Search results for memory impairment

996 hits were found for memory impairment

# Family MCID Name MIFTS Score
1
DMN002 Dementia 65 0.336
2
P ALZ034 Alzheimer Disease 92 0.231
3
P SCH015 Schizophrenia 77 0.226
4
CRB009 Cerebritis 39 0.201
5
P EPL164 Epilepsy 66 0.200
6
NRN002 Neuronitis 41 0.198
7
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.189
8
P ENC018 Encephalopathy 59 0.179
9
LRN003 Learning Disability 49 0.177
10
P HPT021 Hepatitis 69 0.172
11
PSY004 Psychotic Disorder 67 0.164
12
DSS008 Disease of Mental Health 52 0.162
13
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.158
14
ISC004 Ischemia 61 0.157
15
BRN071 Brain Injury 52 0.156
16
END072 Endotheliitis 42 0.151
17
SMN008 Semantic Dementia 44 0.150
18
P NRV007 Nervous System Disease 71 0.139
19
TMP001 Temporal Lobe Epilepsy 50 0.136
20
AMN003 Amnestic Disorder 43 0.132
21
DRG001 Drug Psychosis 38 0.131
22
c CNT035 Central Nervous System Disease 60 0.131
23
VSC002 Vascular Dementia 54 0.130
24
RTR001 Retrograde Amnesia 37 0.129
25
TRM010 Traumatic Brain Injury 52 0.128
26
P LKM002 Leukemia 71 0.128
27
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.125
28
ANX002 Anxiety Disorder 67 0.125
29
IMP003 Impaired Renal Function Disease 34 0.124
30
HV1006 Hiv-1 80 0.124
31
TRN012 Transient Global Amnesia 39 0.120
32
PST028 Post-Traumatic Stress Disorder 57 0.117
33
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.116
34
P ART022 Arthritis 75 0.116
35
MDD011 Mood Disorder 61 0.116
36
P OBS005 Obesity 92 0.112
37
P DYS005 Dyslexia 37 0.112
38
HYP266 Hypoxia 56 0.111
39
MVM001 Movement Disease 49 0.111
40
ADT003 Auditory System Disease 40 0.111
41
P SPC019 Specific Language Impairment 28 0.110
42
SPC010 Speech and Communication Disorders 41 0.109
43
P PRS038 Personality Disorder 62 0.107
44
P LYM118 Lymphoma 69 0.107
45
APH002 Aphasia 54 0.106
46
CRB039 Cerebrovascular Disease 63 0.106
47
PHY002 Physical Disorder 43 0.105
48
SLP005 Sleep Disorder 53 0.105
49
P URF003 Urofacial Syndrome 1 50 0.104
50
STR067 Stroke, Ischemic 75 0.104
51
URN009 Urinary System Disease 50 0.103
52
P BRS047 Breast Cancer 100 0.102
53
P LVR013 Liver Disease 75 0.102
54
ACT084 Acute Stress Disorder 40 0.101
55
ALN001 Aland Island Eye Disease 45 0.101
56
P ENC004 Encephalitis 63 0.101
57
CND002 Conduct Disorder 54 0.101
58
P RHM011 Rheumatoid Arthritis 89 0.099
59
END040 Endogenous Depression 53 0.099
60
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.099
61
MNT002 Mental Depression 53 0.096
62
CRB159 Cerebral Visual Impairment 33 0.096
63
c HPT001 Hepatitis C 68 0.094
64
HDN002 Head Injury 45 0.094
65
TBR010 Tuberculosis 70 0.094
66
PRS013 Prosopagnosia 31 0.093
67
c HPT016 Hepatitis B 64 0.092
68
RDN001 Reading Disorder 34 0.092
69
P ATS007 Autism Spectrum Disorder 65 0.091
70
c HPT003 Hepatitis a 59 0.091
71
P PRK057 Parkinson Disease, Late-Onset 70 0.090
72
GNR004 Generalized Anxiety Disorder 51 0.089
73
BSL008 Basal Ganglia Disease 40 0.088
74
P ATX004 Ataxia 53 0.088
75
PCK002 Pick Disease 68 0.087
76
HYP066 Hyperglycemia 61 0.087
77
P BPL003 Bipolar Disorder 62 0.087
78
AYM001 Ayme-Gripp Syndrome 41 0.087
79
P AST005 Asthma 82 0.086
80
DWN001 Down Syndrome 66 0.086
81
P LPS004 Lupus Erythematosus 64 0.086
82
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.086
83
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.086
84
c HPT073 Hepatitis C Virus 73 0.084
85
c SYS001 Systemic Lupus Erythematosus 86 0.084
86
c ALZ012 Alzheimer Disease 12 32 0.084
87
P KDN018 Kidney Disease 66 0.083
88
NTR005 Nutritional Deficiency Disease 36 0.083
89
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.082
90
ANT019 Anterograde Amnesia 28 0.082
91
DVL001 Developmental Coordination Disorder 36 0.082
92
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.081
93
P INF038 Influenza 72 0.081
94
SPC005 Speech Disorder 41 0.081
95
P MYP004 Myopathy 67 0.081
96
CMM004 Common Variable Immunodeficiency 68 0.080
97
P MNN013 Meningitis 67 0.080
98
ANS006 Anosognosia 25 0.080
99
END030 End Stage Renal Failure 55 0.080
100
BRN028 Brain Cancer 70 0.079
101
ATN002 Autonomic Nervous System Disease 48 0.079
102
P NRP001 Neuropathy 59 0.078
103
TRN015 Transient Cerebral Ischemia 56 0.078
104
ADR009 Adrenal Cortex Disease 39 0.078
105
P INT063 Intellectual Disability 49 0.077
106
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.077
107
c VRL010 Viral Hepatitis 60 0.077
108
P AMY004 Amyloidosis 65 0.076
109
P MYL006 Myeloid Leukemia 66 0.076
110
P AGN002 Agnosia 57 0.076
111
LPD004 Lipoid Nephrosis 48 0.076
112
BRN080 Brain Ischemia 41 0.075
113
P HYP086 Hypothyroidism 64 0.075
114
GLC008 Glucose Metabolism Disease 42 0.075
115
P SZR006 Seizure Disorder 56 0.075
116
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.074
117
FCL014 Focal Epilepsy 55 0.074
118
P CRB088 Cerebral Atrophy 42 0.074
119
MLN008 Melanoma 62 0.073
120
GLT021 Glutaricaciduria, Type I 46 0.073
121
PRP027 Peripheral Vascular Disease 68 0.073
122
SPS057 Spasticity 42 0.072
123
NRM005 Neuromuscular Disease 56 0.072
124
ADJ001 Adjustment Disorder 38 0.072
125
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.072
126
ART111 Artery Disease 55 0.072
127
MLR004 Malaria 83 0.071
128
ACQ007 Acquired Immunodeficiency Syndrome 60 0.071
129
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.071
130
P FRG001 Fragile X Syndrome 69 0.071
131
SBS003 Substance Abuse 54 0.071
132
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.070
133
P SLP006 Sleep Apnea 61 0.070
134
GLB003 Globe Disease 32 0.070
135
VCC001 Vaccinia 46 0.070
136
DMY004 Demyelinating Disease 53 0.070
137
DRG011 Drug Addiction 51 0.070
138
SXL003 Sexual Disorder 42 0.069
139
c CHR089 Chronic Kidney Failure 66 0.069
140
P MSC033 Muscle Disorders 52 0.069
141
c CRN214 Coronary Heart Disease 5 22 0.069
142
ASP001 Asperger Syndrome 50 0.068
143
AMS001 Amusia 22 0.068
144
P THY032 Thyroiditis 54 0.068
145
LYM009 Lymphocytic Choriomeningitis 43 0.068
146
OBS002 Obsessive-Compulsive Disorder 66 0.068
147
ATM052 Autoimmune Disease 1 25 0.068
148
MSC004 Muscle Tissue Disease 34 0.068
149
c PND001 Pain Disorder 54 0.067
150
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.067
151
P NRV006 Nervous System Cancer 60 0.067
152
DRM006 Dermatitis 66 0.067
153
c PRK031 Parkinson Disease 1 51 0.067
154
P HRP006 Herpes Simplex 65 0.066
155
SCH011 Schizotypal Personality Disorder 33 0.066
156
MTH009 Mouth Disease 61 0.066
157
CRB037 Cerebral Palsy 66 0.066
158
BLD054 Blood Protein Disease 37 0.066
159
P ANR007 Anorexia Nervosa 61 0.066
160
PRS047 Prostatitis 56 0.066
161
OBS061 Obstructive Sleep Apnea 66 0.065
162
P HRT032 Heart Disease 75 0.065
163
P PNM007 Pneumonia 68 0.065
164
CRB031 Cerebral Arterial Disease 27 0.065
165
c ALZ039 Alzheimer's Disease 7 26 0.065
166
MCS002 Mucositis 55 0.065
167
P LYM026 Lymphoblastic Leukemia 62 0.065
168
P SPS003 Spastic Diplegia 52 0.065
169
P HPT023 Hepatocellular Carcinoma 92 0.064
170
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.064
171
SCL003 Social Phobia 46 0.064
172
P CHR345 Chronic Pain 50 0.064
173
PRM097 Primary Immunodeficiency Disease 60 0.064
174
c ALZ032 Alzheimer Disease 18 35 0.064
175
CNV002 Conversion Disorder 41 0.064
176
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.064
177
P INF032 Infertility 59 0.064
178
OPT006 Optic Nerve Disease 52 0.064
179
ALC007 Alcohol Dependence 63 0.063
180
TTN003 Tetanus 61 0.063
181
LYM027 Lymphopenia 56 0.063
182
DRG003 Drug Dependence 50 0.063
183
WRN002 Wernicke-Korsakoff Syndrome 44 0.063
184
ACR041 Acromelic Frontonasal Dysostosis 45 0.063
185
BRT030 Birth Defects 43 0.063
186
ALL026 Allergic Hypersensitivity Disease 52 0.063
187
FST001 Foster-Kennedy Syndrome 31 0.063
188
c CHR417 Chronic Graft Versus Host Disease 51 0.063
189
RTN023 Retinitis 50 0.063
190
APR001 Apraxia 51 0.062
191
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.062
192
ANR040 Aneurysm 57 0.062
193
P HNT016 Huntington Disease 80 0.061
194
DYS004 Dyscalculia 27 0.061
195
c SCH051 Schizophrenia 4 28 0.061
196
KDS001 Kid Syndrome 53 0.061
197
P ATP001 Atopic Dermatitis 62 0.061
198
P TCL004 T-Cell Leukemia 47 0.060
199
DVL017 Developmental Prosopagnosia 19 0.060
200
FCL011 Facial Nerve Disease 36 0.060
201
GNC005 Geniculate Ganglionitis 27 0.060
202
HPT019 Hepatic Encephalopathy 56 0.060
203
P TRM003 Tremor 54 0.060
204
CRB004 Cerebral Artery Occlusion 45 0.059
205
ATM054 Autoimmune Disease 3 15 0.059
206
WLL006 Wells Syndrome 59 0.059
207
ART021 Arteriosclerosis 58 0.059
208
HMT018 Hematopoietic Stem Cell Transplantation 41 0.059
209
SPC003 Specific Developmental Disorder 38 0.059
210
LVR012 Liver Cirrhosis 67 0.059
211
c ALZ037 Alzheimer Disease-2 52 0.058
212
GDS001 Good Syndrome 44 0.058
213
WTH001 Withdrawal Disorder 37 0.058
214
C3D001 C3 Deficiency 53 0.058
215
P LTR001 Lateral Sclerosis 53 0.058
216
CYT008 Cytomegalovirus Infection 52 0.058
217
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.058
218
ATH003 Atherosclerosis 65 0.058
219
LMB024 Limbic Encephalitis 38 0.058
220
ATM053 Autoimmune Disease 2 16 0.058
221
CHL071 Child Syndrome 58 0.058
222
PRP019 Peripheral Nervous System Disease 55 0.057
223
SPN369 Spinal Disease 39 0.057
224
P CRN211 Coronary Artery Disease 74 0.057
225
P LNG032 Lung Cancer 95 0.057
226
c ACT073 Acute Leukemia 60 0.057
227
c PRK045 Parkinson Disease 5 40 0.057
228
CYS001 Cystic Fibrosis 83 0.056
229
MYL009 Myelodysplastic Syndrome 73 0.056
230
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.056
231
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.056
232
P HYD006 Hydrocephalus 66 0.056
233
MDY003 Mody, Type Ii 36 0.056
234
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.056
235
CLT003 Colitis 60 0.056
236
c CHR090 Chronic Lymphocytic Leukemia 76 0.056
237
c PRK030 Parkinson Disease 4 38 0.056
238
VSC007 Vascular Disease 67 0.056
239
VRL011 Viral Infectious Disease 55 0.056
240
EXF001 Exfoliation Syndrome 57 0.055
241
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.055
242
c BPL002 Bipolar I Disorder 47 0.055
243
P PNC025 Panic Disorder 60 0.054
244
SBS004 Substance Dependence 47 0.054
245
CHR066 Chronic Fatigue Syndrome 64 0.054
246
P PLN008 Peeling Skin Syndrome 45 0.054
247
P MYC007 Myocardial Infarction 79 0.054
248
P CRD011 Cardiomyopathy 68 0.054
249
P SHR029 Short Syndrome 58 0.054
250
IMM136 Immune System Disease 51 0.054
251
CRB033 Cerebral Degeneration 44 0.054
252
PRM025 Primary Bacterial Infectious Disease 41 0.054
253
c ATM007 Autoimmune Disease of Central Nervous System 25 0.054
254
ETN001 Eating Disorder 58 0.054
255
P ALC004 Alcohol Abuse 59 0.053
256
CNG034 Congestive Heart Failure 72 0.053
257
P DMN033 Dementia, Frontotemporal 62 0.053
258
P PSR002 Psoriasis 61 0.053
259
NSY001 N Syndrome 36 0.053
260
RSP006 Respiratory System Disease 58 0.052
261
DFC004 Deficiency Anemia 64 0.052
262
NSD001 Nose Disease 48 0.052
263
P CRV039 Cervicitis 45 0.052
264
P FTL001 Fetal Alcohol Syndrome 53 0.052
265
c CRN173 Coronary Heart Disease 8 18 0.052
266
P FBR031 Febrile Seizures 53 0.052
267
c CRN175 Coronary Heart Disease 4 19 0.052
268
CRH001 Crohn's Disease 75 0.051
269
P LYM033 Lymphoproliferative Syndrome 56 0.051
270
VSL003 Visual Agnosia 26 0.051
271
LNG099 Lung Disease 64 0.051
272
HYP037 Hyperhomocysteinemia 50 0.051
273
P PRS040 Prostate Cancer 90 0.051
274
PRT037 Pertussis 64 0.050
275
CTS003 Coats Disease 57 0.050
276
BRD004 Borderline Personality Disorder 47 0.050
277
c MLT010 Multiple Personality Disorder 36 0.050
278
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.050
279
P BCL006 B-Cell Lymphomas 65 0.050
280
LYM023 Lymphatic System Cancer 33 0.050
281
c BRN108 Branchiootic Syndrome 1 34 0.050
282
P CTR002 Cataract 58 0.050
283
WLL001 Williams-Beuren Syndrome 60 0.049
284
c MLT093 Multiple Sclerosis 2 18 0.049
285
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.049
286
HRN022 Hearing Loss/deafness 26 0.049
287
P CDS001 Cadasil 55 0.049
288
CHR012 Chronic Granulomatous Disease 65 0.049
289
c MJR008 Major Affective Disorder 2 19 0.049
290
c ADL017 Adult T-Cell Leukemia 60 0.049
291
CNN002 Cannabis Abuse 40 0.049
292
LYM024 Lymphatic System Disease 52 0.049
293
CCN001 Cocaine Dependence 49 0.049
294
INC022 Inclusion-Cell Disease 46 0.049
295
CRT016 Carotid Artery Disease 57 0.049
296
P TBR001 Tuberous Sclerosis 67 0.048
297
SRC014 Sarcoma 66 0.048
298
c ALZ043 Alzheimer's Disease 15 32 0.048
299
c ALZ014 Alzheimer Disease 16 27 0.048
300
HPD002 Hepadnavirus Infection 22 0.048
301
P DYS154 Dystonia 65 0.048
302
c ALZ036 Alzheimer Disease, Type 3 53 0.048
303
TCL003 T Cell Deficiency 45 0.048
304
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.048
305
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.048
306
c PLN017 Peeling Skin Syndrome 1 34 0.048
307
EYC003 Eye Accommodation Disease 24 0.048
308
P ANG001 Angelman Syndrome 61 0.048
309
BNM001 Bone Marrow Cancer 51 0.048
310
ACT118 Acute Non Lymphoblastic Leukemia 30 0.048
311
c LKM061 Leukemia, Acute Myeloid 73 0.047
312
c CHR064 Chronic Monocytic Leukemia 42 0.047
313
VSL004 Visual Cortex Disease 28 0.047
314
ISC006 Ischemic Heart Disease 68 0.047
315
ALX002 Alexithymia 37 0.047
316
c MLT094 Multiple Sclerosis 3 24 0.047
317
c ERL020 Early-Onset Schizophrenia 47 0.047
318
CRB090 Cerebral Hypoxia 45 0.047
319
c ALZ042 Alzheimer's Disease 14 40 0.047
320
P CRT033 Corticobasal Degeneration 47 0.046
321
CRT015 Carotid Artery Occlusion 43 0.046
322
c SCH056 Schizophrenia 15 23 0.046
323
P GLB002 Glioblastoma 68 0.046
324
LSH001 Leishmaniasis 66 0.046
325
P CRT072 Creutzfeldt-Jakob Disease 61 0.046
326
WLF001 Wolff-Parkinson-White Syndrome 56 0.046
327
SML019 Smallpox 54 0.046
328
c CNG006 Congenital Hypothyroidism 60 0.046
329
P CRG003 Crigler-Najjar Syndrome, Type I 59 0.046
330
DYS003 Dysgraphia 36 0.046
331
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.046
332
P ACT135 Acute Graft Versus Host Disease 53 0.046
333
SYN041 Synesthesia 18 0.046
334
P FRD001 Friedreich Ataxia 62 0.046
335
P NRF002 Neurofibromatosis 71 0.046
336
CNN005 Connective Tissue Disease 62 0.046
337
c ALZ002 Alzheimer Disease Type 1 21 0.046
338
GST053 Gastric Cancer 78 0.045
339
INS024 Insulin-Like Growth Factor I 75 0.045
340
P MLT019 Multiple Myeloma 83 0.045
341
P RTT002 Rett Syndrome 77 0.045
342
ATR060 Atrial Standstill, Digenic 51 0.045
343
VTM002 Vitamin B12 Deficiency 44 0.045
344
EYD002 Eye Disease 61 0.045
345
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.045
346
c CHR418 Chronic Leukemia 47 0.045
347
c ACT020 Acute T Cell Leukemia 35 0.045
348
PRM243 Primary Bone Cancer 29 0.045
349
PRV006 Pervasive Developmental Disorder 53 0.045
350
PRD011 Proud Syndrome 42 0.045
351
PNM013 Pneumococcal Meningitis 41 0.045
352
P HML002 Hemolytic Anemia 62 0.045
353
DMN031 Dementia, Lewy Body 58 0.045
354
PRP021 Peripheral Nervous System Neoplasm 46 0.045
355
MRG013 Mirage Syndrome 29 0.045
356
P OVR042 Ovarian Cancer 76 0.044
357
ADM013 Adamantinoma of Long Bones 57 0.044
358
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 53 0.044
359
c HPT015 Hepatitis D 52 0.044
360
RMS001 Rem Sleep Behavior Disorder 41 0.044
361
c CRN177 Coronary Heart Disease 7 20 0.044
362
OCL009 Ocular Cancer 59 0.044
363
RHM027 Rheumatic Disease 58 0.044
364
P ACT074 Acute Lymphocytic Leukemia 56 0.044
365
CHL061 Childhood Leukemia 49 0.044
366
LYM067 Lymphoid Leukemia 44 0.044
367
c PLN021 Peeling Skin Syndrome 3 29 0.044
368
c ALZ041 Alzheimer's Disease 13 23 0.044
369
VND001 Vein Disease 47 0.043
370
BLD053 Blood Platelet Disease 46 0.043
371
c ALZ008 Alzheimer Disease Risk Factor 18 0.043
372
THR024 Thrombosis 57 0.043
373
P PLY019 Polyneuropathy 56 0.043
374
P IDP010 Idiopathic Generalized Epilepsy 61 0.043
375
BRS051 Breast Disease 61 0.043
376
c SVR001 Severe Acute Respiratory Syndrome 57 0.043
377
LYM019 Lymphosarcoma 53 0.043
378
TXC002 Toxic Encephalopathy 51 0.043
379
VSC047 Vascular Malformation 45 0.043
380
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.043
381
c AST037 Asthma 1 28 0.043
382
GRS011 Gerstmann-Straussler Disease 42 0.043
383
DSS010 Dissociative Disorder 32 0.043
384
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.043
385
CHL068 Cholestasis 59 0.043
386
PRV004 Periventricular Leukomalacia 48 0.043
387
LKM006 Leukomalacia 43 0.043
388
c CRN174 Coronary Heart Disease 2 20 0.043
389
MYC002 Mycobacterium Avium Complex Disease 52 0.043
390
P HRP009 Herpes Simplex Encephalitis 47 0.043
391
ACD009 Acid-Labile Subunit, Deficiency of 45 0.043
392
ATM055 Autoimmune Disease 4 15 0.043
393
P ATR011 Atrial Fibrillation 66 0.042
394
ATN004 Autonomic Neuropathy 45 0.042
395
P MDL005 Medulloblastoma 77 0.042
396
BLM002 Bulimia Nervosa 52 0.042
397
PTH002 Pathological Gambling 51 0.042
398
c PLN018 Peeling Skin Syndrome 2 40 0.042
399
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.042
400
SBC016 Subacute Delirium 24 0.042
401
ATS001 Autistic Disorder 63 0.042
402
c ESS001 Essential Tremor 59 0.042
403
ADL002 Adult Syndrome 52 0.042
404
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.042
405
BNC003 Bone Cancer 58 0.042
406
JPN002 Japanese Encephalitis 55 0.042
407
CCN002 Cocaine Abuse 48 0.042
408
P GLM045 Glioma 60 0.042
409
P CRN178 Coronary Heart Disease 6 21 0.042
410
CNT098 Central Core Disease 65 0.041
411
PRN009 Paranoid Schizophrenia 47 0.041
412
ANX004 Anoxia 43 0.041
413
SPS019 Spastic Paraparesis 41 0.041
414
P NRM001 Neuromyelitis Optica 60 0.041
415
P ANT006 Antiphospholipid Syndrome 56 0.041
416
ART002 Arts Syndrome 51 0.041
417
ATP002 Atopy 66 0.041
418
P CSH001 Cushing's Syndrome 65 0.041
419
ALL006 Allergic Asthma 58 0.041
420
BHV002 Behavioral Variant of Frontotemporal Dementia 39 0.041
421
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.041
422
c ACT075 Acute Myocardial Infarction 60 0.041
423
RTN018 Retinal Disease 53 0.041
424
MYL020 Myelomeningocele 51 0.040
425
RMN001 Rumination Disorder 34 0.040
426
P THR014 Thrombocytopenia 64 0.040
427
MLN007 Male Infertility 55 0.040
428
CSY001 C Syndrome 50 0.040
429
P CLR023 Colorectal Cancer 97 0.040
430
HDG012 Hodgkin Lymphoma 77 0.040
431
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.040
432
LYM115 Lymphoma, Non-Hodgkin 63 0.040
433
CHL014 Cholera 53 0.040
434
LKC003 Leukocyte Disease 43 0.040
435
CRN031 Cranial Nerve Disease 40 0.040
436
c MJR007 Major Affective Disorder 1 24 0.040
437
c MLT124 Multiple Sclerosis 5 23 0.040
438
c MLT095 Multiple Sclerosis 4 16 0.040
439
c LKM062 Leukemia, Acute Lymphoblastic 64 0.040
440
MTR014 Motor Neuron Disease 58 0.040
441
c LYM107 Lymphoproliferative Syndrome 2 50 0.040
442
P SDR002 Siderosis 44 0.040
443
NSH001 Nasu-Hakola Disease 44 0.040
444
c CNT015 Central Sleep Apnea 44 0.040
445
SPR066 Superficial Siderosis 34 0.040
446
c TRC078 Trichohepatoenteric Syndrome 2 29 0.040
447
DMN012 Dementia - Subcortical 13 0.040
448
DPH001 Diphtheria 59 0.040
449
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.040
450
P MSC003 Muscular Atrophy 50 0.040
451
HMT002 Hematologic Cancer 64 0.039
452
P NTR004 Neutropenia 59 0.039
453
VSC006 Vascular Cancer 51 0.039
454
P PLM037 Pulmonary Hypertension 79 0.039
455
P ADN016 Adenocarcinoma 69 0.039
456
P DBT005 Diabetes Insipidus 53 0.039
457
PRP080 Peripheral Artery Disease 37 0.039
458
c CRN172 Coronary Heart Disease 3 19 0.039
459
P RBN001 Rubinstein-Taybi Syndrome 64 0.039
460
STT001 Status Epilepticus 59 0.039
461
c HPT007 Hepatitis E 54 0.039
462
NWC001 Newcastle Disease 54 0.039
463
LYM040 Lymphoblastic Lymphoma 53 0.039
464
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.039
465
c PRK025 Parkinson Disease 10 38 0.039
466
OCL011 Ocular Motility Disease 37 0.039
467
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 36 0.039
468
ATM059 Autoimmune Disease 6 22 0.039
469
CRB087 Cerebral Arteriosclerosis 21 0.039
470
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.039
471
MXD001 Mixed Cerebral Palsy 16 0.039
472
SVR004 Severe Combined Immunodeficiency 69 0.038
473
P VLC001 Velocardiofacial Syndrome 62 0.038
474
BDY001 Body Dysmorphic Disorder 39 0.038
475
WHP002 Whiplash 36 0.038
476
P CRN035 Cranial Nerve Palsy 46 0.038
477
SND002 Sneddon Syndrome 44 0.038
478
CRB086 Cerebral Aneurysms 39 0.038
479
c CHR579 Chiari Malformation Type Ii 37 0.038
480
BNL002 Bone Lymphoma 32 0.038
481
IMM068 Immunodeficiency 8 30 0.038
482
P CRB042 Cerebellar Ataxia 63 0.038
483
P SPR098 Supranuclear Palsy, Progressive 56 0.038
484
INT007 Intermediate Coronary Syndrome 50 0.038
485
FML037 Female Breast Cancer 50 0.038
486
P CLL015 Collagen Disease 50 0.038
487
FML039 Female Reproductive System Disease 48 0.038
488
HYP085 Hypothalamic Disease 44 0.038
489
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.038
490
c ADL001 Adult Lymphoma 39 0.038
491
c ALZ040 Alzheimer's Disease 11 27 0.038
492
INT074 Intracranial Arteriosclerosis 14 0.038
493
P INF037 Inflammatory Bowel Disease 63 0.037
494
P ALX003 Alexander Disease 63 0.037
495
P LBR001 Leber Congenital Amaurosis 61 0.037
496
IMM142 Immunodeficiency 50 20 0.037
497
P TRN020 Turner Syndrome 65 0.037
498
GRW007 Growth Hormone Deficiency 50 0.037
499
SPS007 Spastic Cerebral Palsy 44 0.037
500
P INT030 Intracranial Aneurysm 54 0.037
501
P MCR010 Microcephaly 58 0.037
502
P EXN002 Exanthem 57 0.036
503
P CHR562 Chronic Myelocytic Leukemia 41 0.036
504
PRM151 Primary Bone Lymphoma 26 0.036
505
c LKM005 Leukemia, T-Cell, Chronic 20 0.036
506
P CRB019 Cerebral Amyloid Angiopathy 58 0.036
507
IRR002 Irritable Bowel Syndrome 58 0.036
508
DBT010 Diabetic Neuropathy 55 0.036
509
c BCT007 Bacterial Meningitis 54 0.036
510
LND001 Landau-Kleffner Syndrome 35 0.036
511
P GNR027 Generalized Peeling Skin Syndrome 19 0.036
512
P FLL037 Follicular Lymphoma 70 0.036
513
P CNJ013 Conjunctivitis 64 0.036
514
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.036
515
BRN106 Burns 52 0.036
516
c PRK059 Parkinson Disease 8 48 0.036
517
BNG009 Benign Epilepsy with Centrotemporal Spikes 39 0.036
518
c SCH064 Schizophrenia 10 19 0.036
519
P ATX030 Ataxia-Telangiectasia 77 0.036
520
ADR007 Adrenoleukodystrophy 72 0.036
521
P PRD006 Prader-Willi Syndrome 62 0.036
522
FTT001 Fatty Liver Disease 59 0.036
523
c NRF018 Neurofibromatosis, Type 1 67 0.035
524
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.035
525
P ADD001 Addison's Disease 62 0.035
526
VSC011 Vasculitis 62 0.035
527
P WLD002 Waldenstrom Macroglobulinemia 58 0.035
528
ANT011 Antisocial Personality Disorder 47 0.035
529
CHR008 Choroiditis 44 0.035
530
BRN018 Borna Disease 42 0.035
531
BNS002 Bone Structure Disease 37 0.035
532
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.035
533
c PRK022 Parkinson Disease 12 21 0.035
534
SQM006 Squamous Cell Carcinoma 70 0.035
535
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.035
536
BNF002 Bone Fracture 50 0.035
537
LYM017 Lyme Disease 63 0.035
538
BHC003 Behcet Syndrome 60 0.035
539
HMP009 Haemophilus Influenzae 45 0.035
540
c SPN100 Spinocerebellar Ataxia 27 43 0.035
541
SNS023 Sensory System Cancer 43 0.035
542
DYS009 Dysthymic Disorder 37 0.035
543
c SPS072 Spastic Ataxia 1, Autosomal Dominant 27 0.035
544
P LPR003 Leprosy 69 0.034
545
SKN016 Skin Disease 66 0.034
546
P LNG028 Long Qt Syndrome 64 0.034
547
P GT001 Gout 58 0.034
548
ETH011 Ethylmalonic Encephalopathy 56 0.034
549
c PRC016 Pre-Eclampsia 56 0.034
550
ORL011 Oral Cancer 56 0.034
551
CRD118 Cardiovascular Cancer 44 0.034
552
P CRB059 Cerebellar Degeneration 34 0.034
553
P RTN024 Retinoblastoma 74 0.034
554
MSL001 Measles 61 0.034
555
DFF005 Diffuse Large B-Cell Lymphoma 59 0.034
556
MYL031 Myeloproliferative Neoplasm 58 0.034
557
P CHL002 Childhood Absence Epilepsy 55 0.034
558
SKN027 Skin Conditions 43 0.034
559
HYP458 Hyper Ige Syndrome 42 0.034
560
MNS002 Mini Stroke 19 0.034
561
P SML001 Small Cell Carcinoma 56 0.034
562
PRP036 Peripheral T-Cell Lymphoma 45 0.034
563
AGR002 Agoraphobia 44 0.034
564
c GRN014 Grn-Related Frontotemporal Dementia 40 0.034
565
c CNT068 Central Pain Syndrome 29 0.034
566
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 16 0.034
567
P WSK001 Wiskott-Aldrich Syndrome 73 0.033
568
KRT004 Keratitis 71 0.033
569
P OST002 Osteoporosis 64 0.033
570
P ECL001 Eclampsia 54 0.033
571
ADS004 Aids Dementia Complex 39 0.033
572
CRT013 Carotid Stenosis 36 0.033
573
IMM076 Immunodeficiency 24 27 0.033
574
P AGM001 Agammaglobulinemia 64 0.033
575
GLC006 Galactosemia 64 0.033
576
LPP001 Lipoprotein Lipase Deficiency 63 0.033
577
P GLM007 Glomerulonephritis 59 0.033
578
P HMP007 Hemophilia 57 0.033
579
SCK005 Sickle Cell Disease 51 0.033
580
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.033
581
PRN023 Prion Disease 48 0.033
582
PTT009 Pituitary Gland Disease 47 0.033
583
P PNB001 Pineoblastoma 44 0.033
584
SCR011 Scrapie 38 0.033
585
IMM071 Immunodeficiency 12 26 0.033
586
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.033
587
PLR008 Pleurisy 50 0.033
588
c SPN312 Spinocerebellar Ataxia 14 46 0.033
589
CRY004 Cryoglobulinemia 46 0.033
590
DLS001 Delusional Disorder 41 0.033
591
ADP001 Adiposis Dolorosa 36 0.033
592
CRT012 Cortical Blindness 35 0.033
593
PRG033 Progressive Non-Fluent Aphasia 27 0.033
594
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.033
595
BRN049 Brain Tumor, Childhood 20 0.033
596
P MTC003 Metachromatic Leukodystrophy 70 0.033
597
P RCK004 Rickets 61 0.033
598
P GST049 Gastrointestinal System Cancer 60 0.033
599
CFF002 Coffin-Lowry Syndrome 55 0.033
600
P MMB011 Membranous Nephropathy 54 0.033
601
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.033
602
IMM096 Immunodeficiency 30 27 0.033
603
SCK003 Sickle Cell Anemia 71 0.032
604
CHG001 Chagas Disease 67 0.032
605
CHL123 Chlamydia 60 0.032
606
HRY003 Hairy Cell Leukemia 57 0.032
607
P FNC043 Fanconi Anemia, Complementation Group E 55 0.032
608
WHM001 Whim Syndrome 53 0.032
609
BRN004 Brain Edema 52 0.032
610
TCK001 Tick-Borne Encephalitis 50 0.032
611
CHR105 Choreoacanthocytosis 44 0.032
612
c MTR002 Mitral Valve Insufficiency 44 0.032
613
OPP004 Oppositional Defiant Disorder 43 0.032
614
c PRM023 Pre-Malignant Neoplasm 41 0.032
615
FRG010 Fragile X Tremor/ataxia Syndrome 36 0.032
616
P OTS001 Otosclerosis 35 0.032
617
HNS001 Hansen's Disease 30 0.032
618
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 0.032
619
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 16 0.032
620
P THL005 Thalassemia 64 0.032
621
ADN018 Adenoma 58 0.032
622
P HYP024 Hypoparathyroidism 53 0.032
623
SKN023 Skin Tag 44 0.032
624
ATM012 Autoimmune Disease of Blood 35 0.032
625
PST086 Posterior Cortical Atrophy 32 0.032
626
c MYC058 Myocardial Infarction 2 28 0.032
627
P OST012 Osteoarthritis 83 0.031
628
P MYL005 Myelofibrosis 67 0.031
629
P MYS003 Myasthenia Gravis 67 0.031
630
P ART023 Arthropathy 64 0.031
631
CHD001 Chediak-Higashi Syndrome 64 0.031
632
INT075 Intracranial Hypertension 50 0.031
633
c ACT134 Acute Liver Failure 50 0.031
634
CRB027 Cerebellar Disease 47 0.031
635
DDN006 Duodenitis 42 0.031
636
CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 41 0.031
637
MTR028 Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones 32 0.031
638
BRC012 Brucellosis 66 0.030
639
CTN007 Cutaneous Leishmaniasis 62 0.030
640
BLL006 Bullous Pemphigoid 59 0.030
641
P UVT001 Uveitis 58 0.030
642
TRP002 Tropical Spastic Paraparesis 55 0.030
643
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 49 0.030
644
SLP001 Sleeping Sickness 48 0.030
645
P HYP263 Hypersomnia 40 0.030
646
KLV001 Kluver-Bucy Syndrome 38 0.030
647
DPR002 Depersonalization Disorder 35 0.030
648
c PRK051 Parkinson Disease 18 30 0.030
649
FRN030 Frontotemporal Dementia with Parkinsonism-17 29 0.030
650
DMN016 Dementia, Familial, Nonspecific 23 0.030
651
HRP008 Herpes Simiae 12 0.030
652
HRP012 Herpesvirus Simiae B Virus 10 0.030
653
CST001 Costello Syndrome 68 0.030
654
c HMP029 Hemophilia a 63 0.030
655
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.030
656
FCL012 Facial Paralysis 50 0.030
657
FML038 Female Reproductive Organ Cancer 50 0.030
658
CHR001 Churg-Strauss Syndrome 49 0.030
659
ADR012 Adrenal Gland Disease 48 0.030
660
P PRM108 Primary Progressive Multiple Sclerosis 46 0.030
661
PTT037 Pituitary Tumors 45 0.030
662
MTS001 Mutism 43 0.030
663
P BLP003 Blepharospasm 43 0.030
664
MDS022 Mediastinitis 41 0.030
665
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.030
666
c LYM106 Lymphoproliferative Syndrome 1 32 0.030
667
WRT002 Writing Disorder 27 0.030
668
c LKM004 Leukemia, B-Cell, Chronic 24 0.030
669
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.030
670
GLC077 Glucocorticoid Therapy, Response to 16 0.030
671
OBS060 Obesity Due to Sim1 Deficiency 9 0.030
672
P APL001 Aplastic Anemia 75 0.030
673
WRN001 Werner Syndrome 67 0.030
674
PLM001 Pulmonary Tuberculosis 67 0.030
675
P CRN037 Craniosynostosis 66 0.030
676
P LKD001 Leukodystrophy 59 0.030
677
PTT006 Pituitary Adenoma 56 0.030
678
DBT004 Diabetic Polyneuropathy 52 0.030
679
P PRM006 Primary Biliary Cirrhosis 51 0.030
680
SPN041 Spinal Cord Disease 51 0.030
681
STM006 Stomach Disease 50 0.030
682
OVR063 Overnutrition 50 0.030
683
RFL001 Reflex Sympathetic Dystrophy 48 0.030
684
CRV043 Cervical Dystonia 44 0.030
685
ALX001 Alexia 40 0.030
686
ANG049 Angioedema Induced by Ace Inhibitors 34 0.030
687
RFR004 Refractory Hematologic Cancer 28 0.030
688
IMM080 Immunodeficiency 23 27 0.030
689
WLS001 Wilson Disease 72 0.028
690
P NJM001 Nijmegen Breakage Syndrome 67 0.028
691
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.028
692
P PRD008 Periodontitis 63 0.028
693
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.028
694
P DNT015 Dent Disease 61 0.028
695
P RHN004 Rhinitis 60 0.028
696
MRB003 Morbid Obesity 58 0.028
697
MSC077 Muscle Eye Brain Disease 57 0.028
698
P MYP006 Myopia 56 0.028
699
TTH006 Tooth Disease 52 0.028
700
HMG002 Hemoglobinuria 48 0.028
701
NRM004 Neuroma 48 0.028
702
P TRC086 Trichohepatoenteric Syndrome 1 48 0.028
703
CRB085 Cerebral Hemorrhage 46 0.028
704
HRT007 Heart Cancer 46 0.028
705
AMB002 Amblyopia 46 0.028
706
CHR413 Chronic Myocardial Ischemia 41 0.028
707
TRC010 Trichotillomania 40 0.028
708
MNT001 Mantle Cell Lymphoma 72 0.028
709
P PRT013 Portal Hypertension 60 0.028
710
HRP004 Herpes Zoster 56 0.028
711
PLS007 Plasmodium Falciparum Malaria 55 0.028
712
P SYP003 Syphilis 53 0.028
713
MYL001 Myelitis 51 0.028
714
OPT003 Opiate Dependence 50 0.028
715
URB001 Urbach-Wiethe Disease 49 0.028
716
P MRC003 Mercury Poisoning 45 0.028
717
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.028
718
RPR002 Reproductive System Disease 41 0.028
719
SCH003 Schizophreniform Disorder 40 0.028
720
c BNG023 Benign Familial Infantile Epilepsy 39 0.028
721
CRV045 Cervical Intraepithelial Neoplasia 38 0.028
722
CLS049 Classic Phenylketonuria 32 0.028
723
IMM082 Immunodeficiency 18 31 0.028
724
MTH027 Mthfr Deficiency 31 0.028
725
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 29 0.028
726
ADT002 Auditory System Cancer 26 0.028
727
PTC005 Pituicytoma 24 0.028
728
P ANR002 Aniridia 64 0.027
729
ALL003 Allergic Rhinitis 63 0.027
730
c NRF019 Neurofibromatosis, Type 2 62 0.027
731
RBR001 Roberts Syndrome 60 0.027
732
P GRV001 Graves' Disease 59 0.027
733
P MLT074 Multiple Endocrine Neoplasia 56 0.027
734
KRT002 Keratomalacia 52 0.027
735
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.027
736
NNL002 Nonalcoholic Steatohepatitis 50 0.027
737
PRT038 Protein-Energy Malnutrition 49 0.027
738
MLL012 Miller Syndrome 49 0.027
739
IMM065 Immunodeficiency 10 36 0.027
740
MLR007 Male Reproductive System Disease 34 0.027
741
P HRT017 Heart Tumor 32 0.027
742
c MJR006 Major Affective Disorder 5 15 0.027
743
THY028 Thyroid Cancer 69 0.026
744
P PLR004 Pleuropulmonary Blastoma 65 0.026
745
CNT047 Contact Dermatitis 61 0.026
746
ALL010 Allergic Contact Dermatitis 57 0.026
747
TNS005 Tonsillitis 57 0.026
748
c VRL007 Viral Encephalitis 54 0.026
749
SML033 Small Cell Cancer of the Lung, Somatic 54 0.026
750
P CNT005 Central Nervous System Lymphoma 53 0.026
751
c PRM226 Primary Central Nervous System Lymphoma 49 0.026
752
P BRN120 Bronchus Cancer 44 0.026
753
P SKN013 Skin Benign Neoplasm 43 0.026
754
MNN032 Meningococcal Meningitis 42 0.026
755
BNS003 Binswanger's Disease 42 0.026
756
FCT008 Factitious Disorder 41 0.026
757
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.026
758
URT001 Urethritis 41 0.026
759
P CNN004 Connective Tissue Cancer 40 0.026
760
MTH021 Methylmalonic Acidemia with Homocystinuria 37 0.026
761
CHR073 Choreatic Disease 37 0.026
762
P CNT036 Central Nervous System Germ Cell Tumor 37 0.026
763
P HYP111 Hyperprolinemia 33 0.026
764
c PRK026 Parkinson Disease 11 29 0.026
765
MDR006 Moderate and Severe Traumatic Brain Injury 23 0.026
766
DRG016 Drug Induced Dyskinesia 23 0.026
767
IMM103 Immunodeficiency 37 19 0.026
768
CHR321 Chorea and Dementia 16 0.026
769
c MJR003 Major Affective Disorder 6 15 0.026
770
c SML023 Small Cell Lung Cancer, Adult 15 0.026
771
INT031 Integrative Agnosia 9 0.026
772
FML202 Familial Alzheimer-Like Prion Disease 9 0.026
773
P HMC003 Hemochromatosis 72 0.026
774
EWN003 Ewing Sarcoma 66 0.026
775
AND015 Androgen Insensitivity 64 0.026
776
CHR103 Charge Syndrome 62 0.026
777
LPT001 Leptospirosis 62 0.026
778
ACN011 Acne 62 0.026
779
CRD119 Cardiac Arrest 61 0.026
780
CHK001 Chikungunya 54 0.026
781
WST005 West Nile Virus 53 0.026
782
FDL002 Food Allergy 53 0.026
783
P NNT009 Neonatal Diabetes Mellitus 52 0.026
784
CRC006 Carcinoid Syndrome 52 0.026
785
P CRP007 Carpenter Syndrome 51 0.026
786
TRN044 Transposition of the Great Arteries 48 0.026
787
THL018 Thalassemia Major 48 0.026
788
RTN020 Retinal Vascular Disease 48 0.026
789
SYN036 Syncope 47 0.026
790
ACR006 Aceruloplasminemia 45 0.026
791
URT010 Ureteral Obstruction 45 0.026
792
MLL002 Miller Fisher Syndrome 43 0.026
793
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 42 0.026
794
c CNG031 Congenital Nervous System Abnormality 37 0.026
795
FXF002 Fox-Fordyce Disease 36 0.026
796
c CRN176 Coronary Heart Disease 9 18 0.026
797
DVL005 Developmental Dyspraxia 18 0.026
798
CD4004 Cd4 Deficiency 14 0.026
799
P LYN001 Lynch Syndrome 69 0.024
800
GLC037 Glucocorticoid Resistance 62 0.024
801
GNG013 Gingivitis 61 0.024
802
P SYS005 Systemic Scleroderma 61 0.024
803
P SNS014 Sinusitis 60 0.024
804
P DRR001 Diarrhea 60 0.024
805
CHR285 Chronic Myelomonocytic Leukemia 56 0.024
806
PRC002 Paracoccidioidomycosis 55 0.024
807
P WRD001 Waardenburg's Syndrome 55 0.024
808
P LRY019 Laryngitis 54 0.024
809
GNT003 Genital Herpes 53 0.024
810
PRS042 Prostate Disease 52 0.024
811
BRN038 Bronchial Disease 51 0.024
812
MCR004 Macroglobulinemia 50 0.024
813
P SCK002 Sick Sinus Syndrome 50 0.024
814
MSC072 Muscle Cancer 49 0.024
815
MTN003 Motion Sickness 48 0.024
816
P NGH001 Night Blindness 48 0.024
817
INT253 Intestinal Benign Neoplasm 47 0.024
818
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 47 0.024
819
P SYR001 Syringomyelia 47 0.024
820
OST003 Osteonecrosis 45 0.024
821
PTT008 Pituitary Carcinoma 45 0.024
822
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 41 0.024
823
HRN003 Heroin Dependence 40 0.024
824
RCT017 Rectal Disease 40 0.024
825
ATN003 Autonomic Nervous System Neoplasm 40 0.024
826
c PRG001 Progressive Muscular Atrophy 39 0.024
827
P OCY001 Oocyte Maturation Defect 38 0.024
828
P UTR038 Uterine Disease 37 0.024
829
AGR018 Agraphia 36 0.024
830
INF013 Inferior Myocardial Infarction 35 0.024
831
HMC014 Homocysteinemia 35 0.024
832
MLN003 Melancholia 34 0.024
833
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.024
834
CNT017 Central Nervous System Origin Vertigo 24 0.024
835
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.024
836
ADS006 Aids - Neurological Complications 12 0.024
837
c AMY091 Amyotrophic Lateral Sclerosis 1 78 0.022
838
TST021 Testicular Germ Cell Tumor 69 0.022
839
P CLC005 Celiac Disease 68 0.022
840
P CRD013 Cardiofaciocutaneous Syndrome 63 0.022
841
GLB015 Glioblastoma Multiforme 63 0.022
842
VNW001 Von Willebrand's Disease 61 0.022
843
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.022
844
TXC005 Toxic Shock Syndrome 60 0.022
845
P HMN010 Hemangioma 59 0.022
846
ORL015 Oral Squamous Cell Carcinoma 57 0.022
847
SFT003 Soft Tissue Sarcoma 57 0.022
848
P RBL001 Rubella 57 0.022
849
P LPS002 Liposarcoma 55 0.022
850
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 54 0.022
851
ERD001 Erdheim-Chester Disease 52 0.022
852
QDR001 Quadriplegia 52 0.022
853
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.022
854
MRG003 Marginal Zone B-Cell Lymphoma 52 0.022
855
IRN001 Iron Deficiency Anemia 52 0.022
856
HYP005 Hypokalemia 51 0.022
857
CLN019 Colonic Disease 51 0.022
858
STM007 Stomatitis 50 0.022
859
LPR001 Lepromatous Leprosy 50 0.022
860
GLM004 Gliomatosis Cerebri 49 0.022
861
NCT008 Nicotine Dependence, Protection Against 49 0.022
862
RTN003 Retinal Ischemia 48 0.022
863
RTC005 Reticulosarcoma 48 0.022
864
P PLM006 Pulmonary Alveolar Proteinosis 48 0.022
865
RTC009 Reticulum Cell Sarcoma 47 0.022
866
GST009 Gastroschisis 47 0.022
867
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.022
868
IMM105 Immunodeficiency with Hyper-Igm, Type 3 45 0.022
869
c FLL041 Follicular Lymphoma 1 45 0.022
870
MLR006 Male Reproductive Organ Cancer 43 0.022
871
DLY005 Delayed Sleep Phase Syndrome 37 0.022
872
GRM001 Germ Cell and Embryonal Cancer 36 0.022
873
CHL078 Childhood-Onset Schizophrenia 34 0.022
874
FNT004 Fainting 33 0.022
875
CRB040 Cerebrum Cancer 32 0.022
876
PDP001 Pedophilia 30 0.022
877
CRS012 Carasil Syndrome 29 0.022
878
CHL109 Childhood Apraxia of Speech 28 0.022
879
c PRK037 Parkinson Disease 13 27 0.022
880
FNC005 Functional Colonic Disease 27 0.022
881
SPR032 Superficial Siderosis of the Central Nervous System 26 0.022
882
c ADL096 Adult Hepatocellular Carcinoma 24 0.022
883
IMM085 Immunodeficiency 25 23 0.022
884
NRS005 Neurosarcoidosis 23 0.022
885
IMM084 Immunodeficiency 17, Cd3 Gamma Deficient 21 0.022
886
c SPR049 Supranuclear Palsy, Progressive, 2 18 0.022
887
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.022
888
VGS001 Vagus Nerve Disease 18 0.022
889
c ATS173 Autism 18 17 0.022
890
OLF001 Olfactory Nerve Disease 16 0.022
891
c MJR004 Major Affective Disorder 4 16 0.022
892
BSL005 Basal Ganglia Cerebrovascular Disease 9 0.022
893
OMN001 Omenn Syndrome 67 0.020
894
ART005 Arteriovenous Malformation 66 0.020
895
P HYP098 Hypereosinophilic Syndrome 63 0.020
896
TYP007 Typhoid Fever 61 0.020
897
c ATM010 Autoimmune Hemolytic Anemia 60 0.020
898
CMM005 Common Cold 59 0.020
899
P THY023 Thymoma 57 0.020
900
NRN004 Neuroendocrine Tumor 56 0.020
901
c HYP615 Hyperparathyroidism, Familial Primary 56 0.020
902
P WVR001 Weaver Syndrome 56 0.020
903
STF001 Stiff-Person Syndrome 56 0.020
904
P FND001 Fundus Albipunctatus 55 0.020
905
RCT018 Rectal Neoplasm 54 0.020
906
PLS006 Plasmodium Vivax Malaria 53 0.020
907
NRF007 Neurofibroma 53 0.020
908
BLT006 Bilateral Breast Cancer 53 0.020
909
P TRT010 Teratoma 52 0.020
910
STR008 Strongyloidiasis 51 0.020
911
TRY001 Trypanosomiasis 51 0.020
912
RHM028 Rheumatic Heart Disease 50 0.020
913
c MLG079 Malignant Pleural Mesothelioma 50 0.020
914
END035 Endocrine Gland Cancer 49 0.020
915
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.020
916
PST021 Postpartum Depression 49 0.020
917
WHP001 Whipple Disease 49 0.020
918
PYD002 Pyoderma 48 0.020
919
ECT026 Ectopic Pregnancy 48 0.020
920
JCB001 Jacobsen Syndrome 48 0.020
921
VST004 Vestibular Disease 44 0.020
922
EXT033 Extrapulmonary Tuberculosis 44 0.020
923
GRN017 Granulocytopenia 44 0.020
924
P PRL003 Proliferative Glomerulonephritis 43 0.020
925
CMP034 Complete Androgen Insensitivity Syndrome 43 0.020
926
NSS002 Neisseria Meningitidis Infection 43 0.020
927
EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 42 0.020
928
CRY014 Cryptococcal Meningitis 42 0.020
929
SLR001 Sialuria 42 0.020
930
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.020
931
P CYS017 Cystic Teratoma 40 0.020
932
P ARC016 Auriculocondylar Syndrome 1 40 0.020
933
THL010 Thalassemia Minor 39 0.020
934
NRN008 Neuronal Intranuclear Inclusion Disease 39 0.020
935
MHC001 Mhc Class Ii Deficiency 39 0.020
936
BRS090 Breast Reconstruction 38 0.020
937
HRM002 Hermaphroditism 38 0.020
938
PDT001 Pediatric Lymphoma 38 0.020
939
IGG007 Igg4-Related Disease 38 0.020
940
PRP028 Peripheral Vertigo 38 0.020
941
HYP003 Hypermethioninemia 37 0.020
942
c ALP005 Alpha Chain Disease 37 0.020
943
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.020
944
c FNC042 Fanconi Anemia, Complementation Group D2 37 0.020
945
CNT018 Central Nervous System Leukemia 37 0.020
946
BLT001 Bilateral Retinoblastoma 37 0.020
947
c TRN009 Transient Hypogammaglobulinemia of Infancy 36 0.020
948
BRN048 Brain Stem Cancer 36 0.020
949
SPL040 Split Hand 36 0.020
950
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 35 0.020
951
PHT008 Photosensitive Epilepsy 34 0.020
952
HYP231 Hypothalamic Hamartomas 34 0.020
953
LNS003 Lens Disease 33 0.020
954
SPR024 Supratentorial Cancer 33 0.020
955
NMN001 Nominal Aphasia 33 0.020
956
P TRN016 Transient Hypogammaglobulinemia 33 0.020
957
CRV069 Cervix Disease 32 0.020
958
c CNN010 Connective Tissue Benign Neoplasm 32 0.020
959
c ALZ031 Alzheimer Disease 17 32 0.020
960
c CRP022 Carpenter Syndrome 2 31 0.020
961
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.020
962
PRG090 Progressive Relapsing Multiple Sclerosis 30 0.020
963
SPC001 Space Motion Sickness 29 0.020
964
BNM010 Bone Marrow Failure Syndrome 1 29 0.020
965
CNT069 Centrotemporal Epilepsy 28 0.020
966
SBC014 Subclavian Steal Syndrome 28 0.020
967
CRN033 Cranial Nerve Malignant Neoplasm 28 0.020
968
RDT005 Radiation Induced Cancer 28 0.020
969
NNT021 Neonatal Meningitis 28 0.020
970
ENC005 Encephalomalacia 27 0.020
971
IMM036 Immunodeficiency, Isolated 27 0.020
972
CNT023 Central Nervous System Hemangioma 26 0.020
973
YNG002 Young Syndrome 26 0.020
974
CRB014 Cerebral Angioma 24 0.020
975
IMM120 Immunodeficiency 40 24 0.020
976
IMM025 Immunoglobulin a Deficiency 2 24 0.020
977
HDG004 Hodgkin's Granuloma 24 0.020
978
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 23 0.020
979
PRS011 Persian Gulf Syndrome 23 0.020
980
c DYS120 Dyslexia 2 22 0.020
981
IMM088 Immunodeficiency 36 22 0.020
982
BRN027 Brain Angioma 21 0.020
983
HYP002 Hypothalamic Neoplasm 20 0.020
984
CML001 Cumulative Trauma Disorders 18 0.020
985
c BSL039 Basal Ganglia Calcification, Idiopathic, 6 18 0.020
986
HDG006 Hodgkin's Paragranuloma 17 0.020
987
c GRV009 Graves Disease 2 16 0.020
988
SCL044 Scalp Syndrome 15 0.020
989
c INF136 Influenza, Severe 15 0.020
990
PRP010 Prepuce Cancer 15 0.020
991
HRT029 Heart Tumor of the Child 15 0.020
992
WSC001 Wisconsin Syndrome 14 0.020
993
c FRM002 Form Agnosia 14 0.020
994
TCL006 T Cell Immunodeficiency Primary 12 0.020
995
MNT045 Montefiore Syndrome 10 0.020
996
KLV002 Klüver-Bucy Syndrome 2 0.020
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