Search results for alexander disease

322 hits were found for alexander disease

# Family MCID Name MIFTS Score
1
ALX003 Alexander Disease 59 11.994
2
P ALZ034 Alzheimer Disease 88 0.263
3
P LKD001 Leukodystrophy 59 0.256
4
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.181
5
P TRM003 Tremor 54 0.151
6
HMP009 Haemophilus Influenzae 43 0.145
7
P PRK057 Parkinson Disease, Late-Onset 78 0.142
8
BCK006 Back Pain 42 0.139
9
DYS073 Dysphagia 50 0.134
10
SKN016 Skin Disease 63 0.124
11
CRB039 Cerebrovascular Disease 67 0.120
12
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.116
13
P MGL013 Megalencephaly 45 0.114
14
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.114
15
P MYC033 Myoclonus 46 0.114
16
SPS057 Spasticity 45 0.114
17
P DMN002 Dementia 66 0.113
18
ISC004 Ischemia 58 0.110
19
LVR012 Liver Cirrhosis 62 0.110
20
P ENC018 Encephalopathy 61 0.109
21
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.108
22
P VSC011 Vasculitis 62 0.104
23
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.104
24
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.103
25
P ENC004 Encephalitis 61 0.102
26
ATN005 Autonomic Dysfunction 46 0.101
27
P HYD006 Hydrocephalus 66 0.101
28
c SPN225 Spondyloarthropathy 1 73 0.099
29
PTH003 Pathologic Nystagmus 52 0.098
30
P DRR001 Diarrhea 55 0.098
31
PPT005 Peptic Ulcer Disease 59 0.098
32
P RSP003 Respiratory Failure 74 0.097
33
P SZR006 Seizure Disorder 56 0.097
34
P LTR001 Lateral Sclerosis 54 0.095
35
VSL002 Visual Epilepsy 59 0.094
36
CNG034 Congestive Heart Failure 69 0.094
37
P SLP006 Sleep Apnea 69 0.094
38
P SCL018 Scoliosis 60 0.093
39
c ACT027 Acute Pancreatitis 60 0.090
40
PRP016 Paraplegia 52 0.089
41
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.089
42
P DYS154 Dystonia 65 0.089
43
ATH013 Atherosclerosis Susceptibility 65 0.089
44
P HYP265 Hypotonia 43 0.088
45
P AST007 Astrocytoma 51 0.088
46
P SYP003 Syphilis 58 0.088
47
P LPS004 Lupus Erythematosus 61 0.087
48
P MVM001 Movement Disease 63 0.087
49
P GLM045 Glioma 63 0.086
50
GLL048 Glial Tumor 45 0.085
51
P MYP004 Myopathy 70 0.085
52
P LYM118 Lymphoma 68 0.084
53
SPN051 Spondylitis 51 0.084
54
HLX001 Helix Syndrome 47 0.083
55
P MTR014 Motor Neuron Disease 65 0.083
56
HNS001 Hansen's Disease 34 0.082
57
INF009 Inflammatory Spondylopathy 31 0.082
58
P NRP001 Neuropathy 56 0.082
59
ANR007 Anorexia Nervosa 63 0.081
60
DRM006 Dermatitis 61 0.081
61
AGN016 Aging 56 0.080
62
c CNT035 Central Nervous System Disease 52 0.079
63
WST005 West Nile Virus 54 0.079
64
IMP005 Impotence 52 0.079
65
AST005 Asthma 76 0.078
66
PRT036 Peritonitis 64 0.078
67
APH002 Aphasia 57 0.077
68
P LPR021 Leprosy 3 69 0.077
69
c HPT016 Hepatitis B 59 0.077
70
P MLT020 Multiple Sclerosis 72 0.076
71
47X002 47,xyy 49 0.076
72
CYT002 Cytokine Deficiency 42 0.075
73
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.075
74
PLG002 Plague 63 0.074
75
CNS004 Constipation 58 0.074
76
GTR002 Goiter 53 0.073
77
STR067 Stroke, Ischemic 81 0.073
78
ADN018 Adenoma 59 0.073
79
MSL001 Measles 62 0.072
80
CRB037 Cerebral Palsy 69 0.072
81
P PNC044 Pancreatitis 61 0.071
82
P FRN006 Frontotemporal Dementia 68 0.071
83
HMN044 Human Immunodeficiency Virus Type 1 71 0.071
84
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.071
85
PRP030 Purpura 54 0.070
86
c SVR001 Severe Acute Respiratory Syndrome 62 0.070
87
THY029 Thyroid Carcinoma 59 0.070
88
SPS019 Spastic Paraparesis 38 0.069
89
PRT058 Pure Autonomic Failure 59 0.069
90
P HPT023 Hepatocellular Carcinoma 100 0.068
91
TYP007 Typhoid Fever 63 0.068
92
P PNM007 Pneumonia 68 0.068
93
ATS010 Autosomal Recessive Disease 48 0.068
94
ALC007 Alcohol Dependence 66 0.068
95
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.068
96
P SLP005 Sleep Disorder 59 0.067
97
P BLD134 Bladder Cancer 79 0.066
98
P EPL164 Epilepsy 71 0.066
99
P PMP001 Pemphigus 54 0.065
100
LSH001 Leishmaniasis 63 0.065
101
CNT047 Contact Dermatitis 58 0.064
102
WST001 West Syndrome 61 0.064
103
CHR073 Choreatic Disease 52 0.064
104
MLT157 Multiple System Atrophy 1 70 0.064
105
P MTC069 Mitochondrial Disorders 56 0.064
106
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.064
107
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.064
108
TRM010 Traumatic Brain Injury 51 0.063
109
P KLZ004 Kala-Azar 1 41 0.063
110
P NRV007 Nervous System Disease 66 0.063
111
BRR014 Barrett Esophagus 65 0.063
112
BRC012 Brucellosis 64 0.063
113
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.062
114
BLL006 Bullous Pemphigoid 62 0.062
115
KHL003 Kohlschutter-Tonz Syndrome 65 0.062
116
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.062
117
P TRC086 Trichohepatoenteric Syndrome 1 62 0.061
118
SVR004 Severe Combined Immunodeficiency 73 0.061
119
ADL002 Adult Syndrome 70 0.061
120
P TMP001 Temporal Lobe Epilepsy 50 0.060
121
PRT037 Pertussis 65 0.060
122
BRN071 Brain Injury 49 0.060
123
TXC005 Toxic Shock Syndrome 62 0.060
124
THR013 Thoracic Outlet Syndrome 54 0.060
125
P DYS021 Dysautonomia 39 0.060
126
c PRM038 Primary Agammaglobulinemia 44 0.060
127
NTR005 Nutritional Deficiency Disease 62 0.060
128
ERD001 Erdheim-Chester Disease 53 0.060
129
ACN002 Acanthosis Nigricans 60 0.059
130
DNT012 Dental Caries 53 0.059
131
INT075 Intracranial Hypertension 53 0.059
132
c WST009 West Nile Virus Encephalitis 20 0.059
133
P ANR048 Aniridia 1 63 0.058
134
P MCR010 Microcephaly 59 0.058
135
P SNS001 Sensorineural Hearing Loss 60 0.058
136
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.058
137
MLR004 Malaria 81 0.058
138
ACT064 Acute Necrotizing Encephalitis 33 0.058
139
ATX010 Ataxia Neuropathy Spectrum 34 0.057
140
ART002 Arts Syndrome 64 0.057
141
BLD137 Blood Group--Ahonen 16 0.057
142
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.057
143
PNM008 Pneumothorax 56 0.057
144
P ANG001 Angelman Syndrome 69 0.056
145
P ATX030 Ataxia-Telangiectasia 82 0.056
146
MDD011 Mood Disorder 62 0.056
147
P BPL003 Bipolar Disorder 56 0.056
148
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.055
149
P SPS008 Spastic Ataxia 41 0.055
150
AND002 Androgen Insensitivity Syndrome 66 0.055
151
SYN036 Syncope 45 0.055
152
OCL069 Ocular Motor Apraxia 51 0.054
153
PST028 Post-Traumatic Stress Disorder 58 0.054
154
P AXN002 Axenfeld-Rieger Syndrome 59 0.054
155
ATX019 Ataxia with Vitamin E Deficiency 42 0.054
156
P CNR004 Cone-Rod Dystrophy 2 73 0.054
157
P KRB001 Krabbe Disease 69 0.054
158
ALR002 Al-Raqad Syndrome 33 0.053
159
ACT084 Acute Stress Disorder 47 0.053
160
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.053
161
PMP006 Pemphigus Vulgaris, Familial 57 0.052
162
ART001 Arterial Tortuosity Syndrome 66 0.052
163
BRG013 Buerger Disease 58 0.052
164
P ALP106 Alport Syndrome 1, X-Linked 55 0.052
165
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.052
166
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.052
167
CRP001 Carpal Tunnel Syndrome 67 0.052
168
CRT033 Corticobasal Degeneration 57 0.052
169
APR001 Apraxia 52 0.051
170
P PLY017 Polyarteritis Nodosa 58 0.051
171
MYC088 Mycobacterium Avium Complex Infections 29 0.050
172
P ACR001 Aicardi-Goutieres Syndrome 62 0.050
173
c PNS012 Paine Syndrome 61 0.050
174
P KDN017 Kidney Cancer 60 0.050
175
PRS047 Prostatitis 56 0.050
176
HPT082 Hepatic Adenomas, Familial 44 0.050
177
ADP007 Adie Pupil 39 0.050
178
HNM002 Hinman Syndrome 27 0.050
179
c MLG084 Malignant Fibrous Histiocytoma 63 0.050
180
SBC016 Subacute Delirium 44 0.050
181
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.050
182
PPT002 Peptic Ulcer Perforation 36 0.050
183
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.050
184
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.050
185
STT041 Stuttering 52 0.050
186
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.049
187
AND005 Androgen Insensitivity Syndrome, Mild 19 0.049
188
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.049
189
FSC004 Fasciitis 50 0.049
190
P LRY019 Laryngitis 52 0.049
191
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.049
192
MSC007 Muscle Hypertrophy 64 0.049
193
c BCT013 Bacterial Pneumonia 48 0.049
194
c HYD064 Hydrocephalus, Congenital, 1 48 0.048
195
c BLD140 Blood Group, I System 32 0.048
196
ADR007 Adrenoleukodystrophy 75 0.048
197
P CRV039 Cervicitis 49 0.048
198
ACT049 Acute Disseminated Encephalomyelitis 51 0.048
199
CRB009 Cerebritis 37 0.048
200
OBS004 Obstructive Hydrocephalus 46 0.048
201
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.048
202
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
203
HDN002 Head Injury 46 0.047
204
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.047
205
MTY003 Mutyh Polyposis 30 0.047
206
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 50 0.047
207
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.047
208
HRW001 Hair Whorl 36 0.047
209
LGH007 Leigh Syndrome 70 0.047
210
P PTS002 Ptosis 53 0.047
211
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.046
212
STT001 Status Epilepticus 60 0.046
213
CNV004 Canavan Disease 61 0.046
214
MLK003 Melkersson-Rosenthal Syndrome 45 0.046
215
PPL049 Papillon-Lefevre Syndrome 65 0.046
216
NRN002 Neuronitis 32 0.045
217
HMP005 Hemiplegia 55 0.045
218
NCR007 Necrotizing Fasciitis 48 0.045
219
c ALZ056 Alzheimer Disease 3 57 0.044
220
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.044
221
P AXN001 Axonal Neuropathy 36 0.044
222
P MTC133 Mitochondrial Myopathy 49 0.044
223
ERL001 Early Myoclonic Encephalopathy 62 0.044
224
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 0.044
225
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.044
226
SPN019 Spondylolisthesis 51 0.044
227
BLD165 Blood Group, Colton System 20 0.043
228
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.043
229
LMY002 Leiomyoma 52 0.043
230
P ATR001 Atrioventricular Septal Defect 55 0.043
231
SPH010 Sphingolipidosis 47 0.043
232
BRN004 Brain Edema 56 0.042
233
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.042
234
P SPP010 Suppressor of Tumorigenicity 3 51 0.042
235
P CRN035 Cranial Nerve Palsy 42 0.042
236
SPC005 Speech Disorder 43 0.041
237
PMP004 Pemphigus Foliaceus 43 0.041
238
TST014 Testicular Cancer 46 0.041
239
CRY020 Cryptogenic Late-Onset Epileptic Spasms 9 0.041
240
ACR006 Aceruloplasminemia 65 0.041
241
P GLM040 Glioma Susceptibility 1 81 0.041
242
P TCD001 Tic Disorder 53 0.041
243
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.040
244
c DNR003 Duane Retraction Syndrome 1 38 0.040
245
P ANX007 Anauxetic Dysplasia 1 46 0.040
246
CRB033 Cerebral Degeneration 42 0.040
247
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.040
248
SDD001 Sudden Infant Death Syndrome 61 0.040
249
HND015 Hand Skill, Relative 33 0.040
250
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.040
251
c MLG068 Malignant Glioma 46 0.039
252
HYP264 Hypertonia 38 0.039
253
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.039
254
HML054 Hemolytic Disease Due to Fetomaternal Alloimmunization 22 0.039
255
P DYS193 Dystonia 11, Myoclonic 55 0.039
256
CLR030 Clear Cell Renal Cell Carcinoma 53 0.039
257
P TRT019 Torticollis 48 0.039
258
RTN003 Retinal Ischemia 50 0.039
259
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 45 0.039
260
LRN003 Learning Disability 49 0.038
261
WRN003 Wernicke Encephalopathy 47 0.038
262
BHR001 Behr Syndrome 51 0.038
263
P PRC019 Precocious Puberty 46 0.038
264
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.038
265
c CHR353 Charcot-Marie-Tooth Disease, Axonal, Type 2l 40 0.038
266
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.038
267
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.037
268
PST027 Postencephalitic Parkinson Disease 46 0.037
269
c LTN004 Late-Onset Retinal Degeneration 59 0.037
270
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.037
271
CRT012 Cortical Blindness 37 0.037
272
ACH004 Achondroplasia 66 0.037
273
P GNT009 Giant Axonal Neuropathy 45 0.037
274
MYF001 Myofibroma 45 0.037
275
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 57 0.037
276
P RRN010 Rare Neurodegenerative Disease 20 0.037
277
NRM022 Neurometabolic Disease 25 0.036
278
P BNG030 Benign Ependymoma 60 0.036
279
WST010 West Nile Virus Infection 32 0.036
280
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 50 0.036
281
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.036
282
c MLT009 Multiple Cranial Nerve Palsy 25 0.036
283
PSD001 Pseudobulbar Palsy 42 0.035
284
ADR005 Adrenal Carcinoma 58 0.035
285
DLS001 Delusional Disorder 47 0.035
286
GGN002 Gigantism 33 0.035
287
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.035
288
CRT008 Carotid Artery Dissection 33 0.035
289
EXT022 Exotropia 41 0.035
290
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 60 0.034
291
c CNT075 Central Precocious Puberty 46 0.034
292
ACR039 Acromegaloid Hypertrichosis Syndrome 25 0.034
293
ALT003 Alternating Exotropia 34 0.034
294
c DST106 Distal Hereditary Motor Neuronopathy Type 2 34 0.033
295
P STS008 Sotos Syndrome 1 61 0.033
296
EPD050 Epidermolysis Bullosa Simplex with Muscular Dystrophy 56 0.033
297
SBP001 Subependymal Giant Cell Astrocytoma 49 0.033
298
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 35 0.033
299
c MYP072 Myopathy, Myofibrillar, 1 54 0.033
300
c SPL067 Split-Hand/foot Malformation 1 46 0.033
301
c LKD008 Leukodystrophy, Hypomyelinating, 4 34 0.033
302
c MYP082 Myopathy, Myofibrillar, 2 41 0.032
303
HYP007 Hypermobility Syndrome 36 0.032
304
DYS140 Dyskinesia, Familial, with Facial Myokymia 33 0.032
305
P BRN035 Brain Stem Glioma 52 0.032
306
MDD003 Middle Cerebral Artery Infarction 36 0.032
307
c NRN018 Neuronopathy, Distal Hereditary Motor, Type Iic 35 0.032
308
c CTR115 Cataract 16, Multiple Types 37 0.032
309
HYP707 Hypertrophic Olivary Degeneration 17 0.032
310
c MYP079 Myopathy, Myofibrillar, 5 46 0.032
311
c BNG006 Benign Familial Neonatal Epilepsy 50 0.032
312
c CLR102 Ciliary Dyskinesia, Primary, 17 28 0.031
313
EXT039 Extrapontine Myelinolysis 18 0.031
314
P PST016 Posterior Polar Cataract 26 0.031
315
MLT105 Multiple System Atrophy, Cerebellar Type 29 0.031
316
PRM284 Primitive Neuroectodermal Tumor of the Cervix Uteri 24 0.031
317
VST003 Vestibular Nystagmus 25 0.031
318
CTN012 Cutaneous Leiomyosarcoma 29 0.030
319
MDD001 Middle Cranial Fossa Meningioma 22 0.030
320
ERL037 Early-Onset Lamellar Cataract 15 0.030
321
ANG050 Angiocentric Glioma 28 0.030
322
RPT006 Repetitive Stress Injuries 10 0.029
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