Atelectasis
Symptom Information:
Symptom ID: | HPO:0100750 | ||||||||||||||||
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) 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) |
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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) |