Surfactant metabolism dysfunction, pulmonary, 5
MONDO:0013712Any hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene.
Also known as: CSF2RB hereditary pulmonary alveolar proteinosis, hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB, surfactant metabolism dysfunction, pulmonary, 5, surfactant metabolism dysfunction, pulmonary, type 5, Csf2Rb deficiency, Pap due to Csf2Rb deficiency, SMDP5, pulmonary alveolar proteinosis 5
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Disease
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Lung disorder
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Hereditary disease
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Respiratory system disorder
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Lower respiratory tract disorder
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Human disease
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Pulmonary alveolar proteinosis
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Hereditary pulmonary alveolar proteinosis
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Disease of genetic or genomic mechanism
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