Pulmonary artery atresia

Symptom Information:

Symptom ID: HPO:0004935
Synonyms:
Pulmonary atresia [HPO:0004935]
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]
Pulmonary artery atresia [Orphanet:34420]
Pulmonary artery atresia [OMIM:Pulmonary artery atresia]
Pulmonary atresia [OMIM:Pulmonary atresia]
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:0004960 "Absent pulmonary artery" [Orphanet:34420]
Orphanet:34420 "Pulmonary artery stenosis/absence/hypoplasia of the pulmonary branches" [Orphanet:34420]
OMIM: "Pulmonary artery atresia" [OMIM:Pulmonary artery atresia]
OMIM: "Pulmonary atresia" [OMIM:Pulmonary atresia]
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
HPO         Abnormality of the pulmonary artery
MedDRA Congenital cardiac structural defects NEC
Orphanet obsolete Malformation of the heart and great vessels
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 atresia(HPO:0004935)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Congenital cardiac disorders(MedDRA:10010394)
       Congenital cardiac structural defects NEC(MedDRA:10010397)
          Pulmonary artery atresia(HPO:0004935)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2 (OMIM:606217)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Diabetic embryopathy (Orphanet:1926)
FADD-related immunodeficiency (Orphanet:306550)
Ivemark syndrome (Orphanet:97548)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
Matthew-Wood syndrome (Orphanet:2470)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Nephronophthisis 9 (OMIM:613824)
Pulmonary atresia - intact ventricular septum (Orphanet:1208)
Pulmonary atresia with ventricular septal defect (Orphanet:1207)
Werner syndrome (Orphanet:902)