Restrictive deficit on pulmonary function testing
Symptom Information:
Symptom ID: | HPO:0002111 | ||||||||||||
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) Respiratory insufficiency(HPO:0002093) Restrictive deficit on pulmonary function testing(HPO:0002111) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Restrictive ventilatory defect(HPO:0002091) Restrictive deficit on pulmonary function testing(HPO:0002111) Respiratory insufficiency(HPO:0002093) Restrictive deficit on pulmonary function testing(HPO:0002111) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967) Parenchymal lung disorders NEC(MedDRA:10033979) Restrictive deficit on pulmonary function testing(HPO:0002111) |
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Database Frequency: | 25 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Acute interstitial pneumonia | (Orphanet:79126) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Fibrodysplasia ossificans progressiva | (Orphanet:337) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Leigh syndrome | (Orphanet:506) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Native American myopathy | (Orphanet:168572) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
Pulmonary alveolar microlithiasis | (Orphanet:60025) |
Rigid spine syndrome | (Orphanet:97244) |
SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE | (OMIM:608681) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |