Peripheral pulmonary artery stenosis

Symptom Information:

Symptom ID: HPO:0004969
Synonyms:
peripheral pulmonary stenosis [HPO:0004969]
Peripheral pulmonic stenosis [HPO:0004969]
Peripheral pulmonary artery stenosis [OMIM:Peripheral pulmonary artery stenosis]
Peripheral pulmonary stenosis [OMIM:Peripheral pulmonary stenosis]
Peripheral pulmonic stenosis [OMIM:Peripheral pulmonic stenosis]
Peripheral pulmonary stenosis (in some patients) [OMIM:Peripheral pulmonary stenosis (in some patients)]
Quality:
Cross references:
OMIM: "Peripheral pulmonary artery stenosis" [OMIM:Peripheral pulmonary artery stenosis]
OMIM: "Peripheral pulmonary stenosis" [OMIM:Peripheral pulmonary stenosis]
OMIM: "Peripheral pulmonic stenosis" [OMIM:Peripheral pulmonic stenosis]
OMIM: "Peripheral pulmonary stenosis (in some patients)" [OMIM:Peripheral pulmonary stenosis (in some patients)]
Is a (Direct Parents):
HPO         Pulmonary artery stenosis
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)