Search results for lithium

1015 hits were found for lithium

# Family MCID Name MIFTS Score
1
LTH043 Lithium Transport 18 3.336
2
P BPL003 Bipolar Disorder 56 0.910
3
c MJR024 Major Affective Disorder 9 41 0.902
4
c MJR022 Major Affective Disorder 8 38 0.902
5
P MJR007 Major Affective Disorder 1 43 0.435
6
MDD011 Mood Disorder 62 0.421
7
DPR016 Depression 63 0.395
8
P DBT005 Diabetes Insipidus 55 0.378
9
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.352
10
MNT002 Mental Depression 58 0.333
11
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.322
12
c BPL002 Bipolar I Disorder 49 0.315
13
P HYP086 Hypothyroidism 69 0.311
14
HRW001 Hair Whorl 36 0.311
15
c MJR003 Major Affective Disorder 6 33 0.307
16
c MJR006 Major Affective Disorder 5 33 0.307
17
c MJR008 Major Affective Disorder 2 35 0.304
18
P TRM003 Tremor 54 0.301
19
c MJR023 Major Affective Disorder 7 33 0.301
20
c MJR004 Major Affective Disorder 4 28 0.301
21
END040 Endogenous Depression 55 0.298
22
STT001 Status Epilepticus 60 0.296
23
P HYP069 Hyperparathyroidism 63 0.252
24
P NTR004 Neutropenia 63 0.243
25
c HYP595 Hypertension, Essential 84 0.238
26
P HYP076 Hyperthyroidism 55 0.225
27
P MJR001 Major Depressive Disorder 68 0.215
28
P SZR006 Seizure Disorder 56 0.213
29
GTR002 Goiter 53 0.213
30
P KDN018 Kidney Disease 72 0.205
31
VSL002 Visual Epilepsy 59 0.205
32
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.205
33
NRT001 Neurotic Disorder 53 0.203
34
c GRV008 Graves Disease 1 56 0.194
35
P ALZ034 Alzheimer Disease 88 0.167
36
P NRB001 Neuroblastoma 72 0.167
37
P TMP001 Temporal Lobe Epilepsy 50 0.167
38
P PSR002 Psoriasis 62 0.166
39
PST011 Pustulosis of Palm and Sole 52 0.166
40
SCH012 Schizoaffective Disorder 50 0.166
41
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.159
42
ALC007 Alcohol Dependence 66 0.155
43
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.154
44
P LTR001 Lateral Sclerosis 54 0.154
45
c CHR684 Chronic Kidney Disease 70 0.152
46
SBC016 Subacute Delirium 44 0.151
47
TRD006 Tardive Dyskinesia 54 0.149
48
PSY004 Psychotic Disorder 67 0.146
49
P HDC001 Headache 57 0.141
50
OCL069 Ocular Motor Apraxia 51 0.141
51
P ENC018 Encephalopathy 61 0.139
52
P DMN002 Dementia 66 0.136
53
P SCK002 Sick Sinus Syndrome 55 0.134
54
GRN017 Granulocytopenia 44 0.134
55
P SCH015 Schizophrenia 74 0.132
56
NRL004 Neuroleptic Malignant Syndrome 56 0.130
57
P CLS010 Cluster Headache 42 0.130
58
DSS008 Disease of Mental Health 58 0.128
59
c MCR113 Microvascular Complications of Diabetes 3 52 0.128
60
c MCR120 Microvascular Complications of Diabetes 7 47 0.128
61
c MCR130 Microvascular Complications of Diabetes 6 41 0.128
62
c MCR133 Microvascular Complications of Diabetes 4 41 0.128
63
ADN018 Adenoma 59 0.126
64
SNT005 Sinoatrial Node Disease 49 0.126
65
c PRM005 Primary Hyperparathyroidism 58 0.124
66
48X005 48,xyyy 39 0.124
67
P HNT016 Huntington Disease 72 0.122
68
P DBT009 Diabetes Mellitus 64 0.122
69
SPN186 Spinal Cord Injury 60 0.122
70
P NPH012 Nephrotic Syndrome 60 0.122
71
P GRV001 Graves' Disease 55 0.122
72
CND002 Conduct Disorder 51 0.122
73
P LKM002 Leukemia 68 0.120
74
c ACT071 Acute Kidney Failure 60 0.120
75
THY029 Thyroid Carcinoma 59 0.120
76
CHR073 Choreatic Disease 52 0.120
77
END086 End Stage Renal Disease 51 0.120
78
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.120
79
P THY032 Thyroiditis 52 0.118
80
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.116
81
P DRR001 Diarrhea 55 0.114
82
PRT037 Pertussis 65 0.112
83
ANX010 Anxiety 73 0.108
84
P SBS003 Substance Abuse 55 0.108
85
PTH003 Pathologic Nystagmus 52 0.108
86
P MYL006 Myeloid Leukemia 60 0.105
87
P NRP001 Neuropathy 56 0.105
88
HYP005 Hypokalemia 55 0.105
89
P PRS038 Personality Disorder 65 0.103
90
P PHC003 Pheochromocytoma 71 0.098
91
c DBT099 Diabetes Mellitus, Type I 65 0.098
92
ISC004 Ischemia 58 0.098
93
SCH003 Schizophreniform Disorder 56 0.098
94
PRT029 Parathyroid Adenoma 50 0.098
95
SRT004 Serotonin Syndrome 47 0.098
96
ADR040 Adrenal Gland Pheochromocytoma 46 0.098
97
P GLM045 Glioma 63 0.096
98
GLL048 Glial Tumor 45 0.096
99
CHL014 Cholera 59 0.093
100
P RNL007 Renal Tubular Acidosis 51 0.093
101
BRN071 Brain Injury 49 0.093
102
P CNR004 Cone-Rod Dystrophy 2 73 0.091
103
INT067 Interstitial Nephritis 48 0.091
104
P MYC033 Myoclonus 46 0.091
105
P SBR004 Seborrheic Dermatitis 45 0.091
106
P EPL164 Epilepsy 71 0.088
107
P PRP019 Peripheral Nervous System Disease 58 0.088
108
P ALP008 Alopecia 54 0.088
109
AVD001 Avoidant Personality Disorder 51 0.088
110
MTB004 Metabolic Acidosis 50 0.088
111
WTH001 Withdrawal Disorder 48 0.088
112
P HRT032 Heart Disease 75 0.085
113
OBS002 Obsessive-Compulsive Disorder 68 0.085
114
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.085
115
PST028 Post-Traumatic Stress Disorder 58 0.085
116
47X002 47,xyy 49 0.085
117
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.085
118
SVR004 Severe Combined Immunodeficiency 73 0.082
119
KHL003 Kohlschutter-Tonz Syndrome 65 0.082
120
DRM006 Dermatitis 61 0.082
121
GLS018 Glass Syndrome 57 0.082
122
PRS045 Prostatic Hypertrophy 53 0.082
123
PRS021 Prostatic Adenoma 51 0.082
124
PRS129 Prostatic Hyperplasia, Benign 49 0.082
125
P THR014 Thrombocytopenia 67 0.079
126
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.079
127
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.079
128
ACQ007 Acquired Immunodeficiency Syndrome 60 0.079
129
FLT011 Felty Syndrome 52 0.079
130
KLN009 Kleine-Levin Hibernation Syndrome 42 0.079
131
c LKM061 Leukemia, Acute Myeloid 84 0.076
132
c NRF023 Neurofibromatosis, Type Ii 80 0.076
133
HYP056 Hypoglycemia 66 0.076
134
P DYS154 Dystonia 65 0.076
135
P HRP006 Herpes Simplex 65 0.076
136
P BCL017 B-Cell Lymphoma 58 0.076
137
AMN003 Amnestic Disorder 54 0.076
138
TRM010 Traumatic Brain Injury 51 0.076
139
HLX001 Helix Syndrome 47 0.076
140
MYX004 Myxedema 43 0.076
141
CYC005 Cyclothymic Disorder 40 0.076
142
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.073
143
DFC004 Deficiency Anemia 70 0.073
144
P MCH002 Machado-Joseph Disease 62 0.073
145
P ALC033 Alcohol Use Disorder 58 0.073
146
P EXN002 Exanthem 57 0.073
147
CYT002 Cytokine Deficiency 42 0.073
148
MLN003 Melancholia 38 0.073
149
P APL001 Aplastic Anemia 74 0.070
150
P FRG001 Fragile X Syndrome 70 0.070
151
ADL002 Adult Syndrome 70 0.070
152
P TRN020 Turner Syndrome 67 0.070
153
c MGR028 Migraine with or Without Aura 1 67 0.070
154
P VSC007 Vascular Disease 63 0.070
155
ALL026 Allergic Hypersensitivity Disease 62 0.070
156
AGN016 Aging 56 0.070
157
EXP004 Exophthalmos 52 0.070
158
THY030 Thyroid Gland Disease 52 0.070
160
BNR002 Bone Resorption Disease 48 0.070
161
CRB004 Cerebral Artery Occlusion 45 0.070
162
P HYP265 Hypotonia 43 0.070
163
PHY002 Physical Disorder 42 0.070
164
ATX019 Ataxia with Vitamin E Deficiency 42 0.070
165
LBR035 Liberfarb Syndrome 24 0.070
166
GLB015 Glioblastoma Multiforme 75 0.066
167
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
168
DWN001 Down Syndrome 70 0.066
169
P FRN006 Frontotemporal Dementia 68 0.066
170
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.066
171
P MTR014 Motor Neuron Disease 65 0.066
172
PLG002 Plague 63 0.066
173
CNS004 Constipation 58 0.066
174
APH002 Aphasia 57 0.066
175
P PLY019 Polyneuropathy 56 0.066
176
DNT012 Dental Caries 53 0.066
177
P PNC025 Panic Disorder 53 0.066
178
DFF036 Differentiated Thyroid Carcinoma 52 0.066
179
DYS009 Dysthymic Disorder 49 0.066
180
ACT084 Acute Stress Disorder 47 0.066
181
FLL008 Folliculitis 46 0.066
182
P DST107 Distal Renal Tubular Acidosis 42 0.066
183
P HYP263 Hypersomnia 41 0.066
185
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.066
186
P CLR023 Colorectal Cancer 99 0.062
187
P PNC035 Pancreatic Cancer 84 0.062
188
IMM167 Immune Deficiency Disease 78 0.062
189
P PRK057 Parkinson Disease, Late-Onset 78 0.062
190
P OST002 Osteoporosis 74 0.062
191
P MLT020 Multiple Sclerosis 72 0.062
192
c LKM063 Leukemia, Chronic Myeloid 72 0.062
193
P BRG001 Brugada Syndrome 71 0.062
194
CNG034 Congestive Heart Failure 69 0.062
195
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.062
196
LVR012 Liver Cirrhosis 62 0.062
197
INT002 Intermittent Claudication 61 0.062
198
CRD223 Cardiac Arrhythmia 60 0.062
199
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.062
200
ATR057 Atrioventricular Block 55 0.062
201
NPH009 Nephrolithiasis 55 0.062
202
HRY003 Hairy Cell Leukemia 55 0.062
203
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.062
204
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.062
205
APR001 Apraxia 52 0.062
206
INP001 Inappropriate Adh Syndrome 49 0.062
207
PTH002 Pathological Gambling 49 0.062
208
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.062
209
SXL003 Sexual Disorder 47 0.062
210
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.062
211
49X006 49, Xxxxy Syndrome 41 0.062
212
P ART022 Arthritis 69 0.058
213
P LYM118 Lymphoma 68 0.058
214
ACR006 Aceruloplasminemia 65 0.058
215
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.058
216
GT001 Gout 64 0.058
217
CYC010 Cyclic Neutropenia 62 0.058
218
HSH003 Hashimoto Thyroiditis 62 0.058
219
c ACT073 Acute Leukemia 58 0.058
220
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.058
221
THY122 Thyroid Gland Cancer 57 0.058
222
INT303 Intracranial Hypertension, Idiopathic 57 0.058
223
NRN004 Neuroendocrine Tumor 55 0.058
224
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.058
225
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.058
226
HYP060 Hyperinsulinism 54 0.058
227
GLC003 Glucose Intolerance 54 0.058
228
NRT004 Neuritis 52 0.058
229
URM002 Uremia 49 0.058
230
c SPN105 Spinocerebellar Ataxia 4 47 0.058
231
SYN036 Syncope 45 0.058
232
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.058
233
SPN050 Spinocerebellar Degeneration 42 0.058
234
c PRM015 Primary Cerebellar Degeneration 36 0.058
235
SPN187 Spinocerebellar Atrophy 27 0.058
236
CHL079 Children's Interstitial Lung Disease 26 0.058
237
P LNG032 Lung Cancer 98 0.054
238
MYL069 Myeloma, Multiple 85 0.054
239
AST005 Asthma 76 0.054
240
P ATS364 Autism 70 0.054
241
P MYP004 Myopathy 70 0.054
242
CRT072 Creutzfeldt-Jakob Disease 70 0.054
243
BRN024 Bronchitis 68 0.054
244
c ATS007 Autism Spectrum Disorder 67 0.054
245
OST159 Osteogenic Sarcoma 66 0.054
246
c SML038 Small Cell Cancer of the Lung 65 0.054
247
P MVM001 Movement Disease 63 0.054
248
LPD008 Lipid Metabolism Disorder 62 0.054
249
P PLY014 Polycystic Kidney Disease 62 0.054
250
HYP066 Hyperglycemia 61 0.054
251
CNV004 Canavan Disease 61 0.054
252
P MYC008 Myocarditis 59 0.054
253
P CRD246 Cardiovascular System Disease 57 0.054
254
HYP266 Hypoxia 57 0.054
255
ERY051 Erythroleukemia, Familial 56 0.054
256
BRN004 Brain Edema 56 0.054
257
c SPN294 Spinocerebellar Ataxia 1 53 0.054
258
BRD004 Borderline Personality Disorder 53 0.054
259
INT075 Intracranial Hypertension 53 0.054
260
P AST007 Astrocytoma 51 0.054
261
STM007 Stomatitis 50 0.054
262
CCN002 Cocaine Abuse 49 0.054
263
NDL007 Nodular Goiter 47 0.054
264
ALL014 Allergic Encephalomyelitis 38 0.054
265
P CRB059 Cerebellar Degeneration 37 0.054
266
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.054
267
P BRS047 Breast Cancer 97 0.049
268
ESP021 Esophageal Cancer 90 0.049
269
CYS001 Cystic Fibrosis 81 0.049
270
P GLM040 Glioma Susceptibility 1 81 0.049
271
c ATR087 Atrial Standstill 1 75 0.049
272
P RSP003 Respiratory Failure 74 0.049
273
P GRF003 Graft-Versus-Host Disease 72 0.049
274
MLT157 Multiple System Atrophy 1 70 0.049
275
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.049
276
P LKM062 Leukemia, Acute Lymphoblastic 69 0.049
277
PCK003 Pick Disease of Brain 68 0.049
278
P MYS003 Myasthenia Gravis 68 0.049
279
P CRD119 Cardiac Arrest 67 0.049
280
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.049
281
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.049
282
P ANR048 Aniridia 1 63 0.049
283
ANR007 Anorexia Nervosa 63 0.049
284
c BRN108 Branchiootic Syndrome 1 62 0.049
285
P LKD001 Leukodystrophy 59 0.049
286
GST045 Gastroenteritis 59 0.049
287
P GLM007 Glomerulonephritis 57 0.049
288
P FCL005 Focal Segmental Glomerulosclerosis 57 0.049
289
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.049
290
HDR002 Hidradenitis Suppurativa 55 0.049
291
PLM010 Pulmonary Edema 54 0.049
292
IMP005 Impotence 52 0.049
293
KRT009 Keratosis 51 0.049
294
c SCN007 Secondary Hyperparathyroidism 51 0.049
295
PPL021 Papilledema 49 0.049
296
HDR003 Hidradenitis 49 0.049
297
IGG001 Iga Glomerulonephritis 48 0.049
298
P RNL015 Renal Hypertension 47 0.049
299
LYM019 Lymphosarcoma 46 0.049
300
ANR004 Anuria 46 0.049
301
CVD001 Covid-19 44 0.049
302
PRM020 Premenstrual Tension 40 0.049
303
CNN001 Cannabis Dependence 40 0.049
304
P FML187 Familial Hypertension 37 0.049
305
P AXN001 Axonal Neuropathy 36 0.049
306
PSD088 Pseudobulbar Affect 36 0.049
307
c CHR064 Chronic Monocytic Leukemia 33 0.049
308
ADG002 Audiogenic Seizures 25 0.049
309
CPG001 Capgras Syndrome 24 0.049
310
P HPT023 Hepatocellular Carcinoma 100 0.044
311
INS024 Insulin-Like Growth Factor I 79 0.044
312
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.044
313
BRN028 Brain Cancer 74 0.044
314
P RTN024 Retinoblastoma 73 0.044
315
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.044
316
P MYC007 Myocardial Infarction 70 0.044
317
MYL005 Myelofibrosis 70 0.044
318
P LVR013 Liver Disease 68 0.044
319
CRB039 Cerebrovascular Disease 67 0.044
320
THY111 Thyroid Carcinoma, Familial Medullary 67 0.044
321
P HYP098 Hypereosinophilic Syndrome 67 0.044
322
MYC006 Mycosis Fungoides 66 0.044
323
SRC014 Sarcoma 65 0.044
324
c WLM013 Wilms Tumor 1 65 0.044
325
P PRD008 Periodontitis 64 0.044
326
P RHB003 Rhabdomyosarcoma 63 0.044
327
P CRN300 Coronary Heart Disease 1 63 0.044
328
c FNC043 Fanconi Anemia, Complementation Group E 62 0.044
329
c SVR001 Severe Acute Respiratory Syndrome 62 0.044
330
LPP008 Lipoprotein Quantitative Trait Locus 62 0.044
331
P HYP750 Hypertriglyceridemia, Familial 62 0.044
332
OST003 Osteonecrosis 61 0.044
333
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.044
334
P ALP009 Alopecia Areata 60 0.044
335
P ANP001 Anaplastic Large Cell Lymphoma 58 0.044
336
c SPN301 Spinocerebellar Ataxia 2 58 0.044
337
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.044
338
c LKM070 Leukemia, Acute Monocytic 57 0.044
339
P PYL005 Pyelonephritis 56 0.044
340
BCT022 Bacterial Infectious Disease 56 0.044
341
EMB004 Embryonal Carcinoma 56 0.044
342
PNC001 Pancytopenia 54 0.044
343
SPN035 Spindle Cell Sarcoma 53 0.044
344
TXC002 Toxic Encephalopathy 53 0.044
345
c FML008 Familial Retinoblastoma 53 0.044
346
HYP014 Hyperuricemia 52 0.044
347
PNG002 Pain Agnosia 51 0.044
348
TRC010 Trichotillomania 51 0.044
349
PRN009 Paranoid Schizophrenia 50 0.044
350
P TRT019 Torticollis 48 0.044
351
PRP007 Priapism 47 0.044
352
PPL002 Papillary Carcinoma 47 0.044
353
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.044
354
TST014 Testicular Cancer 46 0.044
355
HDN002 Head Injury 46 0.044
356
CYN002 Cyanosis, Transient Neonatal 45 0.044
357
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.044
358
P MLT008 Multinodular Goiter 42 0.044
359
CRV043 Cervical Dystonia 42 0.044
360
c EPS028 Episodic Pain Syndrome, Familial, 3 40 0.044
361
ARG004 Argyria 27 0.044
362
HML018 Homologous Wasting Disease 22 0.044
363
P PRS040 Prostate Cancer 97 0.038
364
P OVR042 Ovarian Cancer 88 0.038
365
P GST053 Gastric Cancer 83 0.038
366
NRL016 Neural Tube Defects 82 0.038
367
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.038
368
STR067 Stroke, Ischemic 81 0.038
369
P LKM071 Leukemia, Chronic Lymphocytic 79 0.038
370
OST012 Osteoarthritis 78 0.038
371
P MDL005 Medulloblastoma 77 0.038
372
END057 Endometrial Cancer 74 0.038
373
P FML018 Familial Mediterranean Fever 73 0.038
374
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.038
375
BRT054 Brittle Bone Disorder 72 0.038
376
P SRC025 Sarcoidosis 1 70 0.038
377
MYL009 Myelodysplastic Syndrome 70 0.038
378
ABT001 Abetalipoproteinemia 69 0.038
379
LYM133 Lymphoma, Hodgkin, Classic 69 0.038
380
MNT001 Mantle Cell Lymphoma 69 0.038
381
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.038
382
P PNM007 Pneumonia 68 0.038
383
c NMN015 Niemann-Pick Disease, Type C1 68 0.038
384
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.038
385
BRK010 Burkitt Lymphoma 67 0.038
386
P FLL037 Follicular Lymphoma 67 0.038
387
P SHW006 Shwachman-Diamond Syndrome 1 67 0.038
388
c RHB024 Rhabdomyosarcoma 2 67 0.038
389
P HYD006 Hydrocephalus 66 0.038
390
P MNN013 Meningitis 66 0.038
391
MYL031 Myeloproliferative Neoplasm 66 0.038
392
TTN003 Tetanus 65 0.038
393
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.038
394
PPL049 Papillon-Lefevre Syndrome 65 0.038
395
P ADL010 Adult Respiratory Distress Syndrome 65 0.038
396
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.038
397
NRR002 Norrie Disease 64 0.038
398
BRC012 Brucellosis 64 0.038
399
P ADN016 Adenocarcinoma 64 0.038
400
MGK001 Megakaryocytic Leukemia 64 0.038
401
c PRC016 Pre-Eclampsia 63 0.038
402
ACT119 Acute Promyelocytic Leukemia 63 0.038
403
c ACT068 Acute Cystitis 63 0.038
404
CLT003 Colitis 62 0.038
405
P VSC011 Vasculitis 62 0.038
406
c NMN013 Niemann-Pick Disease, Type a 62 0.038
407
c PNS012 Paine Syndrome 61 0.038
408
WST001 West Syndrome 61 0.038
409
P ENC004 Encephalitis 61 0.038
410
c WLM018 Wilms Tumor 5 61 0.038
411
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.038
412
SZR001 Sezary's Disease 60 0.038
413
TRG002 Trigeminal Neuralgia 60 0.038
414
OST024 Osteoporosis-Pseudoglioma Syndrome 60 0.038
415
HYD002 Hydronephrosis 60 0.038
416
P GLY013 Glycogen Storage Disease 60 0.038
417
P CHR285 Chronic Myelomonocytic Leukemia 60 0.038
418
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.038
419
P NMN002 Niemann-Pick Disease 59 0.038
420
c SVR003 Severe Congenital Neutropenia 59 0.038
421
PPT005 Peptic Ulcer Disease 59 0.038
422
SRC027 Sarcoma, Synovial 58 0.038
423
RNL024 Renal Glucosuria 58 0.038
424
INC002 Inclusion Body Myositis 58 0.038
425
c NMN016 Niemann-Pick Disease, Type B 58 0.038
426
FBR047 Fibromyalgia 58 0.038
427
LYM027 Lymphopenia 58 0.038
428
P PRN023 Prion Disease 57 0.038
429
P PRV006 Pervasive Developmental Disorder 57 0.038
430
BLR008 Bilirubin Metabolic Disorder 57 0.038
431
CRT033 Corticobasal Degeneration 57 0.038
432
P MYS005 Myositis 56 0.038
433
c ESS001 Essential Tremor 56 0.038
434
SFT003 Soft Tissue Sarcoma 56 0.038
435
P HYP024 Hypoparathyroidism 56 0.038
436
EBS001 Ebstein Anomaly 55 0.038
437
FLR002 Filariasis 55 0.038
439
GNT003 Genital Herpes 54 0.038
440
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.038
441
LYM040 Lymphoblastic Lymphoma 54 0.038
442
P TCD001 Tic Disorder 53 0.038
443
PLS016 Plasma Cell Leukemia 53 0.038
444
P EMB005 Embryonal Rhabdomyosarcoma 53 0.038
445
FNG017 Fungal Infectious Disease 53 0.038
446
P FBR031 Febrile Seizures 53 0.038
447
STT041 Stuttering 52 0.038
448
P DDN001 Duodenal Ulcer 52 0.038
449
MRG003 Marginal Zone B-Cell Lymphoma 52 0.038
450
c ACT135 Acute Graft Versus Host Disease 52 0.038
451
THR004 Thrombocytosis 51 0.038
452
PLS009 Plasma Cell Neoplasm 51 0.038
453
LNG031 Lung Benign Neoplasm 51 0.038
454
HYP081 Hypolipoproteinemia 51 0.038
455
P OVR082 Overgrowth Syndrome 50 0.038
456
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.038
457
DYS073 Dysphagia 50 0.038
458
ATY042 Atypical Chronic Myeloid Leukemia 49 0.038
459
P CRN025 Corneal Dystrophy 49 0.038
460
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.038
461
c FLL041 Follicular Lymphoma 1 49 0.038
462
P CTN015 Cutaneous T Cell Lymphoma 49 0.038
463
LRN003 Learning Disability 49 0.038
464
SBS004 Substance Dependence 48 0.038
465
SCL003 Social Phobia 48 0.038
466
P RNV001 Renovascular Hypertension 48 0.038
467
SPL018 Splenomegaly 48 0.038
468
GRM005 Germ Cell Cancer 47 0.038
469
DRG003 Drug Dependence 47 0.038
470
NRN001 Neuroendocrine Carcinoma 47 0.038
471
RNL077 Renal Fibrosis 47 0.038
472
RTC005 Reticulosarcoma 47 0.038
473
PLS025 Plasmablastic Lymphoma 47 0.038
474
CNT033 Central Nervous System Cancer 47 0.038
475
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.038
476
c SCH079 Schizophrenia 1 46 0.038
477
GST010 Gestational Trophoblastic Neoplasm 46 0.038
478
c DRR009 Diarrhea 6 46 0.038
479
CNT025 Central Pontine Myelinolysis 46 0.038
480
c MLG068 Malignant Glioma 46 0.038
481
MXD026 Mixed Glioma 45 0.038
482
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.038
483
ACT003 Acute Kidney Tubular Necrosis 45 0.038
484
P PRD021 Periodic Paralysis 45 0.038
485
CRT015 Carotid Artery Occlusion 45 0.038
486
PTT037 Pituitary Tumors 44 0.038
487
CNN002 Cannabis Abuse 44 0.038
488
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.038
489
BNM001 Bone Marrow Cancer 43 0.038
490
NSP002 Nasopharyngitis 43 0.038
491
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.038
492
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.038
493
CHR286 Chronic Neutrophilic Leukemia 42 0.038
494
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.038
495
P MLG074 Malignant Mesenchymoma 40 0.038
496
HYP264 Hypertonia 38 0.038
497
FRS012 First-Degree Atrioventricular Block 38 0.038
498
TRP005 Trophoblastic Neoplasm 38 0.038
499
P PST059 Pustular Psoriasis 37 0.038
500
P CRB088 Cerebral Atrophy 37 0.038
501
GLM044 Glomerular Disease 37 0.038
502
c WLM011 Wilms Tumor 6 37 0.038
503
MYT011 Myotonia 34 0.038
504
c PRS136 Prostate Cancer, Hereditary, 6 33 0.038
505
c SCH085 Schizophrenia 2 33 0.038
506
INF013 Inferior Myocardial Infarction 33 0.038
507
c PRS130 Prostate Cancer, Hereditary, 8 32 0.038
508
ACD003 Acid Sphingomyelinase Deficiency 32 0.038
509
HYP645 Hyperthyroxinemia, Dystransthyretinemic 31 0.038
510
HYP029 Hyperthyroxinemia 31 0.038
511
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 0.038
512
MLT116 Multiple System Atrophy, Parkinsonian Type 30 0.038
513
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.038
514
MLT105 Multiple System Atrophy, Cerebellar Type 29 0.038
515
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.038
516
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.038
517
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.038
518
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.038
519
HDG004 Hodgkin's Granuloma 23 0.038
520
HDG006 Hodgkin's Paragranuloma 22 0.038
521
PLT016 Platelet Adenylate Cyclase Activity 16 0.038
522
c SYS001 Systemic Lupus Erythematosus 86 0.031
523
P ATX030 Ataxia-Telangiectasia 82 0.031
524
P RTT002 Rett Syndrome 80 0.031
525
P RHM011 Rheumatoid Arthritis 80 0.031
526
c DLT002 Dilated Cardiomyopathy 79 0.031
527
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.031
528
LPT014 Leptin Deficiency or Dysfunction 74 0.031
529
c HYP836 Hypercholesterolemia, Familial, 1 73 0.031
530
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.031
531
P AMY004 Amyloidosis 70 0.031
532
P OCL013 Oculodentodigital Dysplasia 69 0.031
533
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.031
534
CRP001 Carpal Tunnel Syndrome 67 0.031
535
P PLM037 Pulmonary Hypertension 67 0.031
536
P MLG056 Malignant Hyperthermia 67 0.031
537
GLL008 Gilles De La Tourette Syndrome 66 0.031
538
P MSC005 Muscular Dystrophy 66 0.031
539
P NRV007 Nervous System Disease 66 0.031
540
P AGM001 Agammaglobulinemia 65 0.031
541
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.031
542
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.031
543
CLF027 Cleft Palate, Isolated 64 0.031
544
P GLC113 Galactosemia I 64 0.031
545
c DPH024 Diaphragmatic Hernia, Congenital 63 0.031
546
PHL006 Phelan-Mcdermid Syndrome 62 0.031
547
ATM095 Autoimmune Disease 62 0.031
548
CRN239 Carnitine Deficiency, Systemic Primary 62 0.031
549
TXC005 Toxic Shock Syndrome 62 0.031
550
NTR005 Nutritional Deficiency Disease 62 0.031
551
PSR001 Psoriatic Arthritis 61 0.031
552
P LPS004 Lupus Erythematosus 61 0.031
553
P KDN017 Kidney Cancer 60 0.031
554
TTH002 Tooth Agenesis 60 0.031
555
c ACT027 Acute Pancreatitis 60 0.031
556
LNG099 Lung Disease 60 0.031
557
QFV001 Q Fever 60 0.031
558
ETN001 Eating Disorder 60 0.031
559
DRR014 Darier-White Disease 60 0.031
560
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.031
561
P SLP005 Sleep Disorder 59 0.031
562
PLM033 Pulmonary Embolism 59 0.031
563
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.031
564
BRN002 Bronchiolitis 59 0.031
565
c BNG091 Benign Chronic Pemphigus 58 0.031
566
ERY003 Erythema Multiforme 58 0.031
567
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.031
568
P OPT009 Optic Neuritis 57 0.031
569
IRN002 Iron Metabolism Disease 57 0.031
570
MNR012 Meniere Disease 57 0.031
571
P RHN004 Rhinitis 57 0.031
572
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.031
573
P FTL001 Fetal Alcohol Syndrome 57 0.031
574
VSC002 Vascular Dementia 57 0.031
575
SCH014 Schistosomiasis 57 0.031
576
P FBR017 Fibrosarcoma 56 0.031
577
P MLT074 Multiple Endocrine Neoplasia 56 0.031
578
P MTC069 Mitochondrial Disorders 56 0.031
579
SBC001 Subacute Sclerosing Panencephalitis 56 0.031
580
P PNM006 Pneumoconiosis 56 0.031
581
P GST044 Gastritis 56 0.031
582
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.031
583
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.031
584
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.031
585
P AML002 Amelogenesis Imperfecta 55 0.031
586
URN010 Urinary Tract Obstruction 55 0.031
587
PRP030 Purpura 54 0.031
588
P RST001 Restless Legs Syndrome 54 0.031
589
P INF037 Inflammatory Bowel Disease 54 0.031
590
P ART021 Arteriosclerosis 54 0.031
591
CLR030 Clear Cell Renal Cell Carcinoma 53 0.031
592
P RTN016 Retinal Degeneration 53 0.031
593
P HYP083 Hypopituitarism 53 0.031
594
MTN003 Motion Sickness 53 0.031
595
HYP063 Hypersplenism 53 0.031
596
P LRY019 Laryngitis 52 0.031
597
DMY004 Demyelinating Disease 52 0.031
598
P SML001 Small Cell Carcinoma 52 0.031
599
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.031
600
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.031
601
THR016 Thrombophlebitis 51 0.031
602
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.031
603
BRX001 Bruxism 50 0.031
604
SMT006 Somatoform Disorder 50 0.031
605
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.031
606
HYP017 Hypophosphatemia 50 0.031
607
ENT004 Enthesopathy 49 0.031
608
VCC001 Vaccinia 49 0.031
609
QDR001 Quadriplegia 48 0.031
610
HYP043 Hyperandrogenism 48 0.031
611
CCN001 Cocaine Dependence 48 0.031
612
ANT018 Anthracosis 48 0.031
613
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.031
614
HYP016 Hypochondriasis 47 0.031
615
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.031
616
SMT001 Somatization Disorder 46 0.031
617
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.031
618
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.031
619
PLY012 Polyhydramnios 46 0.031
620
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.031
621
RTR008 Root Resorption 45 0.031
622
c TRC022 Tricuspid Valve Insufficiency 45 0.031
623
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.031
624
TRT001 Teratocarcinoma 45 0.031
625
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.031
626
HPT004 Hepatic Coma 45 0.031
627
c ERL020 Early-Onset Schizophrenia 44 0.031
628
IRT001 Iritis 44 0.031
629
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.031
630
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.031
631
IDP033 Idiopathic Edema 44 0.031
632
AND001 Anodontia 43 0.031
633
URT037 Urethral Stricture 43 0.031
634
PNM013 Pneumococcal Meningitis 42 0.031
635
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.031
636
PCD001 Pica Disease 41 0.031
637
MRP001 Morphine Dependence 41 0.031
638
ANX004 Anoxia 40 0.031
639
IDP064 Idiopathic Neutropenia 40 0.031
640
TNP004 Tn Polyagglutination Syndrome 39 0.031
641
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.031
642
PTY002 Pityriasis Versicolor 38 0.031
643
KLP001 Kleptomania 38 0.031
644
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.031
645
c CHR098 Chronic Pyelonephritis 38 0.031
646
PNC016 Pancreatic Cholera 37 0.031
647
END028 Endemic Goiter 37 0.031
648
GGR001 Geographic Tongue 37 0.031
649
GRN055 Granular Corneal Dystrophy 36 0.031
650
FXD003 Fixed Drug Eruption 35 0.031
651
CHR178 Chromosomal Triplication 35 0.031
652
PST103 Postpartum Psychosis 32 0.031
653
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.031
654
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.031
655
EXN003 Exencephaly 31 0.031
656
CHL078 Childhood-Onset Schizophrenia 30 0.031
657
PST092 Posttransplant Acute Limbic Encephalitis 29 0.031
658
PRP015 Paraphilia Disorder 27 0.031
659
P OVR096 Overlap Myositis 27 0.031
660
EXF003 Exfoliative Dermatitis 27 0.031
661
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.031
662
AND017 Anodontia of Permanent Dentition 23 0.031
663
DPS001 Dipsogenic Diabetes Insipidus 23 0.031
664
CHL098 Childhood Myocerebrohepatopathy Spectrum 19 0.031
665
INT062 Interstitial Myocarditis 18 0.031
666
c TBR025 Tuberous Sclerosis 1 77 0.022
667
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.022
668
ULC004 Ulcerative Colitis 73 0.022
669
c SPN225 Spondyloarthropathy 1 73 0.022
670
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.022
671
P FML011 Familial Adenomatous Polyposis 72 0.022
672
c EXD008 Exudative Vitreoretinopathy 1 71 0.022
673
P HYP061 Hypertrophic Cardiomyopathy 70 0.022
674
P TBR001 Tuberous Sclerosis 70 0.022
675
P KRB001 Krabbe Disease 69 0.022
676
PLM001 Pulmonary Tuberculosis 69 0.022
677
SVR097 Severe Cutaneous Adverse Reaction 69 0.022
678
CRB037 Cerebral Palsy 69 0.022
679
P ANG001 Angelman Syndrome 69 0.022
680
P SYS005 Systemic Scleroderma 68 0.022
681
P MYC084 Mycobacterium Tuberculosis 1 68 0.022
682
RCK004 Rickets 68 0.022
683
PNC129 Pancreatic Adenocarcinoma 68 0.022
684
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.022
685
GST092 Gastroesophageal Reflux 67 0.022
686
P HPT021 Hepatitis 67 0.022
687
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.022
688
PRT010 Parathyroid Carcinoma 67 0.022
689
WLF001 Wolff-Parkinson-White Syndrome 66 0.022
690
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.022
691
P NSP012 Nasopharyngeal Carcinoma 66 0.022
692
P MCR115 Microvascular Complications of Diabetes 5 66 0.022
693
c MCR129 Microvascular Complications of Diabetes 1 66 0.022
694
ART001 Arterial Tortuosity Syndrome 66 0.022
695
P ATR011 Atrial Fibrillation 66 0.022
696
P DRM053 Dermatitis, Atopic 66 0.022
697
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.022
698
P CNJ013 Conjunctivitis 65 0.022
699
KRT019 Keratitis, Hereditary 65 0.022
700
P CLD001 Cleidocranial Dysplasia 65 0.022
701
IRR002 Irritable Bowel Syndrome 65 0.022
702
ATH013 Atherosclerosis Susceptibility 65 0.022
703
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.022
704
PRT036 Peritonitis 64 0.022
705
NRM005 Neuromuscular Disease 64 0.022
706
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.022
707
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.022
708
ART002 Arts Syndrome 64 0.022
709
c CNG006 Congenital Hypothyroidism 64 0.022
710
MSC007 Muscle Hypertrophy 64 0.022
711
P CRN015 Cornelia De Lange Syndrome 64 0.022
712
KRN002 Kearns-Sayre Syndrome 63 0.022
713
P HYP055 Hypoplastic Left Heart Syndrome 63 0.022
714
HYP780 Hypoadrenocorticism, Familial 63 0.022
715
HLT001 Holt-Oram Syndrome 63 0.022
716
c OPT053 Optic Atrophy 1 63 0.022
717
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.022
718
P SPN046 Spinal Muscular Atrophy 62 0.022
719
P TRC086 Trichohepatoenteric Syndrome 1 62 0.022
720
P ART023 Arthropathy 62 0.022
721
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.022
722
MSL001 Measles 62 0.022
723
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.022
724
FTT001 Fatty Liver Disease 61 0.022
725
P PNC044 Pancreatitis 61 0.022
726
RTN017 Retinal Detachment 61 0.022
727
VRL011 Viral Infectious Disease 61 0.022
728
HYP052 Hyperkalemic Periodic Paralysis 61 0.022
729
HRP004 Herpes Zoster 60 0.022
730
DPH001 Diphtheria 60 0.022
731
P VNT002 Ventricular Septal Defect 60 0.022
732
HPT019 Hepatic Encephalopathy 60 0.022
733
ACN002 Acanthosis Nigricans 60 0.022
734
SQM006 Squamous Cell Carcinoma 60 0.022
735
P SNS001 Sensorineural Hearing Loss 60 0.022
736
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.022
737
P CTR002 Cataract 60 0.022
738
ORL011 Oral Cancer 60 0.022
739
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.022
740
c HPT016 Hepatitis B 59 0.022
741
GRD007 Grade Iii Astrocytoma 59 0.022
742
P CYS018 Cystitis 59 0.022
743
ALX003 Alexander Disease 59 0.022
744
GNG013 Gingivitis 59 0.022
745
P GLL022 Guillain-Barre Syndrome 59 0.022
746
SPR004 Supravalvular Aortic Stenosis 58 0.022
747
CRD132 Cardiac Conduction Defect 58 0.022
748
SPT004 Septic Arthritis 58 0.022
749
HYP458 Hyper Ige Syndrome 58 0.022
750
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.022
751
ADR005 Adrenal Carcinoma 58 0.022
752
P URT039 Urticaria 58 0.022
753
P EHL001 Ehlers-Danlos Syndrome 58 0.022
754
EYD002 Eye Disease 58 0.022
755
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 0.022
756
P UVT001 Uveitis 57 0.022
757
BLM002 Bulimia Nervosa 57 0.022
758
c CRN139 Cornelia De Lange Syndrome 1 57 0.022
759
c ACT075 Acute Myocardial Infarction 57 0.022
760
THR024 Thrombosis 57 0.022
761
APH001 Aphthous Stomatitis 57 0.022
762
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.022
763
PNM008 Pneumothorax 56 0.022
764
c LSS005 Lissencephaly 1 56 0.022
765
CMR002 Coumarin Resistance 56 0.022
766
c INT072 Intestinal Pseudo-Obstruction 56 0.022
767
ISL001 Islet Cell Tumor 56 0.022
768
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.022
769
ANN002 Anencephaly 56 0.022
770
MTH009 Mouth Disease 56 0.022
771
GST050 Gastrointestinal System Disease 56 0.022
772
SLC006 Silicosis 56 0.022
773
BRN012 Bronchiolitis Obliterans 55 0.022
774
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.022
775
ADR008 Adrenal Adenoma 55 0.022
776
ICH001 Ichthyosis Vulgaris 55 0.022
777
P EXD001 Exudative Vitreoretinopathy 55 0.022
778
PLV003 Pelvic Inflammatory Disease 55 0.022
779
c BCT007 Bacterial Meningitis 55 0.022
780
P PTT006 Pituitary Adenoma 55 0.022
781
P ALP106 Alport Syndrome 1, X-Linked 55 0.022
782
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.022
783
P DRM007 Dermatitis Herpetiformis 55 0.022
784
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.022
785
HMP005 Hemiplegia 55 0.022
786
P LRY044 Larynx Cancer 55 0.022
787
P CYS039 Cystic Kidney Disease 54 0.022
788
P ICH004 Ichthyosis 54 0.022
789
BRN014 Bronchopneumonia 54 0.022
790
THR013 Thoracic Outlet Syndrome 54 0.022
791
PRC013 Pericarditis 54 0.022
792
DBT010 Diabetic Neuropathy 54 0.022
793
TRC062 Tricuspid Atresia 54 0.022
794
c PST005 Posterior Uveitis 54 0.022
795
NNL006 Non-Alcoholic Steatohepatitis 54 0.022
796
HYP691 Hypomelanosis of Ito 53 0.022
797
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.022
798
FRZ001 Frozen Shoulder 53 0.022
799
P MNC007 Monocytic Leukemia 53 0.022
800
P PTS002 Ptosis 53 0.022
801
NNT012 Neonatal Jaundice 53 0.022
802
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.022
803
GST023 Gastric Ulcer 53 0.022
804
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.022
805
OST011 Osteomalacia 52 0.022
806
P PRG013 Paraganglioma 52 0.022
807
PRS030 Persistent Fetal Circulation Syndrome 52 0.022
808
P HYP730 Hypogonadotropic Hypogonadism 52 0.022
809
ART140 Arteries, Anomalies of 52 0.022
810
P MSC003 Muscular Atrophy 52 0.022
811
ACT200 Acute Monoblastic Leukemia 52 0.022
812
ART074 Aortic Dissection 52 0.022
813
TLN003 Telangiectasis 52 0.022
814
NTR018 Neutrophilia, Hereditary 52 0.022
815
SPS003 Spastic Diplegia 51 0.022
816
MLT134 Multiple Pterygium Syndrome, Lethal Type 51 0.022
817
ILS001 Ileus 51 0.022
818
CLR109 Colorectal Adenocarcinoma 51 0.022
819
MGL001 Megaloblastic Anemia 51 0.022
820
P LCT001 Lactic Acidosis 51 0.022
821
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.022
822
P PRC012 Pericardial Effusion 51 0.022
823
CRV040 Cervix Carcinoma 51 0.022
824
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.022
825
P MMB011 Membranous Nephropathy 50 0.022
826
TMT002 Temtamy Preaxial Brachydactyly Syndrome 50 0.022
827
P FNC004 Fanconi Syndrome 50 0.022
828
P ECL001 Eclampsia 50 0.022
829
PST021 Postpartum Depression 50 0.022
830
THY125 Thyroid Gland Medullary Carcinoma 50 0.022
831
PLC008 Placenta Disease 50 0.022
832
TRY001 Trypanosomiasis 50 0.022
833
NTR046 Neutrophil Migration 50 0.022
834
ILT001 Ileitis 50 0.022
835
HRT011 Heart Septal Defect 50 0.022
836
WRN002 Wernicke-Korsakoff Syndrome 50 0.022
837
BTY001 Butyrylcholinesterase Deficiency 50 0.022
838
c PSR021 Psoriasis 14, Pustular 50 0.022
839
ONC007 Oncocytoma 49 0.022
840
URT001 Urethritis 49 0.022
841
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.022
842
LFT001 Left Bundle Branch Hemiblock 49 0.022
843
BKR002 Baker-Gordon Syndrome 49 0.022
844
MNN009 Meningoencephalitis 49 0.022
845
MTC005 Mitochondrial Metabolism Disease 49 0.022
846
c ACT150 Acute Adrenal Insufficiency 48 0.022
847
BRS064 Bursitis 48 0.022
848
ASP007 Aspiration Pneumonia 48 0.022
849
P CLR019 Color Blindness 48 0.022
850
END062 Endometrial Hyperplasia 48 0.022
851
HMP001 Hemopericardium 48 0.022
852
c MTR002 Mitral Valve Insufficiency 48 0.022
853
FBR032 Fibromuscular Dysplasia 48 0.022
854
c HYD064 Hydrocephalus, Congenital, 1 48 0.022
855
PLC007 Placental Abruption 48 0.022
856
c MLG069 Malignant Hypertension 47 0.022
857
CRC014 Carcinoid Tumors, Intestinal 47 0.022
858
ADN001 Adenosine Deaminase Deficiency 47 0.022
859
CRD001 Cardiac Tamponade 47 0.022
860
c MSC175 Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 1 47 0.022
861
WRN003 Wernicke Encephalopathy 47 0.022
862
LNG020 Lung Oat Cell Carcinoma 47 0.022
863
P CRC039 Coarctation of Aorta 47 0.022
864
CRD137 Cardiogenic Shock 47 0.022
865
P VTR007 Vitreoretinopathy 46 0.022
866
ANT039 Antisynthetase Syndrome 46 0.022
867
ATN005 Autonomic Dysfunction 46 0.022
868
c ACT076 Acute Myocarditis 46 0.022
869
RTN020 Retinal Vascular Disease 46 0.022
870
ALB002 Albinism 46 0.022
871
TTH006 Tooth Disease 46 0.022
872
MDS022 Mediastinitis 46 0.022
873
MTS001 Mutism 46 0.022
874
FCL012 Facial Paralysis 46 0.022
875
EXT033 Extrapulmonary Tuberculosis 46 0.022
876
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.022
877
CHR008 Choroiditis 46 0.022
878
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.022
879
URT010 Ureteral Obstruction 45 0.022
880
BLC012 Bile Acid Malabsorption, Primary 45 0.022
881
AGR002 Agoraphobia 45 0.022
882
MLN073 Melanosis, Neurocutaneous 45 0.022
883
ASP026 Asplenia, Isolated Congenital 44 0.022
884
c CHR579 Chiari Malformation Type Ii 44 0.022
885
c PCH010 Pachyonychia Congenita 3 44 0.022
886
DWR001 Dwarfism 44 0.022
887
FCH001 Fuchs' Endothelial Dystrophy 44 0.022
888
GNG003 Gingival Recession 44 0.022
889
PTY001 Pityriasis Rosea 44 0.022
890
P BLP003 Blepharospasm 44 0.022
891
CRB027 Cerebellar Disease 44 0.022
892
BCT021 Bacterial Sepsis 44 0.022
893
P CRN024 Corneal Disease 44 0.022
894
P MYG005 Myoglobinuria 44 0.022
895
CRB090 Cerebral Hypoxia 44 0.022
896
CLP005 Ciliopathy 43 0.022
897
MND023 Mend Syndrome 43 0.022
898
ADR041 Adrenal Cortical Adenoma 43 0.022
899
TST015 Testicular Disease 43 0.022
900
MDD018 Middle East Respiratory Syndrome 43 0.022
901
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.022
902
P CRN035 Cranial Nerve Palsy 42 0.022
903
ONC003 Oncogenic Osteomalacia 42 0.022
905
DNT014 Dental Pulp Disease 42 0.022
906
P PRT026 Parotitis 42 0.022
907
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.022
908
P RNG032 Ring Chromosome 42 0.022
909
FTL021 Fetal Macrosomia 42 0.022
910
PSD001 Pseudobulbar Palsy 42 0.022
911
OCL052 Ocular Dominance 42 0.022
912
P CHR342 Chiari Malformation 41 0.022
913
CLR033 Color Vision Deficiency 41 0.022
914
LMB024 Limbic Encephalitis 41 0.022
915
PRS063 Paresthesia 41 0.022
916
BSL009 Basal Ganglia Calcification 41 0.022
917
ACT088 Acute Insulin Response 41 0.022
918
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.022
919
P RRT020 Rare Tumor 41 0.022
920
c MCR112 Microvascular Complications of Diabetes 2 41 0.022
921
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 0.022
922
P FNC034 Fanconi Renotubular Syndrome 2 40 0.022
923
HYP540 Hypertension, Diastolic 40 0.022
924
PRM024 Primary Angle-Closure Glaucoma 40 0.022
925
c ACT004 Acute Diarrhea 39 0.022
926
FLL031 Follicular Adenoma 39 0.022
927
ENT001 Enterocele 39 0.022
928
c CHR682 Chronic Bilirubin Encephalopathy 39 0.022
929
SCR011 Scrapie 39 0.022
930
BRN036 Brain Stem Infarction 38 0.022
931
ANT019 Anterograde Amnesia 38 0.022
932
AMN006 Aminoaciduria 38 0.022
933
ALX002 Alexithymia 38 0.022
934
ENT003 Enterobiasis 38 0.022
935
OCL066 Oculogyric Crisis 38 0.022
936
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 38 0.022
937
AMP007 Amphetamine Abuse 37 0.022
938
CRN088 Craniorachischisis 37 0.022
939
UPP004 Upper Respiratory Tract Disease 37 0.022
940
c RTN050 Retinitis Pigmentosa 20 37 0.022
941
CHL013 Cholecystolithiasis 37 0.022
942
SCR003 Secretory Diarrhea 37 0.022
943
P PHC019 Pheochromocytoma-Paraganglioma 36 0.022
944
MYC017 Mycobacterium Kansasii 36 0.022
946
c DRM040 Dermatitis Herpetiformis, Familial 35 0.022
947
PLM011 Plummer's Disease 35 0.022
948
BRK012 Broken Heart Syndrome 35 0.022
949
SCN049 Second-Degree Atrioventricular Block 35 0.022
950
NRD001 Neurodermatitis 35 0.022
951
ATX010 Ataxia Neuropathy Spectrum 34 0.022
952
NNT024 Neonatal Stroke 34 0.022
953
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.022
954
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.022
955
MTH086 Methotrexate Toxicity 33 0.022
956
PRX009 Paroxysmal Hemicrania 33 0.022
957
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.022
958
ACT064 Acute Necrotizing Encephalitis 33 0.022
959
c RCR002 Recurrent Hypersomnia 33 0.022
960
HND015 Hand Skill, Relative 33 0.022
961
TTH030 Teeth, Supernumerary 33 0.022
962
SGT001 Sagittal Sinus Thrombosis 32 0.022
963
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.022
964
NNT010 Nontoxic Goiter 32 0.022
965
c BLD140 Blood Group, I System 32 0.022
966
NRN002 Neuronitis 32 0.022
967
END034 Endocrine Exophthalmos 32 0.022
968
IDM001 Ideomotor Apraxia 32 0.022
969
THY001 Thyroid Crisis 31 0.022
970
LYM157 Lymph Node Carcinoma 31 0.022
971
c PSD093 Pseudohypoaldosteronism, Type Iid 31 0.022
972
P RNL115 Renal Tubular Acidosis, Proximal 31 0.022
973
PLY150 Polykaryocytosis Inducer 31 0.022
974
ISL119 Isolated Optic Neuritis 30 0.022
975
ERY066 Erythema Multiforme Major 30 0.022
976
CRT069 Cortical Malformations, Occipital 30 0.022
977
FNT004 Fainting 30 0.022
978
GLN006 Glandular Cystitis 30 0.022
979
INT042 Internuclear Ophthalmoplegia 30 0.022
980
ACT228 Acute Radiation Syndrome 29 0.022
981
BRN008 Brain Compression 29 0.022
982
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.022
983
SNL009 Senile Plaque Formation 28 0.022
984
ATH004 Athetosis 28 0.022
985
HYP047 Hypertropia 27 0.022
986
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.022
987
DMN026 Dementia Pugilistica 27 0.022
988
MLL004 Mallory-Weiss Syndrome 27 0.022
989
GNT046 Genetic Epilepsy with Febrile Seizures Plus 27 0.022
990
c RNG016 Ring Chromosome 20 27 0.022
991
ACT038 Acute Retrobulbar Neuritis 27 0.022
992
DFF015 Diffuse Glomerulonephritis 26 0.022
993
DFF010 Diffuse Alopecia Areata 26 0.022
994
STR033 Storm Syndrome 26 0.022
995
ETH012 Ethylene Glycol Poisoning 26 0.022
996
HRY002 Hairy Tongue 26 0.022
997
HRP008 Herpes Simiae 25 0.022
998
FTS001 Fetishism 25 0.022
999
TRN006 Transvestism 24 0.022
1000
HYP144 Hyperacusis 23 0.022
1001
FCL074 Facial Spasm 23 0.022
1002
LSS039 Lissencephaly 6 with Microcephaly 23 0.022
1003
SDD004 Sudden Arrhythmia Death Syndrome 22 0.022
1004
CHF001 Chief Cell Adenoma 22 0.022
1005
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 21 0.022
1006
DMN012 Dementia - Subcortical 21 0.022
1007
HYP188 Hypnic Headache 20 0.022
1008
P ACT236 Acute Motor and Sensory Axonal Neuropathy 19 0.022
1009
OBN001 Ouabain Resistance 18 0.022
1010
APR010 Apraxia of Eyelid Opening 18 0.022
1011
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.022
1012
BLD137 Blood Group--Ahonen 16 0.022
1013
MTC196 Mitochondrial Disease with Epilepsy 14 0.022
1014
ORG003 Organic Mood Syndrome 14 0.022
1015
PRM160 Premature Closure of the Arterial Duct 6 0.022
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