Asymmetric septal hypertrophy
Symptom Information:
Symptom ID: | HPO:0001670 | |||
Synonyms: |
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Quality: | ||||
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) Cardiomyopathy(HPO:0001638) Hypertrophic cardiomyopathy(HPO:0001639) Asymmetric septal hypertrophy(HPO:0001670) MedDRA: |
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Database Frequency: | 19 / 7739 | |||
Resource: |
All diseases associated with this symptom:
CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH | (OMIM:212130) |
Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
Cardiomyopathy, familial hypertrophic, 16 | (OMIM:613838) |
Cardiomyopathy, familial hypertrophic, 19 | (OMIM:613875) |
Cardiomyopathy, familial hypertrophic, 2 | (OMIM:115195) |
Cardiomyopathy, familial hypertrophic, 20 | (OMIM:613876) |
Cardiomyopathy, familial hypertrophic, 4 | (OMIM:115197) |
Cardiomyopathy, familial hypertrophic, 6 | (OMIM:600858) |
Cardiomyopathy, familial hypertrophic, 7 | (OMIM:613690) |
Fabry disease | (Orphanet:324) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Friedreich ataxia 1 | (OMIM:229300) |
Leigh syndrome | (Orphanet:506) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Sanfilippo syndrome type A | (Orphanet:79269) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Sanfilippo syndrome type C | (Orphanet:79271) |
Sanfilippo syndrome type D | (Orphanet:79272) |