Search results for "memory impairment"

The MalaCard for "memory impairment" has been retired.
Searching MalaCards for entries containing "memory impairment"

948 hits were found for 'memory impairment'

# Family MCID Name MIFTS Score
1
DMN002 Dementia 64 0.333
2
P ALZ034 Alzheimer Disease 93 0.226
3
P SCH015 Schizophrenia 76 0.224
4
P EPL164 Epilepsy 66 0.199
5
CRB009 Cerebritis 38 0.198
6
NRN002 Neuronitis 42 0.195
7
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.187
8
P ENC018 Encephalopathy 59 0.181
9
PSY004 Psychotic Disorder 67 0.178
10
LRN003 Learning Disability 51 0.178
11
DSS008 Disease of Mental Health 55 0.170
12
P HPT021 Hepatitis 70 0.168
13
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.157
14
ISC004 Ischemia 59 0.154
15
BRN071 Brain Injury 52 0.153
16
SMN008 Semantic Dementia 44 0.149
17
END072 Endotheliitis 42 0.147
18
P NRV007 Nervous System Disease 71 0.140
19
c CNT035 Central Nervous System Disease 59 0.136
20
TMP001 Temporal Lobe Epilepsy 51 0.135
21
HV1006 Hiv-1 82 0.135
22
AMN003 Amnestic Disorder 46 0.131
23
DRG001 Drug Psychosis 40 0.131
24
RTR001 Retrograde Amnesia 40 0.130
25
VSC002 Vascular Dementia 54 0.129
26
TRM010 Traumatic Brain Injury 52 0.126
27
P LKM002 Leukemia 70 0.124
28
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.123
29
ANX002 Anxiety Disorder 69 0.121
30
IMP003 Impaired Renal Function Disease 37 0.119
31
MDD011 Mood Disorder 61 0.118
32
PST028 Post-Traumatic Stress Disorder 57 0.117
33
TRN012 Transient Global Amnesia 39 0.117
34
STR067 Stroke, Ischemic 77 0.113
35
P ART022 Arthritis 75 0.113
36
P DYS005 Dyslexia 39 0.111
37
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.111
38
P LVR013 Liver Disease 72 0.110
39
P OBS005 Obesity 93 0.109
40
HYP266 Hypoxia 55 0.109
41
ADT003 Auditory System Disease 51 0.109
42
P SPC019 Specific Language Impairment 29 0.108
43
SPC010 Speech and Communication Disorders 46 0.107
44
PHY002 Physical Disorder 44 0.107
45
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.107
46
P PRS038 Personality Disorder 61 0.107
47
P LYM118 Lymphoma 70 0.106
48
MVM001 Movement Disease 54 0.106
49
APH002 Aphasia 53 0.106
50
SLP005 Sleep Disorder 53 0.104
51
CND002 Conduct Disorder 56 0.101
52
ALN001 Aland Island Eye Disease 45 0.100
53
P ENC004 Encephalitis 61 0.100
54
ACT084 Acute Stress Disorder 40 0.099
55
P URF003 Urofacial Syndrome 1 52 0.099
56
P BRS047 Breast Cancer 100 0.099
57
URN009 Urinary System Disease 53 0.098
58
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.098
59
MNT002 Mental Depression 54 0.098
60
P RHM011 Rheumatoid Arthritis 88 0.095
61
CRB159 Cerebral Visual Impairment 40 0.094
62
TBR010 Tuberculosis 69 0.093
63
c HPT001 Hepatitis C 68 0.092
64
RDN001 Reading Disorder 39 0.091
65
HDN002 Head Injury 45 0.091
66
c HPT016 Hepatitis B 64 0.091
67
c HPT003 Hepatitis a 59 0.089
68
P ATS007 Autism Spectrum Disorder 64 0.089
69
PCK002 Pick Disease 67 0.087
70
GNR004 Generalized Anxiety Disorder 51 0.087
71
DWN001 Down Syndrome 65 0.086
72
P AST005 Asthma 82 0.086
73
P PRK057 Parkinson Disease, Late-Onset 72 0.086
74
c SYS001 Systemic Lupus Erythematosus 87 0.086
75
P ATX004 Ataxia 53 0.085
76
P LPS004 Lupus Erythematosus 63 0.085
77
P BPL003 Bipolar Disorder 62 0.085
78
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.085
79
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.085
80
AYM001 Ayme-Gripp Syndrome 45 0.085
81
HYP066 Hyperglycemia 60 0.085
82
NTR005 Nutritional Deficiency Disease 39 0.084
83
P PRS013 Prosopagnosia 36 0.084
84
ANT019 Anterograde Amnesia 31 0.084
85
c ALZ012 Alzheimer Disease 12 25 0.083
86
BSL008 Basal Ganglia Disease 43 0.083
87
P MYP004 Myopathy 67 0.082
88
DVL001 Developmental Coordination Disorder 37 0.082
89
c HPT073 Hepatitis C Virus 72 0.082
90
P INF038 Influenza 74 0.081
91
ATN002 Autonomic Nervous System Disease 47 0.080
92
ANS006 Anosognosia 28 0.079
93
P MNN013 Meningitis 65 0.079
94
CMM004 Common Variable Immunodeficiency 67 0.078
95
SPC005 Speech Disorder 43 0.077
96
TRN015 Transient Cerebral Ischemia 56 0.077
97
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.077
98
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.077
99
BRN028 Brain Cancer 70 0.077
100
P NRP001 Neuropathy 60 0.076
101
END030 End Stage Renal Failure 52 0.076
102
ADR009 Adrenal Cortex Disease 41 0.076
103
P INT063 Intellectual Disability 53 0.076
104
c VRL010 Viral Hepatitis 61 0.075
105
LPD004 Lipoid Nephrosis 48 0.075
106
GLC008 Glucose Metabolism Disease 47 0.075
107
P AMY004 Amyloidosis 64 0.075
108
FCL014 Focal Epilepsy 56 0.074
109
P HYP086 Hypothyroidism 65 0.074
110
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.074
111
P AGN002 Agnosia 56 0.074
112
BRN080 Brain Ischemia 41 0.074
113
P CRB088 Cerebral Atrophy 42 0.074
114
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.073
115
P MYL006 Myeloid Leukemia 67 0.072
116
GLT021 Glutaricaciduria, Type I 48 0.072
117
P MSC033 Muscle Disorders 52 0.072
118
P SZR006 Seizure Disorder 57 0.072
119
PRP027 Peripheral Vascular Disease 69 0.071
120
NRM005 Neuromuscular Disease 57 0.071
121
SPS057 Spasticity 42 0.071
122
VCC001 Vaccinia 46 0.070
123
P SLP006 Sleep Apnea 61 0.070
124
GLB003 Globe Disease 35 0.070
125
DRG011 Drug Addiction 51 0.070
126
SBS003 Substance Abuse 56 0.070
127
ART111 Artery Disease 57 0.070
128
P FRG001 Fragile X Syndrome 68 0.070
129
DMY004 Demyelinating Disease 55 0.070
130
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.069
131
ADJ001 Adjustment Disorder 38 0.069
132
c CRN214 Coronary Heart Disease 5 23 0.068
133
AMS001 Amusia 25 0.068
134
LYM009 Lymphocytic Choriomeningitis 43 0.068
135
OBS002 Obsessive-Compulsive Disorder 66 0.068
136
c HYP163 Hyperlipidemia Type 3 34 0.067
137
MLR004 Malaria 79 0.067
138
ATM052 Autoimmune Disease 1 28 0.067
139
P THY032 Thyroiditis 54 0.067
140
P NRV006 Nervous System Cancer 62 0.067
141
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.067
142
c CHR089 Chronic Kidney Failure 66 0.066
143
MSC004 Muscle Tissue Disease 36 0.066
144
SCH011 Schizotypal Personality Disorder 33 0.066
145
P HRP006 Herpes Simplex 65 0.066
146
ASP001 Asperger Syndrome 49 0.066
147
DRM006 Dermatitis 61 0.065
148
SXL003 Sexual Disorder 47 0.065
149
OBS061 Obstructive Sleep Apnea 66 0.065
150
P ANR007 Anorexia Nervosa 63 0.065
151
PRS047 Prostatitis 56 0.065
152
MTH009 Mouth Disease 63 0.065
153
CRB031 Cerebral Arterial Disease 31 0.065
154
c ALZ039 Alzheimer's Disease 7 21 0.065
155
CRB037 Cerebral Palsy 54 0.064
156
BLD054 Blood Protein Disease 40 0.064
157
DRG003 Drug Dependence 53 0.064
158
P PNM007 Pneumonia 66 0.064
159
P CHR345 Chronic Pain 49 0.064
160
P LYM026 Lymphoblastic Leukemia 60 0.063
161
TTN003 Tetanus 61 0.063
162
LYM027 Lymphopenia 54 0.063
163
ACR041 Acromelic Frontonasal Dysostosis 46 0.063
164
BRT030 Birth Defects 43 0.063
165
ALL026 Allergic Hypersensitivity Disease 53 0.063
166
HPT023 Hepatocellular Carcinoma 91 0.063
167
P INF032 Infertility 61 0.063
168
P SPS003 Spastic Diplegia 53 0.063
169
CNV002 Conversion Disorder 42 0.063
170
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.062
171
c PND001 Pain Disorder 55 0.062
172
SCL003 Social Phobia 48 0.062
173
c ALZ032 Alzheimer Disease 18 26 0.062
174
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.062
175
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.062
176
c PRK031 Parkinson Disease 1 55 0.061
177
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.061
178
APR001 Apraxia 48 0.061
179
c CHR417 Chronic Graft Versus Host Disease 50 0.061
180
DYS004 Dyscalculia 28 0.061
181
OPT006 Optic Nerve Disease 51 0.061
182
RTN023 Retinitis 49 0.061
183
KDS001 Kid Syndrome 53 0.061
184
PRM097 Primary Immunodeficiency Disease 61 0.061
185
VRL011 Viral Infectious Disease 59 0.061
186
ANR040 Aneurysm 57 0.061
187
c SCH051 Schizophrenia 4 31 0.061
188
FST001 Foster-Kennedy Syndrome 34 0.060
189
ALC007 Alcohol Dependence 65 0.060
190
P ATP001 Atopic Dermatitis 62 0.059
191
ATM054 Autoimmune Disease 3 18 0.059
192
WRN002 Wernicke-Korsakoff Syndrome 43 0.059
193
CRB004 Cerebral Artery Occlusion 46 0.059
194
HMT018 Hematopoietic Stem Cell Transplantation 41 0.059
195
HPT019 Hepatic Encephalopathy 56 0.058
196
ART021 Arteriosclerosis 59 0.058
197
SPC003 Specific Developmental Disorder 40 0.058
198
CHL071 Child Syndrome 58 0.058
199
WLL006 Wells Syndrome 56 0.058
200
GDS001 Good Syndrome 45 0.058
201
FCL011 Facial Nerve Disease 38 0.058
202
GNC005 Geniculate Ganglionitis 31 0.058
203
P TRM003 Tremor 54 0.058
204
CYT008 Cytomegalovirus Infection 51 0.057
205
C3D001 C3 Deficiency 53 0.057
206
P TCL004 T-Cell Leukemia 46 0.057
207
ATM053 Autoimmune Disease 2 19 0.057
208
LVR012 Liver Cirrhosis 67 0.057
209
P LTR001 Lateral Sclerosis 52 0.057
210
P HRT032 Heart Disease 76 0.057
211
WTH001 Withdrawal Disorder 41 0.057
212
VSC007 Vascular Disease 67 0.057
213
ATH003 Atherosclerosis 62 0.056
214
P HNT016 Huntington Disease 80 0.056
215
P PRP019 Peripheral Nervous System Disease 54 0.056
216
P SHR029 Short Syndrome 60 0.056
217
CYS001 Cystic Fibrosis 86 0.055
218
P CRN211 Coronary Artery Disease 75 0.055
219
MDY003 Mody, Type Ii 38 0.055
220
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.055
221
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.055
222
CLT003 Colitis 59 0.055
223
P LNG032 Lung Cancer 94 0.055
224
c BPL002 Bipolar I Disorder 47 0.055
225
c ALZ037 Alzheimer Disease-2 54 0.054
226
c CHR090 Chronic Lymphocytic Leukemia 74 0.054
227
EXF001 Exfoliation Syndrome 57 0.054
228
NSY001 N Syndrome 39 0.054
229
EYD002 Eye Disease 63 0.054
230
P PNC025 Panic Disorder 60 0.054
231
SBS004 Substance Dependence 50 0.054
232
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 0.054
233
LMB024 Limbic Encephalitis 36 0.054
234
PRM025 Primary Bacterial Infectious Disease 43 0.054
235
c ATM007 Autoimmune Disease of Central Nervous System 28 0.054
236
P PLN008 Peeling Skin Syndrome 47 0.054
237
c PRK045 Parkinson Disease 5 44 0.054
238
RSP006 Respiratory System Disease 62 0.053
239
ETN001 Eating Disorder 60 0.053
240
SPN369 Spinal Disease 41 0.053
241
DFC004 Deficiency Anemia 65 0.053
242
c ACT073 Acute Leukemia 62 0.053
243
P MYC007 Myocardial Infarction 79 0.053
244
P CRD011 Cardiomyopathy 67 0.053
245
IMM136 Immune System Disease 50 0.053
246
CRB033 Cerebral Degeneration 46 0.053
247
MYL009 Myelodysplastic Syndrome 74 0.052
248
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.052
249
c CRN175 Coronary Heart Disease 4 21 0.052
250
P PSR002 Psoriasis 63 0.052
251
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.052
252
NSD001 Nose Disease 52 0.052
253
WLL001 Williams-Beuren Syndrome 61 0.052
254
c PRK030 Parkinson Disease 4 39 0.052
255
P FBR031 Febrile Seizures 52 0.052
256
P FTL001 Fetal Alcohol Syndrome 53 0.051
257
P HYD006 Hydrocephalus 67 0.051
258
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.051
259
VSL003 Visual Agnosia 26 0.051
260
PRT037 Pertussis 64 0.051
261
P ALC004 Alcohol Abuse 60 0.051
262
CRH001 Crohn's Disease 76 0.050
263
P DMN033 Dementia, Frontotemporal 63 0.050
264
P CRV039 Cervicitis 44 0.050
265
ADM013 Adamantinoma of Long Bones 59 0.050
266
BRD004 Borderline Personality Disorder 46 0.050
267
c MLT010 Multiple Personality Disorder 36 0.050
268
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.050
269
P LYM033 Lymphoproliferative Syndrome 53 0.050
270
HYP037 Hyperhomocysteinemia 50 0.050
271
P PRS040 Prostate Cancer 89 0.050
272
CHR066 Chronic Fatigue Syndrome 64 0.050
273
CNN005 Connective Tissue Disease 61 0.049
274
c MLT093 Multiple Sclerosis 2 20 0.049
275
CHR012 Chronic Granulomatous Disease 65 0.049
276
c MJR008 Major Affective Disorder 2 22 0.049
277
P BCL006 B-Cell Lymphomas 64 0.049
278
CCN001 Cocaine Dependence 48 0.049
279
P ANG001 Angelman Syndrome 61 0.048
280
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.048
281
c BRN108 Branchiootic Syndrome 1 36 0.048
282
HPD002 Hepadnavirus Infection 23 0.048
283
P CTR002 Cataract 57 0.048
284
SRC014 Sarcoma 66 0.048
285
CTS003 Coats Disease 57 0.048
286
c ALZ014 Alzheimer Disease 16 23 0.048
287
c ALZ043 Alzheimer's Disease 15 21 0.048
288
c CRN173 Coronary Heart Disease 8 20 0.048
289
CRT016 Carotid Artery Disease 55 0.048
290
HRN022 Hearing Loss/deafness 25 0.048
291
TCL003 T Cell Deficiency 45 0.048
292
c PLN017 Peeling Skin Syndrome 1 33 0.048
293
P CRN178 Coronary Heart Disease 6 24 0.048
294
CNN002 Cannabis Abuse 41 0.048
295
VSL004 Visual Cortex Disease 29 0.048
296
CRB150 Cerebral Creatine Deficiency Syndrome 2 48 0.047
297
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.047
298
ALX002 Alexithymia 37 0.047
299
c MLT094 Multiple Sclerosis 3 26 0.047
300
ISC006 Ischemic Heart Disease 68 0.046
301
ETH011 Ethylmalonic Encephalopathy 59 0.046
302
P DYS154 Dystonia 64 0.046
303
c CNG006 Congenital Hypothyroidism 59 0.046
304
CRB090 Cerebral Hypoxia 48 0.046
305
c ERL020 Early-Onset Schizophrenia 46 0.046
306
c ALZ042 Alzheimer's Disease 14 37 0.046
307
c ADL017 Adult T-Cell Leukemia 58 0.046
308
WLF001 Wolff-Parkinson-White Syndrome 57 0.046
309
SML019 Smallpox 53 0.046
310
CNG034 Congestive Heart Failure 71 0.046
311
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.046
312
SYN041 Synesthesia 19 0.046
313
CRT015 Carotid Artery Occlusion 43 0.046
314
LSH001 Leishmaniasis 62 0.046
315
c ALZ036 Alzheimer Disease, Type 3 51 0.046
316
LYM023 Lymphatic System Cancer 35 0.046
317
P RTT002 Rett Syndrome 78 0.045
318
P CRG003 Crigler-Najjar Syndrome, Type I 58 0.045
319
DYS003 Dysgraphia 38 0.045
320
P GLB002 Glioblastoma 66 0.045
321
P CRB042 Cerebellar Ataxia 64 0.045
322
PRD011 Proud Syndrome 42 0.045
323
c SCH056 Schizophrenia 15 26 0.045
324
INS024 Insulin-Like Growth Factor I 74 0.045
325
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.045
326
BRS051 Breast Disease 62 0.044
327
P HML002 Hemolytic Anemia 60 0.044
328
LYM019 Lymphosarcoma 53 0.044
329
BNM001 Bone Marrow Cancer 52 0.044
330
LYM024 Lymphatic System Disease 50 0.044
331
PRP021 Peripheral Nervous System Neoplasm 50 0.044
332
MRG013 Mirage Syndrome 26 0.044
333
ATR060 Atrial Standstill, Digenic 53 0.044
334
VTM002 Vitamin B12 Deficiency 44 0.044
335
EYC003 Eye Accommodation Disease 26 0.044
336
c ALZ041 Alzheimer's Disease 13 22 0.044
337
LNG099 Lung Disease 62 0.044
338
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.044
339
PRV006 Pervasive Developmental Disorder 50 0.044
340
PNM013 Pneumococcal Meningitis 41 0.044
341
c ALZ002 Alzheimer Disease Type 1 22 0.044
342
GST053 Gastric Cancer 77 0.044
343
TXC002 Toxic Encephalopathy 51 0.043
344
RHM027 Rheumatic Disease 57 0.043
345
CHL061 Childhood Leukemia 48 0.043
346
P MLT019 Multiple Myeloma 80 0.043
347
HMT002 Hematologic Cancer 64 0.043
348
RMS001 Rem Sleep Behavior Disorder 40 0.043
349
c CRN177 Coronary Heart Disease 7 22 0.043
350
BLD053 Blood Platelet Disease 46 0.043
351
c CRN174 Coronary Heart Disease 2 22 0.043
352
P CRT072 Creutzfeldt-Jakob Disease 63 0.043
353
P IDP010 Idiopathic Generalized Epilepsy 61 0.043
354
BNC003 Bone Cancer 45 0.043
355
c ADL001 Adult Lymphoma 41 0.043
356
ACT118 Acute Non Lymphoblastic Leukemia 29 0.043
357
c LKM061 Leukemia, Acute Myeloid 71 0.043
358
P ACT135 Acute Graft Versus Host Disease 53 0.043
359
c CHR064 Chronic Monocytic Leukemia 43 0.043
360
GRS011 Gerstmann-Straussler Disease 42 0.043
361
DSS010 Dissociative Disorder 35 0.043
362
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.043
363
P OVR042 Ovarian Cancer 75 0.043
364
VND001 Vein Disease 52 0.043
365
c ALZ008 Alzheimer Disease Risk Factor 19 0.043
366
P CRT033 Corticobasal Degeneration 46 0.042
367
VSC047 Vascular Malformation 45 0.042
368
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.042
369
c PLN018 Peeling Skin Syndrome 2 35 0.042
370
c AST037 Asthma 1 31 0.042
371
DMN031 Dementia, Lewy Body 60 0.042
372
P ACT074 Acute Lymphocytic Leukemia 55 0.042
373
ACD009 Acid-Labile Subunit, Deficiency of 48 0.042
374
P HRP009 Herpes Simplex Encephalitis 46 0.042
375
SND002 Sneddon Syndrome 44 0.042
376
LYM067 Lymphoid Leukemia 43 0.042
377
IMM127 Immune System Cancer 42 0.042
378
c PLN021 Peeling Skin Syndrome 3 31 0.042
379
ATM055 Autoimmune Disease 4 18 0.042
380
P PLY019 Polyneuropathy 54 0.042
381
P ANT006 Antiphospholipid Syndrome 58 0.042
382
CHL068 Cholestasis 58 0.042
383
PRV004 Periventricular Leukomalacia 48 0.042
384
LKM006 Leukomalacia 42 0.042
385
c SVR001 Severe Acute Respiratory Syndrome 57 0.042
386
JPN002 Japanese Encephalitis 54 0.042
387
CCN002 Cocaine Abuse 47 0.042
388
c ACT020 Acute T Cell Leukemia 39 0.042
389
PTH002 Pathological Gambling 51 0.042
390
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.042
391
SBC016 Subacute Delirium 27 0.042
392
P FRD001 Friedreich Ataxia 62 0.041
393
ATN004 Autonomic Neuropathy 44 0.041
394
CNT098 Central Core Disease 66 0.041
395
CHL014 Cholera 55 0.041
396
INT007 Intermediate Coronary Syndrome 52 0.041
397
P CLL015 Collagen Disease 49 0.041
398
PRN009 Paranoid Schizophrenia 47 0.041
399
ANX004 Anoxia 44 0.041
400
SPS019 Spastic Paraparesis 34 0.041
401
MYL020 Myelomeningocele 50 0.041
402
RMN001 Rumination Disorder 38 0.041
403
P MDL005 Medulloblastoma 77 0.041
404
ATP002 Atopy 63 0.041
405
ALL006 Allergic Asthma 58 0.041
406
BLM002 Bulimia Nervosa 54 0.041
407
P SDR002 Siderosis 44 0.041
408
P ATR011 Atrial Fibrillation 64 0.041
409
P GLM045 Glioma 58 0.041
410
c ESS001 Essential Tremor 61 0.040
411
P THR014 Thrombocytopenia 64 0.040
412
c ACT075 Acute Myocardial Infarction 60 0.040
413
RTN018 Retinal Disease 56 0.040
414
DPH001 Diphtheria 58 0.040
415
c CHR418 Chronic Leukemia 48 0.040
416
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.040
417
MYF002 Myofascial Pain Syndrome 40 0.040
418
LKC003 Leukocyte Disease 47 0.040
419
CRN031 Cranial Nerve Disease 40 0.040
420
c CHR579 Chiari Malformation Type Ii 38 0.040
421
c MJR007 Major Affective Disorder 1 28 0.040
422
c MLT124 Multiple Sclerosis 5 25 0.040
423
c MLT095 Multiple Sclerosis 4 19 0.040
424
P CLR023 Colorectal Cancer 97 0.040
425
HDG012 Hodgkin Lymphoma 73 0.040
426
SKN016 Skin Disease 68 0.040
427
ATS001 Autistic Disorder 59 0.040
428
ADL002 Adult Syndrome 53 0.040
429
P CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 41 0.040
430
P RBN001 Rubinstein-Taybi Syndrome 65 0.040
431
OCL009 Ocular Cancer 62 0.040
432
MTR014 Motor Neuron Disease 59 0.040
433
c PRK059 Parkinson Disease 8 52 0.040
434
NSH001 Nasu-Hakola Disease 45 0.040
435
c CNT015 Central Sleep Apnea 44 0.040
436
SPR066 Superficial Siderosis 33 0.040
437
MLN007 Male Infertility 56 0.039
438
CSY001 C Syndrome 49 0.039
439
P VLC001 Velocardiofacial Syndrome 62 0.039
440
P NRM001 Neuromyelitis Optica 59 0.039
441
c HPT015 Hepatitis D 52 0.039
442
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.039
443
P PLM037 Pulmonary Hypertension 79 0.039
444
CDS001 Cadasil 50 0.039
445
c CRN172 Coronary Heart Disease 3 21 0.039
446
c LKM062 Leukemia, Acute Lymphoblastic 64 0.038
447
NWC001 Newcastle Disease 54 0.038
448
OCL011 Ocular Motility Disease 38 0.038
449
c LYM107 Lymphoproliferative Syndrome 2 34 0.038
450
ATM059 Autoimmune Disease 6 26 0.038
451
CRB087 Cerebral Arteriosclerosis 24 0.038
452
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.038
453
MXD001 Mixed Cerebral Palsy 19 0.038
454
LYM115 Lymphoma, Non-Hodgkin 65 0.038
455
P CRN035 Cranial Nerve Palsy 43 0.038
456
IMM068 Immunodeficiency 8 32 0.038
457
P ADN016 Adenocarcinoma 69 0.038
458
P DBT005 Diabetes Insipidus 53 0.038
459
SVR004 Severe Combined Immunodeficiency 68 0.038
460
BDY001 Body Dysmorphic Disorder 41 0.038
461
WHP002 Whiplash 36 0.038
462
PST086 Posterior Cortical Atrophy 35 0.038
463
P MSC003 Muscular Atrophy 51 0.037
464
PRP080 Peripheral Artery Disease 36 0.037
465
STT001 Status Epilepticus 59 0.037
466
LYM040 Lymphoblastic Lymphoma 54 0.037
467
c HPT007 Hepatitis E 54 0.037
468
MYC002 Mycobacterium Avium Complex Disease 51 0.037
469
FML037 Female Breast Cancer 51 0.037
470
FML039 Female Reproductive System Disease 48 0.037
471
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.037
472
FRG010 Fragile X Tremor/ataxia Syndrome 37 0.037
473
c ALZ040 Alzheimer's Disease 11 20 0.037
474
INT074 Intracranial Arteriosclerosis 14 0.037
475
P LBR001 Leber Congenital Amaurosis 60 0.037
476
P ATX030 Ataxia-Telangiectasia 76 0.037
477
SPS007 Spastic Cerebral Palsy 45 0.037
478
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.037
479
CRB086 Cerebral Aneurysms 39 0.037
480
BNL002 Bone Lymphoma 33 0.037
481
GLC006 Galactosemia 67 0.036
482
P CSH001 Cushing's Syndrome 64 0.036
483
P WLD002 Waldenstrom Macroglobulinemia 62 0.036
484
DBT010 Diabetic Neuropathy 55 0.036
485
c BCT007 Bacterial Meningitis 54 0.036
486
VSC006 Vascular Cancer 54 0.036
487
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.036
488
P GNR027 Generalized Peeling Skin Syndrome 22 0.036
489
GRW007 Growth Hormone Deficiency 48 0.036
490
P FLL037 Follicular Lymphoma 66 0.036
491
P CNJ013 Conjunctivitis 65 0.036
492
BRN106 Burns 52 0.036
493
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.036
494
RPR002 Reproductive System Disease 46 0.036
495
HYP085 Hypothalamic Disease 44 0.036
496
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.035
497
P TRN020 Turner Syndrome 64 0.035
498
FTT001 Fatty Liver Disease 60 0.035
499
ART002 Arts Syndrome 53 0.035
500
c NRF018 Neurofibromatosis, Type 1 68 0.035
501
VSC011 Vasculitis 62 0.035
502
ANT011 Antisocial Personality Disorder 47 0.035
503
SKN027 Skin Conditions 45 0.035
504
CHR008 Choroiditis 43 0.035
505
BRN018 Borna Disease 42 0.035
506
BHV002 Behavioral Variant of Frontotemporal Dementia 38 0.035
507
LND001 Landau-Kleffner Syndrome 36 0.035
508
DMN012 Dementia - Subcortical 14 0.035
509
ORL011 Oral Cancer 55 0.034
510
BNF002 Bone Fracture 47 0.034
511
LYM017 Lyme Disease 63 0.034
512
LKN001 Leukoencephalopathy with Vanishing White Matter 54 0.034
513
SNS023 Sensory System Cancer 46 0.034
514
HMP009 Haemophilus Influenzae 45 0.034
515
c SPN100 Spinocerebellar Ataxia 27 41 0.034
516
DYS009 Dysthymic Disorder 38 0.034
517
c SPS072 Spastic Ataxia 1, Autosomal Dominant 26 0.034
518
c SCH064 Schizophrenia 10 22 0.034
519
P EXN002 Exanthem 57 0.034
520
P SML001 Small Cell Carcinoma 57 0.034
521
PRP036 Peripheral T-Cell Lymphoma 45 0.034
522
AGR002 Agoraphobia 43 0.034
523
c GRN014 Grn-Related Frontotemporal Dementia 43 0.034
524
PRM151 Primary Bone Lymphoma 27 0.034
525
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 15 0.034
526
CMP005 Campomelic Dysplasia 72 0.034
527
MSL001 Measles 61 0.034
528
DFF005 Diffuse Large B-Cell Lymphoma 56 0.034
529
P CHL002 Childhood Absence Epilepsy 56 0.034
530
CHR105 Choreoacanthocytosis 45 0.034
531
c PRK025 Parkinson Disease 10 42 0.034
532
HYP458 Hyper Ige Syndrome 41 0.034
533
BNS002 Bone Structure Disease 36 0.034
534
c TRC078 Trichohepatoenteric Syndrome 2 31 0.034
535
MNS002 Mini Stroke 19 0.034
536
P WSK001 Wiskott-Aldrich Syndrome 72 0.034
537
P LPR003 Leprosy 68 0.034
538
P GT001 Gout 58 0.034
539
P CRB059 Cerebellar Degeneration 32 0.034
540
KRT004 Keratitis 70 0.033
541
P NTR004 Neutropenia 59 0.033
542
CFF002 Coffin-Lowry Syndrome 55 0.033
543
P ECL001 Eclampsia 54 0.033
544
ADS004 Aids Dementia Complex 39 0.033
545
CRT013 Carotid Stenosis 37 0.033
546
IMM076 Immunodeficiency 24 27 0.033
547
P RTN024 Retinoblastoma 75 0.033
548
P ADD001 Addison's Disease 62 0.033
549
P GLM007 Glomerulonephritis 56 0.033
550
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.033
551
SCK005 Sickle Cell Disease 49 0.033
552
PRN023 Prion Disease 48 0.033
553
c MTR002 Mitral Valve Insufficiency 44 0.033
554
SCR011 Scrapie 39 0.033
555
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 34 0.033
556
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.033
557
IMM071 Immunodeficiency 12 28 0.033
558
P NRC002 Narcolepsy 62 0.033
559
PLR008 Pleurisy 50 0.033
560
CRY004 Cryoglobulinemia 47 0.033
561
c SPN312 Spinocerebellar Ataxia 14 46 0.033
562
DLS001 Delusional Disorder 41 0.033
563
ADP001 Adiposis Dolorosa 36 0.033
564
CRT012 Cortical Blindness 36 0.033
565
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.033
566
c LKM005 Leukemia, T-Cell, Chronic 22 0.033
567
BRN049 Brain Tumor, Childhood 21 0.033
568
P OST002 Osteoporosis 64 0.032
569
P ART023 Arthropathy 63 0.032
570
P RCK004 Rickets 59 0.032
571
P MMB011 Membranous Nephropathy 56 0.032
572
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.032
573
IMM096 Immunodeficiency 30 30 0.032
574
CST001 Costello Syndrome 69 0.031
575
SCK003 Sickle Cell Anemia 68 0.031
576
P AGM001 Agammaglobulinemia 64 0.031
577
CHG001 Chagas Disease 62 0.031
578
HRY003 Hairy Cell Leukemia 60 0.031
579
CHL123 Chlamydia 59 0.031
580
P SPR098 Supranuclear Palsy, Progressive 58 0.031
581
P HMP007 Hemophilia 56 0.031
582
WHM001 Whim Syndrome 52 0.031
583
BRN004 Brain Edema 51 0.031
584
TCK001 Tick-Borne Encephalitis 49 0.031
585
PTT009 Pituitary Gland Disease 48 0.031
586
OPP004 Oppositional Defiant Disorder 43 0.031
587
c PRM023 Pre-Malignant Neoplasm 43 0.031
588
P OTS001 Otosclerosis 35 0.031
589
HNS001 Hansen's Disease 29 0.031
590
c LKM055 Leukemia, Acute Lymphoblastic 2 22 0.031
591
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 17 0.031
592
P ALX003 Alexander Disease 64 0.031
593
CHD001 Chediak-Higashi Syndrome 64 0.031
594
ADN018 Adenoma 59 0.031
595
P HYP024 Hypoparathyroidism 52 0.031
596
ATM012 Autoimmune Disease of Blood 37 0.031
597
MTR028 Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones 33 0.031
598
c MYC058 Myocardial Infarction 2 29 0.031
599
BRC012 Brucellosis 65 0.030
600
GLL008 Gilles De La Tourette Syndrome 62 0.030
601
CTN007 Cutaneous Leishmaniasis 62 0.030
602
P ESN007 Eosinophilia 61 0.030
603
P UVT001 Uveitis 59 0.030
604
BLL006 Bullous Pemphigoid 58 0.030
605
TRP002 Tropical Spastic Paraparesis 57 0.030
606
HMG005 Hemoglobinopathy 50 0.030
607
c CNG027 Congenital Hemolytic Anemia 48 0.030
608
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 48 0.030
609
P CHR562 Chronic Myelocytic Leukemia 41 0.030
610
P HYP263 Hypersomnia 40 0.030
611
DPR002 Depersonalization Disorder 35 0.030
612
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.030
613
DMN016 Dementia, Familial, Nonspecific 23 0.030
614
HRP008 Herpes Simiae 15 0.030
615
HRP012 Herpesvirus Simiae B Virus 13 0.030
616
P OST012 Osteoarthritis 82 0.030
617
P MYL005 Myelofibrosis 67 0.030
618
CHR103 Charge Syndrome 64 0.030
619
P CRB019 Cerebral Amyloid Angiopathy 58 0.030
620
c ACT134 Acute Liver Failure 50 0.030
621
CRD118 Cardiovascular Cancer 47 0.030
622
CRB027 Cerebellar Disease 47 0.030
623
SKN023 Skin Tag 46 0.030
624
DDN006 Duodenitis 44 0.030
625
BHC003 Behcet Syndrome 61 0.030
626
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.030
627
FCL012 Facial Paralysis 50 0.030
628
ADR012 Adrenal Gland Disease 49 0.030
629
CHR001 Churg-Strauss Syndrome 49 0.030
630
P PRM108 Primary Progressive Multiple Sclerosis 47 0.030
631
MDS022 Mediastinitis 41 0.030
632
c BNG023 Benign Familial Infantile Epilepsy 41 0.030
633
MTS001 Mutism 40 0.030
634
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.030
635
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 30 0.030
636
MTH027 Mthfr Deficiency 30 0.030
637
WRT002 Writing Disorder 29 0.030
638
NN2002 Non 24 Hour Sleep Wake Disorder 22 0.030
639
GLC077 Glucocorticoid Therapy, Response to 19 0.030
640
P APL001 Aplastic Anemia 73 0.029
641
WLS001 Wilson Disease 72 0.029
642
P MTC003 Metachromatic Leukodystrophy 71 0.029
643
PLM001 Pulmonary Tuberculosis 68 0.029
644
WRN001 Werner Syndrome 67 0.029
645
P NJM001 Nijmegen Breakage Syndrome 66 0.029
646
P MYS003 Myasthenia Gravis 65 0.029
647
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.029
648
P THL005 Thalassemia 61 0.029
649
ANR002 Aniridia 60 0.029
650
P MYP006 Myopia 59 0.029
651
P LKD001 Leukodystrophy 58 0.029
652
INT075 Intracranial Hypertension 53 0.029
653
P PRM006 Primary Biliary Cirrhosis 52 0.029
654
DBT004 Diabetic Polyneuropathy 51 0.029
655
SPN041 Spinal Cord Disease 48 0.029
656
RFL001 Reflex Sympathetic Dystrophy 48 0.029
657
ALX001 Alexia 45 0.029
658
RFR004 Refractory Hematologic Cancer 29 0.029
659
c PRK022 Parkinson Disease 12 24 0.029
660
MNT001 Mantle Cell Lymphoma 70 0.028
661
c HMP029 Hemophilia a 64 0.028
662
P PRT013 Portal Hypertension 59 0.028
663
HRP004 Herpes Zoster 56 0.028
664
PLS007 Plasmodium Falciparum Malaria 54 0.028
665
P SYP003 Syphilis 53 0.028
666
FML038 Female Reproductive Organ Cancer 51 0.028
667
OPT003 Opiate Dependence 50 0.028
668
URB001 Urbach-Wiethe Disease 48 0.028
669
MYL001 Myelitis 48 0.028
670
PTT037 Pituitary Tumors 45 0.028
671
P BLP003 Blepharospasm 44 0.028
672
SCH003 Schizophreniform Disorder 41 0.028
673
CRV045 Cervical Intraepithelial Neoplasia 38 0.028
674
ADT002 Auditory System Cancer 35 0.028
675
c LYM106 Lymphoproliferative Syndrome 1 34 0.028
676
CLS049 Classic Phenylketonuria 33 0.028
677
IMM082 Immunodeficiency 18 31 0.028
678
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 31 0.028
679
c LKM004 Leukemia, B-Cell, Chronic 25 0.028
680
c LKM056 Leukemia, Chronic Lymphocytic 2 24 0.028
681
P NRF019 Neurofibromatosis, Type 2 73 0.028
682
P CRN037 Craniosynostosis 65 0.028
683
P DNT015 Dent Disease 61 0.028
684
P RHN004 Rhinitis 61 0.028
685
RBR001 Roberts Syndrome 59 0.028
686
MSC077 Muscle Eye Brain Disease 56 0.028
687
PTT006 Pituitary Adenoma 55 0.028
688
TTH006 Tooth Disease 52 0.028
689
STM006 Stomach Disease 50 0.028
690
OVR063 Overnutrition 49 0.028
691
HMG002 Hemoglobinuria 49 0.028
692
PRT038 Protein-Energy Malnutrition 49 0.028
693
NRM004 Neuroma 48 0.028
694
P PRD008 Periodontitis 46 0.028
695
AMB002 Amblyopia 46 0.028
696
CRV043 Cervical Dystonia 44 0.028
697
CRB085 Cerebral Hemorrhage 43 0.028
698
TRC010 Trichotillomania 41 0.028
699
CHR413 Chronic Myocardial Ischemia 40 0.028
700
ANG049 Angioedema Induced by Ace Inhibitors 35 0.028
701
P HMC003 Hemochromatosis 72 0.027
702
ALL003 Allergic Rhinitis 64 0.027
703
P CRD013 Cardiofaciocutaneous Syndrome 63 0.027
704
P GRV001 Graves' Disease 61 0.027
705
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.027
706
MRB003 Morbid Obesity 58 0.027
707
P MLT074 Multiple Endocrine Neoplasia 55 0.027
708
NNL002 Nonalcoholic Steatohepatitis 53 0.027
709
P WVR001 Weaver Syndrome 51 0.027
710
HRT007 Heart Cancer 50 0.027
711
MLL012 Miller Syndrome 49 0.027
712
P TRC086 Trichohepatoenteric Syndrome 1 46 0.027
713
IMM065 Immunodeficiency 10 40 0.027
714
MLR007 Male Reproductive System Disease 37 0.027
715
P HRT017 Heart Tumor 35 0.027
716
DVL005 Developmental Dyspraxia 21 0.027
717
c MJR006 Major Affective Disorder 5 18 0.027
718
THY028 Thyroid Cancer 68 0.026
719
P PLR004 Pleuropulmonary Blastoma 64 0.026
720
CNT047 Contact Dermatitis 62 0.026
721
TNS005 Tonsillitis 58 0.026
722
ALL010 Allergic Contact Dermatitis 57 0.026
723
c VRL007 Viral Encephalitis 54 0.026
724
SML033 Small Cell Cancer of the Lung, Somatic 53 0.026
725
P CNT005 Central Nervous System Lymphoma 53 0.026
726
c PRM226 Primary Central Nervous System Lymphoma 49 0.026
727
SLP001 Sleeping Sickness 48 0.026
728
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.026
729
P BRN120 Bronchus Cancer 46 0.026
730
P SKN013 Skin Benign Neoplasm 46 0.026
731
FCT008 Factitious Disorder 43 0.026
732
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.026
733
URT001 Urethritis 40 0.026
734
CHR073 Choreatic Disease 40 0.026
735
P CNT036 Central Nervous System Germ Cell Tumor 39 0.026
736
MNN032 Meningococcal Meningitis 38 0.026
737
P HYP111 Hyperprolinemia 32 0.026
738
c PRK051 Parkinson Disease 18 31 0.026
739
c PRK026 Parkinson Disease 11 30 0.026
740
MDR006 Moderate and Severe Traumatic Brain Injury 24 0.026
741
DRG016 Drug Induced Dyskinesia 21 0.026
742
PRG033 Progressive Non-Fluent Aphasia 19 0.026
743
CHR321 Chorea and Dementia 19 0.026
744
IMM103 Immunodeficiency 37 19 0.026
745
c MJR003 Major Affective Disorder 6 18 0.026
746
c SML023 Small Cell Lung Cancer, Adult 17 0.026
747
INT031 Integrative Agnosia 9 0.026
748
LPP001 Lipoprotein Lipase Deficiency 65 0.025
749
EWN003 Ewing Sarcoma 64 0.025
750
AND015 Androgen Insensitivity 63 0.025
751
ACN011 Acne 63 0.025
752
LPT001 Leptospirosis 63 0.025
753
CRD119 Cardiac Arrest 63 0.025
754
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.025
755
FDL002 Food Allergy 54 0.025
756
KRT002 Keratomalacia 54 0.025
757
WST005 West Nile Virus 53 0.025
758
c LKM060 Leukemia, Acute Lymphoblastic 3 52 0.025
759
P NNT009 Neonatal Diabetes Mellitus 52 0.025
760
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 51 0.025
761
P CRP007 Carpenter Syndrome 49 0.025
762
TRN044 Transposition of the Great Arteries 47 0.025
763
URT010 Ureteral Obstruction 45 0.025
764
MLL002 Miller Fisher Syndrome 43 0.025
765
P NRP041 Neuropathy, Hereditary Sensory, Type Ie 42 0.025
766
c CNG031 Congenital Nervous System Abnormality 39 0.025
767
FXF002 Fox-Fordyce Disease 39 0.025
768
c CRN176 Coronary Heart Disease 9 20 0.025
769
CD4004 Cd4 Deficiency 17 0.025
770
P PRM019 Premature Ovarian Failure 64 0.024
771
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.024
772
GLC037 Glucocorticoid Resistance 62 0.024
773
GNG013 Gingivitis 60 0.024
774
P SNS014 Sinusitis 60 0.024
775
MSM014 Mismatch Repair Cancer Syndrome 59 0.024
776
P SYS005 Systemic Scleroderma 58 0.024
777
PRC002 Paracoccidioidomycosis 55 0.024
778
P OVR049 Ovarian Disease 55 0.024
779
CHR285 Chronic Myelomonocytic Leukemia 55 0.024
780
P LRY019 Laryngitis 55 0.024
781
GNT003 Genital Herpes 54 0.024
782
BRN038 Bronchial Disease 54 0.024
783
PRS042 Prostate Disease 52 0.024
784
IRN001 Iron Deficiency Anemia 51 0.024
785
CRC006 Carcinoid Syndrome 51 0.024
786
CHK001 Chikungunya 50 0.024
787
RTN020 Retinal Vascular Disease 50 0.024
788
MCR004 Macroglobulinemia 50 0.024
789
INT253 Intestinal Benign Neoplasm 50 0.024
790
P SCK002 Sick Sinus Syndrome 50 0.024
791
P NGH001 Night Blindness 49 0.024
792
MTN003 Motion Sickness 48 0.024
793
SYN036 Syncope 47 0.024
794
P SYR001 Syringomyelia 47 0.024
795
OST003 Osteonecrosis 45 0.024
796
P PNB001 Pineoblastoma 44 0.024
797
ATN003 Autonomic Nervous System Neoplasm 43 0.024
798
HRN003 Heroin Dependence 40 0.024
799
c PRG001 Progressive Muscular Atrophy 40 0.024
800
P OCY001 Oocyte Maturation Defect 39 0.024
801
AGR018 Agraphia 39 0.024
802
RCT017 Rectal Disease 39 0.024
803
INF013 Inferior Myocardial Infarction 37 0.024
804
HMC014 Homocysteinemia 34 0.024
805
MLN003 Melancholia 34 0.024
806
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.024
807
OLF001 Olfactory Nerve Disease 21 0.024
808
ADS006 Aids - Neurological Complications 14 0.024
809
NNP013 Non-Polyposis Turcot Syndrome 11 0.024
810
TST021 Testicular Germ Cell Tumor 70 0.022
811
P CLC005 Celiac Disease 67 0.022
812
GLB015 Glioblastoma Multiforme 62 0.022
813
TXC005 Toxic Shock Syndrome 61 0.022
814
VNW001 Von Willebrand's Disease 61 0.022
815
P RBL001 Rubella 56 0.022
816
ORL015 Oral Squamous Cell Carcinoma 56 0.022
817
SFT003 Soft Tissue Sarcoma 56 0.022
818
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 55 0.022
819
QDR001 Quadriplegia 52 0.022
820
NCT008 Nicotine Dependence, Protection Against 52 0.022
821
HYP005 Hypokalemia 51 0.022
822
MSC072 Muscle Cancer 51 0.022
823
CLN019 Colonic Disease 50 0.022
824
P LPS002 Liposarcoma 50 0.022
825
PRG009 Progressive Multifocal Leukoencephalopathy 50 0.022
826
MRG003 Marginal Zone B-Cell Lymphoma 50 0.022
827
STM007 Stomatitis 50 0.022
828
LPR001 Lepromatous Leprosy 49 0.022
829
RTC005 Reticulosarcoma 48 0.022
830
RTN003 Retinal Ischemia 48 0.022
831
JCB001 Jacobsen Syndrome 48 0.022
832
P PLM006 Pulmonary Alveolar Proteinosis 48 0.022
833
RTC009 Reticulum Cell Sarcoma 48 0.022
834
MLR006 Male Reproductive Organ Cancer 47 0.022
835
PRN011 Pernicious Anemia 46 0.022
836
c FLL041 Follicular Lymphoma 1 46 0.022
837
IMM105 Immunodeficiency with Hyper-Igm, Type 3 45 0.022
838
PTT008 Pituitary Carcinoma 44 0.022
839
GST009 Gastroschisis 43 0.022
840
P UTR038 Uterine Disease 40 0.022
841
NRN008 Neuronal Intranuclear Inclusion Disease 39 0.022
842
GRM001 Germ Cell and Embryonal Cancer 39 0.022
843
CNT018 Central Nervous System Leukemia 39 0.022
844
P MRC003 Mercury Poisoning 38 0.022
845
DLY005 Delayed Sleep Phase Syndrome 38 0.022
846
CRB040 Cerebrum Cancer 36 0.022
847
FNT004 Fainting 33 0.022
848
CHL078 Childhood-Onset Schizophrenia 33 0.022
849
PDP001 Pedophilia 31 0.022
850
FNC005 Functional Colonic Disease 30 0.022
851
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 30 0.022
852
CRS012 Carasil Syndrome 29 0.022
853
c PRK037 Parkinson Disease 13 28 0.022
854
CNT017 Central Nervous System Origin Vertigo 28 0.022
855
PRS011 Persian Gulf Syndrome 27 0.022
856
CHL109 Childhood Apraxia of Speech 27 0.022
857
IMM085 Immunodeficiency 25 25 0.022
858
c ATS173 Autism 18 23 0.022
859
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 22 0.022
860
c LKM051 Leukemia, Chronic Lymphocytic 3 22 0.022
861
IMM084 Immunodeficiency 17, Cd3 Gamma Deficient 21 0.022
862
c SPR049 Supranuclear Palsy, Progressive, 2 20 0.022
863
VGS001 Vagus Nerve Disease 20 0.022
864
c MJR004 Major Affective Disorder 4 18 0.022
865
BSL005 Basal Ganglia Cerebrovascular Disease 11 0.022
866
OBS060 Obesity Due to Sim1 Deficiency 9 0.022
867
ART005 Arteriovenous Malformation 65 0.020
868
OMN001 Omenn Syndrome 61 0.020
869
TYP007 Typhoid Fever 61 0.020
870
c ATM010 Autoimmune Hemolytic Anemia 60 0.020
871
CMM005 Common Cold 58 0.020
872
STF001 Stiff-Person Syndrome 56 0.020
873
PRL032 Perlman Syndrome 55 0.020
874
RCT018 Rectal Neoplasm 55 0.020
875
NRN004 Neuroendocrine Tumor 54 0.020
876
P THY023 Thymoma 53 0.020
877
PLS006 Plasmodium Vivax Malaria 53 0.020
878
END035 Endocrine Gland Cancer 52 0.020
879
P TRT010 Teratoma 52 0.020
880
BLT006 Bilateral Breast Cancer 52 0.020
881
TRY001 Trypanosomiasis 52 0.020
882
NRF007 Neurofibroma 52 0.020
883
P DRR001 Diarrhea 51 0.020
884
RHM028 Rheumatic Heart Disease 51 0.020
885
P HYP098 Hypereosinophilic Syndrome 51 0.020
886
STR008 Strongyloidiasis 50 0.020
887
c MLG079 Malignant Pleural Mesothelioma 50 0.020
888
PST021 Postpartum Depression 49 0.020
889
PYD002 Pyoderma 49 0.020
890
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 48 0.020
891
WHP001 Whipple Disease 48 0.020
892
VST004 Vestibular Disease 47 0.020
893
CRB002 Cerebral Primitive Neuroectodermal Tumor 45 0.020
894
P ARC016 Auriculocondylar Syndrome 1 44 0.020
895
EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 44 0.020
896
EXT033 Extrapulmonary Tuberculosis 44 0.020
897
NSS002 Neisseria Meningitidis Infection 43 0.020
898
P PRL003 Proliferative Glomerulonephritis 43 0.020
899
RFT001 Rift Valley Fever 43 0.020
900
THL018 Thalassemia Major 42 0.020
901
CMP034 Complete Androgen Insensitivity Syndrome 42 0.020
902
P CYS017 Cystic Teratoma 41 0.020
903
CNT069 Centrotemporal Epilepsy 40 0.020
904
THL017 Thalassemia Intermedia 40 0.020
905
PDT001 Pediatric Lymphoma 40 0.020
906
BRS090 Breast Reconstruction 39 0.020
907
HRM002 Hermaphroditism 38 0.020
908
THL010 Thalassemia Minor 38 0.020
909
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 38 0.020
910
LNS003 Lens Disease 38 0.020
911
SPR024 Supratentorial Cancer 37 0.020
912
SPL040 Split Hand 37 0.020
913
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.020
914
c ALP005 Alpha Chain Disease 37 0.020
915
c TRN009 Transient Hypogammaglobulinemia of Infancy 37 0.020
916
c FNC042 Fanconi Anemia, Complementation Group D2 35 0.020
917
CRV069 Cervix Disease 34 0.020
918
NMN001 Nominal Aphasia 33 0.020
919
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 33 0.020
920
PRG090 Progressive Relapsing Multiple Sclerosis 33 0.020
921
P TRN016 Transient Hypogammaglobulinemia 32 0.020
922
CRN033 Cranial Nerve Malignant Neoplasm 31 0.020
923
c CRP022 Carpenter Syndrome 2 31 0.020
924
ENC005 Encephalomalacia 28 0.020
925
RDT005 Radiation Induced Cancer 28 0.020
926
IMM025 Immunoglobulin a Deficiency 2 27 0.020
927
IMM036 Immunodeficiency, Isolated 27 0.020
928
HDG004 Hodgkin's Granuloma 26 0.020
929
SPC001 Space Motion Sickness 26 0.020
930
IMM120 Immunodeficiency 40 26 0.020
931
YNG002 Young Syndrome 26 0.020
932
NNT021 Neonatal Meningitis 24 0.020
933
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 24 0.020
934
PTC005 Pituicytoma 23 0.020
935
HYP002 Hypothalamic Neoplasm 23 0.020
936
c DYS120 Dyslexia 2 22 0.020
937
c ALZ031 Alzheimer Disease 17 22 0.020
938
IMM088 Immunodeficiency 36 21 0.020
939
CML001 Cumulative Trauma Disorders 21 0.020
940
HDG006 Hodgkin's Paragranuloma 20 0.020
941
c GRV009 Graves Disease 2 19 0.020
942
c BSL039 Basal Ganglia Calcification, Idiopathic, 6 18 0.020
943
PRP010 Prepuce Cancer 18 0.020
944
SCL044 Scalp Syndrome 17 0.020
945
WSC001 Wisconsin Syndrome 17 0.020
946
HRT029 Heart Tumor of the Child 17 0.020
947
TCL006 T Cell Immunodeficiency Primary 15 0.020
948
MNT045 Montefiore Syndrome 13 0.020