Search results for Phenytoin

844 hits were found for Phenytoin

# Family MCID Name MIFTS Score
1
PHN011 Phenytoin Toxicity 33 3.891
2
FTL007 Fetal Hydantoin Syndrome 29 3.516
3
PHN016 Phenytoin Allergy 14 3.373
4
PHN012 Phenytoin or Carbamazepine Toxicity 18 2.379
5
c OBS333 Obsolete: Susceptibility to Toxic Epidermal Necrolysis Due to Phenytoin Treatment 3 2.379
6
OBS296 Obsolete: Phenytoin Toxicity 1 2.379
7
P SZR006 Seizure Disorder 58 0.402
8
VSL002 Visual Epilepsy 58 0.360
9
STT001 Status Epilepticus 59 0.294
10
GNG012 Gingival Overgrowth 51 0.286
11
P OVR082 Overgrowth Syndrome 50 0.273
12
ALL026 Allergic Hypersensitivity Disease 64 0.260
13
P EPL164 Epilepsy 71 0.252
14
P EXN002 Exanthem 57 0.220
15
ERY003 Erythema Multiforme 57 0.182
16
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.180
17
SVR097 Severe Cutaneous Adverse Reaction 67 0.175
18
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.173
19
PTH003 Pathologic Nystagmus 51 0.171
20
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.169
21
ERY066 Erythema Multiforme Major 28 0.167
22
P HYP098 Hypereosinophilic Syndrome 66 0.160
23
TRM010 Traumatic Brain Injury 53 0.141
24
P ECL001 Eclampsia 51 0.141
25
P ENC018 Encephalopathy 61 0.138
26
BRN071 Brain Injury 49 0.136
27
HDN002 Head Injury 45 0.136
28
FCL014 Focal Epilepsy 54 0.131
29
P EPD016 Epidermolysis Bullosa 53 0.131
30
CLF027 Cleft Palate, Isolated 64 0.124
31
P TMP001 Temporal Lobe Epilepsy 50 0.121
32
URM002 Uremia 49 0.116
33
OCL069 Ocular Motor Apraxia 51 0.113
34
c PRC016 Pre-Eclampsia 63 0.107
35
OST011 Osteomalacia 52 0.107
36
P THR014 Thrombocytopenia 68 0.104
37
CLF001 Cleft Lip 53 0.104
38
RRS014 Rare Surgical Neurologic Disease 32 0.104
39
GRN017 Granulocytopenia 44 0.101
40
P NRB001 Neuroblastoma 71 0.098
41
TRG002 Trigeminal Neuralgia 60 0.098
42
P MYC033 Myoclonus 46 0.098
43
P CRB059 Cerebellar Degeneration 37 0.098
44
P NRP001 Neuropathy 56 0.094
45
P TRM003 Tremor 53 0.094
46
P CRD119 Cardiac Arrest 67 0.091
47
IMM003 Immunoglobulin Alpha Deficiency 45 0.091
48
48X005 48,xyyy 39 0.091
49
P HPT021 Hepatitis 67 0.087
50
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.087
51
DPR016 Depression 63 0.087
52
EXF003 Exfoliative Dermatitis 27 0.087
53
GLB015 Glioblastoma Multiforme 75 0.084
54
P KDN018 Kidney Disease 70 0.084
55
P HYP086 Hypothyroidism 68 0.084
56
P PRP019 Peripheral Nervous System Disease 57 0.084
57
P BPL003 Bipolar Disorder 56 0.084
58
HYP266 Hypoxia 56 0.084
59
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.084
60
P FBR031 Febrile Seizures 51 0.084
61
BNR002 Bone Resorption Disease 48 0.084
62
c MJR024 Major Affective Disorder 9 41 0.084
63
c MJR022 Major Affective Disorder 8 38 0.084
64
P NTR004 Neutropenia 63 0.080
65
P OPT009 Optic Neuritis 56 0.080
66
NRT004 Neuritis 53 0.080
67
CHR073 Choreatic Disease 52 0.080
68
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.080
69
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.080
70
IMM167 Immune Deficiency Disease 78 0.076
71
ACR006 Aceruloplasminemia 73 0.076
72
RCK004 Rickets 69 0.076
73
P LYM118 Lymphoma 68 0.076
74
P LPR021 Leprosy 3 67 0.076
75
PSY004 Psychotic Disorder 67 0.076
76
KRN002 Kearns-Sayre Syndrome 63 0.076
77
P VSC011 Vasculitis 62 0.076
78
c ACT071 Acute Kidney Failure 59 0.076
79
c SVR005 Severe Pre-Eclampsia 49 0.076
80
GLL048 Glial Tumor 45 0.076
81
ANX004 Anoxia 42 0.076
82
HNS001 Hansen's Disease 34 0.076
83
P RSP003 Respiratory Failure 74 0.071
84
ADL002 Adult Syndrome 69 0.071
85
HYP056 Hypoglycemia 66 0.071
86
TTN003 Tetanus 64 0.071
87
P GLM045 Glioma 63 0.071
88
P LPS004 Lupus Erythematosus 61 0.071
89
P PLY019 Polyneuropathy 56 0.071
90
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.071
91
PST047 Post-Traumatic Epilepsy 22 0.071
92
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.067
93
P MNN013 Meningitis 65 0.067
94
DCB001 Decubitus Ulcer 60 0.067
95
GNG013 Gingivitis 59 0.067
96
PRP030 Purpura 55 0.067
97
CLF004 Cleft Lip/palate 54 0.067
98
INT067 Interstitial Nephritis 46 0.067
99
P PRD021 Periodic Paralysis 46 0.067
100
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.067
101
SPS057 Spasticity 41 0.067
102
ALL014 Allergic Encephalomyelitis 39 0.067
103
HRW001 Hair Whorl 36 0.067
104
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.067
105
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.062
106
c MNN043 Meningioma, Familial 74 0.062
107
SVR004 Severe Combined Immunodeficiency 73 0.062
108
P GRF003 Graft-Versus-Host Disease 71 0.062
109
c MGR028 Migraine with or Without Aura 1 69 0.062
110
ALC007 Alcohol Dependence 66 0.062
111
MYC006 Mycosis Fungoides 66 0.062
112
P PRD008 Periodontitis 62 0.062
113
MNN042 Meningioma, Radiation-Induced 62 0.062
114
P MVM001 Movement Disease 61 0.062
115
HYP066 Hyperglycemia 61 0.062
116
CHL068 Cholestasis 60 0.062
117
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.062
118
P ALC033 Alcohol Use Disorder 58 0.062
119
MCS002 Mucositis 55 0.062
120
ATR057 Atrioventricular Block 55 0.062
121
MTN003 Motion Sickness 52 0.062
122
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.062
123
SPN021 Spinal Meningioma 47 0.062
124
SBC016 Subacute Delirium 44 0.062
125
RDC006 Red Cell Aplasia 42 0.062
126
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.062
127
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 39 0.062
128
SCR001 Secretory Meningioma 37 0.062
129
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.062
130
c SYS001 Systemic Lupus Erythematosus 86 0.056
131
MYL069 Myeloma, Multiple 85 0.056
132
P RHM011 Rheumatoid Arthritis 80 0.056
133
DFC004 Deficiency Anemia 75 0.056
134
P ART022 Arthritis 70 0.056
135
P MJR001 Major Depressive Disorder 68 0.056
136
P LKM002 Leukemia 66 0.056
137
P DYS154 Dystonia 65 0.056
138
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.056
139
P NPH012 Nephrotic Syndrome 63 0.056
140
P HYP069 Hyperparathyroidism 62 0.056
141
DRM006 Dermatitis 61 0.056
142
ISC004 Ischemia 60 0.056
143
CRD223 Cardiac Arrhythmia 60 0.056
144
P MYC008 Myocarditis 59 0.056
145
P BND020 Bone Disease 59 0.056
146
END030 End Stage Renal Failure 58 0.056
147
P OPT006 Optic Nerve Disease 57 0.056
148
MNT002 Mental Depression 57 0.056
149
c BCT007 Bacterial Meningitis 55 0.056
150
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.056
151
c ACT134 Acute Liver Failure 51 0.056
152
c SCN007 Secondary Hyperparathyroidism 50 0.056
153
P AST007 Astrocytoma 50 0.056
154
DYS073 Dysphagia 50 0.056
155
47X002 47,xyy 49 0.056
156
IGG001 Iga Glomerulonephritis 48 0.056
157
ATH004 Athetosis 28 0.056
158
NRL016 Neural Tube Defects 82 0.050
159
P GLM040 Glioma Susceptibility 1 81 0.050
160
AST005 Asthma 77 0.050
161
c THR092 Thrombophilia Due to Thrombin Defect 73 0.050
162
ANX010 Anxiety 72 0.050
163
P MYC007 Myocardial Infarction 70 0.050
164
P LKM062 Leukemia, Acute Lymphoblastic 68 0.050
165
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.050
166
P HYD006 Hydrocephalus 65 0.050
167
P MYP004 Myopathy 64 0.050
168
GT001 Gout 63 0.050
169
SKN016 Skin Disease 63 0.050
170
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.050
171
P PSR002 Psoriasis 62 0.050
172
MDD011 Mood Disorder 62 0.050
173
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.050
174
LNG099 Lung Disease 61 0.050
175
P CTR002 Cataract 60 0.050
176
SPN186 Spinal Cord Injury 60 0.050
177
ACQ007 Acquired Immunodeficiency Syndrome 60 0.050
178
HYP052 Hyperkalemic Periodic Paralysis 59 0.050
179
ADN018 Adenoma 58 0.050
180
PST028 Post-Traumatic Stress Disorder 58 0.050
181
P MCR010 Microcephaly 58 0.050
182
DSS008 Disease of Mental Health 57 0.050
183
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.050
184
P DRR001 Diarrhea 57 0.050
185
P ALP008 Alopecia 56 0.050
186
BRN004 Brain Edema 55 0.050
187
P MGL001 Megaloblastic Anemia 55 0.050
188
P LYM031 Lymphocytic Leukemia 55 0.050
189
END040 Endogenous Depression 54 0.050
190
P JNC001 Junctional Epidermolysis Bullosa 54 0.050
191
P ANG015 Angioedema 54 0.050
192
ANL018 Analbuminemia 54 0.050
193
c PRD040 Periodontitis, Chronic 54 0.050
194
CYS005 Cysticercosis 54 0.050
195
CHR100 Chronic Ulcer of Skin 53 0.050
196
PST011 Pustulosis of Palm and Sole 52 0.050
197
P GNG025 Gingival Fibromatosis 51 0.050
198
SCH012 Schizoaffective Disorder 50 0.050
199
P CHR345 Chronic Pain 50 0.050
200
CCN001 Cocaine Dependence 48 0.050
201
CCN002 Cocaine Abuse 48 0.050
202
ACT084 Acute Stress Disorder 48 0.050
203
ANL022 Anal Fistula 47 0.050
204
FBR019 Fibromatosis 44 0.050
205
PNM013 Pneumococcal Meningitis 43 0.050
206
c PRM038 Primary Agammaglobulinemia 43 0.050
207
CLF056 Cleft Lip with or Without Cleft Palate 41 0.050
208
c MLG074 Malignant Mesenchymoma 39 0.050
209
MYT011 Myotonia 35 0.050
210
GNG006 Gingival Hypertrophy 34 0.050
211
CYT018 Cytochrome P450 2d6 Variant 27 0.050
212
P ATX030 Ataxia-Telangiectasia 83 0.044
213
PFF001 Pfeiffer Syndrome 79 0.044
214
P NRF023 Neurofibromatosis, Type Ii 76 0.044
215
P MLT020 Multiple Sclerosis 72 0.044
216
c HYP836 Hypercholesterolemia, Familial, 1 72 0.044
217
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.044
218
HMN044 Human Immunodeficiency Virus Type 1 71 0.044
219
c HPT073 Hepatitis C Virus 70 0.044
220
LYM133 Lymphoma, Hodgkin, Classic 69 0.044
221
CRB039 Cerebrovascular Disease 69 0.044
222
P LVR013 Liver Disease 68 0.044
223
EWN003 Ewing Sarcoma 68 0.044
224
P INF038 Influenza 68 0.044
225
CRB037 Cerebral Palsy 68 0.044
226
P PNM007 Pneumonia 68 0.044
227
c CHR684 Chronic Kidney Disease 66 0.044
228
FCT007 Factor Vii Deficiency 66 0.044
229
P MSC005 Muscular Dystrophy 66 0.044
230
ATH013 Atherosclerosis Susceptibility 66 0.044
231
SRC014 Sarcoma 65 0.044
232
P ATS364 Autism 65 0.044
233
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.044
234
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.044
235
c HPT001 Hepatitis C 63 0.044
236
c ACT068 Acute Cystitis 63 0.044
237
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.044
238
MSS001 Masa Syndrome 62 0.044
239
OST003 Osteonecrosis 61 0.044
240
P MYL006 Myeloid Leukemia 60 0.044
241
P VNT002 Ventricular Septal Defect 60 0.044
242
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.044
243
P BCL017 B-Cell Lymphoma 58 0.044
244
EXT034 Extrinsic Allergic Alveolitis 58 0.044
245
BLR008 Bilirubin Metabolic Disorder 57 0.044
246
P HDC001 Headache 57 0.044
247
THR024 Thrombosis 56 0.044
248
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.044
249
PLS011 Plasmacytoma 56 0.044
250
SFT003 Soft Tissue Sarcoma 56 0.044
251
CMR002 Coumarin Resistance 56 0.044
252
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.044
253
TRD006 Tardive Dyskinesia 55 0.044
254
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.044
255
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.044
256
LYM040 Lymphoblastic Lymphoma 54 0.044
257
THR013 Thoracic Outlet Syndrome 53 0.044
258
c ACT135 Acute Graft Versus Host Disease 51 0.044
259
ILS001 Ileus 51 0.044
260
SPN035 Spindle Cell Sarcoma 51 0.044
261
c HNT004 Huntington Disease-Like 2 49 0.044
262
VTM033 Vitamin K Deficiency Bleeding 48 0.044
263
WTH001 Withdrawal Disorder 48 0.044
264
TBR011 Tuberculous Meningitis 48 0.044
265
SPL018 Splenomegaly 48 0.044
266
PRP007 Priapism 48 0.044
267
PTT037 Pituitary Tumors 44 0.044
268
CYT002 Cytokine Deficiency 44 0.044
269
CRB090 Cerebral Hypoxia 43 0.044
270
P MJR007 Major Affective Disorder 1 43 0.044
271
DRG024 Drug Allergy 43 0.044
272
ORL015 Oral Squamous Cell Carcinoma 43 0.044
273
PRS063 Paresthesia 43 0.044
274
OST115 Osteonecrosis of the Jaw 39 0.044
275
c SYS043 Systemic Lupus Erythematosus 1 38 0.044
276
P MYC026 Myoclonus Epilepsy 35 0.044
277
c MJR008 Major Affective Disorder 2 34 0.044
278
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.044
279
c MJR003 Major Affective Disorder 6 33 0.044
280
c MJR006 Major Affective Disorder 5 33 0.044
281
c MJR023 Major Affective Disorder 7 33 0.044
282
ISL119 Isolated Optic Neuritis 30 0.044
283
c MJR004 Major Affective Disorder 4 28 0.044
284
CTN031 Cutaneous Pseudolymphoma 18 0.044
285
FBR090 Fibro-Adipose Vascular Anomaly 17 0.044
286
P CLR023 Colorectal Cancer 98 0.036
287
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.036
288
P ALZ034 Alzheimer Disease 88 0.036
289
P PNC035 Pancreatic Cancer 84 0.036
290
c HYP595 Hypertension, Essential 84 0.036
291
c LKM061 Leukemia, Acute Myeloid 83 0.036
292
MLR004 Malaria 80 0.036
293
STR067 Stroke, Ischemic 80 0.036
294
c LKM071 Leukemia, Chronic Lymphocytic 79 0.036
295
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.036
296
P SCH015 Schizophrenia 75 0.036
297
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.036
298
c LKM063 Leukemia, Chronic Myeloid 71 0.036
299
P CNR004 Cone-Rod Dystrophy 2 71 0.036
300
P AMY004 Amyloidosis 70 0.036
301
DWN001 Down Syndrome 70 0.036
302
MYL009 Myelodysplastic Syndrome 70 0.036
303
P BRG001 Brugada Syndrome 70 0.036
304
P SYS005 Systemic Scleroderma 70 0.036
305
P TTR001 Tetralogy of Fallot 69 0.036
306
PLY001 Polycythemia Vera 69 0.036
307
BRN024 Bronchitis 68 0.036
308
P ESS003 Essential Thrombocythemia 67 0.036
309
KRT019 Keratitis, Hereditary 67 0.036
310
MYL005 Myelofibrosis 67 0.036
311
BRK010 Burkitt Lymphoma 67 0.036
312
P DMN002 Dementia 67 0.036
313
CMM004 Common Variable Immunodeficiency 67 0.036
314
MNT001 Mantle Cell Lymphoma 66 0.036
315
P FLL037 Follicular Lymphoma 66 0.036
316
OST159 Osteogenic Sarcoma 66 0.036
317
ANG054 Angina Pectoris 66 0.036
318
c RHB024 Rhabdomyosarcoma 2 65 0.036
319
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.036
320
PRT037 Pertussis 65 0.036
321
P TRN020 Turner Syndrome 65 0.036
322
MYL031 Myeloproliferative Neoplasm 65 0.036
323
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.036
324
OST017 Osteomyelitis 64 0.036
325
KHL003 Kohlschutter-Tonz Syndrome 64 0.036
326
P VSC007 Vascular Disease 63 0.036
327
c HPT003 Hepatitis a 63 0.036
328
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.036
329
LSC001 Lesch-Nyhan Syndrome 62 0.036
330
c GLC092 Glaucoma, Primary Open Angle 62 0.036
331
HMT002 Hematologic Cancer 62 0.036
332
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.036
333
NTR005 Nutritional Deficiency Disease 61 0.036
334
P HYP750 Hypertriglyceridemia, Familial 61 0.036
335
P ENC004 Encephalitis 61 0.036
336
c PNS012 Paine Syndrome 61 0.036
337
ERL001 Early Myoclonic Encephalopathy 61 0.036
338
MSL001 Measles 61 0.036
339
ATM095 Autoimmune Disease 61 0.036
340
P EPS003 Episodic Ataxia 60 0.036
341
c PCH015 Pachyonychia Congenita 1 60 0.036
342
ACN002 Acanthosis Nigricans 60 0.036
343
HPT019 Hepatic Encephalopathy 60 0.036
344
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.036
345
INS001 Insulinoma 60 0.036
346
P ALP009 Alopecia Areata 60 0.036
347
WST001 West Syndrome 60 0.036
348
P SCL018 Scoliosis 60 0.036
349
P THL005 Thalassemia 60 0.036
350
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.036
351
BRN002 Bronchiolitis 59 0.036
352
P CHR285 Chronic Myelomonocytic Leukemia 59 0.036
353
PLM033 Pulmonary Embolism 59 0.036
354
P BRS044 Breast Adenocarcinoma 59 0.036
355
PPT005 Peptic Ulcer Disease 58 0.036
356
c ACT073 Acute Leukemia 58 0.036
357
P URT039 Urticaria 58 0.036
358
c DWL002 Dowling-Degos Disease 1 58 0.036
359
LYM021 Lymphadenitis 58 0.036
360
LYM027 Lymphopenia 57 0.036
361
APH001 Aphthous Stomatitis 57 0.036
362
P GLM007 Glomerulonephritis 57 0.036
363
CYT008 Cytomegalovirus Infection 56 0.036
364
PHR003 Pharyngitis 56 0.036
365
AGN016 Aging 56 0.036
366
INT030 Intracranial Aneurysm 56 0.036
367
BRN012 Bronchiolitis Obliterans 56 0.036
368
P MYT023 Myotonia Congenita 55 0.036
369
NRL004 Neuroleptic Malignant Syndrome 55 0.036
370
P PLY018 Polycythemia 55 0.036
371
DBT010 Diabetic Neuropathy 55 0.036
372
P LCH002 Lichen Planus 54 0.036
373
P EPS030 Episodic Kinesigenic Dyskinesia 1 53 0.036
374
P LTR001 Lateral Sclerosis 53 0.036
375
MRG003 Marginal Zone B-Cell Lymphoma 53 0.036
376
INT075 Intracranial Hypertension 53 0.036
377
HMC014 Homocysteinemia 53 0.036
378
P HMR003 Hemorrhagic Disease 52 0.036
379
P PTS002 Ptosis 52 0.036
380
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.036
381
GTR002 Goiter 52 0.036
382
P ACT105 Acute Mountain Sickness 52 0.036
383
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.036
384
c PRM012 Primary Polycythemia 52 0.036
385
c PSR017 Psoriasis 2 52 0.036
386
PLS009 Plasma Cell Neoplasm 51 0.036
387
c VRL010 Viral Hepatitis 51 0.036
388
TLN003 Telangiectasis 51 0.036
389
c FBR084 Fibromatosis, Gingival, 1 51 0.036
390
MYL020 Myelomeningocele 51 0.036
391
ONC002 Onchocerciasis 51 0.036
392
SPL004 Splenic Marginal Zone Lymphoma 51 0.036
393
SMT006 Somatoform Disorder 51 0.036
394
c ALM001 Al Amyloidosis 50 0.036
395
HYP081 Hypolipoproteinemia 50 0.036
396
P HYP077 Hypertrichosis 50 0.036
397
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 50 0.036
398
P SCK005 Sickle Cell Disease 50 0.036
399
VLV047 Volvulus of Midgut 50 0.036
400
HYP080 Hypogonadism 50 0.036
401
HYP748 Hypertelorism 50 0.036
402
P ESN008 Eosinophilic Pneumonia 50 0.036
403
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.036
404
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.036
405
c PSR023 Psoriasis 1 49 0.036
406
P OPN001 Open-Angle Glaucoma 49 0.036
407
BLL003 Bell's Palsy 49 0.036
408
c FLL041 Follicular Lymphoma 1 49 0.036
409
MNN009 Meningoencephalitis 49 0.036
410
ATY042 Atypical Chronic Myeloid Leukemia 49 0.036
411
c THR090 Thrombocythemia 1 49 0.036
412
KRT002 Keratomalacia 48 0.036
413
INT078 Intracranial Thrombosis 48 0.036
414
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.036
415
CHR563 Chronic Eosinophilic Leukemia 48 0.036
416
FCL012 Facial Paralysis 48 0.036
417
ATX019 Ataxia with Vitamin E Deficiency 48 0.036
418
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.036
419
P PRR002 Pure Red-Cell Aplasia 48 0.036
420
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.036
421
SMT001 Somatization Disorder 48 0.036
422
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.036
423
LYM019 Lymphosarcoma 47 0.036
424
PLS025 Plasmablastic Lymphoma 47 0.036
425
HRD005 Hard Palate Cancer 46 0.036
426
RCT020 Rectum Adenocarcinoma 46 0.036
427
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.036
428
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.036
429
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.036
430
GLC084 Glaucoma, Normal Tension 46 0.036
431
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.036
432
EXT010 Extramedullary Plasmacytoma 45 0.036
433
c MLG068 Malignant Glioma 45 0.036
434
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.036
436
CRB027 Cerebellar Disease 45 0.036
437
P BRB001 Beriberi 44 0.036
438
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.036
439
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.036
440
HPT004 Hepatic Coma 43 0.036
441
BNM001 Bone Marrow Cancer 43 0.036
442
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.036
443
P PRT026 Parotitis 42 0.036
444
c PRG011 Progressive Myoclonus Epilepsy 42 0.036
445
P HYP265 Hypotonia 42 0.036
446
TNS007 Taeniasis 41 0.036
447
CHR286 Chronic Neutrophilic Leukemia 41 0.036
448
P RRT020 Rare Tumor 41 0.036
449
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.036
450
HYP064 Hypogonadotropism 40 0.036
451
c PSR028 Psoriasis 7 39 0.036
452
c PSR032 Psoriasis 11 38 0.036
453
c PSR018 Psoriasis 13 38 0.036
454
PRM024 Primary Angle-Closure Glaucoma 38 0.036
455
c HNT011 Huntington Disease-Like 3 38 0.036
457
c PRM340 Primary Adrenal Insufficiency 36 0.036
458
INT025 Intermittent Explosive Disorder 36 0.036
459
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.036
460
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.036
461
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.036
462
c GNR039 Generalized Epilepsy with Febrile Seizures Plus, Type 2 33 0.036
463
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.036
464
MXL016 Maxillonasal Dysplasia, Binder Type 31 0.036
465
PRX035 Paroxysmal Dyskinesia 31 0.036
466
PYR016 Pyridoxine Deficiency 30 0.036
467
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.036
468
c EPL173 Epileptic Encephalopathy, Early Infantile, 47 28 0.036
469
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.036
470
CHL079 Children's Interstitial Lung Disease 27 0.036
471
ADG002 Audiogenic Seizures 26 0.036
472
PGM030 Pigmentation Anomaly of the Skin 25 0.036
473
PRX022 Paroxysmal Choreoathetosis 23 0.036
474
LNR005 Linear Scleroderma 23 0.036
475
HML018 Homologous Wasting Disease 22 0.036
476
NDD001 Nodding Syndrome 21 0.036
478
P HPT023 Hepatocellular Carcinoma 100 0.025
479
P LNG032 Lung Cancer 97 0.025
480
P PRS040 Prostate Cancer 97 0.025
481
P BRS047 Breast Cancer 96 0.025
482
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.025
483
P GST053 Gastric Cancer 83 0.025
484
P MDL005 Medulloblastoma 77 0.025
485
P PRK057 Parkinson Disease, Late-Onset 76 0.025
486
c TBR025 Tuberous Sclerosis 1 76 0.025
487
GST019 Gastrointestinal Stromal Tumor 76 0.025
488
P APL001 Aplastic Anemia 74 0.025
489
END057 Endometrial Cancer 74 0.025
490
CRH001 Crohn's Disease 74 0.025
491
BRN028 Brain Cancer 73 0.025
492
c SPN225 Spondyloarthropathy 1 73 0.025
493
ULC004 Ulcerative Colitis 73 0.025
494
c BTT014 Beta-Thalassemia 72 0.025
495
SCK003 Sickle Cell Anemia 72 0.025
496
P PHC003 Pheochromocytoma 71 0.025
497
PRP027 Peripheral Vascular Disease 71 0.025
498
c TBR026 Tuberous Sclerosis 2 71 0.025
499
P OST001 Osteopetrosis 71 0.025
500
P SRC025 Sarcoidosis 1 70 0.025
501
WLS001 Wilson Disease 70 0.025
502
c GCH015 Gaucher Disease, Type I 70 0.025
503
P TBR001 Tuberous Sclerosis 70 0.025
504
BHC003 Behcet Syndrome 70 0.025
505
P OCL013 Oculodentodigital Dysplasia 69 0.025
506
P SLP006 Sleep Apnea 69 0.025
507
P MYC084 Mycobacterium Tuberculosis 1 68 0.025
508
P MYS003 Myasthenia Gravis 68 0.025
509
P CRN037 Craniosynostosis 68 0.025
510
c FML021 Familial Hypercholesterolemia 68 0.025
511
c ATS007 Autism Spectrum Disorder 67 0.025
512
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.025
513
P OLG002 Oligodendroglioma 67 0.025
514
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.025
515
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.025
516
P ANG001 Angelman Syndrome 67 0.025
517
c MYT021 Myotonic Dystrophy 1 66 0.025
518
PRP001 Propionic Acidemia 66 0.025
519
P ATR011 Atrial Fibrillation 66 0.025
520
ART001 Arterial Tortuosity Syndrome 66 0.025
521
CHG001 Chagas Disease 66 0.025
522
P LNG028 Long Qt Syndrome 65 0.025
523
c SML038 Small Cell Cancer of the Lung 65 0.025
524
P AGM001 Agammaglobulinemia 65 0.025
525
P THY023 Thymoma 65 0.025
526
P DBT009 Diabetes Mellitus 64 0.025
527
P MTR014 Motor Neuron Disease 64 0.025
528
HYP020 Hyperprolactinemia 64 0.025
529
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.025
530
P ADN016 Adenocarcinoma 64 0.025
531
P GCH001 Gaucher's Disease 64 0.025
532
PRP083 Porphyria, Acute Intermittent 63 0.025
533
MSC007 Muscle Hypertrophy 63 0.025
534
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.025
535
LVR012 Liver Cirrhosis 63 0.025
536
P ANR048 Aniridia 1 63 0.025
537
P ADL010 Adult Respiratory Distress Syndrome 63 0.025
538
ANR007 Anorexia Nervosa 63 0.025
539
P HML002 Hemolytic Anemia 62 0.025
540
P ERL057 Early Infantile Epileptic Encephalopathy 62 0.025
541
CLT003 Colitis 62 0.025
542
BDD001 Budd-Chiari Syndrome 62 0.025
543
c ALP101 Alpha-Thalassemia 62 0.025
544
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.025
545
P PRP029 Porphyria 62 0.025
546
P EPL140 Epilepsy, Idiopathic Generalized 61 0.025
547
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.025
548
TXC005 Toxic Shock Syndrome 61 0.025
549
TKY002 Takayasu Arteritis 61 0.025
550
P DRM010 Dermatomyositis 61 0.025
551
ALX003 Alexander Disease 61 0.025
552
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.025
553
c HRD002 Hereditary Angioedema 61 0.025
554
PRT013 Portal Hypertension 60 0.025
555
P LYM033 Lymphoproliferative Syndrome 60 0.025
556
CHR619 Chromosome 2q35 Duplication Syndrome 60 0.025
557
DPH001 Diphtheria 60 0.025
558
SQM006 Squamous Cell Carcinoma 60 0.025
559
HRP004 Herpes Zoster 60 0.025
560
P GLL022 Guillain-Barre Syndrome 59 0.025
561
HYD002 Hydronephrosis 59 0.025
562
P CYS018 Cystitis 59 0.025
563
P TRC086 Trichohepatoenteric Syndrome 1 59 0.025
564
GRD007 Grade Iii Astrocytoma 59 0.025
565
FBR047 Fibromyalgia 59 0.025
566
CRD132 Cardiac Conduction Defect 59 0.025
567
P RBL001 Rubella 58 0.025
568
P INT070 Intestinal Obstruction 58 0.025
569
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.025
570
CRY005 Cryptococcosis 58 0.025
571
P FCL005 Focal Segmental Glomerulosclerosis 58 0.025
572
c EPS042 Episodic Ataxia, Type 1 58 0.025
573
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.025
574
P INF032 Infertility 57 0.025
575
IRN002 Iron Metabolism Disease 57 0.025
576
P PLY041 Polymyositis 57 0.025
577
P UVT001 Uveitis 57 0.025
578
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.025
579
c CHR417 Chronic Graft Versus Host Disease 56 0.025
580
P EPD003 Epidermolysis Bullosa Simplex 56 0.025
581
P EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 56 0.025
582
P DYS193 Dystonia 11, Myoclonic 56 0.025
583
c ACT075 Acute Myocardial Infarction 56 0.025
584
c INT072 Intestinal Pseudo-Obstruction 56 0.025
585
P PLY011 Polycystic Ovary Syndrome 56 0.025
586
P MYS005 Myositis 56 0.025
587
GST050 Gastrointestinal System Disease 56 0.025
588
HMG005 Hemoglobinopathy 55 0.025
589
P GST044 Gastritis 55 0.025
590
HYP005 Hypokalemia 55 0.025
591
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
592
LMB062 Limb Ischemia 55 0.025
593
c GRV008 Graves Disease 1 55 0.025
594
ACT058 Active Peptic Ulcer Disease 55 0.025
595
P HYP076 Hyperthyroidism 55 0.025
596
JVN009 Juvenile Pilocytic Astrocytoma 55 0.025
597
HRY003 Hairy Cell Leukemia 55 0.025
598
P FTL001 Fetal Alcohol Syndrome 55 0.025
599
INT007 Intermediate Coronary Syndrome 55 0.025
600
P DBT005 Diabetes Insipidus 55 0.025
601
PLM010 Pulmonary Edema 55 0.025
602
P PMP001 Pemphigus 55 0.025
603
PYD001 Pyoderma Gangrenosum 54 0.025
604
P ANT006 Antiphospholipid Syndrome 54 0.025
605
CLL003 Cellulitis 54 0.025
606
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.025
607
HMP005 Hemiplegia 54 0.025
608
VGT001 Vogt-Koyanagi-Harada Disease 54 0.025
609
GLS001 Gliosarcoma 54 0.025
610
FRY006 Fryns Microphthalmia Syndrome 54 0.025
611
GLC003 Glucose Intolerance 54 0.025
612
P SPN052 Spondyloarthropathy 54 0.025
613
HST011 Histoplasmosis 54 0.025
614
PNC001 Pancytopenia 54 0.025
615
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.025
616
UNV001 Unverricht-Lundborg Syndrome 54 0.025
617
PRC013 Pericarditis 54 0.025
618
c THY107 Thymoma, Familial 54 0.025
619
PRP016 Paraplegia 53 0.025
620
RFL001 Reflex Sympathetic Dystrophy 53 0.025
621
CCC001 Coccidioidomycosis 53 0.025
622
P HYP730 Hypogonadotropic Hypogonadism 53 0.025
623
PRP036 Peripheral T-Cell Lymphoma 53 0.025
624
P HST010 Histiocytosis 53 0.025
625
P THY032 Thyroiditis 53 0.025
626
PLS007 Plasmodium Falciparum Malaria 52 0.025
627
P CTN003 Cutaneous Lupus Erythematosus 52 0.025
628
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.025
629
PRS045 Prostatic Hypertrophy 52 0.025
630
STT041 Stuttering 52 0.025
631
IMP005 Impotence 52 0.025
632
AGN012 Agnathia-Otocephaly Complex 52 0.025
633
PLM014 Pleomorphic Adenoma 52 0.025
634
GNT002 Giant Cell Glioblastoma 52 0.025
635
TXC002 Toxic Encephalopathy 52 0.025
636
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.025
637
P OLV001 Olivopontocerebellar Atrophy 52 0.025
639
PYD002 Pyoderma 51 0.025
640
THR016 Thrombophlebitis 51 0.025
641
DNT012 Dental Caries 51 0.025
642
PRS021 Prostatic Adenoma 51 0.025
643
MYL001 Myelitis 51 0.025
644
PPT001 Peptic Esophagitis 51 0.025
645
CRY001 Cryptogenic Organizing Pneumonia 51 0.025
646
P LCT001 Lactic Acidosis 51 0.025
647
PNG002 Pain Agnosia 51 0.025
648
FML063 Familial Glucocorticoid Deficiency 51 0.025
649
P HYP040 Hypospadias 51 0.025
650
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.025
651
NRM004 Neuroma 51 0.025
652
GSG001 Gas Gangrene 50 0.025
653
HRT011 Heart Septal Defect 50 0.025
654
LPR001 Lepromatous Leprosy 50 0.025
655
FSC004 Fasciitis 50 0.025
656
c MLG054 Malignant Histiocytosis 50 0.025
657
MTB004 Metabolic Acidosis 50 0.025
658
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 50 0.025
659
ALV002 Alveolar Echinococcosis 50 0.025
660
STM007 Stomatitis 49 0.025
661
P CTN015 Cutaneous T Cell Lymphoma 49 0.025
662
P MTC133 Mitochondrial Myopathy 49 0.025
663
P MYT002 Myotonic Dystrophy 49 0.025
664
SPT005 Spotted Fever 49 0.025
665
INP001 Inappropriate Adh Syndrome 49 0.025
666
PLR007 Pleural Empyema 49 0.025
667
PLC008 Placenta Disease 49 0.025
668
LRN003 Learning Disability 49 0.025
669
CYT005 Cytomegalovirus Retinitis 49 0.025
670
PRS129 Prostatic Hyperplasia, Benign 49 0.025
671
c BPL002 Bipolar I Disorder 49 0.025
672
GYN001 Gynecomastia 49 0.025
673
P CMP008 Compartment Syndrome 48 0.025
674
RFR010 Refractory Anemia 48 0.025
675
c ACT150 Acute Adrenal Insufficiency 48 0.025
676
VTM002 Vitamin B12 Deficiency 48 0.025
677
P CLR019 Color Blindness 48 0.025
678
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.025
679
PRS012 Pars Planitis 48 0.025
680
SXL003 Sexual Disorder 48 0.025
681
FRN020 Frontal Fibrosing Alopecia 48 0.025
682
PLM035 Pulmonary Eosinophilia 48 0.025
683
FLT006 Floating-Harbor Syndrome 48 0.025
684
P NRV006 Nervous System Cancer 48 0.025
685
HLX001 Helix Syndrome 47 0.025
686
ESN015 Eosinophilic Fasciitis 47 0.025
687
CLB002 Clubfoot 47 0.025
688
GRM005 Germ Cell Cancer 47 0.025
689
RGH001 Right Bundle Branch Block 47 0.025
690
NRN001 Neuroendocrine Carcinoma 47 0.025
691
MLT006 Multidrug-Resistant Tuberculosis 47 0.025
692
c BNG006 Benign Familial Neonatal Epilepsy 47 0.025
693
SRT004 Serotonin Syndrome 46 0.025
694
CHR074 Choriocarcinoma 46 0.025
695
P PNT019 Pontocerebellar Hypoplasia 46 0.025
696
EXS001 Exostosis 46 0.025
697
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.025
698
c CNT033 Central Nervous System Cancer 46 0.025
699
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.025
700
ADR040 Adrenal Gland Pheochromocytoma 46 0.025
701
P TRN034 Transverse Myelitis 46 0.025
702
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.025
703
OBS037 Obesity-Hypoventilation Syndrome 45 0.025
704
MCR037 Macroglossia 45 0.025
705
ESP018 Esophageal Candidiasis 45 0.025
706
SYN036 Syncope 45 0.025
707
BRL010 Buruli Ulcer 45 0.025
708
MXD026 Mixed Glioma 45 0.025
709
P SBR004 Seborrheic Dermatitis 45 0.025
710
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 45 0.025
711
ASP004 Asphyxia Neonatorum 45 0.025
712
MTS001 Mutism 45 0.025
713
c EPL082 Epileptic Encephalopathy, Early Infantile, 13 45 0.025
714
KWS001 Kwashiorkor 45 0.025
715
TCL003 T Cell Deficiency 45 0.025
716
CLD007 Cold Agglutinin Disease 45 0.025
717
OLG001 Oligospermia 45 0.025
718
CRB004 Cerebral Artery Occlusion 44 0.025
719
PTY001 Pityriasis Rosea 44 0.025
720
PRL008 Paralytic Ileus 44 0.025
721
P GNT008 Giant Cell Tumor 44 0.025
722
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.025
723
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 44 0.025
724
c FML036 Familial Periodic Paralysis 44 0.025
725
CHD004 Chudley-Mccullough Syndrome 44 0.025
726
GNG003 Gingival Recession 44 0.025
727
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.025
728
SKN005 Skin Atrophy 43 0.025
729
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.025
730
RTT001 Ritter's Disease 43 0.025
731
SCT002 Scotoma 43 0.025
732
PRN049 Paraneoplastic Pemphigus 43 0.025
733
IDP074 Idiopathic Bronchiectasis 43 0.025
734
c ATM101 Autoimmune Gastritis 43 0.025
735
EPC005 Epicanthus 43 0.025
736
ANP009 Anaplastic Oligodendroglioma 43 0.025
737
DSC009 Discoid Lupus Erythematosus 42 0.025
738
DRG002 Drug-Induced Hepatitis 42 0.025
739
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.025
740
PST053 Postherpetic Neuralgia 42 0.025
741
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.025
742
SPC005 Speech Disorder 42 0.025
743
CLR033 Color Vision Deficiency 41 0.025
744
MCR017 Macrocytic Anemia 41 0.025
745
c MNT242 Mental Retardation, Autosomal Dominant 40 41 0.025
746
P FML156 Familial Hyperaldosteronism 41 0.025
747
c HYP057 Hypervitaminosis D 41 0.025
748
PRT012 Prothrombin Deficiency 41 0.025
749
LCR013 Lacrimal Duct Defect 41 0.025
750
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 41 0.025
751
P DMY001 Demyelinating Polyneuropathy 41 0.025
752
NNT049 Nontuberculous Mycobacterial Lung Disease 40 0.025
753
CLP006 Clopidogrel Resistance 40 0.025
754
P CHR342 Chiari Malformation 40 0.025
755
SCR015 Scarlet Fever 40 0.025
756
LNR006 Linear Iga Disease 40 0.025
757
RCK002 Rocky Mountain Spotted Fever 40 0.025
758
SPR126 Superior Semicircular Canal Dehiscence 40 0.025
759
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 40 0.025
760
RTC012 Reticuloendotheliosis, X-Linked 40 0.025
761
ANG049 Angioedema Induced by Ace Inhibitors 40 0.025
762
CRB086 Cerebral Aneurysms 40 0.025
763
SPS019 Spastic Paraparesis 40 0.025
764
PRM329 Premature Aging 39 0.025
765
MLT001 Multiple Chemical Sensitivity 39 0.025
766
ADP007 Adie Pupil 39 0.025
767
ALG001 Algoneurodystrophy 39 0.025
768
SCR011 Scrapie 38 0.025
769
IDP091 Idiopathic Nephrotic Syndrome 38 0.025
770
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.025
771
P CRB088 Cerebral Atrophy 38 0.025
772
c HMG029 Hemoglobin Se Disease 38 0.025
773
SPR024 Supratentorial Cancer 38 0.025
774
ATX010 Ataxia Neuropathy Spectrum 38 0.025
775
FRN014 Fournier Gangrene 37 0.025
776
HPT082 Hepatic Adenomas, Familial 37 0.025
777
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.025
778
P MSN006 Mesenchymoma 36 0.025
779
KKC001 Kikuchi Disease 36 0.025
780
c CHR098 Chronic Pyelonephritis 35 0.025
782
OLG006 Oligoastrocytoma 35 0.025
783
FXD003 Fixed Drug Eruption 35 0.025
784
PLM180 Pulmonary Artery Disease 35 0.025
785
ACT149 Acetaminophen Metabolism 35 0.025
786
c ADL008 Adult Oligodendroglioma 35 0.025
787
c GLM025 Glioma Susceptibility 2 35 0.025
788
NRX001 Neuroaxonal Dystrophy 34 0.025
789
CMP006 Complex Partial Epilepsy 34 0.025
790
PRC054 Perching Syndrome 33 0.025
791
c SBC035 Subacute Cutaneous Lupus Erythematosus 33 0.025
792
c PRS136 Prostate Cancer, Hereditary, 6 33 0.025
793
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.025
794
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.025
795
NRN002 Neuronitis 33 0.025
796
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.025
797
c PRS130 Prostate Cancer, Hereditary, 8 32 0.025
798
KNC002 Knuckle Pads 32 0.025
799
RFR002 Refractory Hairy Cell Leukemia 32 0.025
800
ACT064 Acute Necrotizing Encephalitis 32 0.025
801
MNG003 Mungan Syndrome 32 0.025
802
GRN009 Granulomatous Hepatitis 31 0.025
803
NNT003 Neonatal Thyrotoxicosis 31 0.025
804
INF021 Infant Gynecomastia 31 0.025
805
EXN003 Exencephaly 31 0.025
806
STT009 Sutton Disease 2 30 0.025
808
ANP008 Anaplastic Oligoastrocytoma 30 0.025
809
HNM002 Hinman Syndrome 29 0.025
810
GNT046 Genetic Epilepsy with Febrile Seizures Plus 28 0.025
811
SBD001 Subdural Empyema 28 0.025
813
P MYM016 Moyamoya Angiopathy 27 0.025
814
CLS052 Classic Hairy Cell Leukemia 27 0.025
815
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.025
816
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.025
817
DFF031 Diffuse Alveolar Hemorrhage 26 0.025
818
BLD163 Blood Group, Dombrock System 26 0.025
819
PRD003 Periodontosis 26 0.025
820
c XLN227 X-Linked Chondrodysplasia Punctata 1 25 0.025
821
HYP049 Hypertrophy of Tongue Papillae 24 0.025
822
ANT078 Antipyrine Metabolism 24 0.025
823
KR001 Koro 24 0.025
824
BLD165 Blood Group, Colton System 23 0.025
825
TRM026 Trimethoprim Allergy 23 0.025
826
ORF053 Orofacial Clefting Syndrome 22 0.025
827
LYM053 Lymphomatous Thyroiditis 22 0.025
828
SCN067 Scn1a Seizure Disorders 22 0.025
829
SLF017 Sulfamethoxazole Allergy 21 0.025
830
SSS001 Sessile Serrated Polyposis Cancer Syndrome 21 0.025
831
ABC021 Abacavir Allergy 20 0.025
833
BLD137 Blood Group--Ahonen 19 0.025
834
STX004 Stxbp1 Encephalopathy with Epilepsy 18 0.025
835
EXT039 Extrapontine Myelinolysis 18 0.025
836
c FML159 Familial Periodic Paralyses 17 0.025
837
ORG003 Organic Mood Syndrome 14 0.025
839
MTS004 Metastatic Insulinoma 13 0.025
840
ACH028 Acheiria 13 0.025
841
VTM021 Vitamin K Antagonists Toxicity or Dose Selection 12 0.025
842
ACR040 Acromelanosis 12 0.025
843
CRB080 Cor Biloculare 11 0.025
Content
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