Pulmonary artery atresia
Symptom Information:
Symptom ID: | HPO:0004935 | |||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) 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) |
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Database Frequency: | 12 / 7739 | |||||||||||
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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) |