Pulmonic stenosis

Symptom Information:

Symptom ID: HPO:0001642
Synonyms:
Pulmonary stenosis [HPO:0001642]
Pulmonary valve stenosis [HPO:0001642]
Pulmonic valve stenosis [HPO:0001642]
Pulmonary artery stenosis [Orphanet:34420]
Pulmonary valve stenosis [Orphanet:34180]
Congenital stenosis of pulmonary artery (disorder) [Orphanet:34420]
Pulmonary artery stenosis (disorder) [Orphanet:34420]
Congenital hypoplasia of pulmonary artery (disorder) [Orphanet:34420]
Pulmonic valve stenosis (disorder) [Orphanet:34180]
Pulmonary Stenosis [Orphanet:34420]
Congenital hypoplasia of pulmonary artery [Orphanet:34420]
Congenital stenosis of pulmonary artery [Orphanet:34420]
Pulmonary Valve Stenosis [Orphanet:34180]
Pulmonary Stenosis [Orphanet:34180]
Pulmonary stenosis [OMIM:Pulmonary stenosis]
Pulmonary valve stenosis [OMIM:Pulmonary valve stenosis]
Pulmonic stenosis [OMIM:Pulmonic stenosis]
Pulmonic valve stenosis [OMIM:Pulmonic valve stenosis]
Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches [Orphanet:34420]
Pulmonary valve atresia/stenosis/narrowing [Orphanet:34180]
Pulmonic stenosis [Orphanet:34420]
Pulmonary artery stenosis congenital [Orphanet:34420]
Pulmonic stenosis [Orphanet:34180]
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:0004415 "Pulmonary artery stenosis" [Orphanet:34420]
Orphanet:34420 "Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches" [Orphanet:34420]
Orphanet:34180 "Pulmonary valve atresia/stenosis/narrowing" [Orphanet:34180]
OMIM: "Pulmonary stenosis" [OMIM:Pulmonary stenosis]
OMIM: "Pulmonary valve stenosis" [OMIM:Pulmonary valve stenosis]
OMIM: "Pulmonic stenosis" [OMIM:Pulmonic stenosis]
OMIM: "Pulmonic valve stenosis" [OMIM:Pulmonic valve 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]
UMLS:C0034089 "Pulmonary Valve Stenosis" [Orphanet:34180]
UMLS:C1956257 "Pulmonary Stenosis" [Orphanet:34180]
Is a (Direct Parents):
HPO         Abnormality of the pulmonary valve
MedDRA Pulmonary valvular disorders
Orphanet Abnormality of the heart valves
Orphanet obsolete Malformation of the heart and great vessels
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)
          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)
                      Pulmonic stenosis(HPO:0001642)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Pulmonary valvular disorders(MedDRA:10037445)
          Pulmonic stenosis(HPO:0001642)
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Site specific necrosis and vascular insufficiency NEC(MedDRA:10052781)
          Pulmonic stenosis(HPO:0001642)
Database Frequency: 89 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY (OMIM:614262)
Adams-Oliver syndrome (Orphanet:974)
Alström syndrome (Orphanet:64)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Autosomal recessive infantile hypercalcemia (Orphanet:300547)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARDIOFACIOCUTANEOUS SYNDROME 3 (OMIM:615279)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CARPENTER SYNDROME 1 (OMIM:201000)
CHARGE syndrome (Orphanet:138)
CHST3-related skeletal dysplasia (Orphanet:263463)
CRANIOACROFACIAL SYNDROME (OMIM:122850)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Carpenter syndrome (Orphanet:65759)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Congenital heart block (Orphanet:60041)
Congenital pulmonary valve stenosis (Orphanet:3189)
Costello syndrome (Orphanet:3071)
Diabetic embryopathy (Orphanet:1926)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Emanuel syndrome (Orphanet:96170)
FRONTOOCULAR SYNDROME (OMIM:605321)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Familial retinal arterial macroaneurysm (Orphanet:284247)
Femoral-facial syndrome (Orphanet:1988)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
HETEROTAXY, VISCERAL, 1, X-LINKED (OMIM:306955)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Ivemark syndrome (Orphanet:97548)
KABUKI SYNDROME 2 (OMIM:300867)
KAGAMI-OGATA SYNDROME (OMIM:608149)
Keipert syndrome (Orphanet:2662)
Keutel syndrome (Orphanet:85202)
Koolen-De Vries syndrome (Orphanet:96169)
LEOPARD SYNDROME 1 (OMIM:151100)
Left ventricular noncompaction 2 (OMIM:609470)
MARFANOID HABITUS WITH SITUS INVERSUS (OMIM:609008)
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION (OMIM:249670)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
MUNGAN SYNDROME (OMIM:611376)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
Matthew-Wood syndrome (Orphanet:2470)
McDonough syndrome (Orphanet:2471)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mowat-Wilson syndrome (Orphanet:2152)
NOONAN SYNDROME 1 (OMIM:163950)
NOONAN SYNDROME 3 (OMIM:609942)
NOONAN SYNDROME 4 (OMIM:610733)
NOONAN SYNDROME 6 (OMIM:613224)
NOONAN SYNDROME 7 (OMIM:613706)
NOONAN SYNDROME 8 (OMIM:615355)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 9 (OMIM:613824)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculofaciocardiodental syndrome (Orphanet:2712)
PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS (OMIM:264140)
PULMONIC STENOSIS AND DEAFNESS (OMIM:178651)
PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES (OMIM:178650)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Peters-plus syndrome (Orphanet:709)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Recombinant 8 syndrome (Orphanet:96167)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Supravalvular aortic stenosis (Orphanet:3193)
Syndromic diarrhea (Orphanet:84064)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
VENTRICULAR SEPTAL DEFECT 1 (OMIM:614429)
VENTRICULAR SEPTAL DEFECT 3 (OMIM:614432)
Ventricular septal defect (Orphanet:1480)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
WEILL-MARCHESANI SYNDROME 3 (OMIM:614819)
Weill-Marchesani syndrome (Orphanet:3449)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
Wolfram syndrome 1 (OMIM:222300)
X-linked mandibulofacial dysostosis (Orphanet:1131)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)