surfactant metabolism dysfunction, pulmonary, 1

Preferred Label : surfactant metabolism dysfunction, pulmonary, 1;

MeSH note : aka SMDP1; mutations in SFTPB;

MeSH synonym : pulmonary alveolar proteinosis, congenital, 1; interstitial lung disease due to surfactant protein B deficiency; interstitial lung disease, nonspecific, due to surfactant protein B deficiency;

Related MeSH term : Surfactant Protein B Deficiency; Congenital Surfactant Protein-B Deficiency; Pulmonary Surfactant Protein B, Deficiency of;

Details

Origin ID

C566882;

UMLS CUI

C1968602;

Automatic exact mappings (from CISMeF team)
- Surfactant metabolism dysfunction, pulmonary, 4 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Pulmonary Surfactant Metabolism Dysfunction-1 [NCIt concept]
- Surfactant metabolism dysfunction, pulmonary, 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- lung diseases, interstitial [MeSH Descriptor]
- pulmonary alveolar proteinosis [MeSH Descriptor]
- pulmonary surfactant-associated protein B [MeSH Descriptor]
Record concept(s)
- congenital deficiency of pulmonary surfactant protein B [MeSH concept]
- surfactant metabolism dysfunction, pulmonary, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pulmonary Surfactant Metabolism Dysfunction-1 [NCIt concept]
- Surfactant metabolism dysfunction, pulmonary, 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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