Search results for "memory impairment"

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

947 hits were found for 'memory impairment'

# Family MCID Name MIFTS Score
1
DMN002 Dementia 62 0.329
2
P SCH015 Schizophrenia 78 0.224
3
P ALZ034 Alzheimer Disease 92 0.222
4
P ENC018 Encephalopathy 59 0.200
5
CRB009 Cerebritis 36 0.196
6
P EPL164 Epilepsy 60 0.196
7
NRN002 Neuronitis 40 0.194
8
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 0.185
9
LRN003 Learning Disability 49 0.173
10
DSS008 Disease of Mental Health 48 0.171
11
c CNT035 Central Nervous System Disease 60 0.169
12
P HPT021 Hepatitis 74 0.165
13
TPT001 Tauopathy 51 0.159
14
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.156
15
BRN071 Brain Injury 51 0.152
16
ISC004 Ischemia 56 0.151
17
SMN008 Semantic Dementia 43 0.148
18
P NRV007 Nervous System Disease 71 0.147
19
END072 Endotheliitis 41 0.147
20
DRG001 Drug Psychosis 39 0.137
21
TMP001 Temporal Lobe Epilepsy 47 0.132
22
ANX002 Anxiety Disorder 67 0.132
23
AMN003 Amnestic Disorder 45 0.131
24
RTR001 Retrograde Amnesia 40 0.129
25
PSY004 Psychotic Disorder 62 0.128
26
P LKM002 Leukemia 70 0.127
27
VSC002 Vascular Dementia 41 0.125
28
TRM010 Traumatic Brain Injury 52 0.124
29
HV1006 Hiv-1 80 0.121
30
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.119
31
TRN012 Transient Global Amnesia 38 0.119
32
IMP003 Impaired Renal Function Disease 36 0.117
33
MDD011 Mood Disorder 60 0.116
34
PST028 Post-Traumatic Stress Disorder 55 0.114
35
P OBS005 Obesity 91 0.112
36
P ART022 Arthritis 73 0.111
37
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.110
38
HYP266 Hypoxia 55 0.109
39
P DYS005 Dyslexia 38 0.108
40
P PRS038 Personality Disorder 60 0.107
41
SPC010 Speech and Communication Disorders 42 0.107
42
ADT003 Auditory System Disease 49 0.105
43
P LYM118 Lymphoma 68 0.105
44
MVM001 Movement Disease 45 0.104
45
APH002 Aphasia 52 0.104
46
SLP005 Sleep Disorder 52 0.103
47
CRB039 Cerebrovascular Disease 49 0.100
48
P LVR013 Liver Disease 76 0.100
49
P SPC019 Specific Language Impairment 27 0.100
50
P ENC004 Encephalitis 60 0.100
51
END040 Endogenous Depression 51 0.099
52
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.099
53
ALN001 Aland Island Eye Disease 45 0.099
54
ACT084 Acute Stress Disorder 38 0.097
55
P BRS047 Breast Cancer 100 0.096
56
CND002 Conduct Disorder 54 0.096
57
PHY002 Physical Disorder 43 0.095
58
MNT002 Mental Depression 52 0.094
59
P RHM011 Rheumatoid Arthritis 87 0.094
60
STR067 Stroke, Ischemic 74 0.093
61
HDN002 Head Injury 47 0.093
62
RDN001 Reading Disorder 39 0.092
63
c HPT001 Hepatitis C 68 0.091
64
PCK002 Pick Disease 66 0.091
65
TBR010 Tuberculosis 70 0.091
66
c HPT016 Hepatitis B 61 0.091
67
CRB159 Cerebral Visual Impairment 34 0.090
68
P AST005 Asthma 80 0.089
69
c HPT003 Hepatitis a 55 0.089
70
P ATS007 Autism Spectrum Disorder 64 0.087
71
DWN001 Down Syndrome 65 0.087
72
P PRK057 Parkinson Disease, Late-Onset 72 0.086
73
P ATX004 Ataxia 53 0.085
74
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.085
75
HYP066 Hyperglycemia 61 0.084
76
AYM001 Ayme-Gripp Syndrome 40 0.084
77
ANT019 Anterograde Amnesia 35 0.084
78
c ALZ012 Alzheimer Disease 12 19 0.083
79
c SYS001 Systemic Lupus Erythematosus 87 0.083
80
BSL008 Basal Ganglia Disease 40 0.083
81
GNR004 Generalized Anxiety Disorder 49 0.083
82
P LPS004 Lupus Erythematosus 63 0.083
83
P MYP004 Myopathy 67 0.082
84
P BPL003 Bipolar Disorder 58 0.082
85
c HPT073 Hepatitis C Virus 72 0.082
86
NTR005 Nutritional Deficiency Disease 51 0.081
87
P PRS013 Prosopagnosia 40 0.081
88
DVL001 Developmental Coordination Disorder 36 0.081
89
P INF038 Influenza 71 0.080
90
P MNN013 Meningitis 66 0.079
91
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 56 0.079
92
GLC008 Glucose Metabolism Disease 44 0.078
93
CMM004 Common Variable Immunodeficiency 68 0.078
94
P KDN018 Kidney Disease 64 0.078
95
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.077
96
SPC005 Speech Disorder 41 0.077
97
P NRP001 Neuropathy 57 0.076
98
ADR009 Adrenal Cortex Disease 40 0.076
99
BRN028 Brain Cancer 69 0.076
100
ANS006 Anosognosia 36 0.076
101
END030 End Stage Renal Failure 53 0.076
102
ATN002 Autonomic Nervous System Disease 46 0.075
103
c VRL010 Viral Hepatitis 60 0.075
104
P INT063 Intellectual Disability 46 0.075
105
P AMY004 Amyloidosis 63 0.075
106
LPD004 Lipoid Nephrosis 49 0.075
107
VSC007 Vascular Disease 51 0.074
108
FCL014 Focal Epilepsy 55 0.074
109
P HYP086 Hypothyroidism 63 0.074
110
TRN015 Transient Cerebral Ischemia 57 0.074
111
P CRB088 Cerebral Atrophy 40 0.074
112
GLB003 Globe Disease 34 0.074
113
P AGN002 Agnosia 56 0.073
114
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.073
115
BRN080 Brain Ischemia 42 0.073
116
P MYL006 Myeloid Leukemia 67 0.072
117
GLT021 Glutaricaciduria, Type I 47 0.072
118
MLN008 Melanoma 61 0.072
119
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.071
120
PRP027 Peripheral Vascular Disease 69 0.071
121
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.071
122
P URF003 Urofacial Syndrome 1 51 0.071
123
P FRG001 Fragile X Syndrome 68 0.070
124
VCC001 Vaccinia 46 0.070
125
ART111 Artery Disease 56 0.070
126
NRM005 Neuromuscular Disease 56 0.070
127
P SLP006 Sleep Apnea 60 0.070
128
DMY004 Demyelinating Disease 52 0.070
129
ACQ007 Acquired Immunodeficiency Syndrome 60 0.069
130
P MSC033 Muscle Disorders 52 0.069
131
P SZR006 Seizure Disorder 56 0.069
132
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.069
133
ADJ001 Adjustment Disorder 38 0.069
134
SBS003 Substance Abuse 54 0.069
135
SPS057 Spasticity 41 0.069
136
MVD001 Moved to 60 0.069
137
AMS001 Amusia 24 0.068
138
LYM009 Lymphocytic Choriomeningitis 49 0.068
139
DRG011 Drug Addiction 55 0.068
140
URN009 Urinary System Disease 52 0.068
141
c HYP163 Hyperlipidemia Type 3 52 0.067
142
MLR004 Malaria 80 0.067
143
ATM052 Autoimmune Disease 1 26 0.067
144
OBS002 Obsessive-Compulsive Disorder 66 0.067
145
MSC004 Muscle Tissue Disease 35 0.067
146
P THY032 Thyroiditis 57 0.067
147
MTH009 Mouth Disease 63 0.066
148
c PND001 Pain Disorder 53 0.066
149
SCH011 Schizotypal Personality Disorder 32 0.066
150
c CHR089 Chronic Kidney Failure 67 0.066
151
P HRP006 Herpes Simplex 65 0.066
152
c CRN214 Coronary Heart Disease 5 22 0.066
153
DRM006 Dermatitis 58 0.065
154
ASP001 Asperger Syndrome 49 0.065
155
C3D001 C3 Deficiency 50 0.065
156
KDS001 Kid Syndrome 53 0.065
157
OBS061 Obstructive Sleep Apnea 61 0.065
158
PRS047 Prostatitis 56 0.065
159
CRB031 Cerebral Arterial Disease 31 0.065
160
BLD054 Blood Protein Disease 38 0.064
161
DRG003 Drug Dependence 53 0.064
162
OPT006 Optic Nerve Disease 47 0.064
163
CRB037 Cerebral Palsy 54 0.064
164
P CHR345 Chronic Pain 45 0.064
165
P PNM007 Pneumonia 67 0.064
166
FST001 Foster-Kennedy Syndrome 31 0.064
167
ACR041 Acromelic Frontonasal Dysostosis 45 0.063
168
BRT030 Birth Defects 44 0.063
169
TTN003 Tetanus 62 0.063
170
FRN002 Frontal Lobe Epilepsy 38 0.063
171
WRN002 Wernicke-Korsakoff Syndrome 41 0.063
172
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.063
173
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.063
174
P LYM026 Lymphoblastic Leukemia 60 0.063
175
P INF032 Infertility 61 0.063
176
HPT023 Hepatocellular Carcinoma 90 0.062
177
SCL003 Social Phobia 45 0.062
178
APR001 Apraxia 50 0.062
179
IMM102 Immunodeficiency 14 33 0.062
180
P ANR007 Anorexia Nervosa 63 0.062
181
c ALZ032 Alzheimer Disease 18 23 0.062
182
CNV002 Conversion Disorder 45 0.062
183
P SPS003 Spastic Diplegia 49 0.062
184
P NRV006 Nervous System Cancer 62 0.061
185
CHL071 Child Syndrome 58 0.061
186
c CHR417 Chronic Graft Versus Host Disease 50 0.061
187
c PRK031 Parkinson Disease 1 54 0.061
188
LYM027 Lymphopenia 54 0.061
189
DYS004 Dyscalculia 24 0.061
190
EYD002 Eye Disease 62 0.061
191
ANR040 Aneurysm 56 0.061
192
RTN023 Retinitis 49 0.061
193
SXL003 Sexual Disorder 45 0.060
194
c SCH051 Schizophrenia 4 36 0.060
195
c CNG401 Congenital Heart Disease 67 0.060
196
P ATP001 Atopic Dermatitis 60 0.059
197
ALC007 Alcohol Dependence 66 0.059
198
ATM054 Autoimmune Disease 3 16 0.059
199
CRB004 Cerebral Artery Occlusion 39 0.059
200
HMT018 Hematopoietic Stem Cell Transplantation 39 0.059
201
HPT019 Hepatic Encephalopathy 58 0.058
202
ACD009 Acid-Labile Subunit, Deficiency of 37 0.058
203
WLL006 Wells Syndrome 57 0.058
204
GDS001 Good Syndrome 46 0.058
205
LMB024 Limbic Encephalitis 35 0.058
206
GNC005 Geniculate Ganglionitis 27 0.058
207
FCL011 Facial Nerve Disease 37 0.058
208
PRP019 Peripheral Nervous System Disease 52 0.058
209
P TRM003 Tremor 54 0.058
210
CYT008 Cytomegalovirus Infection 51 0.057
211
ATM053 Autoimmune Disease 2 16 0.057
212
LVR012 Liver Cirrhosis 71 0.057
213
SPC003 Specific Developmental Disorder 39 0.057
214
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.057
215
P SHR029 Short Syndrome 60 0.056
216
P TCL004 T-Cell Leukemia 44 0.056
217
CYS001 Cystic Fibrosis 87 0.055
218
P HYD006 Hydrocephalus 68 0.055
219
ART021 Arteriosclerosis 59 0.055
220
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.055
221
c BPL002 Bipolar I Disorder 45 0.055
222
c ALZ037 Alzheimer Disease-2 36 0.054
223
P LTR001 Lateral Sclerosis 50 0.054
224
CLT003 Colitis 56 0.054
225
c CHR090 Chronic Lymphocytic Leukemia 73 0.054
226
NSY001 N Syndrome 42 0.054
227
VRL011 Viral Infectious Disease 56 0.054
228
MDY003 Mody, Type Ii 36 0.054
229
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.054
230
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.054
231
P PNC025 Panic Disorder 60 0.054
232
SBS004 Substance Dependence 48 0.054
233
c ATM007 Autoimmune Disease of Central Nervous System 29 0.054
234
DFC004 Deficiency Anemia 64 0.054
235
c PRK045 Parkinson Disease 5 43 0.054
236
ETH011 Ethylmalonic Encephalopathy 57 0.053
237
EXF001 Exfoliation Syndrome 56 0.053
238
WTH001 Withdrawal Disorder 36 0.053
239
SPN041 Spinal Cord Disease 50 0.053
240
c ACT073 Acute Leukemia 61 0.053
241
ALL026 Allergic Hypersensitivity Disease 53 0.053
242
CRB033 Cerebral Degeneration 45 0.053
243
P MYC007 Myocardial Infarction 80 0.053
244
P CRD011 Cardiomyopathy 66 0.052
245
CHR066 Chronic Fatigue Syndrome 63 0.052
246
P PLN008 Peeling Skin Syndrome 45 0.052
247
WLL001 Williams-Beuren Syndrome 61 0.052
248
MYL009 Myelodysplastic Syndrome 73 0.052
249
c PRK030 Parkinson Disease 4 38 0.052
250
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.052
251
P CRN178 Coronary Heart Disease 6 22 0.052
252
P FBR031 Febrile Seizures 53 0.052
253
P PSR002 Psoriasis 63 0.051
254
P FTL001 Fetal Alcohol Syndrome 53 0.051
255
P CRN211 Coronary Artery Disease 74 0.051
256
P MYL007 Myeloma 52 0.051
257
c CRN175 Coronary Heart Disease 4 19 0.051
258
P HNT016 Huntington Disease 80 0.051
259
RSP006 Respiratory System Disease 61 0.051
260
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.051
261
ETN001 Eating Disorder 59 0.051
262
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.051
263
VSL003 Visual Agnosia 27 0.051
264
PRT037 Pertussis 63 0.051
265
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.051
266
P ALC004 Alcohol Abuse 57 0.051
267
ATH003 Atherosclerosis 63 0.051
268
P DMN033 Dementia, Frontotemporal 63 0.050
269
VSL004 Visual Cortex Disease 28 0.050
270
c MLT010 Multiple Personality Disorder 36 0.050
271
BRD004 Borderline Personality Disorder 46 0.050
272
PRM025 Primary Bacterial Infectious Disease 42 0.050
273
LNG099 Lung Disease 63 0.050
274
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.050
275
P CRV039 Cervicitis 45 0.050
276
P PRS040 Prostate Cancer 89 0.050
277
P LNG032 Lung Cancer 92 0.050
278
CRH001 Crohn's Disease 76 0.050
279
c BRN108 Branchiootic Syndrome 1 36 0.050
280
CNN005 Connective Tissue Disease 60 0.049
281
CHR012 Chronic Granulomatous Disease 66 0.049
282
LYM024 Lymphatic System Disease 49 0.049
283
P BCL006 B-Cell Lymphomas 64 0.049
284
CCN001 Cocaine Dependence 47 0.049
285
P CTR002 Cataract 57 0.049
286
P ANG001 Angelman Syndrome 62 0.048
287
HPD002 Hepadnavirus Infection 20 0.048
288
HYP037 Hyperhomocysteinemia 49 0.048
289
P TBR001 Tuberous Sclerosis 68 0.048
290
CTS003 Coats Disease 57 0.048
291
c CRN173 Coronary Heart Disease 8 19 0.048
292
c MLT093 Multiple Sclerosis 2 20 0.048
293
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.048
294
CRT016 Carotid Artery Disease 54 0.048
295
HRN022 Hearing Loss/deafness 23 0.048
296
RHM027 Rheumatic Disease 55 0.048
297
NSD001 Nose Disease 51 0.048
298
c MJR008 Major Affective Disorder 2 19 0.048
299
TCL003 T Cell Deficiency 44 0.048
300
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.048
301
CNN002 Cannabis Abuse 37 0.048
302
SRC014 Sarcoma 66 0.047
303
HMT002 Hematologic Cancer 62 0.047
304
c CRN177 Coronary Heart Disease 7 21 0.047
305
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.047
306
c ALZ014 Alzheimer Disease 16 17 0.047
307
CRB150 Cerebral Creatine Deficiency Syndrome 2 47 0.047
308
c PLN017 Peeling Skin Syndrome 1 32 0.047
309
c MLT094 Multiple Sclerosis 3 26 0.047
310
ALX002 Alexithymia 37 0.047
311
c CNG006 Congenital Hypothyroidism 59 0.046
312
CRB090 Cerebral Hypoxia 45 0.046
313
c ERL020 Early-Onset Schizophrenia 44 0.046
314
c ADL017 Adult T-Cell Leukemia 59 0.046
315
SML019 Smallpox 49 0.046
316
CNG034 Congestive Heart Failure 72 0.046
317
P DYS154 Dystonia 62 0.046
318
SYN041 Synesthesia 20 0.046
319
P CRT033 Corticobasal Degeneration 44 0.046
320
CRT015 Carotid Artery Occlusion 43 0.046
321
c ALZ036 Alzheimer Disease, Type 3 49 0.046
322
LYM023 Lymphatic System Cancer 35 0.046
323
P HRT032 Heart Disease 64 0.045
324
P RTT002 Rett Syndrome 77 0.045
325
P CRG003 Crigler-Najjar Syndrome, Type I 57 0.045
326
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.045
327
DYS003 Dysgraphia 34 0.045
328
P CRB042 Cerebellar Ataxia 64 0.045
329
PRD011 Proud Syndrome 42 0.045
330
c SCH056 Schizophrenia 15 25 0.045
331
INS024 Insulin-Like Growth Factor I 75 0.045
332
c CRN174 Coronary Heart Disease 2 19 0.045
333
LSH001 Leishmaniasis 63 0.044
334
P HML002 Hemolytic Anemia 60 0.044
335
BNM001 Bone Marrow Cancer 56 0.044
336
EYC003 Eye Accommodation Disease 25 0.044
337
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 54 0.044
338
PNM013 Pneumococcal Meningitis 41 0.044
339
WLF001 Wolff-Parkinson-White Syndrome 58 0.043
340
TXC002 Toxic Encephalopathy 52 0.043
341
ATR060 Atrial Standstill, Digenic 51 0.043
342
CHL061 Childhood Leukemia 47 0.043
343
PRV006 Pervasive Developmental Disorder 49 0.043
344
c ALZ002 Alzheimer Disease Type 1 16 0.043
345
BLD053 Blood Platelet Disease 44 0.043
346
GST053 Gastric Cancer 52 0.043
347
P CRT072 Creutzfeldt-Jakob Disease 62 0.043
348
P IDP010 Idiopathic Generalized Epilepsy 61 0.043
349
BNC003 Bone Cancer 44 0.043
350
LYM019 Lymphosarcoma 52 0.043
351
PRP021 Peripheral Nervous System Neoplasm 49 0.043
352
ACT118 Acute Non Lymphoblastic Leukemia 27 0.043
353
c ADL001 Adult Lymphoma 40 0.043
354
c LKM061 Leukemia, Acute Myeloid 71 0.043
355
GRS011 Gerstmann-Straussler Disease 44 0.043
356
DSS010 Dissociative Disorder 36 0.043
357
P ACT135 Acute Graft Versus Host Disease 52 0.043
358
c CHR064 Chronic Monocytic Leukemia 42 0.043
359
c MLT019 Multiple Myeloma 77 0.043
360
PRV004 Periventricular Leukomalacia 51 0.043
361
LKM006 Leukomalacia 41 0.043
362
c ALZ008 Alzheimer Disease Risk Factor 17 0.043
363
P LFR001 Li-Fraumeni Syndrome 79 0.042
364
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.042
365
c AST037 Asthma 1 35 0.042
366
RMS001 Rem Sleep Behavior Disorder 40 0.042
367
VSC047 Vascular Malformation 45 0.042
368
DMN031 Dementia, Lewy Body 58 0.042
369
SND002 Sneddon Syndrome 45 0.042
370
P ACT074 Acute Lymphocytic Leukemia 54 0.042
371
P HRP009 Herpes Simplex Encephalitis 46 0.042
372
P CLL015 Collagen Disease 49 0.042
373
LYM067 Lymphoid Leukemia 38 0.042
374
ATM055 Autoimmune Disease 4 16 0.042
375
IMM127 Immune System Cancer 41 0.042
376
P OVR042 Ovarian Cancer 73 0.042
377
P ANT006 Antiphospholipid Syndrome 60 0.042
378
JPN002 Japanese Encephalitis 51 0.042
379
c SVR001 Severe Acute Respiratory Syndrome 56 0.042
380
c ACT020 Acute T Cell Leukemia 38 0.042
381
CCN002 Cocaine Abuse 47 0.042
382
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.042
383
BRS051 Breast Disease 57 0.042
384
PTH002 Pathological Gambling 50 0.042
385
P SDR002 Siderosis 44 0.042
386
SBC016 Subacute Delirium 23 0.042
387
ATS001 Autistic Disorder 60 0.041
388
CHL068 Cholestasis 57 0.041
389
ISC006 Ischemic Heart Disease 54 0.041
390
CNT098 Central Core Disease 68 0.041
391
INT007 Intermediate Coronary Syndrome 52 0.041
392
INC022 Inclusion-Cell Disease 46 0.041
393
CHL014 Cholera 56 0.041
394
c PLN021 Peeling Skin Syndrome 3 30 0.041
395
PRN009 Paranoid Schizophrenia 47 0.041
396
ANX004 Anoxia 45 0.041
397
SPS019 Spastic Paraparesis 34 0.041
398
P FRD001 Friedreich Ataxia 62 0.041
399
RMN001 Rumination Disorder 33 0.041
400
MYL020 Myelomeningocele 50 0.041
401
P MDL005 Medulloblastoma 76 0.041
402
P CSH001 Cushing's Syndrome 65 0.041
403
c PLN018 Peeling Skin Syndrome 2 36 0.041
404
ATP002 Atopy 62 0.041
405
ALL006 Allergic Asthma 59 0.041
406
P SKN013 Skin Benign Neoplasm 38 0.041
407
ATN004 Autonomic Neuropathy 44 0.041
408
c ESS001 Essential Tremor 58 0.040
409
P ATR011 Atrial Fibrillation 63 0.040
410
RTN018 Retinal Disease 55 0.040
411
c ACT075 Acute Myocardial Infarction 61 0.040
412
DPH001 Diphtheria 55 0.040
413
c CHR418 Chronic Leukemia 48 0.040
414
MYF002 Myofascial Pain Syndrome 38 0.040
415
c FTL006 Fetal Alcohol Spectrum Disorder 42 0.040
416
c CHR579 Chiari Malformation Type Ii 38 0.040
417
c MLT124 Multiple Sclerosis 5 24 0.040
418
CRN031 Cranial Nerve Disease 39 0.040
419
c MLT095 Multiple Sclerosis 4 24 0.040
420
P CLR023 Colorectal Cancer 96 0.040
421
HDG012 Hodgkin Lymphoma 75 0.040
422
P VLC001 Velocardiofacial Syndrome 64 0.040
423
P CRB047 Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 39 0.040
424
P RBN001 Rubinstein-Taybi Syndrome 65 0.040
425
NSH001 Nasu-Hakola Disease 46 0.040
426
c PRK059 Parkinson Disease 8 51 0.040
427
OCL009 Ocular Cancer 61 0.040
428
BLM002 Bulimia Nervosa 54 0.040
429
c CNT015 Central Sleep Apnea 43 0.040
430
VTM002 Vitamin B12 Deficiency 45 0.040
431
SPR066 Superficial Siderosis 33 0.040
432
DMN012 Dementia - Subcortical 12 0.040
433
MLN007 Male Infertility 56 0.039
434
CDS001 Cadasil 50 0.039
435
P THR014 Thrombocytopenia 63 0.039
436
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.039
437
BDY001 Body Dysmorphic Disorder 41 0.039
438
P PLM037 Pulmonary Hypertension 78 0.039
439
P GLB002 Glioblastoma 65 0.039
440
P GLM045 Glioma 53 0.039
441
c CRN172 Coronary Heart Disease 3 19 0.039
442
c LKM062 Leukemia, Acute Lymphoblastic 63 0.038
443
NWC001 Newcastle Disease 51 0.038
444
ATM059 Autoimmune Disease 6 23 0.038
445
MXD001 Mixed Cerebral Palsy 15 0.038
446
CRB087 Cerebral Arteriosclerosis 23 0.038
447
LYM115 Lymphoma, Non-Hodgkin 64 0.038
448
IMM068 Immunodeficiency 8 32 0.038
449
P CRN035 Cranial Nerve Palsy 44 0.038
450
LKC003 Leukocyte Disease 45 0.038
451
CSY001 C Syndrome 49 0.038
452
P ADN016 Adenocarcinoma 69 0.038
453
P DBT005 Diabetes Insipidus 53 0.038
454
P LBR001 Leber Congenital Amaurosis 61 0.038
455
c HPT015 Hepatitis D 51 0.038
456
PST086 Posterior Cortical Atrophy 33 0.038
457
WHP002 Whiplash 35 0.038
458
P ATX030 Ataxia-Telangiectasia 78 0.037
459
PRP080 Peripheral Artery Disease 35 0.037
460
STT001 Status Epilepticus 59 0.037
461
FRG010 Fragile X Tremor/ataxia Syndrome 36 0.037
462
P CNJ013 Conjunctivitis 65 0.037
463
c LYM107 Lymphoproliferative Syndrome 2 32 0.037
464
MYC002 Mycobacterium Avium Complex Disease 52 0.037
465
LYM040 Lymphoblastic Lymphoma 51 0.037
466
FML039 Female Reproductive System Disease 49 0.037
467
c ADL052 Adult Acute Lymphocytic Leukemia 41 0.037
468
INT074 Intracranial Arteriosclerosis 14 0.037
469
BNS002 Bone Structure Disease 37 0.037
470
SVR004 Severe Combined Immunodeficiency 71 0.037
471
LND001 Landau-Kleffner Syndrome 36 0.037
472
P MSC003 Muscular Atrophy 51 0.037
473
VND001 Vein Disease 51 0.037
474
ORL011 Oral Cancer 53 0.037
475
BNL002 Bone Lymphoma 34 0.037
476
CRB086 Cerebral Aneurysms 39 0.037
477
c CLL013 Cell Type Cancer 46 0.037
478
GLC006 Galactosemia 64 0.036
479
P NRM001 Neuromyelitis Optica 55 0.036
480
DBT010 Diabetic Neuropathy 55 0.036
481
c BCT007 Bacterial Meningitis 55 0.036
482
BNG009 Benign Epilepsy with Centrotemporal Spikes 42 0.036
483
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.036
484
BRN106 Burns 52 0.036
485
ADM013 Adamantinoma of Long Bones 57 0.036
486
GRW007 Growth Hormone Deficiency 49 0.036
487
SPS007 Spastic Cerebral Palsy 42 0.036
488
ART002 Arts Syndrome 53 0.035
489
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.035
490
FTT001 Fatty Liver Disease 60 0.035
491
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.035
492
P NRF002 Neurofibromatosis 66 0.035
493
P WLD002 Waldenstrom Macroglobulinemia 62 0.035
494
VSC011 Vasculitis 62 0.035
495
VSC006 Vascular Cancer 51 0.035
496
ANT011 Antisocial Personality Disorder 46 0.035
497
BRN018 Borna Disease 43 0.035
498
P GNR027 Generalized Peeling Skin Syndrome 21 0.035
499
CHR008 Choroiditis 43 0.035
500
BHV002 Behavioral Variant of Frontotemporal Dementia 37 0.035
501
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.034
502
c SPN100 Spinocerebellar Ataxia 27 41 0.034
503
c SPS072 Spastic Ataxia 1, Autosomal Dominant 25 0.034
504
LYM017 Lyme Disease 64 0.034
505
RPR002 Reproductive System Disease 45 0.034
506
P FLL037 Follicular Lymphoma 68 0.034
507
c MJR007 Major Affective Disorder 1 27 0.034
508
DYS009 Dysthymic Disorder 37 0.034
509
HMP009 Haemophilus Influenzae 44 0.034
510
c SCH064 Schizophrenia 10 21 0.034
511
SNS023 Sensory System Cancer 45 0.034
512
SKN016 Skin Disease 69 0.034
513
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.034
514
BNF002 Bone Fracture 46 0.034
515
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.034
516
P SML001 Small Cell Carcinoma 54 0.034
517
AGR002 Agoraphobia 41 0.034
518
c GRN014 Grn-Related Frontotemporal Dementia 36 0.034
519
P EXN002 Exanthem 57 0.034
520
PRP036 Peripheral T-Cell Lymphoma 44 0.034
521
PRM151 Primary Bone Lymphoma 26 0.034
522
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 14 0.034
523
CHR105 Choreoacanthocytosis 45 0.034
524
c NRF018 Neurofibromatosis, Type 1 69 0.034
525
IRR002 Irritable Bowel Syndrome 58 0.034
526
P CHL002 Childhood Absence Epilepsy 54 0.034
527
MSL001 Measles 61 0.034
528
OCL011 Ocular Motility Disease 41 0.034
529
MTR014 Motor Neuron Disease 57 0.034
530
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.034
531
HYP458 Hyper Ige Syndrome 43 0.034
532
DFF005 Diffuse Large B-Cell Lymphoma 57 0.034
533
c PRK025 Parkinson Disease 10 41 0.034
534
MNS002 Mini Stroke 18 0.034
535
P WSK001 Wiskott-Aldrich Syndrome 70 0.034
536
P TRN020 Turner Syndrome 64 0.034
537
ADL002 Adult Syndrome 53 0.034
538
P GT001 Gout 58 0.034
539
c PRC016 Pre-Eclampsia 57 0.034
540
P CRB059 Cerebellar Degeneration 30 0.034
541
KRT004 Keratitis 70 0.033
542
CFF002 Coffin-Lowry Syndrome 56 0.033
543
P LNG028 Long Qt Syndrome 67 0.033
544
P ART023 Arthropathy 63 0.033
545
P ECL001 Eclampsia 55 0.033
546
P NTR004 Neutropenia 59 0.033
547
IMM076 Immunodeficiency 24 27 0.033
548
SKN023 Skin Tag 48 0.033
549
CRT013 Carotid Stenosis 35 0.033
550
ADS004 Aids Dementia Complex 47 0.033
551
P RTN024 Retinoblastoma 75 0.033
552
P ADD001 Addison's Disease 60 0.033
553
c TRC078 Trichohepatoenteric Syndrome 2 30 0.033
554
IMM071 Immunodeficiency 12 27 0.033
555
PRN023 Prion Disease 44 0.033
556
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 33 0.033
557
P GLM007 Glomerulonephritis 56 0.033
558
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 31 0.033
559
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.033
560
SCR011 Scrapie 34 0.033
561
P NRC002 Narcolepsy 62 0.033
562
c SPN312 Spinocerebellar Ataxia 14 46 0.033
563
ADP001 Adiposis Dolorosa 44 0.033
564
CRY004 Cryoglobulinemia 47 0.033
565
c CNG027 Congenital Hemolytic Anemia 46 0.033
566
HMG005 Hemoglobinopathy 49 0.033
567
CRT012 Cortical Blindness 36 0.033
568
PLR008 Pleurisy 51 0.033
569
DLS001 Delusional Disorder 40 0.033
570
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 27 0.033
571
c LKM005 Leukemia, T-Cell, Chronic 21 0.033
572
BRN049 Brain Tumor, Childhood 15 0.033
573
P OST002 Osteoporosis 63 0.032
574
IMM096 Immunodeficiency 30 30 0.032
575
P HYP024 Hypoparathyroidism 52 0.032
576
P MMB011 Membranous Nephropathy 53 0.032
577
SCK003 Sickle Cell Anemia 72 0.031
578
CST001 Costello Syndrome 68 0.031
579
WHM001 Whim Syndrome 53 0.031
580
HRY003 Hairy Cell Leukemia 56 0.031
581
CHG001 Chagas Disease 62 0.031
582
P HMP007 Hemophilia 55 0.031
583
TCK001 Tick-Borne Encephalitis 49 0.031
584
CHL123 Chlamydia 60 0.031
585
P OTS001 Otosclerosis 33 0.031
586
SCK005 Sickle Cell Disease 51 0.031
587
BRN004 Brain Edema 51 0.031
588
HYP085 Hypothalamic Disease 43 0.031
589
NN2002 Non 24 Hour Sleep Wake Disorder 23 0.031
590
P AGM001 Agammaglobulinemia 63 0.031
591
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 17 0.031
592
FML037 Female Breast Cancer 49 0.031
593
c LKM055 Leukemia, Acute Lymphoblastic 2 21 0.031
594
HNS001 Hansen's Disease 30 0.031
595
c PRM023 Pre-Malignant Neoplasm 42 0.031
596
CHD001 Chediak-Higashi Syndrome 66 0.031
597
P ALX003 Alexander Disease 64 0.031
598
P RCK004 Rickets 59 0.031
599
P THL005 Thalassemia 61 0.031
600
ADN018 Adenoma 59 0.031
601
c MYC058 Myocardial Infarction 2 28 0.031
602
ATM012 Autoimmune Disease of Blood 36 0.031
603
GLL008 Gilles De La Tourette Syndrome 63 0.030
604
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 38 0.030
605
DMN016 Dementia, Familial, Nonspecific 28 0.030
606
BRC012 Brucellosis 66 0.030
607
BLL006 Bullous Pemphigoid 59 0.030
608
KLV001 Kluver-Bucy Syndrome 37 0.030
609
P ESN007 Eosinophilia 61 0.030
610
CTN007 Cutaneous Leishmaniasis 62 0.030
611
P UVT001 Uveitis 60 0.030
612
DPR002 Depersonalization Disorder 30 0.030
613
P HYP263 Hypersomnia 39 0.030
614
FRN030 Frontotemporal Dementia with Parkinsonism-17 30 0.030
615
P CHR562 Chronic Myelocytic Leukemia 39 0.030
616
HRP008 Herpes Simiae 13 0.030
617
HRP012 Herpesvirus Simiae B Virus 10 0.030
618
CHR103 Charge Syndrome 64 0.030
619
P MYL005 Myelofibrosis 67 0.030
620
c PRM005 Primary Hyperparathyroidism 56 0.030
621
SKN027 Skin Conditions 44 0.030
622
CRB027 Cerebellar Disease 46 0.030
623
DDN006 Duodenitis 44 0.030
624
c ACT134 Acute Liver Failure 46 0.030
625
PTT049 Pituitary Adenoma, Acth-Secreting 52 0.030
626
CRB096 Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants 32 0.030
627
URB001 Urbach-Wiethe Disease 48 0.030
628
BHC003 Behcet Syndrome 60 0.030
629
BRN038 Bronchial Disease 54 0.030
630
FCL012 Facial Paralysis 50 0.030
631
c BNG023 Benign Familial Infantile Epilepsy 40 0.030
632
c CHR092 Chronic Myeloproliferative Disease 50 0.030
633
MTS001 Mutism 38 0.030
634
CHR001 Churg-Strauss Syndrome 48 0.030
635
MDS022 Mediastinitis 37 0.030
636
P MTC003 Metachromatic Leukodystrophy 71 0.029
637
P APL001 Aplastic Anemia 74 0.029
638
WRN001 Werner Syndrome 69 0.029
639
P NJM001 Nijmegen Breakage Syndrome 68 0.029
640
P OST012 Osteoarthritis 81 0.029
641
ANR002 Aniridia 62 0.029
642
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.029
643
P CRB019 Cerebral Amyloid Angiopathy 56 0.029
644
P CRN037 Craniosynostosis 66 0.029
645
TRC010 Trichotillomania 39 0.029
646
P LKD001 Leukodystrophy 58 0.029
647
P MYP006 Myopia 58 0.029
648
P PRM006 Primary Biliary Cirrhosis 55 0.029
649
RFL001 Reflex Sympathetic Dystrophy 45 0.029
650
PLM001 Pulmonary Tuberculosis 69 0.029
651
ALX001 Alexia 42 0.029
652
AMB002 Amblyopia 42 0.029
653
PRT038 Protein-Energy Malnutrition 48 0.029
654
c PRK022 Parkinson Disease 12 22 0.029
655
CRB142 Cerebellar Ataxia, Deafness, and Narcolepsy, Autosomal Dominant 31 0.028
656
c HMP029 Hemophilia a 61 0.028
657
HRP004 Herpes Zoster 56 0.028
658
IMM082 Immunodeficiency 18 31 0.028
659
MNT001 Mantle Cell Lymphoma 72 0.028
660
P BLP003 Blepharospasm 43 0.028
661
PLS007 Plasmodium Falciparum Malaria 56 0.028
662
c LYM106 Lymphoproliferative Syndrome 1 33 0.028
663
P PRT013 Portal Hypertension 61 0.028
664
c LKM004 Leukemia, B-Cell, Chronic 24 0.028
665
VGS001 Vagus Nerve Disease 17 0.028
666
FML038 Female Reproductive Organ Cancer 50 0.028
667
OPT003 Opiate Dependence 49 0.028
668
SCH003 Schizophreniform Disorder 37 0.028
669
c LKM056 Leukemia, Chronic Lymphocytic 2 40 0.028
670
GLC077 Glucocorticoid Therapy, Response to 17 0.028
671
MYL001 Myelitis 35 0.028
672
PTT037 Pituitary Tumors 45 0.028
673
CLS049 Classic Phenylketonuria 23 0.028
674
CRV045 Cervical Intraepithelial Neoplasia 41 0.028
675
WRT002 Writing Disorder 26 0.028
676
WLS001 Wilson Disease 72 0.028
677
P HMC003 Hemochromatosis 71 0.028
678
P DNT015 Dent Disease 61 0.028
679
RBR001 Roberts Syndrome 61 0.028
680
P MYS003 Myasthenia Gravis 64 0.028
681
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.028
682
P RHN004 Rhinitis 59 0.028
683
MSC077 Muscle Eye Brain Disease 54 0.028
684
TTH006 Tooth Disease 52 0.028
685
STM006 Stomach Disease 48 0.028
686
INT075 Intracranial Hypertension 52 0.028
687
HMG002 Hemoglobinuria 49 0.028
688
P PRD008 Periodontitis 46 0.028
689
PTT006 Pituitary Adenoma 54 0.028
690
RFR004 Refractory Hematologic Cancer 27 0.028
691
NRM004 Neuroma 47 0.028
692
CRB085 Cerebral Hemorrhage 40 0.028
693
OVR063 Overnutrition 49 0.028
694
CHR413 Chronic Myocardial Ischemia 39 0.028
695
ALL003 Allergic Rhinitis 67 0.027
696
P CRD013 Cardiofaciocutaneous Syndrome 65 0.027
697
P TRC086 Trichohepatoenteric Syndrome 1 46 0.027
698
c NRF019 Neurofibromatosis, Type 2 62 0.027
699
P GRV001 Graves' Disease 62 0.027
700
HRT007 Heart Cancer 51 0.027
701
IMM065 Immunodeficiency 10 39 0.027
702
ANG049 Angioedema Induced by Ace Inhibitors 35 0.027
703
MRB003 Morbid Obesity 59 0.027
704
P MLT074 Multiple Endocrine Neoplasia 55 0.027
705
c HPT007 Hepatitis E 51 0.027
706
MLR007 Male Reproductive System Disease 36 0.027
707
CRV043 Cervical Dystonia 43 0.027
708
P HRT017 Heart Tumor 34 0.027
709
DVL005 Developmental Dyspraxia 17 0.027
710
ADT005 Auditory Perceptual Disorder 14 0.027
711
THY028 Thyroid Cancer 71 0.026
712
P PLR004 Pleuropulmonary Blastoma 63 0.026
713
SML033 Small Cell Cancer of the Lung, Somatic 53 0.026
714
CNT047 Contact Dermatitis 62 0.026
715
ALL010 Allergic Contact Dermatitis 58 0.026
716
c PRK051 Parkinson Disease 18 30 0.026
717
CHR073 Choreatic Disease 39 0.026
718
SLP001 Sleeping Sickness 48 0.026
719
P HYP111 Hyperprolinemia 33 0.026
720
P SYP003 Syphilis 51 0.026
721
TNS005 Tonsillitis 58 0.026
722
c PRK026 Parkinson Disease 11 30 0.026
723
P BRN120 Bronchus Cancer 43 0.026
724
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.026
725
c PRM226 Primary Central Nervous System Lymphoma 51 0.026
726
BNS003 Binswanger's Disease 30 0.026
727
URT001 Urethritis 39 0.026
728
IMM103 Immunodeficiency 37 18 0.026
729
FCT008 Factitious Disorder 42 0.026
730
P CNT005 Central Nervous System Lymphoma 51 0.026
731
DRG016 Drug Induced Dyskinesia 19 0.026
732
PRG033 Progressive Non-Fluent Aphasia 16 0.026
733
BRN039 Bronchial Neoplasm 35 0.026
734
MNN032 Meningococcal Meningitis 33 0.026
735
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 39 0.026
736
MDR006 Moderate and Severe Traumatic Brain Injury 22 0.026
737
P CNT036 Central Nervous System Germ Cell Tumor 38 0.026
738
INT031 Integrative Agnosia 10 0.026
739
c SML023 Small Cell Lung Cancer, Adult 17 0.026
740
CHR321 Chorea and Dementia 17 0.026
741
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.025
742
EWN003 Ewing Sarcoma 63 0.025
743
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 51 0.025
744
ACN011 Acne 63 0.025
745
AND015 Androgen Insensitivity 64 0.025
746
KRT002 Keratomalacia 50 0.025
747
P SYS005 Systemic Scleroderma 60 0.025
748
MLL012 Miller Syndrome 43 0.025
749
LPT001 Leptospirosis 65 0.025
750
c NRP041 Neuropathy, Hereditary Sensory, Type Ie 35 0.025
751
LPP001 Lipoprotein Lipase Deficiency 63 0.025
752
IRN001 Iron Deficiency Anemia 51 0.025
753
c MTR002 Mitral Valve Insufficiency 42 0.025
754
SSC001 Susac Syndrome 28 0.025
755
MLL002 Miller Fisher Syndrome 43 0.025
756
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.025
757
PTT009 Pituitary Gland Disease 45 0.025
758
WST005 West Nile Virus 50 0.025
759
FXF002 Fox-Fordyce Disease 37 0.025
760
P NNT009 Neonatal Diabetes Mellitus 50 0.025
761
FDL002 Food Allergy 56 0.025
762
OPP004 Oppositional Defiant Disorder 42 0.025
763
c MJR006 Major Affective Disorder 5 17 0.025
764
c CNG031 Congenital Nervous System Abnormality 39 0.025
765
URT010 Ureteral Obstruction 45 0.025
766
CD4004 Cd4 Deficiency 15 0.025
767
P PRM019 Premature Ovarian Failure 65 0.024
768
MSM014 Mismatch Repair Cancer Syndrome 60 0.024
769
JCB001 Jacobsen Syndrome 49 0.024
770
CRD119 Cardiac Arrest 63 0.024
771
P CRP007 Carpenter Syndrome 49 0.024
772
P WRD001 Waardenburg's Syndrome 56 0.024
773
PRC002 Paracoccidioidomycosis 57 0.024
774
GLC037 Glucocorticoid Resistance 57 0.024
775
MTN003 Motion Sickness 48 0.024
776
GNT003 Genital Herpes 55 0.024
777
GNG013 Gingivitis 61 0.024
778
CHK001 Chikungunya 49 0.024
779
P SNS014 Sinusitis 66 0.024
780
PRS042 Prostate Disease 50 0.024
781
P NGH001 Night Blindness 49 0.024
782
ADR012 Adrenal Gland Disease 49 0.024
783
c CHR285 Chronic Myelomonocytic Leukemia 54 0.024
784
CRC006 Carcinoid Syndrome 51 0.024
785
P OVR049 Ovarian Disease 54 0.024
786
OST003 Osteonecrosis 45 0.024
787
P SYR001 Syringomyelia 44 0.024
788
P SCK002 Sick Sinus Syndrome 49 0.024
789
CHL109 Childhood Apraxia of Speech 29 0.024
790
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 21 0.024
791
OLF001 Olfactory Nerve Disease 20 0.024
792
INT253 Intestinal Benign Neoplasm 48 0.024
793
RCT017 Rectal Disease 35 0.024
794
P LRY019 Laryngitis 55 0.024
795
MCR004 Macroglobulinemia 48 0.024
796
MHC002 Mhc Class I Deficiency 34 0.024
797
c PRG001 Progressive Muscular Atrophy 39 0.024
798
RTN020 Retinal Vascular Disease 49 0.024
799
HRN003 Heroin Dependence 40 0.024
800
SYN036 Syncope 45 0.024
801
INF013 Inferior Myocardial Infarction 36 0.024
802
MLN003 Melancholia 36 0.024
803
ADS006 Aids - Neurological Complications 12 0.024
804
NNP013 Non-Polyposis Turcot Syndrome 12 0.024
805
HMC014 Homocysteinemia 32 0.024
806
P SPR098 Supranuclear Palsy, Progressive 57 0.022
807
P PLZ001 Pelizaeus-Merzbacher Disease 63 0.022
808
P CLC005 Celiac Disease 67 0.022
809
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 55 0.022
810
CRS012 Carasil Syndrome 30 0.022
811
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.022
812
TST021 Testicular Germ Cell Tumor 67 0.022
813
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 28 0.022
814
NCT008 Nicotine Dependence, Protection Against 51 0.022
815
P RBL001 Rubella 54 0.022
816
IMM084 Immunodeficiency 17, Cd3 Gamma Deficient 20 0.022
817
c FLL041 Follicular Lymphoma 1 45 0.022
818
TXC005 Toxic Shock Syndrome 61 0.022
819
c ATS173 Autism 18 21 0.022
820
IMM105 Immunodeficiency with Hyper-Igm, Type 3 23 0.022
821
ADT002 Auditory System Cancer 32 0.022
822
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.022
823
IMM085 Immunodeficiency 25 25 0.022
824
MLR006 Male Reproductive Organ Cancer 46 0.022
825
c PRK037 Parkinson Disease 13 27 0.022
826
HYP005 Hypokalemia 52 0.022
827
P UTR038 Uterine Disease 38 0.022
828
DLY005 Delayed Sleep Phase Syndrome 37 0.022
829
SFT003 Soft Tissue Sarcoma 55 0.022
830
NRN008 Neuronal Intranuclear Inclusion Disease 41 0.022
831
CLN019 Colonic Disease 50 0.022
832
GLM004 Gliomatosis Cerebri 48 0.022
833
P PLM006 Pulmonary Alveolar Proteinosis 46 0.022
834
RTC005 Reticulosarcoma 46 0.022
835
CNT017 Central Nervous System Origin Vertigo 27 0.022
836
MSC072 Muscle Cancer 47 0.022
837
STM007 Stomatitis 50 0.022
838
PTT008 Pituitary Carcinoma 45 0.022
839
RTC009 Reticulum Cell Sarcoma 46 0.022
840
P MRC003 Mercury Poisoning 38 0.022
841
MTH027 Mthfr Deficiency 23 0.022
842
AGR018 Agraphia 38 0.022
843
PRS011 Persian Gulf Syndrome 20 0.022
844
CRB040 Cerebrum Cancer 36 0.022
845
GST009 Gastroschisis 31 0.022
846
PDP001 Pedophilia 29 0.022
847
P PRM108 Primary Progressive Multiple Sclerosis 47 0.022
848
CNT018 Central Nervous System Leukemia 38 0.022
849
CHL078 Childhood-Onset Schizophrenia 32 0.022
850
P LPS002 Liposarcoma 50 0.022
851
c LKM051 Leukemia, Chronic Lymphocytic 3 21 0.022
852
ATN003 Autonomic Nervous System Neoplasm 43 0.022
853
FNC005 Functional Colonic Disease 32 0.022
854
GRM001 Germ Cell and Embryonal Cancer 38 0.022
855
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 19 0.022
856
ORL015 Oral Squamous Cell Carcinoma 55 0.022
857
c SPR049 Supranuclear Palsy, Progressive, 2 19 0.022
858
c MJR004 Major Affective Disorder 4 19 0.022
859
MRG003 Marginal Zone B-Cell Lymphoma 50 0.022
860
RTN003 Retinal Ischemia 48 0.022
861
FNT004 Fainting 33 0.022
862
BSL005 Basal Ganglia Cerebrovascular Disease 10 0.022
863
OBS060 Obesity Due to Sim1 Deficiency 9 0.022
864
SPR032 Superficial Siderosis of the Central Nervous System 24 0.022
865
PRL032 Perlman Syndrome 55 0.020
866
CMM005 Common Cold 58 0.020
867
STF001 Stiff-Person Syndrome 54 0.020
868
RCT018 Rectal Neoplasm 53 0.020
869
c ATM010 Autoimmune Hemolytic Anemia 59 0.020
870
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 36 0.020
871
STR008 Strongyloidiasis 51 0.020
872
ART005 Arteriovenous Malformation 63 0.020
873
P ACT117 Acute Myelomonocytic Leukemia 46 0.020
874
c FNC042 Fanconi Anemia, Complementation Group D2 32 0.020
875
OMN001 Omenn Syndrome 61 0.020
876
TYP007 Typhoid Fever 61 0.020
877
QDR001 Quadriplegia 51 0.020
878
IMM036 Immunodeficiency, Isolated 26 0.020
879
MHC001 Mhc Class Ii Deficiency 39 0.020
880
HYP003 Hypermethioninemia 37 0.020
881
IMM025 Immunoglobulin a Deficiency 2 27 0.020
882
WHP001 Whipple Disease 49 0.020
883
P ARC016 Auriculocondylar Syndrome 1 44 0.020
884
PLS006 Plasmodium Vivax Malaria 52 0.020
885
DBT001 Diabetic Ketoacidosis 45 0.020
886
P HYP098 Hypereosinophilic Syndrome 48 0.020
887
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 38 0.020
888
HDG004 Hodgkin's Granuloma 25 0.020
889
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 25 0.020
890
NRN004 Neuroendocrine Tumor 54 0.020
891
P DRR001 Diarrhea 60 0.020
892
c CRP022 Carpenter Syndrome 2 30 0.020
893
c BSL039 Basal Ganglia Calcification, Idiopathic, 6 18 0.020
894
BRM003 Biermer's Disease 22 0.020
895
END035 Endocrine Gland Cancer 50 0.020
896
LNS003 Lens Disease 37 0.020
897
PHT008 Photosensitive Epilepsy 34 0.020
898
RFT001 Rift Valley Fever 42 0.020
899
IMM120 Immunodeficiency 40 24 0.020
900
c DYS120 Dyslexia 2 21 0.020
901
NRF007 Neurofibroma 53 0.020
902
PST021 Postpartum Depression 49 0.020
903
CMP034 Complete Androgen Insensitivity Syndrome 42 0.020
904
IMM088 Immunodeficiency 36 21 0.020
905
P TRT010 Teratoma 49 0.020
906
CRV069 Cervix Disease 31 0.020
907
c MLG079 Malignant Pleural Mesothelioma 54 0.020
908
NSS002 Neisseria Meningitidis Infection 33 0.020
909
CNT069 Centrotemporal Epilepsy 16 0.020
910
NMN001 Nominal Aphasia 28 0.020
911
SPR024 Supratentorial Cancer 36 0.020
912
HYP231 Hypothalamic Hamartomas 35 0.020
913
TRY001 Trypanosomiasis 51 0.020
914
YNG002 Young Syndrome 25 0.020
915
CRN033 Cranial Nerve Malignant Neoplasm 31 0.020
916
HDG006 Hodgkin's Paragranuloma 18 0.020
917
BLT006 Bilateral Breast Cancer 50 0.020
918
P THY023 Thymoma 57 0.020
919
PRG090 Progressive Relapsing Multiple Sclerosis 31 0.020
920
SPL040 Split Hand 35 0.020
921
PRP010 Prepuce Cancer 17 0.020
922
c ALP005 Alpha Chain Disease 36 0.020
923
c TRN009 Transient Hypogammaglobulinemia of Infancy 38 0.020
924
PTC005 Pituicytoma 24 0.020
925
HYP002 Hypothalamic Neoplasm 21 0.020
926
c GRV009 Graves Disease 2 18 0.020
927
RDT005 Radiation Induced Cancer 26 0.020
928
SCL044 Scalp Syndrome 17 0.020
929
P CYS017 Cystic Teratoma 40 0.020
930
HRT029 Heart Tumor of the Child 16 0.020
931
c ALZ031 Alzheimer Disease 17 16 0.020
932
CRB002 Cerebral Primitive Neuroectodermal Tumor 42 0.020
933
EXT033 Extrapulmonary Tuberculosis 45 0.020
934
c MJR003 Major Affective Disorder 6 17 0.020
935
NNT021 Neonatal Meningitis 23 0.020
936
PDT001 Pediatric Lymphoma 39 0.020
937
SPC001 Space Motion Sickness 30 0.020
938
ENC005 Encephalomalacia 26 0.020
939
TCL006 T Cell Immunodeficiency Primary 13 0.020
940
THL010 Thalassemia Minor 38 0.020
941
WSC001 Wisconsin Syndrome 16 0.020
942
P PRL003 Proliferative Glomerulonephritis 40 0.020
943
P TRN016 Transient Hypogammaglobulinemia 33 0.020
944
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 29 0.020
945
BRS090 Breast Reconstruction 38 0.020
946
DPB001 Deep Brain Stimulation for Parkinson's Disease 23 0.020
947
MNT045 Montefiore Syndrome 11 0.020