Additional Disease Briefs

striatonigral degeneration, childhood-onset

Also known as: Lenk-Ploski syndrome, SNDC, childhood-onset basal ganglia degeneration syndrome, striatonigral Degeneration, childhood-onset, striatonigral degeneration, childhood-onset; SNDC

striatonigral degeneration, infantile, mitochondrial

Also known as: bilateral striatal Necrosis, infantile, mitochondrial, infantile bilateral striatal Necrosis, mitochondrial, striatonigral degeneration, infantile, mitochondrial

stromal corneal dystrophy

Also known as: corneal dystrophy (disease) of substantia propria of cornea, corneal stromal dystrophy, stromal dystrophy, substantia propria of cornea corneal dystrophy (disease)

stromal keratitis

Stromme syndrome

Also known as: CILD31, STROMS, Stromme syndrome, apple peel syndrome with microcephaly and ocular anomalies, apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome, ciliary dyskinesia, primary, 31, ciliary dyskinesia, primary, 31, formerly, ciliary dyskinesia, primary, type 31, jejunal atresia with microcephaly and ocular anomalies, jejunal atresia-microcephaly-ocular anomalies syndrome, lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome, lethal foetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome, primary ciliary dyskinesia 31

strongyloidiasis

Also known as: Anguilluliasis, Anguillulosis, disseminated strongyloidiasis, infection by Strongyloides

struma ovarii

Also known as: struma ovarii, struma ovarii (morphologic abnormality), struma ovarii NOS (morphologic abnormality)

STT3A-congenital disorder of glycosylation

Also known as: CDG Iw, CDG syndrome type Iw, CDG-Iw, CDG1W, STT3A-CDG, STT3A-congenital disorder of glycosylation, congenital disorder of glycosylation type 1w, congenital disorder of glycosylation type Iw, congenital disorder of glycosylation, type Iw, congenital disorder of glycosylation, type Iw, autosomal recessive

STT3B-congenital disorder of glycosylation

Also known as: CDG IX, CDG syndrome type IX, CDG-Ix, CDG1X, STT3B-CDG, STT3B-congenital disorder of glycosylation, carbohydrate deficient glycoprotein syndrome type IX, congenital disorder of glycosylation type 1x, congenital disorder of glycosylation type IX, congenital disorder of glycosylation, type IX