Abnormality of the tricuspid valve
Symptom Information:
| Symptom ID: | HPO:0001702 | ||
| Synonyms: |
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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 atrioventricular valves(HPO:0006705) Abnormality of the tricuspid valve(HPO:0001702) MedDRA: |
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| Database Frequency: | 32 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
| 16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
| 22q11.2 deletion syndrome | (Orphanet:567) |
| 3C syndrome | (Orphanet:7) |
| Angio-osteohypertrophic syndrome | (Orphanet:2346) |
| Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
| Autosomal recessive Robinow syndrome | (Orphanet:1507) |
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Coffin-Lowry syndrome | (Orphanet:192) |
| Congenital pericardium anomaly | (Orphanet:2846) |
| Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
| Criss-cross heart | (Orphanet:1461) |
| Dislocation of the hip - dysmorphism | (Orphanet:2412) |
| Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
| Distal monosomy 19p13.3 | (Orphanet:96129) |
| Ebstein malformation | (Orphanet:1880) |
| Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
| Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
| Faciocardiorenal syndrome | (Orphanet:1973) |
| GMS syndrome | (Orphanet:2090) |
| Geleophysic dysplasia | (Orphanet:2623) |
| Heart defects - limb shortening | (Orphanet:1354) |
| Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
| Klippel-Trénaunay syndrome | (Orphanet:90308) |
| Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
| Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
| Polyvalvular heart disease syndrome | (Orphanet:228410) |
| Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
| Pulmonary arterial hypertension | (Orphanet:182090) |
| Pulmonary atresia - intact ventricular septum | (Orphanet:1208) |
| Thoraco-abdominal enteric duplication | (Orphanet:1759) |
| Umbilical cord ulceration - intestinal atresia | (Orphanet:3405) |