Knowledge (XXG)

Category:Neurogenetic disorders

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Severe intellectual disability-progressive spastic diplegia syndrome
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The following 27 pages are in this category, out of 27 total.
181:Hereditary sensory and autonomic neuropathy type I 20:This category has only the following subcategory. 205:Mandibulofacial dysostosis-microcephaly syndrome 98:Biotin-thiamine-responsive basal ganglia disease 8: 176:Hereditary sensory and autonomic neuropathy 53:Pages in category "Neurogenetic disorders" 285:TRPM3-related neurodevelopmental disorder 110:Congenital distal spinal muscular atrophy 81:Athabaskan brainstem dysgenesis syndrome 58:This list may not reflect recent changes 268:SYNGAP1-related intellectual disability 171:Hereditary motor and sensory neuropathy 309:Congenital disorders of nervous system 142:Distal spinal muscular atrophy type 1 7: 137:Dentatorubral–pallidoluysian atrophy 115:Congenital fiber type disproportion 62: 33: 22: 14: 154:FBXW7 neurodevelopmental syndrome 1: 71:Allan–Herndon–Dudley syndrome 304:Genetic disorders by system 325: 234:Pontocerebellar hypoplasia 193:Kohlschütter–Tönz syndrome 222:Neotenic complex syndrome 258:Salt and pepper syndrome 132:Dejerine–Sottas disease 37:Spinal muscular atrophy 93:Beck–Fahrner syndrome 246:Roussy–Lévy syndrome 159:Fragile X syndrome 280:Tourette syndrome 76:Asperger syndrome 316: 127:GLUT1 deficiency 42: 35: 324: 323: 319: 318: 317: 315: 314: 313: 294: 293: 292: 291: 290: 289: 272: 250: 238: 226: 214: 210:McLeod syndrome 197: 185: 163: 146: 119: 102: 85: 50: 49: 48: 47: 44: 43: 32: 12: 11: 5: 322: 320: 312: 311: 306: 296: 295: 288: 287: 282: 276: 273: 271: 270: 265: 260: 254: 251: 249: 248: 242: 239: 237: 236: 230: 227: 225: 224: 218: 215: 213: 212: 207: 201: 198: 196: 195: 189: 186: 184: 183: 178: 173: 167: 164: 162: 161: 156: 150: 147: 145: 144: 139: 134: 129: 123: 120: 118: 117: 112: 106: 103: 101: 100: 95: 89: 86: 84: 83: 78: 73: 67: 64: 63: 54: 51: 46: 45: 31: 30: 27: 24: 23: 18: 15: 13: 10: 9: 6: 4: 3: 2: 321: 310: 307: 305: 302: 301: 299: 286: 283: 281: 278: 277: 274: 269: 266: 264: 261: 259: 256: 255: 252: 247: 244: 243: 240: 235: 232: 231: 228: 223: 220: 219: 216: 211: 208: 206: 203: 202: 199: 194: 191: 190: 187: 182: 179: 177: 174: 172: 169: 168: 165: 160: 157: 155: 152: 151: 148: 143: 140: 138: 135: 133: 130: 128: 125: 124: 121: 116: 113: 111: 108: 107: 104: 99: 96: 94: 91: 90: 87: 82: 79: 77: 74: 72: 69: 68: 65: 61: 59: 52: 38: 34: 29: 28: 25: 21: 17:Subcategories 16: 55: 19: 41:(1 C, 21 P) 298:Categories 300:: 60:. 39:‎ 275:T 253:S 241:R 229:P 217:N 200:M 188:K 166:H 149:F 122:D 105:C 88:B 66:A 26:S

Index


Spinal muscular atrophy
This list may not reflect recent changes
Allan–Herndon–Dudley syndrome
Asperger syndrome
Athabaskan brainstem dysgenesis syndrome
Beck–Fahrner syndrome
Biotin-thiamine-responsive basal ganglia disease
Congenital distal spinal muscular atrophy
Congenital fiber type disproportion
GLUT1 deficiency
Dejerine–Sottas disease
Dentatorubral–pallidoluysian atrophy
Distal spinal muscular atrophy type 1
FBXW7 neurodevelopmental syndrome
Fragile X syndrome
Hereditary motor and sensory neuropathy
Hereditary sensory and autonomic neuropathy
Hereditary sensory and autonomic neuropathy type I
Kohlschütter–Tönz syndrome
Mandibulofacial dysostosis-microcephaly syndrome
McLeod syndrome
Neotenic complex syndrome
Pontocerebellar hypoplasia
Roussy–Lévy syndrome
Salt and pepper syndrome
Severe intellectual disability-progressive spastic diplegia syndrome
SYNGAP1-related intellectual disability
Tourette syndrome
TRPM3-related neurodevelopmental disorder

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