Bronchomalacia
Symptom Information:
Symptom ID: | HPO:0002780 | ||||
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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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of the upper respiratory tract(HPO:0002087) Abnormality of the tracheobronchial system(HPO:0005607) Abnormality of the bronchi(HPO:0002109) Bronchomalacia(HPO:0002780) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Bronchial disorders (excl neoplasms)(MedDRA:10006436) Bronchial conditions NEC(MedDRA:10006429) Bronchomalacia(HPO:0002780) |
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Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Costello syndrome | (Orphanet:3071) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
Pfeiffer syndrome | (Orphanet:710) |
White forelock with malformations | (Orphanet:2475) |