Abnormality of the pulmonary artery
Symptom Information:
| Symptom ID: | HPO:0004414 | ||
| Synonyms: |
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| Quality: | |||
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| 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) MedDRA: |
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| Database Frequency: | 50 / 7739 | ||
| Resource: |
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) |