Additional Disease Briefs

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

Sydenham chorea

symbrachydactyly of hand and foot, bilateral

symbrachydactyly of hand and foot, unilateral

symbrachydactyly of hands and feet

Also known as: De Smet-Fabry-Fryns syndrome, frints de Smet Fabry Fryns syndrome, symbrachydactyly of the hand and foot

symmetrical thalamic calcifications

Also known as: bilateral symmetrical thalamic gliosis

sympathetic ophthalmia

Also known as: sympathetic ophthalmia, sympathetic uveitis