surfactant metabolism dysfunction, pulmonary, 4

Preferred Label : surfactant metabolism dysfunction, pulmonary, 4;

MeSH note : mutation in CSF2RA;

MeSH synonym : PAP due to CSF2RA deficiency; CSF2RA deficiency; pulmonary alveolar proteinosis, congenital, 4;

Details

Origin ID

C567461;

UMLS CUI

C2677877;

Currated CISMeF NLP mapping
- Surfactant metabolism dysfunction, pulmonary, 4 [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- pulmonary alveolar proteinosis [MeSH Descriptor]
Record concept(s)
- surfactant metabolism dysfunction, pulmonary, 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Surfactant metabolism dysfunction, pulmonary, 4 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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