Search results for alzheimer disease familial

604 hits were found for alzheimer disease familial

# Family MCID Name MIFTS Score
1
P ALZ034 Alzheimer Disease 95 12.199
2
c ALZ056 Alzheimer Disease 3 41 6.716
3
c ALZ049 Alzheimer Disease 2 59 6.302
4
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 5.711
5
c ALZ054 Alzheimer Disease 4 43 4.802
6
c ALZ057 Alzheimer Disease 10 21 4.023
7
c ALZ050 Alzheimer Disease 5 44 3.946
8
c ALZ016 Alzheimer Disease 8 22 3.887
9
c ALZ053 Alzheimer Disease 7 21 3.850
10
c ALZ012 Alzheimer Disease 12 20 3.661
11
c ALZ058 Alzheimer Disease 11 19 3.505
12
c ALZ002 Alzheimer Disease Type 1 15 3.044
13
c ERL006 Early-Onset Familial Alzheimer Disease 38 2.271
14
ALZ052 Alzheimer Disease, Familial Early-Onset, with Coexisting Amyloid and Prion Pathology 10 1.550
15
FML202 Familial Alzheimer-Like Prion Disease 12 1.534
16
DMN002 Dementia 68 0.872
17
P ENC018 Encephalopathy 58 0.568
18
AGN016 Aging 65 0.526
19
c CNT035 Central Nervous System Disease 65 0.499
20
NRN002 Neuronitis 43 0.455
21
CRB009 Cerebritis 41 0.368
22
P AMY004 Amyloidosis 69 0.359
23
VSC002 Vascular Dementia 58 0.316
24
FRN006 Frontotemporal Dementia 70 0.254
25
c BLD140 Blood Group, I System 37 0.237
26
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.208
27
MNT002 Mental Depression 60 0.204
28
P PRK057 Parkinson Disease, Late-Onset 78 0.195
29
DWN001 Down Syndrome 70 0.193
30
ART140 Arteries, Anomalies of 51 0.187
31
P NRV007 Nervous System Disease 75 0.186
32
CRB039 Cerebrovascular Disease 68 0.184
33
P HRT032 Heart Disease 80 0.180
34
END072 Endotheliitis 46 0.176
35
c ALZ062 Alzheimer Disease 19 26 0.175
36
PCK003 Pick Disease of Brain 66 0.171
37
ANX010 Anxiety 72 0.169
38
P BRS047 Breast Cancer 100 0.168
39
P SCH015 Schizophrenia 71 0.167
40
P DBT009 Diabetes Mellitus 72 0.165
41
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.163
42
PSY004 Psychotic Disorder 72 0.161
43
SMN008 Semantic Dementia 41 0.161
44
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.157
45
P LTR001 Lateral Sclerosis 58 0.156
46
DMN031 Dementia, Lewy Body 66 0.154
47
P ANR048 Aniridia 1 68 0.153
48
P THY032 Thyroiditis 56 0.153
49
BRC012 Brucellosis 71 0.153
50
APH002 Aphasia 58 0.150
51
P HYP607 Hypercholesterolemia, Familial 81 0.148
52
P CRN018 Coronary Artery Anomaly 69 0.148
53
SPS057 Spasticity 41 0.147
54
ANR038 Anorexia Nervosa 1 21 0.144
55
BLD137 Blood Group--Ahonen 17 0.144
56
VSC007 Vascular Disease 71 0.143
57
P EPL164 Epilepsy 70 0.141
58
P KDN018 Kidney Disease 69 0.140
59
P FML018 Familial Mediterranean Fever 73 0.139
60
CRT072 Creutzfeldt-Jakob Disease 65 0.139
61
RTN023 Retinitis 52 0.139
62
P HYD006 Hydrocephalus 68 0.134
63
ISC004 Ischemia 66 0.134
64
SPS003 Spastic Diplegia 55 0.132
65
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.132
66
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.130
67
P MLT020 Multiple Sclerosis 85 0.130
68
P NRB001 Neuroblastoma 73 0.129
69
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.128
70
P CRB088 Cerebral Atrophy 38 0.128
71
P LKM002 Leukemia 75 0.127
72
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.126
73
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.126
74
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.126
75
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.126
76
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.126
77
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.126
78
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.126
79
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.126
80
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.126
81
PST086 Posterior Cortical Atrophy 38 0.125
82
P ART022 Arthritis 77 0.125
83
P HPT021 Hepatitis 75 0.124
84
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.124
85
P NRP001 Neuropathy 63 0.124
86
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.123
87
PRN023 Prion Disease 51 0.122
88
MVM001 Movement Disease 40 0.121
89
P ART021 Arteriosclerosis 62 0.119
90
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.118
91
SPS019 Spastic Paraparesis 33 0.118
92
HYD061 Hydrocephalus, Normal-Pressure 47 0.117
93
ALR002 Al-Raqad Syndrome 30 0.117
94
P PNC044 Pancreatitis 64 0.117
95
APR001 Apraxia 52 0.115
96
CRT033 Corticobasal Degeneration 51 0.115
97
P LVR013 Liver Disease 76 0.114
98
CLS047 Classic Progressive Supranuclear Palsy Syndrome 25 0.114
99
SLP005 Sleep Disorder 59 0.113
100
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.113
101
PRS047 Prostatitis 59 0.110
102
P CLR023 Colorectal Cancer 98 0.109
103
P CTR002 Cataract 60 0.108
104
BRN071 Brain Injury 54 0.108
105
P RHM011 Rheumatoid Arthritis 91 0.106
106
MDD011 Mood Disorder 64 0.105
107
ATM095 Autoimmune Disease 66 0.104
108
LNG099 Lung Disease 67 0.104
109
MLN008 Melanoma 72 0.100
110
CRH001 Crohn's Disease 80 0.100
111
BSL008 Basal Ganglia Disease 44 0.100
112
AST005 Asthma 83 0.099
113
P TRM003 Tremor 54 0.099
114
SPC010 Speech and Communication Disorders 40 0.098
115
P HYP086 Hypothyroidism 62 0.094
116
HYP266 Hypoxia 61 0.093
117
P DYS021 Dysautonomia 47 0.092
118
HPT082 Hepatic Adenomas, Familial 52 0.092
119
P PRS040 Prostate Cancer 88 0.091
120
P HRP006 Herpes Simplex 70 0.090
121
GRN014 Grn-Related Frontotemporal Dementia 34 0.090
122
P OST002 Osteoporosis 75 0.090
123
P LYM118 Lymphoma 71 0.090
124
MRG013 Mirage Syndrome 44 0.089
125
P MYC007 Myocardial Infarction 81 0.089
126
P MYS005 Myositis 63 0.089
127
ADN018 Adenoma 63 0.089
128
FRN030 Frontotemporal Dementia with Parkinsonism-17 22 0.088
129
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.088
130
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.087
131
THR024 Thrombosis 61 0.086
132
c CHR089 Chronic Kidney Failure 72 0.086
133
P PNM007 Pneumonia 70 0.086
134
MGR028 Migraine with or Without Aura 1 55 0.085
135
PRM153 Primary Progressive Apraxia of Speech 21 0.085
136
P MSC005 Muscular Dystrophy 66 0.085
137
HDC001 Headache 55 0.083
138
P MYP004 Myopathy 69 0.083
139
TRM010 Traumatic Brain Injury 54 0.083
140
CNG034 Congestive Heart Failure 74 0.083
141
LPD008 Lipid Metabolism Disorder 59 0.082
142
BNS003 Binswanger's Disease 43 0.082
143
MTR014 Motor Neuron Disease 62 0.082
144
P DYS154 Dystonia 61 0.081
145
INC002 Inclusion Body Myositis 64 0.081
146
MLT157 Multiple System Atrophy 1 65 0.080
147
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.080
148
P GRF003 Graft-Versus-Host Disease 72 0.080
149
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.079
150
P RNG031 Ring Chromosome Y Syndrome 29 0.079
151
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.079
152
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.079
153
BRN106 Burns 57 0.078
154
SPC005 Speech Disorder 44 0.078
155
CRB085 Cerebral Hemorrhage 47 0.078
156
c TRC078 Trichohepatoenteric Syndrome 2 34 0.078
157
MYC033 Myoclonus 40 0.078
158
c MCL042 Macular Degeneration, Age-Related, 1 79 0.077
159
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.077
160
P SLP006 Sleep Apnea 65 0.077
161
c CHR579 Chiari Malformation Type Ii 42 0.077
162
P MJR001 Major Depressive Disorder 70 0.077
163
P HNT016 Huntington Disease 78 0.076
164
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.076
165
P CLC063 Celiac Disease 1 65 0.076
166
c ESS001 Essential Tremor 58 0.076
167
CHR008 Choroiditis 47 0.076
168
P PRD008 Periodontitis 67 0.075
169
NRM005 Neuromuscular Disease 60 0.075
170
GT001 Gout 60 0.074
171
WLS001 Wilson Disease 72 0.074
172
P BPL003 Bipolar Disorder 61 0.074
173
c ALZ045 Alzheimer Disease 9 22 0.074
174
LGP003 Logopenic Progressive Aphasia 23 0.074
175
CLT003 Colitis 63 0.073
176
FTL002 Fatal Familial Insomnia 49 0.073
177
INS024 Insulin-Like Growth Factor I 83 0.072
178
P ENC004 Encephalitis 66 0.072
179
P OPN001 Open-Angle Glaucoma 51 0.072
180
GLC008 Glucose Metabolism Disease 38 0.072
181
LKD001 Leukodystrophy 57 0.071
182
P NMN002 Niemann-Pick Disease 68 0.071
183
P ADN016 Adenocarcinoma 71 0.071
184
ALP046 Alport Syndrome, X-Linked 74 0.071
185
BHV002 Behavioral Variant of Frontotemporal Dementia 41 0.070
186
P CRV039 Cervicitis 49 0.070
187
CHR073 Choreatic Disease 40 0.070
188
P GLM045 Glioma 61 0.069
189
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.069
190
P PRP029 Porphyria 62 0.069
191
P MYL006 Myeloid Leukemia 69 0.069
192
P PSR002 Psoriasis 65 0.069
193
ALC007 Alcohol Dependence 65 0.069
194
P SZR006 Seizure Disorder 55 0.068
195
VRL011 Viral Infectious Disease 64 0.068
196
P MCR010 Microcephaly 57 0.068
197
P MYP006 Myopia 56 0.067
198
c BRN108 Branchiootic Syndrome 1 47 0.066
199
CYS001 Cystic Fibrosis 85 0.066
200
P MTC003 Metachromatic Leukodystrophy 72 0.066
201
ATM052 Autoimmune Disease 1 30 0.066
202
P HPT023 Hepatocellular Carcinoma 94 0.066
203
P TYS001 Tay-Sachs Disease 71 0.066
204
ULC004 Ulcerative Colitis 80 0.065
205
c MTR002 Mitral Valve Insufficiency 46 0.065
206
P AGN002 Agnosia 61 0.064
207
HYP060 Hyperinsulinism 56 0.064
208
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.064
209
RHM027 Rheumatic Disease 62 0.064
210
ACR006 Aceruloplasminemia 65 0.063
211
P MNN013 Meningitis 71 0.063
212
ATN005 Autonomic Dysfunction 51 0.063
213
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.063
214
BRN080 Brain Ischemia 45 0.063
215
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.063
216
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.062
217
HDN002 Head Injury 48 0.062
218
PRD007 Periodontal Disease 64 0.062
219
P TRC086 Trichohepatoenteric Syndrome 1 54 0.062
220
CRB193 Cerebral Amyloid Angiopathy, App-Related 36 0.062
221
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.061
222
RTN018 Retinal Disease 56 0.061
223
GLC003 Glucose Intolerance 58 0.061
224
PRP016 Paraplegia 53 0.061
225
IDM001 Ideomotor Apraxia 38 0.060
226
SNL009 Senile Plaque Formation 26 0.060
227
P RTN016 Retinal Degeneration 56 0.060
228
ALZ029 Alzheimer Disease Mitochondrial 25 0.060
229
BRS051 Breast Disease 67 0.060
230
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.059
231
P LYM026 Lymphoblastic Leukemia 66 0.059
232
P ANX007 Anauxetic Dysplasia 1 36 0.059
233
c GLC092 Glaucoma, Primary Open Angle 58 0.059
234
DYS073 Dysphagia 47 0.059
235
ALX001 Alexia 44 0.059
236
GTP001 Gait Apraxia 38 0.059
237
VSL003 Visual Agnosia 33 0.059
238
MTH009 Mouth Disease 64 0.058
239
APN008 Apnea, Obstructive Sleep 67 0.058
240
P INF038 Influenza 77 0.057
241
CRB008 Cerebral Atherosclerosis 42 0.057
242
P HYP750 Hypertriglyceridemia, Familial 55 0.056
243
c LKM061 Leukemia, Acute Myeloid 81 0.056
244
PHN003 Phenylketonuria 73 0.056
245
P OLV001 Olivopontocerebellar Atrophy 51 0.056
246
ADP007 Adie Pupil 41 0.056
247
NRL016 Neural Tube Defects 79 0.055
248
PST011 Pustulosis of Palm and Sole 47 0.055
249
MYL069 Myeloma, Multiple 86 0.055
250
OVR063 Overnutrition 53 0.055
251
RST001 Restless Legs Syndrome 54 0.055
252
OBS002 Obsessive-Compulsive Disorder 68 0.055
253
P DRR001 Diarrhea 60 0.055
254
c CRB176 Cerebral Amyloid Angiopathy, Itm2b-Related, 1 35 0.054
255
P WSK001 Wiskott-Aldrich Syndrome 76 0.054
256
HMT018 Hematopoietic Stem Cell Transplantation 58 0.054
257
TMP001 Temporal Lobe Epilepsy 54 0.054
258
P EXN002 Exanthem 62 0.054
259
GNR004 Generalized Anxiety Disorder 53 0.054
260
P INF032 Infertility 59 0.053
261
P THR014 Thrombocytopenia 65 0.053
262
INT074 Intracranial Arteriosclerosis 14 0.053
263
PRG033 Progressive Non-Fluent Aphasia 48 0.053
264
P NRC002 Narcolepsy 64 0.053
265
P PRS038 Personality Disorder 65 0.053
266
SCR011 Scrapie 40 0.052
267
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.052
268
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.052
269
SYN058 Synucleinopathy 42 0.052
270
P ATX030 Ataxia-Telangiectasia 80 0.052
271
ALX003 Alexander Disease 58 0.052
272
OST012 Osteoarthritis 88 0.052
273
PRP030 Purpura 61 0.052
274
CHL123 Chlamydia 64 0.052
275
P FCL005 Focal Segmental Glomerulosclerosis 60 0.051
276
c FML346 Familial Adenomatous Polyposis 1 63 0.051
277
P ALC004 Alcohol Abuse 63 0.051
278
PLT031 Platelet Membrane Fluidity 29 0.051
279
RCK004 Rickets 63 0.051
280
CRD119 Cardiac Arrest 63 0.051
281
AND002 Androgen Insensitivity Syndrome 57 0.050
282
HDR002 Hidradenitis Suppurativa 54 0.050
283
HDR003 Hidradenitis 47 0.050
284
ADR007 Adrenoleukodystrophy 72 0.050
285
LYM019 Lymphosarcoma 58 0.050
286
MLR004 Malaria 86 0.050
287
P MYL005 Myelofibrosis 75 0.050
288
c HPT016 Hepatitis B 68 0.049
289
ILT001 Ileitis 52 0.049
290
PRD004 Prediabetes Syndrome 46 0.049
291
DMY004 Demyelinating Disease 58 0.049
292
TTR011 Tetraploidy 49 0.049
293
RTN209 Retinoschisis 1, X-Linked, Juvenile 56 0.049
294
EXF001 Exfoliation Syndrome 55 0.048
295
ICH054 Ichthyosis, X-Linked 59 0.048
296
MNN009 Meningoencephalitis 49 0.048
297
P ANG001 Angelman Syndrome 61 0.048
298
HYP066 Hyperglycemia 64 0.048
299
P CNJ013 Conjunctivitis 67 0.048
300
KR002 Kuru 39 0.048
301
HML018 Homologous Wasting Disease 18 0.048
302
P MYC026 Myoclonus Epilepsy 35 0.048
303
SCH014 Schistosomiasis 62 0.048
304
P SDR002 Siderosis 48 0.048
305
ETN001 Eating Disorder 61 0.047
306
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.047
307
SYN036 Syncope 46 0.047
308
SNS001 Sensorineural Hearing Loss 59 0.047
309
NRS003 Neurosyphilis 44 0.047
310
PST028 Post-Traumatic Stress Disorder 59 0.047
311
BLD163 Blood Group, Dombrock System 23 0.047
312
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.047
313
c WLM011 Wilms Tumor 6 44 0.047
314
PRM290 Premature Centromere Division 19 0.047
315
AGR018 Agraphia 38 0.046
316
ENT004 Enthesopathy 38 0.046
317
LVR012 Liver Cirrhosis 73 0.046
318
P SCK002 Sick Sinus Syndrome 53 0.046
319
P HRP009 Herpes Simplex Encephalitis 50 0.046
320
BLL006 Bullous Pemphigoid 64 0.046
321
GLB002 Glioblastoma 74 0.046
322
HMT002 Hematologic Cancer 64 0.046
323
c BLM008 Bulimia Nervosa 2 53 0.045
324
CYT008 Cytomegalovirus Infection 57 0.045
325
P FRG001 Fragile X Syndrome 69 0.045
326
LRN003 Learning Disability 49 0.045
327
CRB033 Cerebral Degeneration 42 0.045
328
SPR066 Superficial Siderosis 40 0.045
329
P SBS003 Substance Abuse 57 0.045
330
DFC004 Deficiency Anemia 62 0.045
331
FXF002 Fox-Fordyce Disease 40 0.045
332
c PRC016 Pre-Eclampsia 65 0.045
333
TTN003 Tetanus 65 0.044
334
RTR001 Retrograde Amnesia 40 0.044
335
NRT004 Neuritis 55 0.044
336
P HRD009 Hereditary Wilms' Tumor 46 0.044
337
ART004 Aortic Atherosclerosis 48 0.044
338
P AST007 Astrocytoma 66 0.044
339
IRN001 Iron Deficiency Anemia 55 0.044
340
P SPN301 Spinocerebellar Ataxia 2 56 0.044
341
P SYR001 Syringomyelia 49 0.043
342
MNK001 Menkes Disease 64 0.043
343
GTL001 Gitelman Syndrome 62 0.043
344
P ECL001 Eclampsia 57 0.043
345
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.043
346
BRN028 Brain Cancer 72 0.043
347
c HPT003 Hepatitis a 63 0.043
348
TRD006 Tardive Dyskinesia 59 0.043
349
CPG001 Capgras Syndrome 25 0.043
350
P AST055 Asthma-Related Traits 1 18 0.043
351
HYP080 Hypogonadism 54 0.043
352
VTM002 Vitamin B12 Deficiency 46 0.043
353
ACT049 Acute Disseminated Encephalomyelitis 52 0.043
354
CRV043 Cervical Dystonia 45 0.043
355
P PRD006 Prader-Willi Syndrome 66 0.043
356
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 54 0.043
357
PST027 Postencephalitic Parkinson Disease 30 0.042
358
THY030 Thyroid Gland Disease 51 0.042
359
SBS004 Substance Dependence 51 0.042
360
P CRB059 Cerebellar Degeneration 40 0.042
361
MRT001 Muir-Torre Syndrome 59 0.042
362
DRG003 Drug Dependence 51 0.042
363
PRP019 Peripheral Nervous System Disease 53 0.042
364
P FNC043 Fanconi Anemia, Complementation Group E 52 0.042
365
IRR002 Irritable Bowel Syndrome 63 0.042
366
HMS001 Hemosiderosis 50 0.042
367
P LCT001 Lactic Acidosis 51 0.042
368
P CMM008 Communicating Hydrocephalus 35 0.042
369
MNG003 Mungan Syndrome 34 0.042
370
P END044 Endometriosis 71 0.042
371
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.041
372
SPN041 Spinal Cord Disease 54 0.041
373
P TXP001 Toxoplasmosis 65 0.041
374
GST033 Gestational Diabetes 62 0.041
375
DYS004 Dyscalculia 30 0.041
376
CNN003 Conn's Syndrome 70 0.041
377
P PRM006 Primary Biliary Cirrhosis 55 0.040
378
CRD223 Cardiac Arrhythmia 52 0.040
379
STR067 Stroke, Ischemic 84 0.040
380
c BPL002 Bipolar I Disorder 50 0.040
381
PNN005 Panencephalitis, Subacute Sclerosing 44 0.040
382
c ART101 Aortic Valve Disease 2 65 0.040
383
LMB024 Limbic Encephalitis 42 0.040
384
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.040
385
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.040
386
TRN015 Transient Cerebral Ischemia 58 0.040
387
P ANT006 Antiphospholipid Syndrome 59 0.040
388
c CTR119 Cataract 32, Multiple Types 32 0.040
389
KLV001 Kluver-Bucy Syndrome 41 0.040
390
RNL024 Renal Glucosuria 50 0.040
391
BNF002 Bone Fracture 56 0.040
392
PNM001 Pneumocystosis 55 0.040
393
P STR001 Striatonigral Degeneration 34 0.039
394
MYS004 Myiasis 34 0.039
395
PLS009 Plasma Cell Neoplasm 51 0.039
396
PRT037 Pertussis 70 0.039
397
ARL004 Aural Atresia, Congenital 27 0.039
398
c WLM018 Wilms Tumor 5 49 0.039
399
PRM008 Parametritis 29 0.039
400
WLL001 Williams-Beuren Syndrome 63 0.038
401
c ERL020 Early-Onset Schizophrenia 51 0.038
402
P ACH003 Achromatopsia 57 0.038
403
P CHR084 Chromosomal Disease 40 0.038
404
VCC001 Vaccinia 50 0.038
405
IRN002 Iron Metabolism Disease 45 0.038
406
c HMC039 Hemochromatosis, Type 1 71 0.038
407
PST055 Postural Hypotension 40 0.037
408
P BLM007 Bulimia Nervosa 1 53 0.037
409
HMR039 Hemorrhage, Intracerebral 57 0.037
410
P FRD012 Friedreich Ataxia 1 58 0.037
411
ATX010 Ataxia Neuropathy Spectrum 29 0.037
412
PRT038 Protein-Energy Malnutrition 52 0.037
413
NRX001 Neuroaxonal Dystrophy 40 0.037
414
GLB015 Glioblastoma Multiforme 68 0.037
415
P ENC011 Encephalomyopathy 40 0.037
416
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.037
417
ADS004 Aids Dementia Complex 42 0.037
418
LBR002 Leber Hereditary Optic Neuropathy 57 0.036
419
P CRB174 Cerebral Amyloid Angiopathy, Itm2b-Related, 2 36 0.036
420
P PRS013 Prosopagnosia 34 0.036
421
SKN019 Skin Melanoma 63 0.036
422
ECH002 Echolalia 35 0.036
423
FML304 Familial Isolated Dilated Cardiomyopathy 36 0.036
424
BLM001 Bloom Syndrome 62 0.036
425
HYP064 Hypogonadotropism 38 0.036
426
BRX001 Bruxism 51 0.036
427
P AXN002 Axenfeld-Rieger Syndrome 53 0.036
428
PRK066 Parkinsonism with Spasticity, X-Linked 31 0.035
429
c PRG011 Progressive Myoclonus Epilepsy 40 0.035
430
PTH002 Pathological Gambling 53 0.035
431
P PNC025 Panic Disorder 57 0.035
432
LNS003 Lens Disease 37 0.035
433
PSD088 Pseudobulbar Affect 31 0.035
434
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.035
435
CGN007 Cognitive Function 1, Social 27 0.035
436
ATH013 Atherosclerosis Susceptibility 59 0.035
437
LMY002 Leiomyoma 58 0.035
438
FCT004 Factor Xii Deficiency 50 0.035
439
GND003 Gonadal Disease 32 0.035
440
MTC004 Mitochondrial Encephalomyopathy 42 0.034
441
P JVN024 Juvenile Hereditary Hemochromatosis 22 0.034
442
WVR001 Weaver Syndrome 61 0.034
443
BRG013 Buerger Disease 62 0.034
444
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.034
445
AMS001 Amusia 25 0.034
446
CTR172 Citrullinemia, Classic 58 0.034
447
APC009 Apocrine Gland Secretion, Variation in 29 0.034
448
SPN186 Spinal Cord Injury 67 0.034
449
SCH012 Schizoaffective Disorder 51 0.034
450
EMB004 Embryonal Carcinoma 59 0.034
451
PRS064 Persistent Vegetative State 32 0.034
452
PFF001 Pfeiffer Syndrome 74 0.034
453
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.034
454
HMC014 Homocysteinemia 49 0.034
455
SDD001 Sudden Infant Death Syndrome 61 0.034
456
BRL010 Buruli Ulcer 51 0.033
457
ATH004 Athetosis 24 0.033
458
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 40 0.033
459
MSL001 Measles 64 0.033
460
WGN006 Wegener Granulomatosis 71 0.033
461
c PRK090 Parkinson Disease 3, Autosomal Dominant 37 0.033
462
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.033
463
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 36 0.033
464
TRT001 Teratocarcinoma 41 0.033
465
GNG011 Gingival Disease 50 0.033
466
AND020 Androgen Insensitivity, Partial 49 0.033
467
TRN007 Transsexualism 44 0.033
468
MHR001 Mohr-Tranebjaerg Syndrome 39 0.033
469
ECT026 Ectopic Pregnancy 52 0.033
470
PNG002 Pain Agnosia 41 0.033
471
ADR012 Adrenal Gland Disease 51 0.033
472
c HYP396 Hypercholesterolemia, Autosomal Recessive 37 0.033
473
STT001 Status Epilepticus 60 0.033
474
GNG004 Ganglioglioma 51 0.032
475
P PNM006 Pneumoconiosis 55 0.032
476
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 37 0.032
477
FTL009 Fetal Akinesia Deformation Sequence 54 0.032
478
c HYP293 Hypophosphatasia, Adult 48 0.032
479
FNT004 Fainting 36 0.032
480
ALN001 Aland Island Eye Disease 39 0.032
481
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 0.032
482
TRN069 Transsexuality 23 0.032
483
CHL014 Cholera 56 0.032
484
RTC003 Root Caries 38 0.032
485
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 38 0.032
486
CRB026 Cerebellar Astrocytoma 39 0.032
487
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.032
488
IMM162 Immunoglobulin E Concentration, Serum 16 0.032
489
c PRK085 Parkinson Disease 1, Autosomal Dominant 31 0.031
490
FND001 Fundus Albipunctatus 54 0.031
491
WRN003 Wernicke Encephalopathy 47 0.031
492
c PRM039 Primary Angiitis of the Central Nervous System 26 0.031
493
EPT021 Epithelial Recurrent Erosion Dystrophy 35 0.031
494
ACR008 Acrocallosal Syndrome 56 0.031
495
TRG017 Trigeminal Trophic Syndrome 15 0.031
496
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.031
497
ARS001 Aarskog-Scott Syndrome 55 0.031
498
MYD002 Myd88 Deficiency 49 0.031
499
ADL060 Adult Polyglucosan Body Disease 32 0.031
500
c MYT020 Myotonic Dystrophy 2 56 0.031
501
LMY014 Leiomyoma, Uterine 61 0.030
502
PLY158 Polyglucosan Body Neuropathy, Adult Form 29 0.030
503
PLG002 Plague 55 0.030
504
JJN008 Jejunoileitis 41 0.030
505
ANX004 Anoxia 49 0.030
506
NMN001 Nominal Aphasia 36 0.030
507
P SJG008 Sjogren Syndrome 58 0.030
508
BRD004 Borderline Personality Disorder 50 0.030
509
VRT003 Vertebrobasilar Insufficiency 31 0.030
510
CRN031 Cranial Nerve Disease 45 0.030
511
c MLG068 Malignant Glioma 66 0.030
512
c PCH012 Pachyonychia Congenita 2 47 0.030
513
CRB087 Cerebral Arteriosclerosis 20 0.030
514
AND005 Androgen Insensitivity Syndrome, Mild 16 0.030
515
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.030
516
PRM236 Primary Biliary Cholangitis 56 0.030
517
SLT014 Salt and Pepper Developmental Regression Syndrome 37 0.030
518
WLF002 Wolf-Hirschhorn Syndrome 54 0.030
519
RTN185 Retinal Dysplasia, Primary 21 0.029
520
ESN005 Eosinophilic Gastroenteritis 56 0.029
521
ATM021 Autoimmune Inner Ear Disease 34 0.029
522
SPR038 Supranuclear Ocular Palsy 21 0.029
523
P SCL057 Scoliosis, Isolated 1 28 0.029
524
c CLR131 Ciliary Dyskinesia, Primary, 1 54 0.029
525
DFF012 Differentiating Neuroblastoma 34 0.029
526
CD4001 Cd45 Deficiency 28 0.029
527
P GLM040 Glioma Susceptibility 1 51 0.029
528
KRN002 Kearns-Sayre Syndrome 59 0.029
529
SVN002 Sveinsson Chorioretinal Atrophy 29 0.029
530
PRN009 Paranoid Schizophrenia 49 0.029
531
c LSS005 Lissencephaly 1 46 0.028
532
P MTC133 Mitochondrial Myopathy 53 0.028
533
SMT008 Smith-Magenis Syndrome 54 0.028
534
MTC097 Mitochondrial Complex Iv Deficiency 55 0.028
535
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 40 0.028
536
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 34 0.028
537
SRT004 Serotonin Syndrome 51 0.028
538
ALP097 Alopecia Universalis Congenita 40 0.028
539
P GRS003 Griscelli Syndrome 58 0.027
540
PRT055 Prieto X-Linked Mental Retardation Syndrome 30 0.027
541
OCL006 Ocular Hypertension 51 0.027
542
FCL044 Fecal Incontinence 38 0.027
543
c HYP292 Hypophosphatasia, Infantile 48 0.027
544
RNS001 Raine Syndrome 45 0.027
545
P RNV001 Renovascular Hypertension 48 0.027
546
CRB004 Cerebral Artery Occlusion 46 0.027
547
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 35 0.027
548
BRN041 Bornholm Eye Disease 25 0.027
549
DYS009 Dysthymic Disorder 42 0.027
550
HNM002 Hinman Syndrome 25 0.027
551
ADR013 Adrenal Gland Hyperfunction 54 0.027
552
END040 Endogenous Depression 53 0.027
553
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 33 0.027
554
ISL119 Isolated Optic Neuritis 23 0.027
555
OCL011 Ocular Motility Disease 31 0.027
556
PRR013 Prurigo Nodularis 39 0.027
557
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.027
558
APR006 Apert Syndrome 69 0.026
559
PRT058 Pure Autonomic Failure 60 0.026
560
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 49 0.026
561
P CHR342 Chiari Malformation 45 0.026
562
ASY002 Asymptomatic Neurosyphilis 34 0.026
563
EPD070 Epidermoid Cysts 46 0.026
564
PLY039 Polymorphic Reticulosis 22 0.026
565
ANR009 Aneurysmal Bone Cysts 46 0.026
566
CYT018 Cytochrome P450 2d6 Variant 13 0.026
567
c LYD012 Leydig Cell Hypoplasia, Type I 34 0.026
568
MNS002 Mini Stroke 23 0.026
569
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.026
570
CLL002 Collecting Duct Carcinoma 43 0.026
571
SWT003 Sweat Gland Disease 42 0.026
572
CHR178 Chromosomal Triplication 35 0.026
573
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 37 0.026
574
DYS032 Dystrophinopathies 43 0.025
575
DYS006 Dysembryoplastic Neuroepithelial Tumor 37 0.025
576
BRS050 Breast Cyst 36 0.025
577
P GRN010 Granular Cell Tumor 47 0.025
578
DSS008 Disease of Mental Health 51 0.025
579
HRT007 Heart Cancer 46 0.025
580
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 0.025
581
P PRT008 Proteus Syndrome 67 0.025
582
GNT031 Genitopatellar Syndrome 43 0.025
583
NTR027 Neutrophil Actin Dysfunction 23 0.025
584
HYP572 Hypoganglionosis 31 0.025
585
SKN023 Skin Tag 41 0.024
586
MTR031 Motor Neuro-Ophthalmic Disorders 20 0.024
587
MTN003 Motion Sickness 52 0.024
588
SLV025 Salivary Gland Adenoma, Pleomorphic 29 0.024
589
APL024 Apolipoprotein C-Iii Deficiency 20 0.024
590
P BRS044 Breast Adenocarcinoma 58 0.024
591
PSD029 Pseudocholinesterase Deficiency 38 0.024
592
URN022 Urinary Tract Infections, Recurrent 29 0.024
593
SCR016 Scrotal Carcinoma 35 0.024
594
LBR030 Leber Optic Atrophy 38 0.024
595
IMM105 Immunodeficiency with Hyper-Igm, Type 3 42 0.024
596
BRN034 Brain Meningioma 22 0.024
597
PRM087 Premature Chromatid Separation Trait 20 0.023
598
STR094 Stromme Syndrome 34 0.023
599
STV003 Stuve-Wiedemann Syndrome 38 0.023
600
ARG004 Argyria 21 0.023
601
MYF001 Myofibroma 42 0.022
602
ANT019 Anterograde Amnesia 29 0.022
603
MSC148 Musical Perfect Pitch 19 0.022
604
HDC005 Headache Associated with Sexual Activity 17 0.021
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