Pulmonary insufficiency

Symptom Information:

Symptom ID: HPO:0010444
Synonyms:
Pulmonary incompetence [HPO:0010444]
Puolmonary valve insufficiency [HPO:0010444]
Pulmonary valve insufficiency [Orphanet:34160]
Pulmonic valve regurgitation (disorder) [Orphanet:34160]
Pulmonary Valve Insufficiency [Orphanet:34160]
Pulmonary insufficiency [OMIM:Pulmonary insufficiency]
Pulmonary valve anomaly/incompetence/insufficiency/regurgitation [Orphanet:34160]
Pulmonary valve incompetence [Orphanet:34160]
Pulmonary valve incompetence [MedDRA:10037448]
Pulmonary incompetence [MedDRA:10037448]
Pulmonary valve regurgitation [MedDRA:10037448]
Pulmonary valve insufficiency [MedDRA:10037448]
Pulmonary valve regurgitation [OMIM:Pulmonary valve regurgitation]
Quality:
Cross references:
Orphanet:34160 "Pulmonary valve anomaly/incompetence/insufficiency/regurgitation" [Orphanet:34160]
OMIM: "Pulmonary insufficiency" [OMIM:Pulmonary insufficiency]
OMIM: "Pulmonary valve regurgitation" [OMIM:Pulmonary valve regurgitation]
UMLS:C0034088 "Pulmonary Valve Insufficiency" [Orphanet:34160]
Is a (Direct Parents):
Orphanet Abnormality of the pulmonary valve
Orphanet Abnormality of the heart valves
HPO         Abnormality of the pulmonary valve
MedDRA Pulmonary 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 heart valves(HPO:0001654)
                   Abnormality of the pulmonary valve(HPO:0001641)
                      Pulmonary insufficiency(HPO:0010444)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Pulmonary valvular disorders(MedDRA:10037445)
          Pulmonary insufficiency(HPO:0010444)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB (OMIM:614437)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Jeune syndrome (Orphanet:474)
Lethal Larsen-like syndrome (Orphanet:2371)
MUNGAN SYNDROME (OMIM:611376)
Nephronophthisis 2 (OMIM:602088)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Osteogenesis imperfecta type 2 (Orphanet:216804)
Pseudoxanthoma elasticum (Orphanet:758)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Tropical endomyocardial fibrosis (Orphanet:75565)