Pulmonary artery stenosis

Symptom Information:

Symptom ID: HPO:0004415
Synonyms:
Congenital stenosis of pulmonary artery (disorder) [Orphanet:34420]
Pulmonary artery stenosis (disorder) [Orphanet:34420]
Congenital hypoplasia of pulmonary artery (disorder) [Orphanet:34420]
Pulmonary artery stenosis [Orphanet:34420]
Pulmonary Stenosis [Orphanet:34420]
Congenital hypoplasia of pulmonary artery [Orphanet:34420]
Congenital stenosis of pulmonary artery [Orphanet:34420]
Pulmonary artery stenosis [OMIM:Pulmonary artery stenosis]
Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches [Orphanet:34420]
Pulmonic stenosis [Orphanet:34420]
Pulmonary artery stenosis congenital [Orphanet:34420]
Pulmonary artery stenosis [MedDRA:10037338]
Pulmonary valve stenosis [MedDRA:10037450]
Pulmonary stenosis [MedDRA:10037450]
Pulmonic stenosis [MedDRA:10037450]
Stenosis pulmonic valve [MedDRA:10037450]
Pulmonary artery stenosis congenital [MedDRA:10037339]
Congenital infundibular stenosis [MedDRA:10037339]
Congenital pulmonary artery stenosis [MedDRA:10037339]
Congenital pulmonary stenosis [MedDRA:10037339]
Infundibular pulmonic stenosis, congenital [MedDRA:10037339]
Pulmonic stenosis congenital [MedDRA:10037339]
Pulmonary artery stenosis (1 patient) [OMIM:Pulmonary artery stenosis (1 patient)]
Pulmonary artery stenosis (in some patients) [OMIM:Pulmonary artery stenosis (in some patients)]
Pulmonary stenosis (1 patient) [OMIM:Pulmonary stenosis (1 patient)]
Pulmonary stenosis (in some patients) [OMIM:Pulmonary stenosis (in some patients)]
Pulmonary stenosis (rare) [OMIM:Pulmonary stenosis (rare)]
Pulmonary valve stenosis (rare) [OMIM:Pulmonary valve stenosis (rare)]
Pulmonic stenosis (40%) [OMIM:Pulmonic stenosis (40%)]
Pulmonic stenosis (in some patients) [OMIM:Pulmonic stenosis (in some patients)]
Pulmonic valve stenosis (rare) [OMIM:Pulmonic valve stenosis (rare)]
Quality:
Cross references:
HPO:0004971 "Pulmonary artery hypoplasia" [Orphanet:34420]
HPO:0001642 "Pulmonic stenosis" [Orphanet:34420]
Orphanet:34420 "Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches" [Orphanet:34420]
OMIM: "Pulmonary artery stenosis" [OMIM:Pulmonary artery stenosis]
OMIM: "Pulmonary artery stenosis (1 patient)" [OMIM:Pulmonary artery stenosis (1 patient)]
OMIM: "Pulmonary artery stenosis (in some patients)" [OMIM:Pulmonary artery stenosis (in some patients)]
OMIM: "Pulmonary stenosis (1 patient)" [OMIM:Pulmonary stenosis (1 patient)]
OMIM: "Pulmonary stenosis (in some patients)" [OMIM:Pulmonary stenosis (in some patients)]
OMIM: "Pulmonary stenosis (rare)" [OMIM:Pulmonary stenosis (rare)]
OMIM: "Pulmonary valve stenosis (rare)" [OMIM:Pulmonary valve stenosis (rare)]
OMIM: "Pulmonic stenosis (40%)" [OMIM:Pulmonic stenosis (40%)]
OMIM: "Pulmonic stenosis (in some patients)" [OMIM:Pulmonic stenosis (in some patients)]
OMIM: "Pulmonic valve stenosis (rare)" [OMIM:Pulmonic valve stenosis (rare)]
UMLS:C0238397 "Pulmonary artery stenosis" [Orphanet:34420]
UMLS:C1956257 "Pulmonary Stenosis" [Orphanet:34420]
UMLS:C0265910 "Congenital hypoplasia of pulmonary artery" [Orphanet:34420]
UMLS:C0265911 "Congenital stenosis of pulmonary artery" [Orphanet:34420]
Is a (Direct Parents):
HPO         Abnormality of the pulmonary artery
Orphanet Pulmonic stenosis
Orphanet obsolete Malformation of the heart and great vessels
MedDRA Pulmonary valvular disorders
MedDRA Site specific necrosis and vascular insufficiency NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the pulmonary vasculature(HPO:0004930)
                Abnormality of the pulmonary artery(HPO:0004414)
                   Pulmonary artery stenosis(HPO:0004415)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Pulmonary valvular disorders(MedDRA:10037445)
          Pulmonary artery stenosis(HPO:0004415)
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Site specific necrosis and vascular insufficiency NEC(MedDRA:10052781)
          Pulmonary artery stenosis(HPO:0004415)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
Adams-Oliver syndrome (Orphanet:974)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal recessive omodysplasia (Orphanet:93329)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
Diabetic embryopathy (Orphanet:1926)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
LEOPARD SYNDROME 1 (OMIM:151100)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Mowat-Wilson syndrome (Orphanet:2152)
Nephronophthisis 16 (OMIM:615382)
Noonan syndrome (Orphanet:648)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Supravalvular aortic stenosis (Orphanet:3193)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
VENTRICULAR SEPTAL DEFECT 1 (OMIM:614429)
VENTRICULAR SEPTAL DEFECT 3 (OMIM:614432)
Werner syndrome (Orphanet:902)