Abnormality of the myocardium
Symptom Information:
Symptom ID: | HPO:0001637 | |||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the myocardium(HPO:0001637) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) |
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Database Frequency: | 76 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALG1-CDG | (Orphanet:79327) |
Adult Still's disease | (Orphanet:829) |
Antisynthetase syndrome | (Orphanet:81) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Atrial standstill 2 | (OMIM:615745) |
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2J | (Orphanet:140922) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2T | (Orphanet:363623) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Behçet disease | (Orphanet:117) |
CREST syndrome | (Orphanet:90290) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
Cardiomyopathy, familial hypertrophic, 15 | (OMIM:613255) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Cardiomyopathy, fatal fetal, due to myocardial calcification | (OMIM:300829) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Cogan syndrome | (Orphanet:1467) |
D-2-@HYDROXYGLUTARIC ACIDURIA 1 | (OMIM:600721) |
Dermatomyositis | (Orphanet:221) |
Distal myopathy with posterior leg and anterior hand involvement | (Orphanet:63273) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fabry disease | (Orphanet:324) |
Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form | (Orphanet:308712) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form | (Orphanet:308684) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form | (Orphanet:308698) |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form | (Orphanet:308670) |
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form | (Orphanet:308655) |
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form | (Orphanet:308638) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Kawasaki disease | (Orphanet:2331) |
Kearns-Sayre syndrome | (Orphanet:480) |
Left ventricular noncompaction 1 | (OMIM:604169) |
Left ventricular noncompaction 10 | (OMIM:615396) |
Legionellosis | (Orphanet:549) |
Lyell syndrome | (Orphanet:537) |
MUSCULAR DYSTROPHY, SCAPULOHUMERAL | (OMIM:600416) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
Malignant atrophic papulosis | (Orphanet:679) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Mixed connective tissue disease | (Orphanet:809) |
Neonatal intrahepatic cholestasis due to citrin deficiency | (Orphanet:247598) |
Neutral lipid storage myopathy | (Orphanet:98908) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Peripartum cardiomyopathy | (Orphanet:563) |
Relapsing polychondritis | (Orphanet:728) |
Rheumatic fever | (Orphanet:3099) |
Scleroderma | (Orphanet:801) |
Scrub typhus | (Orphanet:83317) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Sialidosis type 1 | (Orphanet:812) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Systemic capillary leak syndrome | (Orphanet:188) |
TRAPS syndrome | (Orphanet:32960) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Thymoma | (Orphanet:99867) |
Uhl anomaly | (Orphanet:3403) |
VENTRICULAR TACHYCARDIA, FAMILIAL | (OMIM:192605) |
Whipple disease | (Orphanet:3452) |
Wolfram syndrome 1 | (OMIM:222300) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |