Restrictive ventilatory defect
Symptom Information:
Symptom ID: | HPO:0002091 | |||||||
Synonyms: |
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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) Abnormality of lung morphology(HPO:0002088) Restrictive ventilatory defect(HPO:0002091) 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 ventilatory defect(HPO:0002091) |
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Database Frequency: | 46 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Adult Still's disease | (Orphanet:829) |
Adult pulmonary Langerhans cell histiocytosis | (Orphanet:99874) |
Antisynthetase syndrome | (Orphanet:81) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Cogan syndrome | (Orphanet:1467) |
Common variable immunodeficiency | (Orphanet:1572) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Dermatomyositis | (Orphanet:221) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Eosinophilic granuloma | (Orphanet:99871) |
Fibrodysplasia ossificans progressiva | (Orphanet:337) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 3 | (Orphanet:77261) |
Granulomatosis with polyangiitis | (Orphanet:900) |
HERMANSKY-PUDLAK SYNDROME 1 | (OMIM:203300) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Juvenile dermatomyositis | (Orphanet:93672) |
Kawasaki disease | (Orphanet:2331) |
Legionellosis | (Orphanet:549) |
Lyell syndrome | (Orphanet:537) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
Muckle-Wells syndrome | (Orphanet:575) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Polymyositis | (Orphanet:732) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4 | (OMIM:300770) |
Scheie syndrome | (Orphanet:93474) |
Scleroderma | (Orphanet:801) |
Scrub typhus | (Orphanet:83317) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Typhoid | (Orphanet:99745) |