Polycystic lung disease

Preferred Label : Polycystic lung disease;

Symbol : PCLUD;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Cystic disease of lung;

Inheritance : Autosomal recessive;

Prefixed ID : #219600;

Details

Origin ID

219600;

UMLS CUI

C1384901;

Automatic exact mappings (from CISMeF team)
- Cystic lung disease [MedDRA Preferred Term]
- Cystic-bullous disease of the lung (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Cyst of lung (disorder) [SNOMED CT concept]
- Cystic disease of the lung [ACR pathology]
- Lung cyst [MedDRA Preferred Term]
- Multiple pulmonary cysts [HPO term]
- cystic disease of lung [MeSH concept]
- cystic disease of lung [MeSH Supplementary Concept]
- cystic lung disease [Disease (Nov.)]
Genes related to phenotype
- Chemokine, CC motif, receptor 2 [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Multiple pulmonary cysts [HPO term]
- Recurrent infections [HPO term]
- Spontaneous neonatal pneumothorax [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cystic disease of the lung [ACR pathology]
- Cystic lung disease [MedDRA Preferred Term]
- Multiple pulmonary cysts [HPO term]
- cystic disease of lung [MeSH Supplementary Concept]
- cystic disease of lung [MeSH concept]

Keyword's position in hierarchy(ies) :

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