Asymmetric septal hypertrophy

Symptom Information:

Symptom ID: HPO:0001670
Synonyms:
Asymmetric septal hypertrophy [OMIM:Asymmetric septal hypertrophy]
Asymmetric septal hypertrophy (in some patients) [OMIM:Asymmetric septal hypertrophy (in some patients)]
Hypertrophy, asymmetric septal (variable) [OMIM:Hypertrophy, asymmetric septal (variable)]
Quality:
Cross references:
OMIM: "Asymmetric septal hypertrophy" [OMIM:Asymmetric septal hypertrophy]
OMIM: "Asymmetric septal hypertrophy (in some patients)" [OMIM:Asymmetric septal hypertrophy (in some patients)]
OMIM: "Hypertrophy, asymmetric septal (variable)" [OMIM:Hypertrophy, asymmetric septal (variable)]
Is a (Direct Parents):
HPO         Hypertrophic cardiomyopathy
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:
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)