Abnormal respiratory system morphology
Symptom Information:
Symptom ID: | HPO:0012252 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) MedDRA: |
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Database Frequency: | 14 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant hypophosphatemic rickets | (Orphanet:89937) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
Congenital pulmonary airway malformation | (Orphanet:2444) |
Congenital unilateral hypoplasia of depressor anguli oris | (Orphanet:1166) |
Familial spontaneous pneumothorax | (Orphanet:2903) |
Hydrolethalus | (Orphanet:2189) |
Hypoplasminogenemia | (Orphanet:722) |
Isolated polycystic liver disease | (Orphanet:2924) |
Juvenile xanthogranuloma | (Orphanet:158000) |
Neurofibromatosis type 1 | (Orphanet:636) |
Tracheobronchomegaly | (Orphanet:3347) |
Tuberous sclerosis | (Orphanet:805) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
White forelock with malformations | (Orphanet:2475) |