Nervous%20System%20Disorders
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Records Return:
(54)
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Description | Omim Number | Sample Count |
ALEXANDER DISEASE; ALXDRD | 203450 | 3 |
ALZHEIMER DISEASE; AD | 104300 | 2 |
AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1 | 105400 | 9 |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1 | 213600 | 1 |
CANAVAN DISEASE | 271900 | 5 |
CEROID LIPOFUSCINOSIS, NEURONAL, 1; CLN1 | 256730 | 13 |
CEROID LIPOFUSCINOSIS, NEURONAL, 2; CLN2 | 204500 | 11 |
CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3 | 204200 | 6 |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D | 601472 | 1 |
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A | 118220 | 1 |
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B | 118200 | 1 |
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1 | 302800 | 6 |
DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; DRPLA | 125370 | 3 |
DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 3; DEE3 | 609304 | 1 |
EPILEPSY, IDIOPATHIC GENERALIZED; EIG | 600669 | 5 |
EPILEPSY, MYOCLONIC JUVENILE; EJM | 254770 | 3 |
FETAL AKINESIA DEFORMATION SEQUENCE 1; FADS1 | 208150 | 1 |
FRIEDREICH ATAXIA; FRDA | 229300 | 53 |
GILLES DE LA TOURETTE SYNDROME; GTS | 137580 | 55 |
HUNTINGTON DISEASE; HD | 143100 | 147 |
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