Additional Disease Briefs

silver-Russell syndrome due to maternal uniparental disomy of chromosome 7

Also known as: Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 7, UPD(7)mat

Silverman-Handmaker type dyssegmental dysplasia

Also known as: Anisospondylic Camptomicromelic dwarfism, Silverman-Handmaker type, Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type, DDSH, dyssegmental dwarfism Silverman-Handmaker type, dyssegmental dwarfism, Silverman-Handmaker type, dyssegmental dysplasia Silverman-Handmaker type, dyssegmental dysplasia, Silverman-Handmaker type

SIM1-related Prader-Willi-like syndrome

Also known as: PWS-like due to a point mutation, PWS-like due to point mutation, Prader-Willi-like syndrome due to a point mutation, SIM1-related PWLS

simple cryoglobulinemia

Also known as: cryoglobulinemia type 1

Simpson-Golabi-Behmel syndrome type 1

Also known as: DGSX Golabi-Rosen syndrome, GPC3 Simpson-Golabi-Behmel syndrome, Golabi-Rosen syndrome, SGBS1, Sgbs, Simpson dysmorphia syndrome, Simpson-Golabi-Behmel syndrome caused by mutation in GPC3, Simpson-Golabi-Behmel syndrome type 1, Simpson-Golabi-Behmel syndrome, type 1, Simpson-Golabi-Behmel syndrome, type 1, X-linked recessive, bulldog syndrome, dysplasia gigantism syndrome, X-linked

Simpson-Golabi-Behmel syndrome type 2

Also known as: OFD1 Simpson-Golabi-Behmel syndrome, SGBS2, Sgbs2, Simpson-Golabi-Behmel syndrome caused by mutation in OFD1, Simpson-Golabi-Behmel syndrome, type 2, Simpson-Golabi-Behmel syndrome, type 2, X-linked recessive, lethal variant of Simpson-Golabi-Behmel syndrome

SIN3A-related intellectual disability syndrome

SIN3A-related intellectual disability syndrome due to a point mutation

Sinding-Larsen-Johansson disease

Also known as: Osteochondrosis of patella, aseptic necrosis of patella