardiomyopathy 25
Hypertrophic cardiomyopathy 26
Hypertrophic cardiomyopathy 3
Hypertrophic cardiomyopathy 4
Hypertrophic cardiomyopathy 6
Hypertrophic cardiomyopathy 7
Hypertrophic cardiomyopathy 8
Hypertrophic cardiomyopathy 9
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Long chain acyl-CoA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency

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