Peripheral pulmonary artery stenosis
Symptom Information:
Symptom ID: | HPO:0004969 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) Peripheral pulmonary artery stenosis(HPO:0004969) MedDRA: |
||||||
Database Frequency: | 9 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alagille syndrome due to a NOTCH2 point mutation | (Orphanet:261629) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Isobutyryl-CoA dehydrogenase deficiency | (Orphanet:79159) |
Keutel syndrome | (Orphanet:85202) |
Williams syndrome | (Orphanet:904) |
Zunich-Kaye syndrome | (Orphanet:3474) |