Additional Disease Briefs

supranuclear palsy, progressive, 3

Also known as: PSNP3, supranuclear palsy, progressive, 3

supratip dysplasia

supravalvular aortic stenosis

Also known as: SVAS, aortic supravalvular stenosis, supra-valvular aortic stenosis, supravalvar aortic stenosis, supravalvar aortic stenosis, Eisenberg type, supravalvular aortic stenosis, supravalvular aortic stenosis (disease)

supravalvular pulmonary stenosis

Also known as: pulmonary supravalvular stenosis

surfactant metabolism dysfunction, pulmonary, 1

Also known as: SMDP1, interstitial lung disease due to SP-B dysfunction, interstitial lung disease due to surfactant Protein B deficiency, interstitial lung disease, nonspecific, due to surfactant Protein B deficiency, neonatal acute respiratory distress due to SP-B deficiency, neonatal acute respiratory distress due to surfactant protein B deficiency, pulmonary alveolar proteinosis, congenital, 1, pulmonary surfactant protein B, deficiency of, surfactant metabolism dysfunction, pulmonary, 1, surfactant metabolism dysfunction, pulmonary, type 1SMDP1, interstitial lung disease due to SP-B dysfunction, interstitial lung disease due to surfactant Protein B deficiency, interstitial lung disease, nonspecific, due to surfactant Protein B deficiency, neonatal acute respiratory distress due to SP-B deficiency, neonatal acute respiratory distress due to surfactant protein B deficiency, pulmonary alveolar proteinosis, congenital, 1, pulmonary surfactant protein B, deficiency of, surfactant metabolism dysfunction, pulmonary, 1, surfactant metabolism dysfunction, pulmonary, type 1

surfactant metabolism dysfunction, pulmonary, 2

Also known as: SMDP2, desquamative interstitial pneumonitis due to surfactant Protein C deficiency, interstitial lung disease due to surfactant Protein C deficiency, pulmonary alveolar proteinosis, congenital, 2, surfactant metabolism dysfunction, pulmonary, 2

surfactant metabolism dysfunction, pulmonary, 4

Also known as: Csf2Ra deficiency, Pap due to Csf2Ra deficiency, SMDP4, pulmonary alveolar proteinosis, congenital, 4, surfactant metabolism dysfunction, pulmonary, 4, surfactant metabolism dysfunction, pulmonary, type 4

surfactant metabolism dysfunction, pulmonary, 5

Also known as: CSF2RB hereditary pulmonary alveolar proteinosis, Csf2Rb deficiency, Pap due to Csf2Rb deficiency, SMDP5, hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB, pulmonary alveolar proteinosis 5, surfactant metabolism dysfunction, pulmonary, 5, surfactant metabolism dysfunction, pulmonary, type 5

susceptibility to respiratory infections associated with CD8alpha chain mutation

Also known as: CD8 deficiency, familial, familial CD8 deficiency, susceptibility to respiratory infections associated with CD8alpha chain mutation