Tricuspid regurgitation
Symptom Information:
Symptom ID: | HPO:0005180 | |||||||||||||||||
Synonyms: |
|
|||||||||||||||||
Quality: | ||||||||||||||||||
Cross references: |
|
|||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||
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 tricuspid valve(HPO:0001702) Tricuspid regurgitation(HPO:0005180) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Tricuspid valvular disorders(MedDRA:10044637) Tricuspid regurgitation(HPO:0005180) |
|||||||||||||||||
Database Frequency: | 20 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Atrial fibrillation, familial, 10 | (OMIM:614022) |
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL | (OMIM:212093) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
Cardiomyopathy, dilated, 1S | (OMIM:613426) |
Congenital heart block | (Orphanet:60041) |
Congenital valvular dysplasia | (Orphanet:1864) |
Costello syndrome | (Orphanet:3071) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Fabry disease | (Orphanet:324) |
Familial cutaneous collagenoma | (Orphanet:53296) |
Familial isolated restrictive cardiomyopathy | (Orphanet:75249) |
GMS syndrome | (Orphanet:2090) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
MUNGAN SYNDROME | (OMIM:611376) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Neonatal hemochromatosis | (Orphanet:446) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pulmonary venoocclusive disease | (Orphanet:31837) |