Nervous System Diseases | Page 12

1250 diseases found in 13 pages

S Diseases

Spinocerebellar ataxia 11 Spinocerebellar ataxia 12 Spinocerebellar ataxia 13 Spinocerebellar ataxia 14 Spinocerebellar ataxia 15 Spinocerebellar ataxia 17 Spinocerebellar ataxia 18 Spinocerebellar ataxia 19 and 22 Spinocerebellar ataxia 2 Spinocerebellar ataxia 20 Spinocerebellar ataxia 21 Spinocerebellar ataxia 23 Spinocerebellar ataxia 25 Spinocerebellar ataxia 26 Spinocerebellar ataxia 27 Spinocerebellar ataxia 28 Spinocerebellar ataxia 29 Spinocerebellar ataxia 3 Spinocerebellar ataxia 30 Spinocerebellar ataxia 31 Spinocerebellar ataxia 34 Spinocerebellar ataxia 4 Spinocerebellar ataxia 5 Spinocerebellar ataxia 7 Spinocerebellar ataxia 8 Spinocerebellar ataxia 9 Spinocerebellar ataxia autosomal recessive 3 Spinocerebellar ataxia autosomal recessive 4 Spinocerebellar ataxia autosomal recessive 5 Spinocerebellar ataxia autosomal recessive 6 Spinocerebellar ataxia autosomal recessive 7 Spinocerebellar ataxia autosomal recessive 8 Spinocerebellar ataxia autosomal recessive with axonal neuropathy Spinocerebellar ataxia type 6 Spinocerebellar ataxia with dysmorphism Spinocerebellar ataxia X-linked type 2 Spinocerebellar ataxia X-linked type 3 Spinocerebellar ataxia X-linked type 4 Spinocerebellar degeneration and corneal dystrophy Split hand urinary anomalies spina bifida Split spinal cord malformation Spondyloepiphyseal dysplasia congenita SRD5A3-CDG (CDG-Iq) SSR4-CDG STAC3 Disorder Status epilepticus Steinfeld syndrome Stiff person syndrome Stocco dos Santos syndrome Striatonigral degeneration infantile Sturge-Weber syndrome Subacute sclerosing panencephalitis Subcortical band heterotopia Subependymal giant cell astrocytoma Subependymoma Succinic semialdehyde dehydrogenase deficiency Susac syndrome Symmetrical thalamic calcifications

T Diseases

Tangier disease TANGO2-Related Metabolic Encephalopathy and Arrhythmias Tarlov cysts Tay-Sachs disease Telfer Sugar Jaeger syndrome Tel Hashomer camptodactyly syndrome Temple-Baraitser syndrome Temple syndrome Temporal epilepsy, familial Temtamy syndrome Tethered cord syndrome Thoracic dysplasia hydrocephalus syndrome Thoracic outlet syndromes Thyrotoxic periodic paralysis TMEM165-CDG (CDG-IIk) Toriello-Carey syndrome Tourette syndrome Tranebjaerg Svejgaard syndrome Transverse myelitis Trichinosis Trichorhinophalangeal syndrome type 2 Trigeminal neuralgia Triosephosphate isomerase deficiency Triple A syndrome Troyer syndrome Tuberous sclerosis Tubular aggregate myopathy Tumefactive multiple sclerosis Typical congenital nemaline myopathy Tyrosine hydroxylase deficiency Tyrosinemia type 1

U Diseases

Ullrich congenital muscular dystrophy Unverricht-Lundborg disease

V Diseases

Van Benthem-Driessen-Hanveld syndrome Van Den Bosch syndrome Variant Creutzfeldt-Jakob disease Variegate porphyria Vein of Galen aneurysm Vici syndrome Viljoen Kallis Voges syndrome Visual snow syndrome VLCAD deficiency

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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