Pulmonary artery hypoplasia
Symptom Information:
Symptom ID: | HPO:0004971 | ||||||||||||||||||||||||||||||||
Synonyms: |
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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 hypoplasia(HPO:0004971) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Site specific necrosis and vascular insufficiency NEC(MedDRA:10052781) Pulmonary artery hypoplasia(HPO:0004971) Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Pulmonary valvular disorders(MedDRA:10037445) Pulmonary artery hypoplasia(HPO:0004971) |
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Database Frequency: | 15 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Cardiomyopathy, dilated, 1S | (OMIM:613426) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Keutel syndrome | (Orphanet:85202) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
MICROPHTHALMIA, SYNDROMIC 9 | (OMIM:601186) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Nephronophthisis 16 | (OMIM:615382) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
VENTRICULAR SEPTAL DEFECT 1 | (OMIM:614429) |
VENTRICULAR SEPTAL DEFECT 3 | (OMIM:614432) |
Werner syndrome | (Orphanet:902) |