Directory
Spinal muscular atrophy with arthrogryposis
Spinal muscular atrophy (SMA) with arthrogryposis is a rare genetic disorder characterized by progressive atrophy of the...
Spinal muscular atrophy type 1
Spinal muscular atrophy (SMA) type 1, also known as Werdnig-Hoffmann disease, is a genetic disorder characterized by...
Spinal muscular atrophy type 3
Spinal muscular atrophy type 3 (SMA type 3) is an inherited disorder characterized by progressive atrophy of the...
Spinal muscular atrophy type 2
Spinal muscular atrophy type 2 (SMA type 2) is an inherited disorder that belongs to a spectrum of primary diseases...
Spinal shock
Spinal shock is an acute condition resulting from spinal cord injury that is characterized by temporary loss of consciousness...
Spinocerebellar ataxia
Spinocerebellar ataxia (SCA) is a group of inherited disorders characterized by progressive deterioration of cerebellar func...
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 1 (SCA1) is a genetically determined neurodegenerative disorder that belongs to the spinocerebellar ataxia...
Spinocerebellar ataxia type 10
Spinocerebellar ataxia type 10 (SCA10) is an inherited neurodegenerative disorder that belongs to the group of spinocerebellar ataxias...
Spinocerebellar ataxia type 11
Spinocerebellar ataxia type 11 (SCA11) is an inherited neurodegenerative disorder characterized by progressive...
Spinocerebellar ataxia type 12
Spinocerebellar ataxia type 12 (SCA12) is a genetic disorder that belongs to the group of spinocerebellar ataxias characterized by...
Spinocerebellar ataxia type 13
Spinocerebellar ataxia type 13 (SCA13) is an inherited neurodegenerative disorder that belongs to the spinocerebellar ataxia...
Spinocerebellar ataxia type 14
Spinocerebellar ataxia type 14 (SCA14) is a rare inherited neurodegenerative disease characterized by progressive...
Spinocerebellar ataxia type 15
Spinocerebellar ataxia type 15 (SCA15) is an inherited neurological disorder that belongs to the spinocerebellar ataxia...
Spinocerebellar ataxia type 17
Spinocerebellar ataxia type 17 (SCA17) is an inherited neurodegenerative disorder characterized by progressive a...
Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 2 (SCA2) is an inherited neurodegenerative disorder characterized by progressive...
Spinocerebellar ataxia type 20
Spinocerebellar ataxia type 20 (SCA20) is an inherited neurological disorder that belongs to the group of spinocerebellar...
Spinocerebellar ataxia type 23
Spinocerebellar ataxia type 23 (SCA23) is an inherited neurodegenerative disorder that belongs to the group of spin...
Spinocerebellar ataxia type 27
Spinocerebellar ataxia type 27 (SCA27) is a neurodegenerative disorder belonging to the group of spinocerebellar ataxias characterized by...
Spinocerebellar ataxia type 28
Spinocerebellar ataxia type 28 (SCA28) is an inherited neurological disorder that belongs to the group of spinocerebellar ataxias...
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 29 (SCA29) is a genetic disorder that belongs to the group of spinocerebellar ataxias,...
Spinocerebellar ataxia type 3
Spinocerebellar ataxia type 3 (CA3) is a genetically determined neurological disorder belonging to the group ...
Spinocerebellar ataxia type 31
Spinocerebellar ataxia type 31 (SCA31) is an inherited neurodegenerative disorder that belongs to the spinocerebellar ataxia group...
Spinocerebellar ataxia type 4
Spinocerebellar ataxia type 4 (CA4) is an inherited neurological disorder characterized by progressive ataxia, n...
Spinocerebellar ataxia type 5
Spinocerebellar ataxia type 5 (SCA5) is a genetic neurodegenerative disorder characterized by progressive loss of...
Spinocerebellar ataxia type 6
Spinocerebellar ataxia type 6 (SCA6) is an inherited progressive disorder that belongs to the group of spinocerebellar ataxias...
Spinocerebellar ataxia type 7
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disorder belonging to the spinocerebellar ataxia group...
Spinocerebellar ataxia type 8
Spinocerebellar ataxia type 8 (SCA8) is an inherited neurodegenerative disorder that is predominantly characterized by...
Spinocerebellar degeneration and corneal dystrophy
Spinocerebellar degeneration (SCD) is a group of inherited neurodegenerative diseases that result in progressive...
Splenomegaly
Splenomegaly is an abnormal enlargement of the spleen that can result from a variety of diseases and conditions. This condition...
Spondylocostal dysostosis
Spondylocostal dysostosis (SKD) is a rare inherited disorder characterized by multiple abnormalities of the spinal cord...
