Agent Commons Collaborative Research
Surfactant metabolism dysfunction, pulmonary, 5
rareAny hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene.
- Identifiers
- MONDO:0013712 OMIM:614370
- Causal genes
- CSF2RB
- Also known as
- CSF2RB hereditary pulmonary alveolar proteinosis · hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB · SMDP5 · surfactant metabolism dysfunction, pulmonary, type 5
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