Absent pulmonary artery

Symptom Information:

Symptom ID: HPO:0004960
Synonyms:
Pulmonary artery atresia [Orphanet:34420]
Congenital atresia of pulmonary artery (disorder) [Orphanet:34420]
Agenesis of pulmonary artery (disorder) [Orphanet:34420]
Pulmonary artery atresia (disorder) [Orphanet:34420]
Agenesis of pulmonary artery [Orphanet:34420]
Absent pulmonary artery [OMIM:Absent pulmonary artery]
Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches [Orphanet:34420]
Pulmonary artery atresia [MedDRA:10037337]
Pulmonary artery atresia (rare) [OMIM:Pulmonary artery atresia (rare)]
Quality:
Cross references:
HPO:0004935 "Pulmonary artery atresia" [Orphanet:34420]
Orphanet:34420 "Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches" [Orphanet:34420]
OMIM: "Absent pulmonary artery" [OMIM:Absent pulmonary artery]
OMIM: "Pulmonary artery atresia (rare)" [OMIM:Pulmonary artery atresia (rare)]
UMLS:C0265905 "Agenesis of pulmonary artery" [Orphanet:34420]
UMLS:C0265908 "Pulmonary artery atresia" [Orphanet:34420]
Is a (Direct Parents):
Orphanet Pulmonic stenosis
Orphanet obsolete Malformation of the heart and great vessels
HPO         Abnormality of the pulmonary artery
MedDRA Congenital cardiac structural defects NEC
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)
                   Absent pulmonary artery(HPO:0004960)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Congenital cardiac disorders(MedDRA:10010394)
       Congenital cardiac structural defects NEC(MedDRA:10010397)
          Absent pulmonary artery(HPO:0004960)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Acro-cardio-facial syndrome (Orphanet:2008)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
Werner syndrome (Orphanet:902)