Abnormality of the pulmonary artery

Symptom Information:

Symptom ID: HPO:0004414
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the pulmonary vasculature
Is a (Whole tree): HPO:
    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)
Database Frequency: 50 / 7739

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
3q29 microdeletion syndrome (Orphanet:65286)
8p23.1 microdeletion syndrome (Orphanet:251071)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Adams-Oliver syndrome (Orphanet:974)
Alagille syndrome (Orphanet:52)
Aniridia - cerebellar ataxia - intellectual deficit (Orphanet:1065)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Brachydactyly-long thumb syndrome (Orphanet:2946)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Congenital pulmonary valve stenosis (Orphanet:3189)
Congenital rubella syndrome (Orphanet:290)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Congenital unilateral pulmonary hypoplasia (Orphanet:2258)
Conotruncal heart malformations (Orphanet:2445)
Diabetic embryopathy (Orphanet:1926)
Duodenal atresia (Orphanet:1203)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Gastrocutaneous syndrome (Orphanet:2069)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Heart defects - limb shortening (Orphanet:1354)
Juvenile polyposis syndrome (Orphanet:2929)
Kallmann syndrome - heart disease (Orphanet:2326)
Keutel syndrome (Orphanet:85202)
Kleefstra syndrome (Orphanet:261494)
Klippel-Trénaunay syndrome (Orphanet:90308)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lowry-MacLean syndrome (Orphanet:2409)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
PAGOD syndrome (Orphanet:991)
PHAVER syndrome (Orphanet:2876)
Pericardial and diaphragmatic defect (Orphanet:2847)
Peters-plus syndrome (Orphanet:709)
Pulmonary atresia - intact ventricular septum (Orphanet:1208)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Recombinant 8 syndrome (Orphanet:96167)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Uhl anomaly (Orphanet:3403)
Waardenburg syndrome type 2 (Orphanet:895)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
X-linked mandibulofacial dysostosis (Orphanet:1131)