Reduced vital capacity
Symptom Information:
| Symptom ID: | HPO:0002792 | ||||
| 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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Reduced vital capacity(HPO:0002792) MedDRA: Investigations(MedDRA:10022891) Respiratory and pulmonary investigations (excl blood gases)(MedDRA:10038668) Respiratory and pulmonary function diagnostic procedures(MedDRA:10037385) Reduced vital capacity(HPO:0002792) |
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| Database Frequency: | 17 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
| Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
| Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
| Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
| Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
| Classic multiminicore myopathy | (Orphanet:324604) |
| Cryptogenic organizing pneumonia | (Orphanet:1302) |
| Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
| Desquamative interstitial pneumonia | (Orphanet:98852) |
| Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
| Distal spinal muscular atrophy type 3 | (Orphanet:139547) |
| Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
| Idiopathic pulmonary fibrosis | (Orphanet:2032) |
| MYOPATHY, MYOSIN STORAGE | (OMIM:608358) |
| NEMALINE MYOPATHY 4 | (OMIM:609285) |
| Non-specific interstitial pneumonia | (Orphanet:91364) |
| Rigid spine syndrome | (Orphanet:97244) |