Pulmonary insufficiency
Symptom Information:
Symptom ID: | HPO:0010444 | |||||||||||||
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) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the heart valves(HPO:0001654) Abnormality of the pulmonary valve(HPO:0001641) Pulmonary insufficiency(HPO:0010444) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Pulmonary valvular disorders(MedDRA:10037445) Pulmonary insufficiency(HPO:0010444) |
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Database Frequency: | 11 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Jeune syndrome | (Orphanet:474) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
MUNGAN SYNDROME | (OMIM:611376) |
Nephronophthisis 2 | (OMIM:602088) |
OSTEOGENESIS IMPERFECTA, TYPE II | (OMIM:166210) |
Osteogenesis imperfecta type 2 | (Orphanet:216804) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |
Tropical endomyocardial fibrosis | (Orphanet:75565) |