Myocardial fibrosis
Symptom Information:
| Symptom ID: | HPO:0001685 | ||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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| 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) Myocardial fibrosis(HPO:0001685) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Myocardial disorders NEC(MedDRA:10028590) Myocardial fibrosis(HPO:0001685) |
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| Database Frequency: | 30 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| AL amyloidosis | (Orphanet:85443) |
| Alström syndrome | (Orphanet:64) |
| Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
| Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
| CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 | (OMIM:617047) |
| Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
| Cardiomyopathy, dilated, 1D | (OMIM:601494) |
| Cardiomyopathy, dilated, 1DD | (OMIM:613172) |
| Cardiomyopathy, dilated, 1FF | (OMIM:613286) |
| Cardiomyopathy, dilated, 1M | (OMIM:607482) |
| Cardiomyopathy, dilated, 1Q | (OMIM:609915) |
| Cardiomyopathy, dilated, 1V | (OMIM:613697) |
| Cardiomyopathy, dilated, 2B | (OMIM:614672) |
| Cardiomyopathy, dilated, 3B | (OMIM:302045) |
| Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
| Cardiomyopathy, familial hypertrophic, 2 | (OMIM:115195) |
| Cardiomyopathy, familial hypertrophic, 21 | (OMIM:614676) |
| Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
| Congenital heart block | (Orphanet:60041) |
| Fabry disease | (Orphanet:324) |
| Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
| Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
| Hypertaurinuric cardiomyopathy | (OMIM:145350) |
| Left ventricular noncompaction 8 | (OMIM:615373) |
| Limited cutaneous systemic sclerosis | (Orphanet:220402) |
| MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
| Mulibrey nanism | (Orphanet:2576) |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
| Uhl anomaly | (Orphanet:3403) |
| Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |