Abnormality of the myocardium

Symptom Information:

Symptom ID: HPO:0001637
Synonyms:
Myocardium anomaly [Orphanet:34560]
Cardiomyopathy (disorder) [Orphanet:34560]
Myocardial disease (disorder) [Orphanet:34560]
Cardiomyopathies [Orphanet:34560]
Myocardium anomalies/myocarditis [Orphanet:34560]
Cardiomyopathy [Orphanet:34560]
Cardiomyopathy [MedDRA:10007636]
Cardiomyopathy in other diseases classified elsewhere [MedDRA:10007636]
Cardiomyopathy NOS [MedDRA:10007636]
Cardiomyopathy primary NOS [MedDRA:10007636]
Cardiomyopathy secondary NOS [MedDRA:10007636]
Degeneration myocardial [MedDRA:10007636]
Myocardial degeneration [MedDRA:10007636]
Myocardial disorder [MedDRA:10007636]
Myocardosis [MedDRA:10007636]
Nutritional and metabolic cardiomyopathy [MedDRA:10007636]
Obscure cardiomyopathy of Africa [MedDRA:10007636]
Other primary cardiomyopathies [MedDRA:10007636]
Secondary cardiomyopathy, unspecified [MedDRA:10007636]
Non-ischaemic cardiomyopathy [MedDRA:10007636]
Non-ischemic cardiomyopathy [MedDRA:10007636]
Cardiomyopathy primary [MedDRA:10007636]
Cardiomyopathy secondary [MedDRA:10007636]
Myocardiodystrophy [MedDRA:10007636]
Cardiomyopathy (1 patient) [OMIM:Cardiomyopathy (1 patient)]
Cardiomyopathy (CVS+) [OMIM:Cardiomyopathy (CVS+)]
Cardiomyopathy (in 2 of 4 patients from 1 family) [OMIM:Cardiomyopathy (in 2 of 4 patients from 1 family)]
Cardiomyopathy (in a subset of patients) [OMIM:Cardiomyopathy (in a subset of patients)]
Cardiomyopathy (in some patients) [OMIM:Cardiomyopathy (in some patients)]
Cardiomyopathy (in some) [OMIM:Cardiomyopathy (in some)]
Cardiomyopathy (less common) [OMIM:Cardiomyopathy (less common)]
Cardiomyopathy (rare) [OMIM:Cardiomyopathy (rare)]
Cardiomyopathy (reported in 1 family) [OMIM:Cardiomyopathy (reported in 1 family)]
Cardiomyopathy (reported in 1 patient) [OMIM:Cardiomyopathy (reported in 1 patient)]
Cardiomyopathy (reported in 2 patients) [OMIM:Cardiomyopathy (reported in 2 patients)]
Cardiomyopathy (severe form) [OMIM:Cardiomyopathy (severe form)]
Cardiomyopathy (type II, congenital) [OMIM:Cardiomyopathy (type II, congenital)]
Cardiomyopathy (uncommon) [OMIM:Cardiomyopathy (uncommon)]
Cardiomyopathy (variable) [OMIM:Cardiomyopathy (variable)]
No cardiomyopathy [OMIM:No cardiomyopathy]
Myocarditis [MedDRA:10028606]
Myocarditis (disorder) [Orphanet:34560]
Myocarditis [Orphanet:34560]
Myocardial disorders [MedDRA:10028593]
Cardiomyopathies [MedDRA:10007635]
Quality:
Cross references:
HPO:0001638 "Cardiomyopathy" [Orphanet:34560]
Orphanet:34560 "Myocardium anomalies/myocarditis" [Orphanet:34560]
OMIM: "Cardiomyopathy (1 patient)" [OMIM:Cardiomyopathy (1 patient)]
OMIM: "Cardiomyopathy (CVS+)" [OMIM:Cardiomyopathy (CVS+)]
OMIM: "Cardiomyopathy (in 2 of 4 patients from 1 family)" [OMIM:Cardiomyopathy (in 2 of 4 patients from 1 family)]
OMIM: "Cardiomyopathy (in a subset of patients)" [OMIM:Cardiomyopathy (in a subset of patients)]
OMIM: "Cardiomyopathy (in some patients)" [OMIM:Cardiomyopathy (in some patients)]
OMIM: "Cardiomyopathy (in some)" [OMIM:Cardiomyopathy (in some)]
OMIM: "Cardiomyopathy (less common)" [OMIM:Cardiomyopathy (less common)]
OMIM: "Cardiomyopathy (rare)" [OMIM:Cardiomyopathy (rare)]
OMIM: "Cardiomyopathy (reported in 1 family)" [OMIM:Cardiomyopathy (reported in 1 family)]
OMIM: "Cardiomyopathy (reported in 1 patient)" [OMIM:Cardiomyopathy (reported in 1 patient)]
OMIM: "Cardiomyopathy (reported in 2 patients)" [OMIM:Cardiomyopathy (reported in 2 patients)]
OMIM: "Cardiomyopathy (severe form)" [OMIM:Cardiomyopathy (severe form)]
OMIM: "Cardiomyopathy (type II, congenital)" [OMIM:Cardiomyopathy (type II, congenital)]
OMIM: "Cardiomyopathy (uncommon)" [OMIM:Cardiomyopathy (uncommon)]
OMIM: "Cardiomyopathy (variable)" [OMIM:Cardiomyopathy (variable)]
OMIM: "No cardiomyopathy" [OMIM:No cardiomyopathy]
UMLS:C0878544 "Cardiomyopathies" [Orphanet:34560]
UMLS:C0027059 "Myocarditis" [Orphanet:34560]
Is a (Direct Parents):
HPO         Myocarditis
HPO         obsolete Malformation of the heart and great vessels
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Abnormal morphology of myocardial trabeculae
MedDRA Cardiac disorders
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)
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)