Tricuspid atresia

Symptom Information:

Symptom ID: HPO:0011662
Synonyms:
Tricuspid valve atresia [Orphanet:34100]
Congenital atresia of tricuspid valve (disorder) [Orphanet:34100]
Right atrioventricular valve atresia (disorder) [Orphanet:34100]
Tricuspid Atresia [Orphanet:34100]
Tricuspid atresia [OMIM:Tricuspid atresia]
tricuspid valve atresia/stenosis/narrowing [Orphanet:34100]
Congenital tricuspid valve atresia [Orphanet:34100]
Congenital tricuspid valve atresia [MedDRA:10049767]
Quality:
Cross references:
Orphanet:34100 "tricuspid valve atresia/stenosis/narrowing" [Orphanet:34100]
OMIM: "Tricuspid atresia" [OMIM:Tricuspid atresia]
UMLS:C0243002 "Tricuspid Atresia" [Orphanet:34100]
Is a (Direct Parents):
Orphanet Tricuspid stenosis
HPO         Abnormality of the tricuspid valve
Orphanet Abnormality of the heart valves
MedDRA Tricuspid 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 tricuspid valve(HPO:0001702)
                      Tricuspid atresia(HPO:0011662)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Tricuspid valvular disorders(MedDRA:10044637)
          Tricuspid atresia(HPO:0011662)
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
Diabetic embryopathy (Orphanet:1926)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Nephronophthisis 9 (OMIM:613824)