Restrictive deficit on pulmonary function testing

Symptom Information:

Symptom ID: HPO:0002111
Synonyms:
Restrictive deficit on pulmonary function tests [HPO:0002111]
Restrictive respiratory disease [HPO:0002111]
Restrictive respiratory syndrome [HPO:0002111]
Restrictive lung disease [Orphanet:33800]
Restrictive lung disease (disorder) [Orphanet:33800]
Restrictive pulmonary disease [Orphanet:33800]
Restrictive respiratory disease [OMIM:Restrictive respiratory disease]
Restrictive respiratory insufficiency [OMIM:Restrictive respiratory insufficiency]
Restrictive respiratory syndrome [OMIM:Restrictive respiratory syndrome]
Interstitial/restrictive pneumopathy/restrictive respiratory syndrome [Orphanet:33800]
Restrictive pulmonary disease [MedDRA:10048667]
Restrictive pulmonary disease [OMIM:Restrictive pulmonary disease]
Quality:
Cross references:
HPO:0002091 "Restrictive lung disease" [Orphanet:33800]
Orphanet:33800 "Interstitial/restrictive pneumopathy/restrictive respiratory syndrome" [Orphanet:33800]
OMIM: "Restrictive respiratory disease" [OMIM:Restrictive respiratory disease]
OMIM: "Restrictive respiratory insufficiency" [OMIM:Restrictive respiratory insufficiency]
OMIM: "Restrictive respiratory syndrome" [OMIM:Restrictive respiratory syndrome]
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         Respiratory insufficiency
MedDRA Parenchymal lung disorders NEC
HPO         Restrictive ventilatory defect
Orphanet Abnormality of the respiratory system
Orphanet Restrictive ventilatory defect
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)
                Respiratory insufficiency(HPO:0002093)
                   Restrictive deficit on pulmonary function testing(HPO:0002111)
                Restrictive ventilatory defect(HPO:0002091)
                   Restrictive deficit on pulmonary function testing(HPO:0002111)
          Functional respiratory abnormality(HPO:0002795)
             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)
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)