Search results for Valproic Acid

921 hits were found for Valproic Acid

# Family MCID Name MIFTS Score
1
VLP002 Valproate Embryopathy 45 6.695
2
P SZR006 Seizure Disorder 59 0.397
3
NRL016 Neural Tube Defects 83 0.385
4
VSL002 Visual Epilepsy 58 0.357
5
P BPL003 Bipolar Disorder 59 0.338
6
c MJR024 Major Affective Disorder 9 42 0.335
7
c MJR022 Major Affective Disorder 8 39 0.335
8
P ATS364 Autism 68 0.300
9
P NRB010 Neuroblastoma 1 66 0.296
10
P LVR013 Liver Disease 71 0.291
11
P ENC018 Encephalopathy 64 0.290
12
P GLM045 Glioma 64 0.286
13
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.283
14
GLL048 Glial Tumor 48 0.281
15
FTT001 Fatty Liver Disease 63 0.268
16
GLB002 Glioblastoma 74 0.268
17
P CLR023 Colorectal Cancer 100 0.268
18
GLB015 Glioblastoma Multiforme 60 0.268
19
c ATS007 Autism Spectrum Disorder 69 0.267
20
P MYL006 Myeloid Leukemia 61 0.263
21
P LKM002 Leukemia 69 0.263
22
c LKM061 Leukemia, Acute Myeloid 84 0.257
23
ACT119 Acute Promyelocytic Leukemia 63 0.254
24
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.251
25
P EPL164 Epilepsy 73 0.251
26
c MGR028 Migraine with or Without Aura 1 70 0.242
27
48X005 48,xyyy 37 0.239
28
P BRS047 Breast Cancer 99 0.235
29
P KDN018 Kidney Disease 73 0.231
30
CHL068 Cholestasis 61 0.229
31
LPD008 Lipid Metabolism Disorder 64 0.226
32
OCL069 Ocular Motor Apraxia 53 0.225
33
MTB004 Metabolic Acidosis 48 0.223
34
LVR012 Liver Cirrhosis 67 0.221
35
ISC004 Ischemia 62 0.218
36
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.217
37
STT001 Status Epilepticus 61 0.213
38
P PRS040 Prostate Cancer 97 0.212
39
HLX001 Helix Syndrome 46 0.210
40
HYP014 Hyperuricemia 52 0.208
41
MYL009 Myelodysplastic Syndrome 72 0.205
42
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.205
43
P DRR001 Diarrhea 55 0.203
44
ALL026 Allergic Hypersensitivity Disease 65 0.203
45
P LYM031 Lymphocytic Leukemia 56 0.196
46
BRN071 Brain Injury 51 0.195
47
P PNC044 Pancreatitis 61 0.195
48
P LNG032 Lung Cancer 99 0.194
49
GST092 Gastroesophageal Reflux 68 0.193
50
P THR014 Thrombocytopenia 67 0.192
51
P HPT023 Hepatocellular Carcinoma 99 0.190
52
HYP056 Hypoglycemia 68 0.190
53
TRM010 Traumatic Brain Injury 54 0.188
54
HYP060 Hyperinsulinism 55 0.187
55
HMN044 Human Immunodeficiency Virus Type 1 73 0.187
56
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.187
57
P PNC035 Pancreatic Cancer 86 0.186
58
P NRF023 Neurofibromatosis, Type Ii 77 0.186
59
MDD011 Mood Disorder 62 0.184
60
HYP066 Hyperglycemia 63 0.178
61
P ALZ034 Alzheimer Disease 90 0.178
62
P OVR042 Ovarian Cancer 89 0.177
63
P NTR004 Neutropenia 64 0.176
64
P MSC003 Muscular Atrophy 52 0.175
65
BNR002 Bone Resorption Disease 51 0.174
66
c ACT210 Acute Respiratory Distress Syndrome 59 0.174
67
P HNT016 Huntington Disease 72 0.173
68
GT001 Gout 63 0.173
69
ATM095 Autoimmune Disease 62 0.173
70
P CRN300 Coronary Heart Disease 1 59 0.172
71
MYL069 Myeloma, Multiple 85 0.172
72
c ACT027 Acute Pancreatitis 60 0.170
73
DFC004 Deficiency Anemia 77 0.170
74
P HYP750 Hypertriglyceridemia, Familial 62 0.170
75
P VSC007 Vascular Disease 65 0.168
76
P BLD134 Bladder Cancer 79 0.167
77
THY029 Thyroid Carcinoma 62 0.167
78
OST159 Osteogenic Sarcoma 67 0.167
79
SPN186 Spinal Cord Injury 63 0.166
80
c MLG068 Malignant Glioma 46 0.165
81
EXN003 Exencephaly 32 0.164
82
P HYP086 Hypothyroidism 70 0.163
83
47X002 47,xyy 49 0.162
84
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.161
85
P OST002 Osteoporosis 79 0.161
86
c RHB024 Rhabdomyosarcoma 2 64 0.160
87
HRW001 Hair Whorl 36 0.159
88
CYT002 Cytokine Deficiency 46 0.159
89
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.157
90
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.157
91
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.157
92
SQM006 Squamous Cell Carcinoma 60 0.156
93
P TRM003 Tremor 55 0.156
94
DPR016 Depression 64 0.155
95
PRT037 Pertussis 66 0.155
96
c PCH010 Pachyonychia Congenita 3 43 0.154
97
P AST007 Astrocytoma 52 0.154
98
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.154
99
DRM006 Dermatitis 63 0.153
100
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.153
101
c HYP836 Hypercholesterolemia, Familial, 1 74 0.153
102
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.152
103
P LTR001 Lateral Sclerosis 56 0.152
104
CRV035 Cervical Cancer 77 0.151
105
ALC007 Alcohol Dependence 68 0.151
106
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.151
107
P NRP001 Neuropathy 57 0.151
108
NNL006 Non-Alcoholic Steatohepatitis 53 0.150
109
P CRN018 Coronary Artery Anomaly 67 0.150
110
c CHR684 Chronic Kidney Disease 68 0.149
111
P ALP008 Alopecia 58 0.149
112
HYP266 Hypoxia 58 0.148
113
c SML038 Small Cell Cancer of the Lung 67 0.148
114
HPT004 Hepatic Coma 42 0.147
115
P ESP024 Esophagitis 62 0.146
116
P ADN016 Adenocarcinoma 65 0.146
117
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.145
118
ADN018 Adenoma 60 0.145
119
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.143
120
P EXN002 Exanthem 58 0.142
121
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.142
122
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.142
123
RTN023 Retinitis 46 0.141
124
NRR001 Neuroretinitis 46 0.141
125
ART140 Arteries, Anomalies of 60 0.141
126
P MJR007 Major Affective Disorder 1 44 0.141
127
P DBT009 Diabetes Mellitus 66 0.140
128
P SPN046 Spinal Muscular Atrophy 65 0.139
129
OVR082 Overgrowth Syndrome 51 0.138
130
SRC014 Sarcoma 67 0.138
131
SPN035 Spindle Cell Sarcoma 57 0.138
132
MNT002 Mental Depression 60 0.138
133
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.138
134
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.137
135
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.137
136
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.137
137
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.137
138
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.137
139
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.137
140
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.137
141
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.137
142
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.137
143
CRB004 Cerebral Artery Occlusion 38 0.137
144
c LKM071 Leukemia, Chronic Lymphocytic 81 0.136
145
P RTN008 Retinitis Pigmentosa 77 0.136
146
P LYM118 Lymphoma 70 0.136
147
ADL002 Adult Syndrome 62 0.136
148
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.135
149
P MYC007 Myocardial Infarction 74 0.135
150
P TRN020 Turner Syndrome 66 0.135
151
MLN008 Melanoma 68 0.135
152
BND020 Bone Disease 60 0.135
153
END030 End Stage Renal Failure 60 0.134
154
c ACT073 Acute Leukemia 59 0.134
155
P MYP004 Myopathy 63 0.134
156
P CNR004 Cone-Rod Dystrophy 2 72 0.134
157
c LKM004 Leukemia, B-Cell, Chronic 35 0.134
158
URM002 Uremia 50 0.133
159
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.133
160
c HYP595 Hypertension, Essential 87 0.133
161
DYS014 Dyspepsia 51 0.133
162
HPT019 Hepatic Encephalopathy 60 0.133
163
c ACT071 Acute Kidney Failure 60 0.133
164
IMM167 Immune Deficiency Disease 79 0.133
165
DWN001 Down Syndrome 70 0.133
166
ATX019 Ataxia with Vitamin E Deficiency 46 0.131
167
P HDC001 Headache 59 0.131
168
CRB039 Cerebrovascular Disease 71 0.130
169
TRT001 Teratocarcinoma 44 0.130
170
HMC014 Homocysteinemia 54 0.130
171
P DMN002 Dementia 68 0.129
172
P HRP006 Herpes Simplex 66 0.129
173
P PLY011 Polycystic Ovary Syndrome 58 0.128
174
BRN028 Brain Cancer 75 0.128
175
c CHR064 Chronic Monocytic Leukemia 43 0.128
176
EMB004 Embryonal Carcinoma 57 0.127
177
c INH020 Inherited Metabolic Disorder 51 0.127
178
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.126
179
LNG099 Lung Disease 62 0.125
180
NTR005 Nutritional Deficiency Disease 61 0.125
181
LNG031 Lung Benign Neoplasm 52 0.125
182
P SCH015 Schizophrenia 76 0.125
183
P BCL017 B-Cell Lymphoma 61 0.125
184
ALL014 Allergic Encephalomyelitis 40 0.125
185
P GLM040 Glioma Susceptibility 1 68 0.124
186
CHL014 Cholera 58 0.123
187
STR067 Stroke, Ischemic 82 0.123
188
P RSP003 Respiratory Failure 75 0.123
189
P LCT001 Lactic Acidosis 52 0.122
190
ANX010 Anxiety 75 0.121
191
P TMP001 Temporal Lobe Epilepsy 53 0.120
192
LYM019 Lymphosarcoma 48 0.120
193
P HPT021 Hepatitis 69 0.119
194
GLC003 Glucose Intolerance 55 0.119
195
MXD026 Mixed Glioma 36 0.119
196
P MLT020 Multiple Sclerosis 73 0.119
197
P HYP098 Hypereosinophilic Syndrome 67 0.118
198
ACQ007 Acquired Immunodeficiency Syndrome 61 0.118
199
CHL079 Children's Interstitial Lung Disease 27 0.118
200
P RTN024 Retinoblastoma 74 0.117
201
c FML008 Familial Retinoblastoma 46 0.117
202
SVR004 Severe Combined Immunodeficiency 74 0.116
203
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.116
204
c MJR003 Major Affective Disorder 6 34 0.116
205
c MJR006 Major Affective Disorder 5 34 0.116
206
SBC016 Subacute Delirium 43 0.116
207
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.116
208
c HPT001 Hepatitis C 62 0.115
209
c MJR008 Major Affective Disorder 2 35 0.115
210
c MJR023 Major Affective Disorder 7 34 0.115
211
c MJR004 Major Affective Disorder 4 29 0.115
212
PLM033 Pulmonary Embolism 60 0.115
213
P PRP019 Peripheral Nervous System Disease 64 0.115
214
P LKM062 Leukemia, Acute Lymphoblastic 68 0.115
215
c ACT075 Acute Myocardial Infarction 59 0.115
216
SFT003 Soft Tissue Sarcoma 57 0.114
217
CLF027 Cleft Palate, Isolated 67 0.113
218
PPL022 Papilloma 56 0.113
219
ADR007 Adrenoleukodystrophy 72 0.113
220
P MYC033 Myoclonus 47 0.113
221
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.113
222
P CRD119 Cardiac Arrest 71 0.113
223
HYP005 Hypokalemia 55 0.113
224
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.113
225
P LPS004 Lupus Erythematosus 62 0.112
226
STM007 Stomatitis 51 0.112
227
c SYS001 Systemic Lupus Erythematosus 88 0.112
228
RCK004 Rickets 70 0.112
229
THR024 Thrombosis 58 0.112
230
BRN004 Brain Edema 57 0.111
231
P MSC005 Muscular Dystrophy 68 0.111
232
ADR022 Adrenomyeloneuropathy 39 0.111
233
P MDL005 Medulloblastoma 78 0.111
234
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.111
235
P RTN016 Retinal Degeneration 56 0.110
236
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.110
237
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.110
238
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.110
239
SQM002 Squamous Cell Papilloma 49 0.110
240
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.109
241
P CTR002 Cataract 62 0.108
242
KRT002 Keratomalacia 47 0.107
243
AGN016 Aging 58 0.107
244
P PRP029 Porphyria 58 0.106
245
P MJR001 Major Depressive Disorder 69 0.106
246
c ACT068 Acute Cystitis 63 0.106
247
CHR073 Choreatic Disease 52 0.105
248
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.105
249
c ACT134 Acute Liver Failure 53 0.105
250
c LRG017 Large Intestine Cancer 53 0.104
251
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.104
252
OST003 Osteonecrosis 62 0.104
253
PNG002 Pain Agnosia 52 0.103
254
c PRS136 Prostate Cancer, Hereditary, 6 34 0.103
255
c PRS130 Prostate Cancer, Hereditary, 8 33 0.103
256
P PLY019 Polyneuropathy 55 0.103
257
RRS014 Rare Surgical Neurologic Disease 33 0.102
258
c THR092 Thrombophilia Due to Thrombin Defect 74 0.102
259
P HYP265 Hypotonia 43 0.102
260
TXC005 Toxic Shock Syndrome 63 0.102
261
FCL014 Focal Epilepsy 56 0.102
262
SPP010 Suppressor of Tumorigenicity 3 54 0.102
263
P CHR345 Chronic Pain 52 0.101
264
SCH012 Schizoaffective Disorder 50 0.101
265
ESP021 Esophageal Cancer 90 0.101
266
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.101
267
c DWL002 Dowling-Degos Disease 1 59 0.101
268
c HPT016 Hepatitis B 63 0.100
269
P MNN013 Meningitis 67 0.100
270
PRT036 Peritonitis 66 0.100
271
PPT001 Peptic Esophagitis 47 0.100
272
P RCT021 Rectum Cancer 54 0.100
273
P PLM037 Pulmonary Hypertension 69 0.100
274
ERL001 Early Myoclonic Encephalopathy 60 0.100
275
RYS001 Reye Syndrome 49 0.099
276
BRK010 Burkitt Lymphoma 68 0.099
277
c LKM063 Leukemia, Chronic Myeloid 74 0.099
278
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.098
279
P NSP012 Nasopharyngeal Carcinoma 67 0.098
280
EYD002 Eye Disease 59 0.098
281
c PRM038 Primary Agammaglobulinemia 45 0.098
282
PSY004 Psychotic Disorder 68 0.098
283
BLR008 Bilirubin Metabolic Disorder 58 0.097
284
ATS010 Autosomal Recessive Disease 49 0.097
285
LYM133 Lymphoma, Hodgkin, Classic 70 0.097
286
CLN015 Colon Adenocarcinoma 65 0.097
287
P ALC033 Alcohol Use Disorder 58 0.097
288
CRB037 Cerebral Palsy 69 0.097
289
CHR074 Choriocarcinoma 47 0.097
290
P THL005 Thalassemia 62 0.096
291
DBT010 Diabetic Neuropathy 56 0.096
292
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.096
293
P END044 Endometriosis 63 0.095
295
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.094
296
KPS004 Kaposi Sarcoma 75 0.094
297
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.094
298
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.094
299
P NPH012 Nephrotic Syndrome 65 0.094
300
GRD007 Grade Iii Astrocytoma 59 0.093
301
P GLY013 Glycogen Storage Disease 59 0.093
302
P RHB003 Rhabdomyosarcoma 62 0.093
303
ANN002 Anencephaly 55 0.093
304
c MLG074 Malignant Mesenchymoma 50 0.093
305
P MCR115 Microvascular Complications of Diabetes 5 67 0.093
306
P FBR017 Fibrosarcoma 57 0.093
307
P ATR011 Atrial Fibrillation 67 0.092
308
c VRL010 Viral Hepatitis 56 0.092
309
MCS002 Mucositis 56 0.092
310
P CHL002 Childhood Absence Epilepsy 60 0.092
311
CNS004 Constipation 59 0.092
312
TTN003 Tetanus 62 0.091
313
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.090
314
P SRC025 Sarcoidosis 1 72 0.090
315
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.090
316
P GRF003 Graft-Versus-Host Disease 71 0.090
317
P SCK005 Sickle Cell Disease 53 0.090
318
P RTN018 Retinal Disease 53 0.089
319
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.089
320
ERY003 Erythema Multiforme 57 0.087
321
P TCL004 T-Cell Leukemia 48 0.087
322
c LKM005 Leukemia, T-Cell, Chronic 35 0.087
323
P SPN237 Spina Bifida Aperta 21 0.087
324
TRN018 Transitional Cell Carcinoma 57 0.086
325
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.086
326
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.086
327
MLR004 Malaria 82 0.086
328
P LNG064 Lung Cancer Susceptibility 3 79 0.085
329
c FNC043 Fanconi Anemia, Complementation Group E 64 0.085
330
P KDN017 Kidney Cancer 60 0.085
331
SVR097 Severe Cutaneous Adverse Reaction 66 0.085
332
PNC001 Pancytopenia 54 0.085
333
ERY066 Erythema Multiforme Major 29 0.085
334
ENH001 Enhanced S-Cone Syndrome 56 0.085
335
P PRK057 Parkinson Disease, Late-Onset 77 0.085
336
PRP030 Purpura 56 0.085
337
MNN042 Meningioma, Radiation-Induced 64 0.084
338
ORL015 Oral Squamous Cell Carcinoma 44 0.084
339
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.084
340
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.084
341
P PLM036 Pulmonary Fibrosis 66 0.084
342
IDP011 Idiopathic Interstitial Pneumonia 65 0.084
343
NWC001 Newcastle Disease 45 0.084
344
c MNN043 Meningioma, Familial 74 0.083
345
SPN021 Spinal Meningioma 40 0.083
346
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.083
347
SCR001 Secretory Meningioma 38 0.083
348
P FNC004 Fanconi Syndrome 48 0.083
349
SPL018 Splenomegaly 48 0.083
350
P BNG032 Benign Mesothelioma 47 0.082
351
LPT014 Leptin Deficiency or Dysfunction 72 0.082
352
CHL065 Cholangiocarcinoma 68 0.082
353
THY122 Thyroid Gland Cancer 59 0.082
354
OVR094 Ovarian Epithelial Cancer 39 0.082
355
HDN002 Head Injury 47 0.081
356
SKN019 Skin Melanoma 68 0.081
357
THY030 Thyroid Gland Disease 53 0.081
358
INT079 Intrahepatic Cholangiocarcinoma 54 0.081
359
49X002 49,xxxxy Syndrome 39 0.081
360
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.080
361
P SBS003 Substance Abuse 56 0.080
362
GLS001 Gliosarcoma 56 0.080
363
P AMY004 Amyloidosis 71 0.079
364
RNL077 Renal Fibrosis 49 0.079
365
DSS009 Disseminated Intravascular Coagulation 58 0.079
366
LYM040 Lymphoblastic Lymphoma 54 0.079
367
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.078
368
EWN003 Ewing Sarcoma 69 0.078
369
WST001 West Syndrome 61 0.078
370
P PRS038 Personality Disorder 66 0.078
371
WTH001 Withdrawal Disorder 47 0.078
372
MNT001 Mantle Cell Lymphoma 69 0.077
373
END057 Endometrial Cancer 74 0.077
374
ANR040 Aneurysm 60 0.077
375
c BPL002 Bipolar I Disorder 48 0.077
376
STT004 Steatorrhea 39 0.077
377
P OLG002 Oligodendroglioma 67 0.077
378
P MVM001 Movement Disease 63 0.077
379
HYP081 Hypolipoproteinemia 51 0.076
380
HMS001 Hemosiderosis 54 0.076
381
P FBR031 Febrile Seizures 54 0.076
382
MSL001 Measles 61 0.076
383
P HYD006 Hydrocephalus 68 0.075
384
c CNG216 Congenital Hydrocephalus 55 0.075
385
NRT001 Neurotic Disorder 53 0.075
386
P CND004 Candidiasis 61 0.075
387
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.075
388
P ALP009 Alopecia Areata 61 0.075
389
SPS057 Spasticity 38 0.075
390
P SCL018 Scoliosis 61 0.075
391
TRN015 Transient Cerebral Ischemia 62 0.074
392
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.074
393
CHR178 Chromosomal Triplication 36 0.074
394
ERY051 Erythroleukemia, Familial 58 0.073
395
P MLN007 Male Infertility 57 0.073
396
HYP043 Hyperandrogenism 48 0.073
397
P BRN035 Brain Stem Glioma 51 0.073
398
ACR006 Aceruloplasminemia 74 0.073
399
HYP017 Hypophosphatemia 48 0.073
400
c HNT004 Huntington Disease-Like 2 48 0.072
401
c HNT011 Huntington Disease-Like 3 37 0.072
402
c PNS012 Paine Syndrome 61 0.072
403
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.072
404
THY111 Thyroid Carcinoma, Familial Medullary 68 0.072
405
END040 Endogenous Depression 55 0.072
406
DYS073 Dysphagia 52 0.072
407
P MTR014 Motor Neuron Disease 66 0.071
408
SPN221 Spina Bifida Occulta 36 0.071
409
TLN003 Telangiectasis 53 0.071
410
c CNT033 Central Nervous System Cancer 51 0.071
411
P SHR001 Short Bowel Syndrome 50 0.071
412
P MYC008 Myocarditis 60 0.071
413
c ADL017 Adult T-Cell Leukemia 59 0.071
414
AMN003 Amnestic Disorder 55 0.070
415
SPN041 Spinal Cord Disease 57 0.070
416
DFF005 Diffuse Large B-Cell Lymphoma 56 0.070
417
P DYS154 Dystonia 65 0.070
418
DSS008 Disease of Mental Health 66 0.070
419
VRL011 Viral Infectious Disease 62 0.070
420
PNC129 Pancreatic Adenocarcinoma 69 0.070
421
NRN004 Neuroendocrine Tumor 59 0.070
422
P VNW001 Von Willebrand's Disease 64 0.070
423
SCK003 Sickle Cell Anemia 74 0.069
424
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.069
425
P EPN002 Ependymoma 61 0.069
426
RFR010 Refractory Anemia 50 0.069
427
FCT007 Factor Vii Deficiency 65 0.069
428
P TRT010 Teratoma 52 0.069
429
HPT022 Hepatoblastoma 58 0.069
430
CMP006 Complex Partial Epilepsy 32 0.069
431
P NRV006 Nervous System Cancer 55 0.068
432
P DNG005 Dengue Virus 57 0.068
433
c BNG030 Benign Ependymoma 48 0.068
434
c OVR114 Ovarian Cancer 1 39 0.068
435
HYD002 Hydronephrosis 58 0.068
436
P HYP040 Hypospadias 54 0.068
437
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.068
438
EWN002 Ewing's Family of Tumors 48 0.068
439
P PNC025 Panic Disorder 53 0.068
440
DMY004 Demyelinating Disease 54 0.068
441
HRT011 Heart Septal Defect 52 0.068
442
MYL020 Myelomeningocele 51 0.068
443
P FLL037 Follicular Lymphoma 67 0.068
444
MSC007 Muscle Hypertrophy 65 0.067
445
IMP005 Impotence 53 0.067
446
MSC157 Muscular Dystrophy, Duchenne Type 70 0.067
447
SCR011 Scrapie 37 0.067
448
MCR017 Macrocytic Anemia 41 0.067
449
P PRV006 Pervasive Developmental Disorder 58 0.067
450
P TBR001 Tuberous Sclerosis 72 0.066
451
NRT004 Neuritis 52 0.066
452
c CHR682 Chronic Bilirubin Encephalopathy 36 0.066
453
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.066
454
BTN004 Biotin Deficiency 38 0.066
455
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.066
456
MLT157 Multiple System Atrophy 1 71 0.066
457
HMT002 Hematologic Cancer 64 0.066
458
IMM064 Immunodeficiency, Common Variable, 10 51 0.066
459
P PTT006 Pituitary Adenoma 53 0.066
460
ADG002 Audiogenic Seizures 25 0.066
461
HDG004 Hodgkin's Granuloma 27 0.065
462
HDG006 Hodgkin's Paragranuloma 23 0.065
463
GLS018 Glass Syndrome 51 0.065
464
MCR004 Macroglobulinemia 50 0.065
465
RTC005 Reticulosarcoma 48 0.065
466
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.065
467
SPR008 Supratentorial Primitive Neuroectodermal Tumor 39 0.064
468
PRP083 Porphyria, Acute Intermittent 62 0.064
469
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.064
470
BRD004 Borderline Personality Disorder 51 0.064
471
VSC002 Vascular Dementia 57 0.064
472
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.064
473
ACT084 Acute Stress Disorder 42 0.064
474
URT010 Ureteral Obstruction 46 0.063
475
AND014 Androgenic Alopecia 41 0.063
476
PST028 Post-Traumatic Stress Disorder 60 0.063
477
CLF001 Cleft Lip 53 0.063
478
INT075 Intracranial Hypertension 54 0.063
479
c ACT135 Acute Graft Versus Host Disease 52 0.063
480
P FRG001 Fragile X Syndrome 69 0.063
481
CYT008 Cytomegalovirus Infection 58 0.063
482
c LTN004 Late-Onset Retinal Degeneration 49 0.063
483
P PRN023 Prion Disease 57 0.063
484
CHC001 Chickenpox 53 0.063
485
LYM027 Lymphopenia 58 0.062
486
SCH003 Schizophreniform Disorder 49 0.062
487
c FLL041 Follicular Lymphoma 1 50 0.062
488
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.062
489
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.062
490
P ALP061 Alopecia, Androgenetic, 1 51 0.062
491
HMG005 Hemoglobinopathy 57 0.062
492
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.062
493
PPL049 Papillon-Lefevre Syndrome 63 0.061
494
P ORL007 Oral Cavity Cancer 57 0.061
495
c LBR014 Leber Congenital Amaurosis 4 55 0.061
496
P TXP001 Toxoplasmosis 61 0.061
497
TRP002 Tropical Spastic Paraparesis 49 0.061
498
KRN002 Kearns-Sayre Syndrome 64 0.061
499
CRC021 Carcinosarcoma 62 0.060
500
GLM004 Gliomatosis Cerebri 50 0.060
501
c BTT014 Beta-Thalassemia 73 0.060
502
KRT019 Keratitis, Hereditary 69 0.060
503
MCR013 Microphthalmia 62 0.060
504
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 36 0.060
505
PRP036 Peripheral T-Cell Lymphoma 53 0.060
506
GRN017 Granulocytopenia 46 0.059
507
NRM005 Neuromuscular Disease 62 0.059
508
TXC002 Toxic Encephalopathy 54 0.059
509
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.059
510
P FCL005 Focal Segmental Glomerulosclerosis 63 0.059
511
DFF037 Diffuse Intrinsic Pontine Glioma 43 0.059
512
P PRC012 Pericardial Effusion 51 0.059
513
HMP001 Hemopericardium 44 0.059
514
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.059
515
P SNS001 Sensorineural Hearing Loss 62 0.058
516
P FTL001 Fetal Alcohol Syndrome 56 0.058
517
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.058
518
PLS025 Plasmablastic Lymphoma 48 0.058
519
P CRB088 Cerebral Atrophy 43 0.058
520
P VNT002 Ventricular Septal Defect 61 0.058
521
P HYP058 Hypervitaminosis a 45 0.058
522
P ATX030 Ataxia-Telangiectasia 83 0.058
523
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.058
524
TRD006 Tardive Dyskinesia 58 0.058
525
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 55 0.058
526
INT002 Intermittent Claudication 60 0.057
527
P SLP005 Sleep Disorder 58 0.057
528
WST005 West Nile Virus 56 0.057
529
P VSC018 Visceral Steatosis 34 0.057
530
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 55 0.057
531
P LYM033 Lymphoproliferative Syndrome 62 0.057
532
GST020 Gastric Antral Vascular Ectasia 42 0.057
533
CYT018 Cytochrome P450 2d6 Variant 28 0.057
534
FBR047 Fibromyalgia 60 0.056
535
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.056
536
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.056
537
c INF023 Inflammatory Breast Carcinoma 52 0.056
538
P HMN032 Human Herpesvirus 8 49 0.056
539
OBS002 Obsessive-Compulsive Disorder 69 0.056
540
LRN003 Learning Disability 51 0.056
541
P CRN037 Craniosynostosis 69 0.056
542
P JVN007 Juvenile Absence Epilepsy 47 0.056
543
GRM010 Germ Cells Tumors 35 0.056
544
P NRC002 Narcolepsy 56 0.056
545
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.055
546
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 60 0.055
547
PLC005 Placental Insufficiency 55 0.055
548
HRP004 Herpes Zoster 58 0.055
549
LYM012 Lymphoplasmacytic Lymphoma 62 0.055
550
THR012 Thoracic Cancer 51 0.055
551
c HMC039 Hemochromatosis, Type 1 73 0.055
552
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.055
553
GST019 Gastrointestinal Stromal Tumor 76 0.054
554
NRF007 Neurofibroma 63 0.054
555
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.054
556
P ANG015 Angioedema 54 0.054
557
RTN003 Retinal Ischemia 52 0.054
558
ACT003 Acute Kidney Tubular Necrosis 42 0.054
559
PHT008 Photosensitive Epilepsy 34 0.054
560
BRN049 Brain Tumor, Childhood 30 0.054
561
c MST023 Mesothelioma, Malignant 59 0.054
562
PTH003 Pathologic Nystagmus 53 0.054
563
EXC002 Exocrine Pancreatic Insufficiency 41 0.054
564
P RTT002 Rett Syndrome 81 0.054
565
HMR039 Hemorrhage, Intracerebral 59 0.054
566
LYM009 Lymphocytic Choriomeningitis 45 0.054
567
P ASP006 Aspergillosis 67 0.053
568
CRN036 Craniopharyngioma 65 0.053
569
P ATR010 Atrial Heart Septal Defect 61 0.053
570
MRG003 Marginal Zone B-Cell Lymphoma 55 0.053
571
LPD004 Lipoid Nephrosis 48 0.053
572
PSD088 Pseudobulbar Affect 37 0.053
573
OST011 Osteomalacia 51 0.053
574
c SPN393 Spinal Muscular Atrophy, Type I 53 0.053
575
c SPN394 Spinal Muscular Atrophy, Type Iii 49 0.053
576
INT067 Interstitial Nephritis 46 0.053
577
PYR016 Pyridoxine Deficiency 31 0.053
578
P PLY006 Polydactyly 58 0.053
579
P MGR001 Migraine Without Aura 47 0.053
580
CRB086 Cerebral Aneurysms 41 0.053
581
c TBR025 Tuberous Sclerosis 1 74 0.053
582
P EPL140 Epilepsy, Idiopathic Generalized 62 0.052
583
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.052
584
ORG002 Organic Acidemia 43 0.052
585
RDN001 Reading Disorder 42 0.052
586
CLR030 Clear Cell Renal Cell Carcinoma 54 0.052
587
c NRF024 Neurofibromatosis, Type I 72 0.051
588
P MLN069 Melanoma, Uveal 59 0.051
589
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 48 0.051
590
P BLR006 Biliary Tract Disease 49 0.051
591
WLL004 Wallerian Degeneration 40 0.051
592
PLY100 Polyploidy 41 0.051
593
c EPL133 Epilepsy, Juvenile Absence 1 40 0.051
594
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.051
595
MYL057 Myelopathy, Htlv-1-Associated 40 0.051
596
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 36 0.051
597
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.051
598
PRM042 Primary Effusion Lymphoma 55 0.051
599
CLS047 Classic Progressive Supranuclear Palsy Syndrome 30 0.051
600
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.051
601
MYL031 Myeloproliferative Neoplasm 66 0.050
602
P HMN010 Hemangioma 62 0.050
603
ARG002 Argininosuccinic Aciduria 59 0.050
604
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.050
605
PNM008 Pneumothorax 56 0.050
606
P OPT009 Optic Neuritis 55 0.050
607
P MCR010 Microcephaly 56 0.050
608
P MCH002 Machado-Joseph Disease 61 0.050
609
HYP063 Hypersplenism 51 0.050
610
c SPL067 Split-Hand/foot Malformation 1 49 0.050
611
ISL121 Isolated Split Hand-Split Foot Malformation 46 0.050
612
LPG001 Lipogranulomatosis 29 0.050
613
MYL005 Myelofibrosis 69 0.050
614
KHL003 Kohlschutter-Tonz Syndrome 63 0.050
615
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.050
616
P CHR285 Chronic Myelomonocytic Leukemia 60 0.050
617
CLL003 Cellulitis 56 0.050
618
INT030 Intracranial Aneurysm 57 0.049
619
P MYG005 Myoglobinuria 43 0.049
620
FLL027 Fallopian Tube Carcinoma 64 0.049
621
BTN003 Biotinidase Deficiency 56 0.049
622
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 56 0.049
623
P SBR004 Seborrheic Dermatitis 41 0.049
624
RTN020 Retinal Vascular Disease 49 0.049
625
ADN027 Adenomyosis 55 0.049
626
CLL014 Cll/sll 44 0.049
627
IDP091 Idiopathic Nephrotic Syndrome 43 0.049
628
CVT001 Cavitary Optic Disc Anomalies 39 0.049
629
P RST001 Restless Legs Syndrome 54 0.048
630
P ANL018 Analbuminemia 51 0.048
631
P CHR071 Charcot-Marie-Tooth Disease 65 0.048
632
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 62 0.048
633
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.048
634
TTH006 Tooth Disease 47 0.048
635
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.048
636
BLD131 Bladder Urothelial Carcinoma 62 0.048
637
THY125 Thyroid Gland Medullary Carcinoma 52 0.048
638
PLC006 Placental Choriocarcinoma 33 0.048
639
ANS011 Anus Cancer 49 0.048
640
HYL004 Hyaline Fibromatosis Syndrome 49 0.048
641
CYS009 Cystadenoma 43 0.048
642
CRB026 Cerebellar Astrocytoma 31 0.048
643
SPC030 Specific Language Disorder 27 0.048
644
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.048
645
BLD053 Blood Platelet Disease 51 0.048
646
END041 Endometrial Adenocarcinoma 64 0.047
647
CMR002 Coumarin Resistance 56 0.047
648
c MLG079 Malignant Pleural Mesothelioma 43 0.047
649
c ACT020 Acute T Cell Leukemia 54 0.047
650
DRG024 Drug Allergy 43 0.047
651
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.047
652
ORP003 Oropharynx Cancer 55 0.047
653
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.047
654
c DYS119 Dystonia 9 45 0.047
655
BNS007 Bone Sarcoma 44 0.047
656
P PHT010 Photoparoxysmal Response 1 39 0.047
657
CHL057 Childhood Brain Stem Glioma 19 0.047
658
CHL009 Childhood Cerebral Astrocytoma 15 0.047
659
CRT072 Creutzfeldt-Jakob Disease 67 0.047
660
INT066 Interstitial Lung Disease 61 0.047
661
INT303 Intracranial Hypertension, Idiopathic 52 0.047
662
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.047
663
MNG007 Manganese Poisoning 28 0.047
664
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.046
665
NRL018 Neural Tube Defects, Folate-Sensitive 50 0.046
666
OCL022 Ocular Melanoma 54 0.046
667
VGN017 Vaginal Cancer 51 0.046
668
CHL018 Childhood Medulloblastoma 46 0.046
669
END035 Endocrine Gland Cancer 46 0.046
670
SPN040 Spinal Cancer 44 0.046
671
PDT014 Pediatric Ependymoma 33 0.046
672
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.046
673
GNT002 Giant Cell Glioblastoma 52 0.046
674
GNG012 Gingival Overgrowth 52 0.046
675
BHR001 Behr Syndrome 47 0.046
676
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.045
677
P DBT005 Diabetes Insipidus 54 0.045
678
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.045
680
HMT008 Hematuria, Benign Familial 53 0.045
681
NCT003 N-Acetylglutamate Synthase Deficiency 42 0.045
682
HRT012 Heart Valve Disease 56 0.045
683
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.045
684
P ENC008 Encephalocele 47 0.045
685
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.045
686
DFF036 Differentiated Thyroid Carcinoma 53 0.044
687
CRV040 Cervix Carcinoma 52 0.044
688
P RNV001 Renovascular Hypertension 49 0.044
689
TST014 Testicular Cancer 49 0.044
690
INT052 Intestinal Volvulus 44 0.044
691
ERD001 Erdheim-Chester Disease 51 0.044
692
c SPN395 Spinal Muscular Atrophy, Type Ii 47 0.044
693
c NPH049 Nephrotic Syndrome, Type 2 45 0.044
694
c NLD016 Nail Disorder, Nonsyndromic Congenital, 10 42 0.044
695
ANS025 Anus Benign Neoplasm 34 0.044
696
RFL002 Reflex Epilepsy 33 0.044
697
PDT015 Pediatric Supratentorial Ependymoma 31 0.044
698
PDT016 Pediatric Infratentorial Ependymoma 29 0.044
699
CHL003 Childhood Spinal Cord Tumor 14 0.044
700
CHK001 Chikungunya 55 0.044
701
SPS019 Spastic Paraparesis 40 0.044
702
SMT001 Somatization Disorder 45 0.044
703
GLL008 Gilles De La Tourette Syndrome 66 0.043
704
P TCD001 Tic Disorder 55 0.043
705
P MTC133 Mitochondrial Myopathy 53 0.043
706
ACR041 Acromelic Frontonasal Dysostosis 50 0.043
707
P PLR004 Pleuropulmonary Blastoma 68 0.043
708
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 68 0.043
709
CST005 Castleman Disease 54 0.043
710
P LPC002 Lip Cancer 47 0.043
711
P CNT036 Central Nervous System Germ Cell Tumor 28 0.043
712
P DMN001 Diamond-Blackfan Anemia 69 0.043
713
NRL005 Neurilemmoma 62 0.043
714
c INV001 Invasive Aspergillosis 48 0.043
715
ASP003 Aseptic Meningitis 51 0.042
716
CCN002 Cocaine Abuse 48 0.042
717
SPR126 Superior Semicircular Canal Dehiscence 39 0.042
718
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.042
719
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.042
720
LYM007 Lymphangioleiomyomatosis 67 0.042
721
CNN010 Connective Tissue Benign Neoplasm 44 0.042
722
SRV001 Survival Motor Neuron Spinal Muscular Atrophy 25 0.042
723
ADN011 Adenoid Cystic Carcinoma 71 0.042
724
P LMY004 Leiomyosarcoma 63 0.042
725
c LCL006 Localized Scleroderma 61 0.042
726
ALV005 Alveolar Soft Part Sarcoma 56 0.042
727
P THR015 Thrombophilia 51 0.042
728
VLV011 Vulvovaginal Candidiasis 50 0.042
729
SXL003 Sexual Disorder 49 0.042
730
EPL131 Epilepsy, Pyridoxine-Dependent 47 0.042
731
LNN001 Lennox-Gastaut Syndrome 56 0.041
732
FCL012 Facial Paralysis 53 0.041
733
PNC119 Pancreatic Neuroendocrine Tumor 48 0.041
734
P CLS010 Cluster Headache 44 0.041
735
CRC014 Carcinoid Tumors, Intestinal 49 0.041
736
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
737
P SDR003 Sideroblastic Anemia 47 0.041
738
MTB016 Metabolic Myopathy 34 0.041
739
c WLF013 Wolfram Syndrome 1 56 0.041
740
P PHR004 Pharynx Cancer 51 0.041
741
MLR006 Male Reproductive Organ Cancer 43 0.041
742
c PST022 Posterior Uveal Melanoma 39 0.041
743
PHB003 Phobia, Specific 39 0.041
744
HYP748 Hypertelorism 50 0.041
745
EMB015 Embryonal Tumor with Multilayered Rosettes 29 0.041
746
c PRT132 Protoporphyria, Erythropoietic, 1 59 0.040
747
GNR004 Generalized Anxiety Disorder 55 0.040
748
OPT003 Opiate Dependence 50 0.040
749
GLC008 Glucose Metabolism Disease 47 0.040
750
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.040
751
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.040
752
CND002 Conduct Disorder 52 0.040
753
VSL006 Visual Pathway and Hypothalamic Glioma, Childhood 7 0.039
754
CRN239 Carnitine Deficiency, Systemic Primary 56 0.039
755
AVD001 Avoidant Personality Disorder 45 0.039
756
ANG049 Angioedema Induced by Ace Inhibitors 41 0.039
757
P PHC014 Phocomelia 25 0.039
758
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.039
759
NRN001 Neuroendocrine Carcinoma 48 0.039
760
CLB002 Clubfoot 44 0.039
761
P HYP263 Hypersomnia 42 0.039
763
CCN001 Cocaine Dependence 48 0.038
764
ANP009 Anaplastic Oligodendroglioma 44 0.038
765
OLG022 Oligoasthenoteratozoospermia 34 0.038
766
NRM022 Neurometabolic Disease 26 0.038
767
FCT005 Factor Xiii Deficiency 50 0.038
768
c CNG389 Congenital Disorder of Glycosylation, Type Iim 48 0.038
769
c ACQ017 Acquired Von Willebrand Syndrome 42 0.038
770
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.037
771
FND002 Fundus Dystrophy 52 0.037
772
SBS004 Substance Dependence 48 0.037
773
SYD002 Sydenham Chorea 44 0.036
774
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.036
775
c INH030 Inherited Retinal Disorder 48 0.036
776
FBR019 Fibromatosis 47 0.036
777
P PRT026 Parotitis 43 0.036
778
LKS001 Leukostasis 43 0.036
779
SPC010 Speech and Communication Disorders 46 0.036
780
CNN001 Cannabis Dependence 41 0.036
781
CNN002 Cannabis Abuse 40 0.036
782
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.036
783
SMT006 Somatoform Disorder 51 0.035
784
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.035
785
HYD061 Hydrocephalus, Normal-Pressure 49 0.034
786
OPD006 Opioid Addiction 49 0.034
787
HYP348 Hyperglycinuria 42 0.034
788
THR123 Thrombotic Microangiopathy 41 0.034
789
c ADL008 Adult Oligodendroglioma 40 0.034
790
P STR001 Striatonigral Degeneration 38 0.034
791
c RST012 Restless Legs Syndrome 1 34 0.034
792
BNG009 Benign Epilepsy with Centrotemporal Spikes 52 0.034
793
c THR048 Thrombocytopenia 4 31 0.034
794
CHR158 Charles Bonnet Syndrome 23 0.034
795
P RNL100 Renal Hypodysplasia/aplasia 1 61 0.033
796
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 59 0.033
797
P SLV026 Salivary Gland Carcinoma 58 0.033
798
OPD001 Opioid Abuse 42 0.033
799
DFF031 Diffuse Alveolar Hemorrhage 28 0.033
800
FTL073 Fetal Anticonvulsant Syndrome 26 0.033
801
DMN031 Dementia, Lewy Body 66 0.032
802
ONC002 Onchocerciasis 50 0.032
803
BRX001 Bruxism 49 0.032
804
PLM035 Pulmonary Eosinophilia 47 0.032
805
PHY002 Physical Disorder 42 0.032
806
TRC097 Tracheomalacia 38 0.032
807
EXF003 Exfoliative Dermatitis 28 0.032
808
P PLG001 Pelger-Huet Anomaly 49 0.032
809
CNT106 Centralopathic Epilepsy 36 0.032
810
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 36 0.032
811
FMR017 Femur, Unilateral Bifid, with Monodactylous Ectrodactyly 23 0.032
812
FMR007 Femur Bifid with Monodactylous Ectrodactyly 14 0.032
813
CRN080 Craniofacial and Skeletal Defects 4 0.032
814
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.031
815
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 36 0.031
816
RFR009 Refractory Cytopenia with Multilineage Dysplasia 32 0.031
817
SDD004 Sudden Arrhythmia Death Syndrome 23 0.031
818
PRT010 Parathyroid Carcinoma 67 0.030
819
NVS017 Nevus, Epidermal 66 0.030
820
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 51 0.030
821
SPC005 Speech Disorder 44 0.030
822
HSD004 Hsd10 Mitochondrial Disease 42 0.030
823
UTR043 Uterine Sarcoma 40 0.030
824
MNN017 Mononeuropathy 38 0.030
825
IMM162 Immunoglobulin E Concentration, Serum 29 0.030
826
TBL029 Tubulin, Beta 29 0.030
827
DDN011 Duodenal Atresia 49 0.030
828
P LFR001 Li-Fraumeni Syndrome 71 0.029
829
c GLY004 Glycogen Storage Disease V 60 0.029
830
P PLY147 Polydactyly, Postaxial, Type A1 57 0.029
831
c THR071 Thrombocytopenia 1 50 0.029
832
c RCR022 Recurrent Acute Pancreatitis 46 0.029
833
PRT011 Protein C Deficiency 45 0.029
834
TRC010 Trichotillomania 45 0.029
835
c SCH079 Schizophrenia 1 44 0.029
836
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 41 0.029
837
c LFR007 Li-Fraumeni Syndrome 2 41 0.029
838
CDQ001 Cauda Equina Syndrome 39 0.029
839
P MNN007 Meningocele 37 0.029
840
PCD001 Pica Disease 33 0.029
841
CD4008 Cd4/cd8 T-Cell Ratio 21 0.029
842
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.028
843
P CRB045 Cerebellar Hypoplasia 53 0.028
844
P HYP077 Hypertrichosis 51 0.028
845
PHL006 Phelan-Mcdermid Syndrome 51 0.028
846
c OPT053 Optic Atrophy 1 51 0.028
847
P EPT012 Epithelioid Sarcoma 49 0.028
848
TLP001 Talipes Equinovarus 45 0.028
849
P PRX014 Proximal Spinal Muscular Atrophy 44 0.028
851
CYC005 Cyclothymic Disorder 34 0.028
852
NRL008 Neural Crest Tumor 26 0.028
853
INT358 Intestinal Polyposis Syndrome 26 0.028
854
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.027
855
P EPS003 Episodic Ataxia 60 0.027
856
P DYS193 Dystonia 11, Myoclonic 55 0.027
857
OCL008 Oculopharyngeal Muscular Dystrophy 50 0.027
858
OPP004 Oppositional Defiant Disorder 50 0.027
859
P OPT070 Optic Nerve Hypoplasia, Bilateral 47 0.027
860
CYC008 Cyclic Vomiting Syndrome 46 0.027
861
CRV043 Cervical Dystonia 45 0.027
862
VCT001 Vacterl Association 43 0.027
863
P CHR342 Chiari Malformation 42 0.027
864
SKL017 Skeletal Dysplasias 41 0.027
865
AMP007 Amphetamine Abuse 39 0.027
866
DGT005 Digital Arthropathy-Brachydactyly, Familial 36 0.027
867
SPS016 Spasmodic Dysphonia 32 0.027
868
DRG016 Drug Induced Dyskinesia 24 0.027
870
OBS635 Obsolete: Laryngeal Dyskinesia 24 0.027
871
LPM007 Lipomyelomeningocele 23 0.027
872
c EPS035 Episodic Ataxia, Type 2 58 0.025
873
P WLF004 Wolfram Syndrome 58 0.025
874
KLN009 Kleine-Levin Hibernation Syndrome 46 0.025
875
c HLP023 Holoprosencephaly 1 44 0.025
876
TCL003 T Cell Deficiency 44 0.025
877
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 44 0.025
878
P DCR003 Dacryoadenitis 42 0.025
879
INT025 Intermittent Explosive Disorder 40 0.025
880
PHN011 Phenytoin Toxicity 34 0.025
881
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.025
882
c PST106 Post-Cardiac Arrest Syndrome 31 0.025
883
FTL007 Fetal Hydantoin Syndrome 28 0.025
884
P SPN042 Spinal Cord Ependymoma 27 0.025
885
EPL230 Epilepsy with Myoclonic-Atonic Seizures 27 0.025
886
2MT001 2-Methyl-3-Hydroxybutyric Aciduria 26 0.025
887
DMN012 Dementia - Subcortical 22 0.025
888
NDD001 Nodding Syndrome 21 0.025
889
c RFR015 Refractory Anemia with Excess Blasts Type 1 16 0.025
890
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 62 0.023
891
SPT006 Septooptic Dysplasia 60 0.023
892
P MLT007 Multiple Epiphyseal Dysplasia 56 0.023
893
c RBN021 Rubinstein-Taybi Syndrome 1 55 0.023
894
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 0.023
895
P RNL028 Renal Tubular Dysgenesis 51 0.023
896
P APL006 Aplasia Cutis Congenita 49 0.023
897
c OTP007 Otopalatodigital Syndrome, Type Ii 46 0.023
898
ACH001 Acheiropody 45 0.023
899
NLS001 Nelson Syndrome 44 0.023
900
c OTP006 Otopalatodigital Syndrome, Type I 42 0.023
901
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 41 0.023
902
c SPN398 Spinal Muscular Atrophy, Type Iv 40 0.023
903
SLV003 Salivary Gland Disease 40 0.023
904
c ATR031 Atrial Septal Defect 4 40 0.023
905
ALG027 Al-Gazali-Bakalinova Syndrome 37 0.023
906
ASK001 Askin's Tumor 35 0.023
907
MCL057 Macular Dystrophy with Central Cone Involvement 32 0.023
908
HMC012 Hemicrania Continua 29 0.023
909
BRS061 Breast Sarcoma 28 0.023
910
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 27 0.023
911
c TRS012 Trisomy 22 26 0.023
912
c ERL003 Early Onset Absence Epilepsy 24 0.023
913
PRX022 Paroxysmal Choreoathetosis 23 0.023
914
MYC001 Myoclonic Cerebellar Dyssynergia 23 0.023
915
c EPL201 Epilepsy, Familial Adult Myoclonic, 1 23 0.023
916
P SCN067 Scn1a Seizure Disorders 21 0.023
917
PST047 Post-Traumatic Epilepsy 20 0.023
918
MSC017 Mosaic Trisomy 22 20 0.023
919
c EPL053 Epilepsy, Familial Adult Myoclonic, 3 19 0.023
920
CTN020 Cutaneous Sclerosis 18 0.023
921
CRB080 Cor Biloculare 11 0.023
Content
Loading form....