Abnormality of the tricuspid valve

Symptom Information:

Symptom ID: HPO:0001702
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the atrioventricular valves
Is a (Whole tree): HPO:
    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)
Database Frequency: 32 / 7739

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)