The search resulted in 108 diseases.
Orphanet:111 Barth syndrome
Orphanet:1344 Atrial standstill
Orphanet:1345 Cardiomyopathy-cataract-hip spine disease
Orphanet:1359 Carney complex
Orphanet:137675 Histiocytoid cardiomyopathy
Orphanet:1493 Vici syndrome
Orphanet:154 Familial isolated dilated cardiomyopathy
Orphanet:158 Carnitine uptake deficiency
Orphanet:183 Eosinophilic granulomatosis with polyangiitis
Orphanet:2022 Endomyocardial fibroelastosis
Orphanet:208600 Papillary fibroelastoma of the heart
Orphanet:217093 Mucopolysaccharidosis type 2, attenuated form
Orphanet:217622 Sensorineural deafness with dilated cardiomyopathy
Orphanet:2331 Kawasaki disease
Orphanet:2515 Microcephaly-cardiomyopathy syndrome
Orphanet:26791 Multiple acyl-CoA dehydrogenase deficiency
Orphanet:289377 Early-onset myopathy with fatal cardiomyopathy
Orphanet:300751 Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Orphanet:314637 Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Orphanet:324 Fabry disease
Orphanet:324410 X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
Orphanet:3282 Multifocal atrial tachycardia
Orphanet:3283 His bundle tachycardia
Orphanet:329874 Idiopathic giant cell myocarditis
Orphanet:3403 Uhl anomaly
Orphanet:34217 Naxos disease
Orphanet:352563 Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Orphanet:363618 LMNA-related cardiocutaneous progeria syndrome
Orphanet:369913 Combined oxidative phosphorylation defect type 17
Orphanet:45452 Idiopathic neonatal atrial flutter
Orphanet:5 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Orphanet:54260 Left ventricular noncompaction
Orphanet:550 MELAS
Orphanet:563 Peripartum cardiomyopathy
Orphanet:57777 Cirrhotic cardiomyopathy
Orphanet:580 Mucopolysaccharidosis type 2
Orphanet:59306 McLeod neuroacanthocytosis syndrome
Orphanet:60041 Congenital heart block
Orphanet:615 Familial atrial myxoma
Orphanet:64 Alström syndrome
Orphanet:65282 Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Orphanet:66529 Tako-Tsubo cardiomyopathy
Orphanet:66634 Dilated cardiomyopathy with ataxia
Orphanet:746 Mitochondrial trifunctional protein deficiency
Orphanet:75565 Tropical endomyocardial fibrosis
Orphanet:77259 Gaucher disease type 1
Orphanet:77260 Gaucher disease type 2
Orphanet:77261 Gaucher disease type 3
Orphanet:797 Sarcoidosis
Orphanet:85443 AL amyloidosis
Orphanet:85451 ATTRV122I amyloidosis
Orphanet:874 Adult heart tumor
Orphanet:90291 Systemic sclerosis
Orphanet:93473 Hurler syndrome
Orphanet:93476 Hurler-Scheie syndrome
Orphanet:93567 Pediatric systemic sclerosis
Orphanet:98896 Duchenne muscular dystrophy
Orphanet:99901 Acyl-CoA dehydrogenase 9 deficiency
OMIM:115197 Cardiomyopathy, familial hypertrophic, 4
OMIM:192600 Cardiomyopathy, familial hypertrophic, 1
OMIM:229300 Friedreich ataxia 1
OMIM:302045 Cardiomyopathy, dilated, 3B
OMIM:600858 Cardiomyopathy, familial hypertrophic, 6
OMIM:600884 Cardiomyopathy, dilated, 1B
OMIM:601493 Cardiomyopathy, dilated, 1C
OMIM:601494 Cardiomyopathy, dilated, 1D
OMIM:602086 Arrhythmogenic right ventricular dysplasia, familial, 3
OMIM:604169 Left ventricular noncompaction 1
OMIM:604400 Arrhythmogenic right ventricular dysplasia, familial, 5
OMIM:604765 Cardiomyopathy, dilated, 1I
OMIM:606685 Cardiomyopathy, dilated, 1L
OMIM:607450 Arrhythmogenic right ventricular dysplasia, familial, 8
OMIM:607482 Cardiomyopathy, dilated, 1M
OMIM:608569 Cardiomyopathy, dilated, 1O
OMIM:608751 Cardiomyopathy, familial hypertrophic, 8
OMIM:609040 Arrhythmogenic right ventricular dysplasia, familial, 9
OMIM:609909 Cardiomyopathy, dilated, 1P
OMIM:610193 Arrhythmogenic right ventricular dysplasia, familial, 10
OMIM:611407 Cardiomyopathy, dilated, 1W
OMIM:611528 Arrhythmogenic right ventricular dysplasia, familial, 12
OMIM:611615 Cardiomyopathy, dilated, 1X
OMIM:611878 Cardiomyopathy, dilated, 1Y
OMIM:611879 Cardiomyopathy, dilated, 1Z
OMIM:611880 Cardiomyopathy, dilated, 2A
OMIM:612877 Cardiomyopathy, dilated, 1BB
OMIM:613122 Cardiomyopathy, dilated, 1CC
OMIM:613172 Cardiomyopathy, dilated, 1DD
OMIM:613251 Cardiomyopathy, familial hypertrophic, 14
OMIM:613252 Cardiomyopathy, dilated, 1EE
OMIM:613286 Cardiomyopathy, dilated, 1FF
OMIM:613424 Cardiomyopathy, dilated, 1R
OMIM:613426 Cardiomyopathy, dilated, 1S
OMIM:613690 Cardiomyopathy, familial hypertrophic, 7
OMIM:613694 Cardiomyopathy, dilated, 1U
OMIM:613697 Cardiomyopathy, dilated, 1V
OMIM:613740 Cardiomyopathy, dilated, 1T
OMIM:613881 Cardiomyopathy, dilated, 1HH
OMIM:614672 Cardiomyopathy, dilated, 2B
OMIM:614676 Cardiomyopathy, familial hypertrophic, 21
OMIM:615184 Cardiomyopathy, dilated, 1II
OMIM:615373 Left ventricular noncompaction 8
OMIM:615396 Left ventricular noncompaction 10
OMIM:609470 Left ventricular noncompaction 2
OMIM:615745 Atrial standstill 2
OMIM:615248 Cardiomyopathy, dilated, 1KK
Orphanet:436242 Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
OMIM:609915 Cardiomyopathy, dilated, 1Q