Restrictive ventilatory defect

Symptom Information:

Symptom ID: HPO:0002091
Synonyms:
Restrictive lung disease (disorder) [Orphanet:33800]
Restrictive pulmonary disease [Orphanet:33800]
Restrictive lung disease [Orphanet:33800]
Restrictive lung disease [OMIM:Restrictive lung disease]
Interstitial/restrictive pneumopathy/restrictive respiratory syndrome [Orphanet:33800]
Restrictive pulmonary disease [MedDRA:10048667]
Restrictive pulmonary disease [OMIM:Restrictive pulmonary disease]
Quality:
Cross references:
HPO:0002111 "Restrictive respiratory insufficiency" [Orphanet:33800]
Orphanet:33800 "Interstitial/restrictive pneumopathy/restrictive respiratory syndrome" [Orphanet:33800]
OMIM: "Restrictive lung disease" [OMIM:Restrictive lung disease]
OMIM: "Restrictive pulmonary disease" [OMIM:Restrictive pulmonary disease]
UMLS:C0877013 "Restrictive pulmonary disease" [Orphanet:33800]
UMLS:C0085581 "Restrictive lung disease" [Orphanet:33800]
Is a (Direct Parents):
HPO         Abnormality of lung morphology
MedDRA Parenchymal lung disorders NEC
Orphanet Abnormality of the respiratory system
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)
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)