Mitral stenosis

Symptom Information:

Symptom ID: HPO:0001718
Synonyms:
Mitral valve stenosis [HPO:0001718]
Mitral valve stenosis [Orphanet:34060]
Mitral valve stenosis (disorder) [Orphanet:34060]
Mitral Valve Stenosis [Orphanet:34060]
Mitral stenosis [OMIM:Mitral stenosis]
Mitral valve stenosis [OMIM:Mitral valve stenosis]
Mitral valve atresia/stenosis/narrowing [Orphanet:34060]
Mitral valve stenosis [MedDRA:10027733]
Mitral stenosis [MedDRA:10027733]
Mitral stenosis rheumatic [MedDRA:10027733]
Rheumatic mitral stenosis [MedDRA:10027733]
Mitral valve stenosis (uncommon) [OMIM:Mitral valve stenosis (uncommon)]
Quality:
Cross references:
Orphanet:34060 "Mitral valve atresia/stenosis/narrowing" [Orphanet:34060]
OMIM: "Mitral stenosis" [OMIM:Mitral stenosis]
OMIM: "Mitral valve stenosis" [OMIM:Mitral valve stenosis]
OMIM: "Mitral valve stenosis (uncommon)" [OMIM:Mitral valve stenosis (uncommon)]
UMLS:C0026269 "Mitral Valve Stenosis" [Orphanet:34060]
Is a (Direct Parents):
HPO         Abnormality of the mitral valve
Orphanet Abnormality of the heart valves
MedDRA Mitral valvular 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 atrioventricular valves(HPO:0006705)
                   Abnormality of the mitral valve(HPO:0001633)
                      Mitral stenosis(HPO:0001718)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Mitral valvular disorders(MedDRA:10027723)
          Mitral stenosis(HPO:0001718)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
CHST3-related skeletal dysplasia (Orphanet:263463)
Carney complex (Orphanet:1359)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Geleophysic dysplasia (Orphanet:2623)
Mowat-Wilson syndrome (Orphanet:2152)
Sneddon syndrome (Orphanet:820)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)