Abnormality of the pulmonary valve

Symptom Information:

Symptom ID: HPO:0001641
Synonyms:
Pulmonary valve anomaly [Orphanet:34160]
Congenital pulmonary valve abnormality (disorder) [Orphanet:34160]
Congenital pulmonary valve abnormality [Orphanet:34160]
Pulmonary valve anomaly/incompetence/insufficiency/regurgitation [Orphanet:34160]
Congenital pulmonary valve disorder [Orphanet:34160]
Congenital pulmonary valve disorder [MedDRA:10061075]
Anomalies of pulmonary valve, congenital [MedDRA:10061075]
Congenital pulmonary valve anomaly, unspecified [MedDRA:10061075]
Congenital pulmonary valve disorder NOS [MedDRA:10061075]
Other congenital anomalies of pulmonary valve [MedDRA:10061075]
Quality:
Cross references:
Orphanet:34160 "Pulmonary valve anomaly/incompetence/insufficiency/regurgitation" [Orphanet:34160]
UMLS:C0265830 "Congenital pulmonary valve abnormality" [Orphanet:34160]
Is a (Direct Parents):
Orphanet Abnormality of the heart valves
HPO         Abnormality of the heart valves
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)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Pulmonary valvular disorders(MedDRA:10037445)
          Abnormality of the pulmonary valve(HPO:0001641)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microdeletion syndrome (Orphanet:276413)
22q11.2 deletion syndrome (Orphanet:567)
8p23.1 microduplication syndrome (Orphanet:251076)
Adams-Oliver syndrome (Orphanet:974)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Autosomal dominant cutis laxa (Orphanet:90348)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Brittle cornea syndrome (Orphanet:90354)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Costello syndrome (Orphanet:3071)
Criss-cross heart (Orphanet:1461)
Distal monosomy 19p13.3 (Orphanet:96129)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Holoprosencephaly (Orphanet:2162)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteopetrosis (Orphanet:2781)
Polyvalvular heart disease syndrome (Orphanet:228410)
Townes-Brocks syndrome (Orphanet:857)
Weill-Marchesani syndrome (Orphanet:3449)
X-linked mandibulofacial dysostosis (Orphanet:1131)
Zunich-Kaye syndrome (Orphanet:3474)