Atelectasis

Symptom Information:

Symptom ID: HPO:0100750
Synonyms:
Pulmonary atelectasis [HPO:0100750]
Atelectasis (disorder) [Orphanet:33600]
Atelectasis [Orphanet:33600]
Atelectasis [OMIM:Atelectasis]
Atelectasia/pulmonary collapse [Orphanet:33600]
Collapse of lung [Orphanet:33600]
Pneumothorax [MedDRA:10035759]
Collapse of lung [MedDRA:10035759]
Pneumothorax (excl traumatic) [MedDRA:10035759]
Pneumothorax NOS [MedDRA:10035759]
Pulmonary collapse [MedDRA:10035759]
Tension pneumothorax [MedDRA:10035759]
Atelectasis [MedDRA:10003598]
Lobar collapse [MedDRA:10003598]
Partial atelectasis [MedDRA:10003598]
Pneumothorax (rare) [OMIM:Pneumothorax (rare)]
Quality:
Cross references:
Orphanet:33600 "Atelectasia/pulmonary collapse" [Orphanet:33600]
OMIM: "Atelectasis" [OMIM:Atelectasis]
OMIM: "Pneumothorax (rare)" [OMIM:Pneumothorax (rare)]
UMLS:C0004144 "Atelectasis" [Orphanet:33600]
Is a (Direct Parents):
MedDRA Parenchymal lung disorders NEC
MedDRA Pneumothorax and pleural effusions NEC
HPO         Abnormality of lung morphology
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)
                Atelectasis(HPO:0100750)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Pleural disorders(MedDRA:10035597)
       Pneumothorax and pleural effusions NEC(MedDRA:10035761)
          Atelectasis(HPO:0100750)
    Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967)
       Parenchymal lung disorders NEC(MedDRA:10033979)
          Atelectasis(HPO:0100750)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
CILIARY DYSKINESIA, PRIMARY, 21 (OMIM:615294)
CILIARY DYSKINESIA, PRIMARY, 29 (OMIM:615872)
Desquamative interstitial pneumonia (Orphanet:98852)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Infant acute respiratory distress syndrome (Orphanet:70587)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
Lymphangioleiomyomatosis (Orphanet:538)
MUCUS INSPISSATION OF RESPIRATORY TRACT (OMIM:253240)
Oculocerebrorenal syndrome (Orphanet:534)
Primary ciliary dyskinesia - retinitis pigmentosa (Orphanet:247522)
ROWLEY-ROSENBERG SYNDROME (OMIM:268500)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Waardenburg syndrome type 3 (Orphanet:896)