Search results for zinc acetate

1423 hits were found for zinc acetate

# Family MCID Name MIFTS Score
1
P DRR001 Diarrhea 55 0.323
2
P PRS040 Prostate Cancer 97 0.316
3
IRN002 Iron Metabolism Disease 58 0.246
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.225
5
P NRF023 Neurofibromatosis, Type Ii 77 0.225
6
c PRS136 Prostate Cancer, Hereditary, 6 34 0.224
7
c PRS130 Prostate Cancer, Hereditary, 8 33 0.224
8
ACR005 Acrodermatitis 35 0.212
9
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 54 0.210
10
48X005 48,xyyy 37 0.202
11
ENT007 Enteropathica 27 0.202
12
P BRS047 Breast Cancer 99 0.199
13
DRM006 Dermatitis 63 0.199
14
P MLT020 Multiple Sclerosis 73 0.198
15
P ADN016 Adenocarcinoma 65 0.196
16
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.196
17
DFC004 Deficiency Anemia 77 0.192
18
HMN044 Human Immunodeficiency Virus Type 1 73 0.189
19
LVR012 Liver Cirrhosis 67 0.189
20
P ALP008 Alopecia 58 0.188
21
DWN001 Down Syndrome 70 0.188
22
P KDN018 Kidney Disease 73 0.185
23
P END044 Endometriosis 63 0.182
25
P INF032 Infertility 60 0.181
26
CLT003 Colitis 63 0.180
27
P SZR006 Seizure Disorder 59 0.178
28
LMY002 Leiomyoma 52 0.173
29
P DBT009 Diabetes Mellitus 66 0.172
30
c RHB024 Rhabdomyosarcoma 2 64 0.171
31
GST023 Gastric Ulcer 53 0.167
32
CRV035 Cervical Cancer 77 0.167
33
VSL002 Visual Epilepsy 58 0.165
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.164
35
END057 Endometrial Cancer 74 0.163
36
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.161
37
P LTR001 Lateral Sclerosis 56 0.161
38
HYP066 Hyperglycemia 63 0.160
39
ALL026 Allergic Hypersensitivity Disease 65 0.158
40
P LVR013 Liver Disease 71 0.157
41
CMM005 Common Cold 57 0.156
42
NTR005 Nutritional Deficiency Disease 61 0.155
43
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.155
44
HLX001 Helix Syndrome 46 0.154
45
P CTR002 Cataract 62 0.153
46
P INF037 Inflammatory Bowel Disease 57 0.152
47
CYT002 Cytokine Deficiency 46 0.148
48
P CLR023 Colorectal Cancer 100 0.146
49
CHL079 Children's Interstitial Lung Disease 27 0.145
50
P ALZ034 Alzheimer Disease 90 0.145
51
HYP080 Hypogonadism 51 0.145
52
P PLY011 Polycystic Ovary Syndrome 58 0.145
53
KRT002 Keratomalacia 47 0.144
54
P LKM002 Leukemia 69 0.144
55
MYF001 Myofibroma 40 0.144
56
IMM167 Immune Deficiency Disease 79 0.144
57
P PNM007 Pneumonia 71 0.143
58
HYP064 Hypogonadotropism 40 0.142
59
ULC004 Ulcerative Colitis 75 0.141
60
P OST002 Osteoporosis 79 0.140
61
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.139
62
PRS045 Prostatic Hypertrophy 55 0.139
63
ATX019 Ataxia with Vitamin E Deficiency 46 0.138
64
AMN001 Amenorrhea 54 0.138
65
ACQ007 Acquired Immunodeficiency Syndrome 61 0.137
66
HYP056 Hypoglycemia 68 0.137
67
HRW001 Hair Whorl 36 0.136
68
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.134
69
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.134
70
ADN018 Adenoma 60 0.134
71
BNR002 Bone Resorption Disease 51 0.134
72
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.134
73
P EPL164 Epilepsy 73 0.134
74
INS024 Insulin-Like Growth Factor I 79 0.133
75
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.132
76
P PSR002 Psoriasis 63 0.132
77
END030 End Stage Renal Failure 60 0.132
78
PST011 Pustulosis of Palm and Sole 51 0.131
79
c ACT004 Acute Diarrhea 38 0.129
80
P HPT023 Hepatocellular Carcinoma 99 0.129
81
c CHR684 Chronic Kidney Disease 68 0.128
82
P PRC019 Precocious Puberty 48 0.128
83
IRN001 Iron Deficiency Anemia 59 0.128
84
P NTR004 Neutropenia 64 0.128
85
47X002 47,xyy 49 0.128
86
ATH013 Atherosclerosis Susceptibility 68 0.126
87
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.126
88
ATM095 Autoimmune Disease 62 0.125
89
P RHM011 Rheumatoid Arthritis 82 0.124
90
P NRB010 Neuroblastoma 1 66 0.124
91
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.123
92
CRH001 Crohn's Disease 75 0.122
93
ISC004 Ischemia 62 0.122
94
P ENC018 Encephalopathy 64 0.121
95
c PCH010 Pachyonychia Congenita 3 43 0.121
96
ALL014 Allergic Encephalomyelitis 40 0.120
97
ALC007 Alcohol Dependence 68 0.120
98
SKN016 Skin Disease 64 0.120
99
P OVR042 Ovarian Cancer 89 0.120
100
P THL005 Thalassemia 62 0.119
101
P TRN020 Turner Syndrome 66 0.119
102
P LYM031 Lymphocytic Leukemia 56 0.119
103
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.119
104
c HYP595 Hypertension, Essential 87 0.118
105
CYS001 Cystic Fibrosis 84 0.118
106
MTB004 Metabolic Acidosis 48 0.118
107
DPR016 Depression 64 0.118
108
P HYP086 Hypothyroidism 70 0.118
109
P EXN002 Exanthem 58 0.118
110
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.118
111
PRS021 Prostatic Adenoma 52 0.117
112
P HRT032 Heart Disease 78 0.116
113
P NRP001 Neuropathy 57 0.116
114
P LNG032 Lung Cancer 99 0.116
115
P VSC007 Vascular Disease 65 0.115
116
P CRN018 Coronary Artery Anomaly 67 0.115
117
P LYM118 Lymphoma 70 0.115
118
c HYP836 Hypercholesterolemia, Familial, 1 74 0.115
119
P HRP006 Herpes Simplex 66 0.114
120
P MYC007 Myocardial Infarction 74 0.113
121
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.113
122
P SCK005 Sickle Cell Disease 53 0.113
123
WLS001 Wilson Disease 69 0.113
124
LPD008 Lipid Metabolism Disorder 64 0.113
125
ESP021 Esophageal Cancer 90 0.113
126
CNT047 Contact Dermatitis 58 0.112
127
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.112
128
ADL002 Adult Syndrome 62 0.112
129
LMY014 Leiomyoma, Uterine 57 0.111
130
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.110
131
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.110
132
c ACT071 Acute Kidney Failure 60 0.110
133
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.110
134
GLL048 Glial Tumor 48 0.110
135
c ACT210 Acute Respiratory Distress Syndrome 59 0.110
136
AGN016 Aging 58 0.110
137
PRS129 Prostatic Hyperplasia, Benign 49 0.110
138
P GLM045 Glioma 64 0.109
139
P CRN300 Coronary Heart Disease 1 59 0.109
140
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.108
141
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.108
142
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.108
143
HYP005 Hypokalemia 55 0.108
144
GLB002 Glioblastoma 74 0.107
145
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.107
146
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.107
147
GLB015 Glioblastoma Multiforme 60 0.106
148
CHL014 Cholera 58 0.106
149
P MYL006 Myeloid Leukemia 61 0.105
150
P PNC035 Pancreatic Cancer 86 0.105
151
MTH071 Methane Production 26 0.105
152
P ART022 Arthritis 71 0.105
153
MNT002 Mental Depression 60 0.104
154
P GST053 Gastric Cancer 85 0.102
155
GLC003 Glucose Intolerance 55 0.102
156
URM002 Uremia 50 0.102
157
CNG034 Congestive Heart Failure 69 0.102
158
OST012 Osteoarthritis 80 0.102
159
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.102
160
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.102
161
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.102
162
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.102
163
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.102
164
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.102
165
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.102
166
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.102
167
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.102
168
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.102
169
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.102
170
TRM010 Traumatic Brain Injury 54 0.101
171
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.100
172
CRV045 Cervical Intraepithelial Neoplasia 41 0.100
173
PPL052 Papillomatosis, Confluent and Reticulated 34 0.099
174
HPT004 Hepatic Coma 42 0.099
175
LNG099 Lung Disease 62 0.099
176
HYP266 Hypoxia 58 0.099
177
BCT022 Bacterial Infectious Disease 57 0.099
178
HPT019 Hepatic Encephalopathy 60 0.098
179
END062 Endometrial Hyperplasia 49 0.098
180
BRN071 Brain Injury 51 0.098
181
RCK004 Rickets 70 0.097
182
LSH001 Leishmaniasis 64 0.097
183
P KLZ004 Kala-Azar 1 43 0.097
184
P CLC063 Celiac Disease 1 66 0.097
185
P DRM053 Dermatitis, Atopic 68 0.097
186
MYM001 Myoma 52 0.097
187
P RTN024 Retinoblastoma 74 0.096
188
c FML008 Familial Retinoblastoma 46 0.096
189
c LKM061 Leukemia, Acute Myeloid 84 0.096
190
P MLN007 Male Infertility 57 0.096
191
c MCR120 Microvascular Complications of Diabetes 7 48 0.096
192
PPT005 Peptic Ulcer Disease 60 0.095
193
P BCL017 B-Cell Lymphoma 61 0.095
194
SCK003 Sickle Cell Anemia 74 0.095
195
ART140 Arteries, Anomalies of 60 0.095
196
c PRC016 Pre-Eclampsia 63 0.094
197
DYS015 Dysentery 45 0.094
198
P PNC044 Pancreatitis 61 0.094
199
INS001 Insulinoma 60 0.093
200
P DMN002 Dementia 68 0.093
201
P LKM062 Leukemia, Acute Lymphoblastic 68 0.093
202
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.093
203
SQM006 Squamous Cell Carcinoma 60 0.093
204
SPP011 Suppression of Tumorigenicity 12 61 0.093
205
DNT012 Dental Caries 52 0.092
206
MYL069 Myeloma, Multiple 85 0.092
207
LYM027 Lymphopenia 58 0.092
208
EYD002 Eye Disease 59 0.092
209
FTT001 Fatty Liver Disease 63 0.091
210
P HPT021 Hepatitis 69 0.090
211
AST005 Asthma 80 0.090
212
ANR007 Anorexia Nervosa 64 0.089
213
AZS001 Azoospermia 51 0.089
214
c ACT075 Acute Myocardial Infarction 59 0.088
215
P PRD008 Periodontitis 66 0.088
216
P PRP019 Peripheral Nervous System Disease 64 0.088
217
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.088
218
ATS010 Autosomal Recessive Disease 49 0.087
219
GST045 Gastroenteritis 60 0.087
220
TXC005 Toxic Shock Syndrome 63 0.087
221
PPL022 Papilloma 56 0.087
222
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.087
223
HYP081 Hypolipoproteinemia 51 0.087
224
TTN003 Tetanus 62 0.087
225
P HYP076 Hyperthyroidism 55 0.087
226
c BTT014 Beta-Thalassemia 73 0.086
227
P CND004 Candidiasis 61 0.086
228
P ALP009 Alopecia Areata 61 0.086
229
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.085
230
OST159 Osteogenic Sarcoma 67 0.085
231
P ATS364 Autism 68 0.085
232
P MCR115 Microvascular Complications of Diabetes 5 67 0.085
233
IMP005 Impotence 53 0.085
234
MDD011 Mood Disorder 62 0.085
235
STM007 Stomatitis 51 0.085
236
HYP043 Hyperandrogenism 48 0.084
237
c HPT001 Hepatitis C 62 0.084
238
MLN008 Melanoma 68 0.084
239
P LPR021 Leprosy 3 67 0.083
240
HNS001 Hansen's Disease 35 0.083
241
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.083
242
BRR014 Barrett Esophagus 67 0.083
243
ARG004 Argyria 28 0.083
244
ORL011 Oral Cancer 62 0.083
245
c SML038 Small Cell Cancer of the Lung 67 0.083
246
SQM002 Squamous Cell Papilloma 49 0.083
247
MCS002 Mucositis 56 0.083
248
ACT119 Acute Promyelocytic Leukemia 63 0.083
249
c ACT027 Acute Pancreatitis 60 0.083
250
CHL068 Cholestasis 61 0.082
251
P SKN015 Skin Carcinoma 67 0.082
252
P SBR004 Seborrheic Dermatitis 41 0.082
253
GST033 Gestational Diabetes 58 0.081
254
NRL016 Neural Tube Defects 83 0.081
255
PLM001 Pulmonary Tuberculosis 72 0.081
256
P RHN004 Rhinitis 59 0.081
257
SXL003 Sexual Disorder 49 0.081
258
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.081
259
GNG013 Gingivitis 60 0.081
260
HYP025 Hyperphosphatemia 47 0.081
261
MLR004 Malaria 82 0.080
262
BND020 Bone Disease 60 0.080
263
PRT038 Protein-Energy Malnutrition 56 0.080
264
P GST044 Gastritis 58 0.080
265
P ART021 Arteriosclerosis 56 0.080
266
HMS001 Hemosiderosis 54 0.080
267
SPP010 Suppressor of Tumorigenicity 3 54 0.080
268
ANX010 Anxiety 75 0.079
269
P ADL010 Adult Respiratory Distress Syndrome 61 0.079
270
P KDN017 Kidney Cancer 60 0.079
271
ACR007 Acromegaly 70 0.079
272
GLS018 Glass Syndrome 51 0.079
273
CNS004 Constipation 59 0.079
274
P DDN001 Duodenal Ulcer 50 0.079
275
c FML035 Familial Hyperlipidemia 56 0.078
276
P NPH012 Nephrotic Syndrome 65 0.078
277
c PNS012 Paine Syndrome 61 0.078
278
RHM027 Rheumatic Disease 56 0.077
279
HYP060 Hyperinsulinism 55 0.077
280
P HML002 Hemolytic Anemia 64 0.077
281
P ASP006 Aspergillosis 67 0.077
282
P INS002 in Situ Carcinoma 55 0.077
283
P RRH023 Rare Hereditary Hemochromatosis 41 0.077
284
c HPT073 Hepatitis C Virus 74 0.077
285
CLN015 Colon Adenocarcinoma 65 0.077
286
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.077
287
THR024 Thrombosis 58 0.077
288
ALL010 Allergic Contact Dermatitis 56 0.077
289
c MCR113 Microvascular Complications of Diabetes 3 55 0.077
290
END041 Endometrial Adenocarcinoma 64 0.077
291
PLM010 Pulmonary Edema 56 0.076
292
CRB004 Cerebral Artery Occlusion 38 0.076
293
P BLD134 Bladder Cancer 79 0.076
294
P HYP069 Hyperparathyroidism 64 0.075
295
49X002 49,xxxxy Syndrome 39 0.075
296
c HPT016 Hepatitis B 63 0.075
297
c WLM018 Wilms Tumor 5 63 0.075
298
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.075
299
P RTN018 Retinal Disease 53 0.075
300
c HYP272 Hypercholesterolemia, Familial, 3 44 0.075
301
P NGH001 Night Blindness 48 0.075
302
c MCR130 Microvascular Complications of Diabetes 6 42 0.075
303
c MCR133 Microvascular Complications of Diabetes 4 42 0.075
304
BRK010 Burkitt Lymphoma 68 0.075
305
LYM133 Lymphoma, Hodgkin, Classic 70 0.074
306
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.074
307
GST050 Gastrointestinal System Disease 57 0.074
308
c ACT068 Acute Cystitis 63 0.074
309
P TRM003 Tremor 55 0.074
310
LYM019 Lymphosarcoma 48 0.074
311
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.074
312
HVY002 Heavy Metal Poisoning 23 0.073
313
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.073
314
OVR094 Ovarian Epithelial Cancer 39 0.073
315
PRS047 Prostatitis 57 0.073
316
c ATR087 Atrial Standstill 1 76 0.073
317
P ALC033 Alcohol Use Disorder 58 0.073
318
TST023 Testotoxicosis 35 0.073
319
c FML157 Familial Male-Limited Precocious Puberty 33 0.073
320
SPN186 Spinal Cord Injury 63 0.073
321
c LKM071 Leukemia, Chronic Lymphocytic 81 0.072
322
P CNJ013 Conjunctivitis 67 0.072
323
c MCR129 Microvascular Complications of Diabetes 1 67 0.072
324
P THY032 Thyroiditis 52 0.072
325
P INT143 Interstitial Cystitis 62 0.071
326
c LKM004 Leukemia, B-Cell, Chronic 35 0.071
327
P MYP004 Myopathy 63 0.071
328
c SYS001 Systemic Lupus Erythematosus 88 0.071
329
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.071
330
OCL069 Ocular Motor Apraxia 53 0.070
331
P MNN013 Meningitis 67 0.070
332
P NSP012 Nasopharyngeal Carcinoma 67 0.070
333
PRT036 Peritonitis 66 0.070
334
HYP781 Hypoascorbemia 48 0.070
335
P CHR345 Chronic Pain 52 0.070
336
KRT009 Keratosis 52 0.070
337
MYL009 Myelodysplastic Syndrome 72 0.070
338
P LPS004 Lupus Erythematosus 62 0.070
339
PLM017 Pulmonary Alveolar Microlithiasis 54 0.070
340
ALL003 Allergic Rhinitis 69 0.069
341
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.069
342
c LRG017 Large Intestine Cancer 53 0.069
343
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.069
344
OTT002 Otitis Media 71 0.069
345
BRN024 Bronchitis 70 0.069
346
P BPL003 Bipolar Disorder 59 0.069
347
c MJR024 Major Affective Disorder 9 42 0.069
348
c MJR022 Major Affective Disorder 8 39 0.069
349
P BRS044 Breast Adenocarcinoma 59 0.069
350
SVR004 Severe Combined Immunodeficiency 74 0.069
351
P HYP750 Hypertriglyceridemia, Familial 62 0.069
352
c ACT073 Acute Leukemia 59 0.069
353
P MSC005 Muscular Dystrophy 68 0.069
354
ETN001 Eating Disorder 61 0.069
355
PST092 Posttransplant Acute Limbic Encephalitis 29 0.069
356
P SLP006 Sleep Apnea 71 0.069
357
c FNC043 Fanconi Anemia, Complementation Group E 64 0.069
358
c THR092 Thrombophilia Due to Thrombin Defect 74 0.069
359
P PHC003 Pheochromocytoma 71 0.069
360
ADR040 Adrenal Gland Pheochromocytoma 51 0.069
361
CNN003 Conn's Syndrome 78 0.068
362
c PLY105 Polycystic Ovary Syndrome 1 38 0.068
363
BLR008 Bilirubin Metabolic Disorder 58 0.068
364
c ATS007 Autism Spectrum Disorder 69 0.068
365
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.068
366
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.068
367
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.068
368
PRT037 Pertussis 66 0.068
369
P OPT006 Optic Nerve Disease 59 0.067
370
DWR001 Dwarfism 45 0.067
371
P MJR001 Major Depressive Disorder 69 0.067
372
P SCH015 Schizophrenia 76 0.067
373
P PLM037 Pulmonary Hypertension 69 0.067
374
SRC014 Sarcoma 67 0.067
375
P GLM007 Glomerulonephritis 58 0.067
376
c PRM038 Primary Agammaglobulinemia 45 0.067
377
KHL003 Kohlschutter-Tonz Syndrome 63 0.067
378
MST005 Mastitis 55 0.067
379
P MNC007 Monocytic Leukemia 52 0.067
380
RTN023 Retinitis 46 0.067
381
NRR001 Neuroretinitis 46 0.067
382
CHR178 Chromosomal Triplication 36 0.067
383
OLG001 Oligospermia 44 0.067
384
PRM020 Premenstrual Tension 48 0.066
385
PTT037 Pituitary Tumors 47 0.066
386
P FBR017 Fibrosarcoma 57 0.066
387
P MTR014 Motor Neuron Disease 66 0.066
388
BRN004 Brain Edema 57 0.066
389
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.066
390
KHN001 Kuhnt-Junius Degeneration 45 0.066
391
P UVT001 Uveitis 58 0.065
392
SPN035 Spindle Cell Sarcoma 57 0.065
393
P LNG064 Lung Cancer Susceptibility 3 79 0.065
394
PLC008 Placenta Disease 51 0.065
395
c SCN007 Secondary Hyperparathyroidism 52 0.065
396
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.065
397
GST092 Gastroesophageal Reflux 68 0.065
398
c ACT134 Acute Liver Failure 53 0.065
399
PRP027 Peripheral Vascular Disease 72 0.064
400
P TCL004 T-Cell Leukemia 48 0.064
401
c LKM005 Leukemia, T-Cell, Chronic 35 0.064
402
ERY051 Erythroleukemia, Familial 58 0.064
403
P ATR011 Atrial Fibrillation 67 0.063
404
ENT004 Enthesopathy 46 0.063
405
ART016 Aortic Aneurysm 71 0.063
406
c VRL010 Viral Hepatitis 56 0.063
407
P HDC001 Headache 59 0.063
408
ANV001 Anovulation 47 0.063
409
P AMY004 Amyloidosis 71 0.063
410
PNC129 Pancreatic Adenocarcinoma 69 0.063
411
THY029 Thyroid Carcinoma 62 0.063
412
LNG031 Lung Benign Neoplasm 52 0.063
413
c MLG068 Malignant Glioma 46 0.062
414
ANR040 Aneurysm 60 0.062
415
P MYC084 Mycobacterium Tuberculosis 1 69 0.062
416
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.062
418
P CHR012 Chronic Granulomatous Disease 69 0.061
419
OVR029 Ovarian Hyperstimulation Syndrome 63 0.061
420
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.061
421
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.061
422
TLN003 Telangiectasis 53 0.061
423
P HYP098 Hypereosinophilic Syndrome 67 0.061
424
GTR002 Goiter 54 0.061
425
KWS001 Kwashiorkor 46 0.061
426
CLF027 Cleft Palate, Isolated 67 0.061
427
CHG001 Chagas Disease 66 0.061
428
P ECL001 Eclampsia 53 0.061
429
HMP009 Haemophilus Influenzae 46 0.061
430
c NGH026 Night Blindness, Congenital Stationary, Type 1a 46 0.060
431
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.060
432
c MNN043 Meningioma, Familial 74 0.060
433
MNN042 Meningioma, Radiation-Induced 64 0.060
434
P OTT001 Otitis Externa 41 0.060
435
SPN021 Spinal Meningioma 40 0.060
436
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.060
437
SCR001 Secretory Meningioma 38 0.060
438
ORL005 Oral Candidiasis 56 0.060
439
PNG002 Pain Agnosia 52 0.060
440
P OPN001 Open-Angle Glaucoma 50 0.060
441
P RSP003 Respiratory Failure 75 0.060
442
P ESP024 Esophagitis 62 0.060
443
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.060
444
P HNT016 Huntington Disease 72 0.060
445
HMG005 Hemoglobinopathy 57 0.060
446
FCT007 Factor Vii Deficiency 65 0.060
447
PLR008 Pleurisy 50 0.060
448
c MCR112 Microvascular Complications of Diabetes 2 42 0.060
449
P PRP029 Porphyria 58 0.059
450
P FTL001 Fetal Alcohol Syndrome 56 0.059
451
SCH014 Schistosomiasis 57 0.059
452
ORL015 Oral Squamous Cell Carcinoma 44 0.059
453
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.059
454
PLY150 Polykaryocytosis Inducer 31 0.059
455
P MSC003 Muscular Atrophy 52 0.059
456
P THR014 Thrombocytopenia 67 0.059
457
CRB039 Cerebrovascular Disease 71 0.059
458
DMY004 Demyelinating Disease 54 0.059
459
OVR082 Overgrowth Syndrome 51 0.059
460
GT001 Gout 63 0.058
461
PLS011 Plasmacytoma 57 0.058
462
PST021 Postpartum Depression 51 0.058
464
BRS051 Breast Disease 59 0.058
465
CHR100 Chronic Ulcer of Skin 53 0.058
466
P RTN008 Retinitis Pigmentosa 77 0.058
467
c WLM013 Wilms Tumor 1 69 0.058
468
P CRD119 Cardiac Arrest 71 0.058
469
P SYS005 Systemic Scleroderma 68 0.058
470
DSS008 Disease of Mental Health 66 0.058
471
P BNG032 Benign Mesothelioma 47 0.058
472
ENT011 Enterocolitis 51 0.058
473
P PRK057 Parkinson Disease, Late-Onset 77 0.058
474
c DWL002 Dowling-Degos Disease 1 59 0.058
475
HDN002 Head Injury 47 0.058
476
STR067 Stroke, Ischemic 82 0.058
477
P URT039 Urticaria 61 0.058
478
CMR002 Coumarin Resistance 56 0.058
479
HMT018 Hematopoietic Stem Cell Transplantation 54 0.058
480
ALC009 Alcoholic Liver Cirrhosis 53 0.057
481
MCL006 Macular Retinal Edema 52 0.057
482
P INT068 Intestinal Disease 56 0.057
483
GLC036 Glucagonoma 45 0.057
484
LPT014 Leptin Deficiency or Dysfunction 72 0.057
485
P VSC011 Vasculitis 64 0.057
486
PCD001 Pica Disease 33 0.057
487
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.057
488
APH001 Aphthous Stomatitis 56 0.057
489
STT009 Sutton Disease 2 31 0.057
490
STT001 Status Epilepticus 61 0.056
491
ANG054 Angina Pectoris 66 0.056
492
VRL011 Viral Infectious Disease 62 0.056
493
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 58 0.056
494
P PRN023 Prion Disease 57 0.056
495
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.056
496
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.056
497
HLC007 Helicobacter Pylori Infection 61 0.056
498
P GRV001 Graves' Disease 57 0.056
499
P LCH002 Lichen Planus 55 0.056
500
IRR002 Irritable Bowel Syndrome 65 0.056
501
PPL001 Papillary Adenoma 42 0.056
502
RTN017 Retinal Detachment 62 0.056
503
P PYL005 Pyelonephritis 58 0.056
504
CHC001 Chickenpox 53 0.056
505
DYS014 Dyspepsia 51 0.056
506
c LKM063 Leukemia, Chronic Myeloid 74 0.056
507
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 57 0.055
508
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.055
509
BRN028 Brain Cancer 75 0.055
510
KRT019 Keratitis, Hereditary 69 0.055
511
WTH001 Withdrawal Disorder 47 0.055
512
SBC016 Subacute Delirium 43 0.055
513
P CNR004 Cone-Rod Dystrophy 2 72 0.055
514
c DLT002 Dilated Cardiomyopathy 81 0.055
515
c HPT003 Hepatitis a 60 0.054
516
NWB001 Newborn Respiratory Distress Syndrome 58 0.054
517
P ALP061 Alopecia, Androgenetic, 1 51 0.054
518
HYP020 Hyperprolactinemia 62 0.054
519
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.054
520
CHL065 Cholangiocarcinoma 68 0.054
521
INT079 Intrahepatic Cholangiocarcinoma 54 0.054
522
AND014 Androgenic Alopecia 41 0.054
523
P OVR049 Ovarian Disease 55 0.054
524
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.054
525
ACT011 Acute Contagious Conjunctivitis 35 0.054
526
c ALP101 Alpha-Thalassemia 63 0.054
527
THY030 Thyroid Gland Disease 53 0.054
528
P SRC025 Sarcoidosis 1 72 0.054
529
P GRF003 Graft-Versus-Host Disease 71 0.054
530
PSY004 Psychotic Disorder 68 0.054
531
PLM033 Pulmonary Embolism 60 0.054
532
c PSR017 Psoriasis 2 55 0.054
533
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.054
534
P OVR046 Ovarian Cyst 50 0.054
535
P HMR005 Hemorrhoid 47 0.054
536
TRP009 Triple X Syndrome 42 0.054
537
PRN019 Perinatal Necrotizing Enterocolitis 55 0.053
538
P ENC004 Encephalitis 64 0.053
539
INT002 Intermittent Claudication 60 0.053
540
c PRM196 Premature Ovarian Failure 1 70 0.053
541
P GLM040 Glioma Susceptibility 1 68 0.053
542
ADR057 Adrenogenital Syndrome 33 0.053
543
P MDL005 Medulloblastoma 78 0.053
544
IMM064 Immunodeficiency, Common Variable, 10 51 0.053
545
PHR003 Pharyngitis 56 0.052
546
VCC001 Vaccinia 50 0.052
547
GRW007 Growth Hormone Deficiency 48 0.052
548
RSC001 Rosacea 55 0.052
549
CHL123 Chlamydia 60 0.052
550
DBT010 Diabetic Neuropathy 56 0.052
551
P RCT021 Rectum Cancer 54 0.052
552
LYM040 Lymphoblastic Lymphoma 54 0.052
553
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.052
554
P RTT002 Rett Syndrome 81 0.052
555
BRS099 Breast Ductal Carcinoma 63 0.052
556
P RHB003 Rhabdomyosarcoma 62 0.052
557
HYP014 Hyperuricemia 52 0.052
558
P EHL001 Ehlers-Danlos Syndrome 60 0.052
559
EMB004 Embryonal Carcinoma 57 0.052
560
P RTN016 Retinal Degeneration 56 0.052
561
GYN001 Gynecomastia 49 0.052
562
BCK006 Back Pain 44 0.052
563
INF021 Infant Gynecomastia 32 0.052
564
P ATX030 Ataxia-Telangiectasia 83 0.052
565
P DYS154 Dystonia 65 0.052
566
c BRN108 Branchiootic Syndrome 1 62 0.052
567
DPH001 Diphtheria 61 0.052
568
BRN056 Bronchopulmonary Dysplasia 57 0.052
569
P INT070 Intestinal Obstruction 60 0.052
570
P HYP730 Hypogonadotropic Hypogonadism 54 0.052
571
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.052
572
NRT004 Neuritis 52 0.051
573
c PSR023 Psoriasis 1 50 0.051
574
c PSR028 Psoriasis 7 40 0.051
575
c PSR018 Psoriasis 13 40 0.051
576
c PSR032 Psoriasis 11 40 0.051
577
MSL001 Measles 61 0.051
578
c INV001 Invasive Aspergillosis 48 0.051
579
CYT018 Cytochrome P450 2d6 Variant 28 0.051
580
BRN002 Bronchiolitis 60 0.051
581
SNL007 Senile Cataract 41 0.051
582
CVT001 Cavitary Optic Disc Anomalies 39 0.051
583
c HMC039 Hemochromatosis, Type 1 73 0.051
584
CRC006 Carcinoid Syndrome 55 0.051
585
P DBT005 Diabetes Insipidus 54 0.051
586
P PLM036 Pulmonary Fibrosis 66 0.051
587
IDP011 Idiopathic Interstitial Pneumonia 65 0.051
588
P SBS003 Substance Abuse 56 0.051
589
DMP001 Dumping Syndrome 44 0.051
590
c BSL007 Basal Cell Carcinoma 68 0.051
591
VSC002 Vascular Dementia 57 0.051
592
P AST007 Astrocytoma 52 0.051
593
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.050
594
SKN019 Skin Melanoma 68 0.050
595
P SCL018 Scoliosis 61 0.050
596
P MCR010 Microcephaly 56 0.050
597
P PLY019 Polyneuropathy 55 0.050
598
P PRM006 Primary Biliary Cirrhosis 54 0.050
599
P TRT010 Teratoma 52 0.050
600
GST020 Gastric Antral Vascular Ectasia 42 0.050
601
KPS004 Kaposi Sarcoma 75 0.050
602
PRP030 Purpura 56 0.050
603
CND006 Candida Glabrata 33 0.050
604
ALC006 Alcoholic Hepatitis 60 0.049
605
SFT003 Soft Tissue Sarcoma 57 0.049
606
P PMP001 Pemphigus 56 0.049
607
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.049
608
DRM011 Dermatophytosis 49 0.049
609
c DRM054 Dermatitis, Atopic, 2 45 0.049
610
c CHR682 Chronic Bilirubin Encephalopathy 36 0.049
611
PRS042 Prostate Disease 42 0.049
612
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.049
613
P PTT006 Pituitary Adenoma 53 0.049
614
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.049
615
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.049
616
DYS073 Dysphagia 52 0.049
617
P KRT007 Keratoconus 51 0.049
618
AMN003 Amnestic Disorder 55 0.048
619
ANX004 Anoxia 44 0.048
620
CHR066 Chronic Fatigue Syndrome 61 0.048
621
P LRY044 Larynx Cancer 59 0.048
622
PRM236 Primary Biliary Cholangitis 57 0.048
623
CLR109 Colorectal Adenocarcinoma 51 0.048
624
ORL013 Oral Lichen Planus 47 0.048
625
ACD008 Acid-Labile Subunit Deficiency 55 0.048
626
MYL031 Myeloproliferative Neoplasm 66 0.048
627
DCB001 Decubitus Ulcer 54 0.048
628
P FBR031 Febrile Seizures 54 0.048
629
HSH003 Hashimoto Thyroiditis 63 0.048
630
P ART023 Arthropathy 61 0.048
631
END040 Endogenous Depression 55 0.048
632
PLG002 Plague 54 0.048
633
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.048
634
P PRS038 Personality Disorder 66 0.048
635
ADR016 Adrenal Cortical Carcinoma 51 0.048
636
TND005 Tendinitis 45 0.048
637
ADR004 Adrenal Cortical Adenocarcinoma 44 0.048
638
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.047
639
ENH001 Enhanced S-Cone Syndrome 56 0.047
640
SHG001 Shigellosis 54 0.047
641
FDL002 Food Allergy 52 0.047
642
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.047
643
PSR001 Psoriatic Arthritis 63 0.047
644
c INH020 Inherited Metabolic Disorder 51 0.047
645
P CYS018 Cystitis 59 0.047
646
DSS009 Disseminated Intravascular Coagulation 58 0.047
647
PRP036 Peripheral T-Cell Lymphoma 53 0.047
648
PRT013 Portal Hypertension 61 0.047
649
P INF038 Influenza 69 0.047
650
IMM136 Immune System Disease 52 0.047
651
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.047
652
c ATM011 Autoimmune Hepatitis 63 0.046
653
P LCT001 Lactic Acidosis 52 0.046
654
OPT003 Opiate Dependence 50 0.046
655
c HNT004 Huntington Disease-Like 2 48 0.046
656
RDN001 Reading Disorder 42 0.046
657
SPS057 Spasticity 38 0.046
658
c GRV008 Graves Disease 1 55 0.046
659
ORL004 Oral Submucous Fibrosis 55 0.046
660
HYP780 Hypoadrenocorticism, Familial 60 0.046
661
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.046
662
c INF071 Inflammatory Bowel Disease 1 66 0.046
663
CRD223 Cardiac Arrhythmia 61 0.046
664
P HMP007 Hemophilia 58 0.046
665
TBC004 Tobacco Addiction 65 0.046
666
P MYC008 Myocarditis 60 0.046
667
VSC003 Visceral Leishmaniasis 55 0.046
668
PLP001 Pulpitis 48 0.046
669
P TMP001 Temporal Lobe Epilepsy 53 0.045
670
P MYT002 Myotonic Dystrophy 52 0.045
671
ANG005 Anogenital Venereal Wart 51 0.045
672
NWC001 Newcastle Disease 45 0.045
673
MYT026 Myotonia Atrophica 25 0.045
674
MSC007 Muscle Hypertrophy 65 0.045
675
NRT001 Neurotic Disorder 53 0.045
676
ILS001 Ileus 51 0.045
677
DRY001 Dry Eye Syndrome 50 0.045
678
BCK003 Background Diabetic Retinopathy 37 0.045
679
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.045
680
RRS014 Rare Surgical Neurologic Disease 33 0.045
681
P OPT009 Optic Neuritis 55 0.045
682
CLC006 Calcinosis 48 0.045
683
PRS063 Paresthesia 46 0.045
684
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.045
685
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.045
686
c SPN225 Spondyloarthropathy 1 74 0.045
687
CNN005 Connective Tissue Disease 68 0.045
688
P GND004 Gonadal Dysgenesis 47 0.045
689
SKN005 Skin Atrophy 41 0.045
690
c FNC027 Fanconi Anemia, Complementation Group a 81 0.044
691
PNC001 Pancytopenia 54 0.044
692
P ANL018 Analbuminemia 51 0.044
693
ULC007 Ulcerative Stomatitis 41 0.044
694
EWN003 Ewing Sarcoma 69 0.044
695
c MST023 Mesothelioma, Malignant 59 0.044
696
CRT017 Cartilage Disease 54 0.044
697
RNL077 Renal Fibrosis 49 0.044
698
TNG003 Tongue Cancer 57 0.044
699
HND015 Hand Skill, Relative 33 0.044
700
c PRD040 Periodontitis, Chronic 56 0.044
701
OST011 Osteomalacia 51 0.044
702
P SHR001 Short Bowel Syndrome 50 0.044
703
P FLL037 Follicular Lymphoma 67 0.043
704
HRY003 Hairy Cell Leukemia 57 0.043
705
c OVR114 Ovarian Cancer 1 39 0.043
706
CRP001 Carpal Tunnel Syndrome 68 0.043
707
c FML001 Familial Atrial Fibrillation 67 0.043
708
P THY023 Thymoma 64 0.043
709
OST003 Osteonecrosis 62 0.043
710
HRP004 Herpes Zoster 58 0.043
711
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.043
712
MXD026 Mixed Glioma 36 0.043
713
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.043
714
APN008 Apnea, Obstructive Sleep 64 0.043
715
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.043
716
ERY003 Erythema Multiforme 57 0.043
717
P HYP040 Hypospadias 54 0.043
718
EXP004 Exophthalmos 53 0.043
719
c INF145 Infantile Liver Failure Syndrome 1 50 0.043
720
c MLG074 Malignant Mesenchymoma 50 0.043
721
KRT013 Keratolytic Winter Erythema 45 0.043
722
FDB001 Foodborne Botulism 53 0.042
723
BLL006 Bullous Pemphigoid 63 0.042
724
P SNS001 Sensorineural Hearing Loss 62 0.042
725
P SJG008 Sjogren Syndrome 57 0.042
726
MTH009 Mouth Disease 56 0.042
727
P END046 Endometritis 49 0.042
728
PPT001 Peptic Esophagitis 47 0.042
729
P HYP058 Hypervitaminosis a 45 0.042
730
P HYP061 Hypertrophic Cardiomyopathy 68 0.042
731
CRC021 Carcinosarcoma 62 0.042
732
TNS005 Tonsillitis 58 0.042
733
P TRC086 Trichohepatoenteric Syndrome 1 57 0.042
734
TRN018 Transitional Cell Carcinoma 57 0.042
735
PMP006 Pemphigus Vulgaris, Familial 56 0.042
736
PLR007 Pleural Empyema 44 0.042
737
c MGR028 Migraine with or Without Aura 1 70 0.042
738
P RTN022 Retinal Vein Occlusion 50 0.042
739
P TXP001 Toxoplasmosis 61 0.042
740
CLL003 Cellulitis 56 0.042
741
CRV040 Cervix Carcinoma 52 0.042
742
PYD002 Pyoderma 51 0.042
743
SLP001 Sleeping Sickness 47 0.042
744
P BLP003 Blepharospasm 43 0.042
745
LKP003 Leukoplakia 40 0.042
746
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.042
747
P OCL013 Oculodentodigital Dysplasia 65 0.042
748
c SCL052 Scleroderma, Familial Progressive 62 0.042
749
KRT001 Keratoconjunctivitis Sicca 53 0.042
750
P OCY003 Oocyte Maturation Defect 1 44 0.042
751
ATM052 Autoimmune Disease 1 38 0.042
752
c HNT011 Huntington Disease-Like 3 37 0.042
753
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.042
754
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.041
755
HMT002 Hematologic Cancer 64 0.041
756
NRM005 Neuromuscular Disease 62 0.041
757
APH002 Aphasia 56 0.041
758
PNM008 Pneumothorax 56 0.041
759
P HYP024 Hypoparathyroidism 56 0.041
760
FCT001 Factor Viii Deficiency 54 0.041
761
c CHR418 Chronic Leukemia 52 0.041
762
BNN003 Bone Inflammation Disease 51 0.041
763
CRD137 Cardiogenic Shock 50 0.041
764
FBR054 Fibroma 45 0.041
765
RSP007 Respiratory Distress Syndrome, Infant 31 0.041
766
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.041
767
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.041
768
GNT003 Genital Herpes 54 0.041
769
RTN003 Retinal Ischemia 52 0.041
770
PHN003 Phenylketonuria 73 0.041
771
LPR001 Lepromatous Leprosy 50 0.041
772
P NRV007 Nervous System Disease 68 0.041
773
BCT002 Bacterial Vaginosis 52 0.041
774
PLL012 Pollen Allergy 46 0.041
775
MCR011 Microinvasive Gastric Cancer 43 0.041
776
P CRD132 Cardiac Conduction Defect 61 0.040
777
HRT012 Heart Valve Disease 56 0.040
778
PTT009 Pituitary Gland Disease 54 0.040
779
SCH003 Schizophreniform Disorder 49 0.040
780
NPH010 Nephrosclerosis 46 0.040
781
c ACT150 Acute Adrenal Insufficiency 46 0.040
782
IDP033 Idiopathic Edema 44 0.040
783
NRV004 Nerve Compression Syndrome 35 0.040
784
GST040 Gastric Adenocarcinoma 67 0.040
785
VRC005 Varicose Veins 61 0.040
786
ALL006 Allergic Asthma 56 0.040
787
CRH005 Crohn's Colitis 56 0.040
788
URT049 Urate Oxidase, Pseudogene 26 0.040
789
MSC157 Muscular Dystrophy, Duchenne Type 70 0.040
790
CMM004 Common Variable Immunodeficiency 69 0.040
791
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.040
792
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.040
793
HPT014 Hepatorenal Syndrome 49 0.040
794
SPL018 Splenomegaly 48 0.040
795
BHR001 Behr Syndrome 47 0.040
796
TRC003 Trichomoniasis 46 0.040
797
CYN002 Cyanosis, Transient Neonatal 45 0.040
798
ACT003 Acute Kidney Tubular Necrosis 42 0.040
799
P APL001 Aplastic Anemia 76 0.039
800
c HMP029 Hemophilia a 69 0.039
801
P MYS003 Myasthenia Gravis 68 0.039
802
c MCL013 Mucolipidosis Iv 60 0.039
803
P BNC003 Bone Cancer 56 0.039
804
RHM001 Rheumatic Fever 56 0.039
805
P ANG015 Angioedema 54 0.039
806
TXC002 Toxic Encephalopathy 54 0.039
807
P PTS002 Ptosis 53 0.039
808
NNL006 Non-Alcoholic Steatohepatitis 53 0.039
809
RFR010 Refractory Anemia 50 0.039
810
ATN005 Autonomic Dysfunction 48 0.039
811
MYC006 Mycosis Fungoides 67 0.039
812
P LMY004 Leiomyosarcoma 63 0.039
813
P CHR285 Chronic Myelomonocytic Leukemia 60 0.039
814
ADR005 Adrenal Carcinoma 58 0.039
815
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.039
816
SYN007 Synovitis 55 0.039
817
c THY107 Thymoma, Familial 55 0.039
818
VGN023 Vaginitis 54 0.039
819
c GLL024 Gallbladder Disease 1 53 0.039
820
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
821
RDC002 Radiculopathy 51 0.039
822
CRC014 Carcinoid Tumors, Intestinal 49 0.039
823
c BPL002 Bipolar I Disorder 48 0.039
824
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.039
825
HDG004 Hodgkin's Granuloma 27 0.039
826
HDG006 Hodgkin's Paragranuloma 23 0.039
827
P AGM001 Agammaglobulinemia 66 0.039
828
HDR002 Hidradenitis Suppurativa 58 0.039
829
PNC034 Pancreas Disease 51 0.039
830
BLR001 Biliary Atresia 51 0.039
831
c PNC106 Pancreatic Agenesis 1 50 0.039
832
HDR003 Hidradenitis 48 0.039
833
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.039
834
P SDR002 Siderosis 42 0.039
835
c BLP048 Blepharospasm, Benign Essential 38 0.039
836
P MYP006 Myopia 58 0.039
837
CLF001 Cleft Lip 53 0.039
838
CRN030 Coronary Stenosis 49 0.039
839
P PLL002 Pellagra 47 0.039
840
ANP008 Anaplastic Oligoastrocytoma 31 0.039
841
CYT008 Cytomegalovirus Infection 58 0.038
842
P SML001 Small Cell Carcinoma 55 0.038
843
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.038
844
NTR046 Neutrophil Migration 49 0.038
845
OPD006 Opioid Addiction 49 0.038
846
CHR074 Choriocarcinoma 47 0.038
847
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.038
848
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.038
849
TND004 Tendinopathy 44 0.038
850
c SBR001 Seborrheic Infantile Dermatitis 36 0.038
851
P ANP001 Anaplastic Large Cell Lymphoma 62 0.037
852
APP008 Appendicitis 61 0.037
853
GLS001 Gliosarcoma 56 0.037
854
P THR015 Thrombophilia 51 0.037
855
c CNT016 Central Retinal Vein Occlusion 48 0.037
856
c SYS043 Systemic Lupus Erythematosus 1 39 0.037
857
c PRM340 Primary Adrenal Insufficiency 37 0.037
858
GRM010 Germ Cells Tumors 35 0.037
859
ACR006 Aceruloplasminemia 74 0.037
860
CRB037 Cerebral Palsy 69 0.037
861
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.037
862
ACN002 Acanthosis Nigricans 62 0.037
863
c DNG003 Dengue Disease 61 0.037
864
P CRN028 Corneal Ulcer 49 0.037
865
INT067 Interstitial Nephritis 46 0.037
866
DNT006 Dental Pulp Necrosis 37 0.037
867
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 34 0.037
868
TRY004 Trypanosomiasis, Human East-African 25 0.037
869
OST017 Osteomyelitis 65 0.037
870
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.037
871
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.037
872
P SYP003 Syphilis 59 0.037
873
INT007 Intermediate Coronary Syndrome 58 0.037
874
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.037
876
CHL004 Cholelithiasis 50 0.037
877
GST049 Gastrointestinal System Cancer 49 0.037
878
CRN027 Corneal Neovascularization 48 0.037
879
PRC003 Proctitis 44 0.037
880
P MJR007 Major Affective Disorder 1 44 0.037
881
ENT001 Enterocele 44 0.037
882
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.037
883
c MJR003 Major Affective Disorder 6 34 0.037
884
c MJR006 Major Affective Disorder 5 34 0.037
885
BRN049 Brain Tumor, Childhood 30 0.037
886
P SLM003 Salmonellosis 54 0.037
887
CRY005 Cryptococcosis 51 0.037
888
c SVR005 Severe Pre-Eclampsia 50 0.037
889
CRT015 Carotid Artery Occlusion 44 0.037
890
EXC002 Exocrine Pancreatic Insufficiency 41 0.037
891
PCK003 Pick Disease of Brain 63 0.037
892
P PLY014 Polycystic Kidney Disease 61 0.037
893
GLB001 Gilbert Syndrome 58 0.037
894
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.037
895
ISL003 Isolated Growth Hormone Deficiency 50 0.037
896
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.037
897
BHV002 Behavioral Variant of Frontotemporal Dementia 49 0.037
898
c ART101 Aortic Valve Disease 2 67 0.036
899
CRN036 Craniopharyngioma 65 0.036
900
PPL049 Papillon-Lefevre Syndrome 63 0.036
901
c LCL006 Localized Scleroderma 61 0.036
902
IGR001 Ige Responsiveness, Atopic 61 0.036
903
FBR047 Fibromyalgia 60 0.036
904
HMR039 Hemorrhage, Intracerebral 59 0.036
905
P HYP726 Hypercalcemia, Infantile, 1 58 0.036
906
c BCT007 Bacterial Meningitis 56 0.036
907
ECH003 Echinococcosis 54 0.036
908
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.036
909
FCL012 Facial Paralysis 53 0.036
910
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.036
911
TST014 Testicular Cancer 49 0.036
912
GLC096 Galactorrhea 44 0.036
913
FNC007 Functioning Pituitary Adenoma 44 0.036
914
CYS009 Cystadenoma 43 0.036
915
c ADL017 Adult T-Cell Leukemia 59 0.036
916
CNV004 Canavan Disease 56 0.036
917
P MYS005 Myositis 54 0.036
918
c ACT135 Acute Graft Versus Host Disease 52 0.036
919
P CLL015 Collagen Disease 46 0.036
920
MLG164 Malignant Epithelial Tumor of Ovary 27 0.036
921
c EXD008 Exudative Vitreoretinopathy 1 69 0.035
922
TYP007 Typhoid Fever 61 0.035
923
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.035
924
P HYP265 Hypotonia 43 0.035
925
STT004 Steatorrhea 39 0.035
926
SCR003 Secretory Diarrhea 36 0.035
927
PYR009 Pyridoxine Deficiency Anemia 32 0.035
928
EXN003 Exencephaly 32 0.035
929
OBS002 Obsessive-Compulsive Disorder 69 0.034
930
P HYD006 Hydrocephalus 68 0.034
931
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.034
932
PST028 Post-Traumatic Stress Disorder 60 0.034
933
P MMP001 Mumps 57 0.034
934
c CNG216 Congenital Hydrocephalus 55 0.034
935
SPS003 Spastic Diplegia 53 0.034
936
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.034
937
THR004 Thrombocytosis 52 0.034
938
P CTN015 Cutaneous T Cell Lymphoma 52 0.034
939
PRP080 Peripheral Artery Disease 51 0.034
940
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.034
941
PLR022 Pleural Disease 50 0.034
942
c BCT013 Bacterial Pneumonia 49 0.034
943
RNL011 Renal Osteodystrophy 49 0.034
944
P HMN032 Human Herpesvirus 8 49 0.034
945
GRN017 Granulocytopenia 46 0.034
946
PLY100 Polyploidy 41 0.034
947
c HMG029 Hemoglobin Se Disease 40 0.034
948
SPR126 Superior Semicircular Canal Dehiscence 39 0.034
949
DGR001 Digeorge Syndrome 61 0.034
950
P PRD006 Prader-Willi Syndrome 60 0.034
951
HMC014 Homocysteinemia 54 0.034
952
CLN045 Colonic Benign Neoplasm 52 0.034
953
P LCT002 Lactose Intolerance 51 0.034
954
P DRM007 Dermatitis Herpetiformis 50 0.034
955
VTM002 Vitamin B12 Deficiency 48 0.034
956
IDP070 Idiopathic Scoliosis 39 0.034
957
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.034
958
P BRN022 Bronchiectasis 60 0.034
959
P GLL020 Gallbladder Disease 60 0.034
960
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.034
961
EXT034 Extrinsic Allergic Alveolitis 58 0.034
962
P SLP005 Sleep Disorder 58 0.034
963
P EPD016 Epidermolysis Bullosa 54 0.034
964
P CHL066 Cholangitis 53 0.034
965
CHR005 Chorioamnionitis 51 0.034
966
ACR041 Acromelic Frontonasal Dysostosis 50 0.034
967
IGG001 Iga Glomerulonephritis 50 0.034
968
PRD004 Prediabetes Syndrome 49 0.034
969
TST015 Testicular Disease 49 0.034
970
GRM005 Germ Cell Cancer 47 0.034
971
DBT006 Diabetic Macular Edema 46 0.034
972
SPP008 Suppurative Otitis Media 46 0.034
973
LWC001 Low Compliance Bladder 45 0.034
974
c ADN012 Adenocarcinoma in Situ 43 0.034
975
GST071 Gastrointestinal Carcinoma 42 0.034
976
PTT003 Pituitary-Dependent Cushing's Disease 42 0.034
977
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.034
978
KLD004 Keloid Disorder 41 0.034
979
CHP002 Chops Syndrome 41 0.034
980
MYF002 Myofascial Pain Syndrome 39 0.034
981
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.034
982
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.034
983
ANS012 Anus Disease 37 0.034
984
c MJR008 Major Affective Disorder 2 35 0.034
985
c MJR023 Major Affective Disorder 7 34 0.034
986
c MJR004 Major Affective Disorder 4 29 0.034
987
SCL001 Scalp Dermatosis 20 0.034
988
ADR007 Adrenoleukodystrophy 72 0.034
989
MYL005 Myelofibrosis 69 0.034
990
SPN041 Spinal Cord Disease 57 0.034
991
c ADL096 Adult Hepatocellular Carcinoma 56 0.034
992
c LKM070 Leukemia, Acute Monocytic 55 0.034
993
MCN017 Meconium Ileus 54 0.034
994
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.034
995
P RNL015 Renal Hypertension 47 0.034
996
DFF003 Diffuse Scleroderma 43 0.034
997
MMM006 Mammographic Density 43 0.034
998
PST053 Postherpetic Neuralgia 43 0.034
999
TRP005 Trophoblastic Neoplasm 38 0.034
1000
PSD088 Pseudobulbar Affect 37 0.034
1001
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.033
1002
P LPS002 Liposarcoma 62 0.033
1003
P PRV006 Pervasive Developmental Disorder 58 0.033
1004
P CHN012 Chondrosarcoma 57 0.033
1005
ORP003 Oropharynx Cancer 55 0.033
1006
P ICH004 Ichthyosis 55 0.033
1007
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.033
1008
P HYP083 Hypopituitarism 53 0.033
1009
LMB062 Limb Ischemia 50 0.033
1010
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.033
1011
P TRC031 Trichorhinophalangeal Syndrome 41 0.033
1012
MCC012 Mccune-Albright Syndrome 70 0.032
1013
SVR097 Severe Cutaneous Adverse Reaction 66 0.032
1014
THY122 Thyroid Gland Cancer 59 0.032
1015
TRG002 Trigeminal Neuralgia 58 0.032
1016
KRT006 Keratoconjunctivitis 53 0.032
1017
HMT008 Hematuria, Benign Familial 53 0.032
1018
P MYC033 Myoclonus 47 0.032
1019
ADR041 Adrenal Cortical Adenoma 44 0.032
1020
CRB086 Cerebral Aneurysms 41 0.032
1021
P TST026 Testicular Germ Cell Cancer 40 0.032
1022
LCH009 Lichen Sclerosus 39 0.032
1023
LYM053 Lymphomatous Thyroiditis 23 0.032
1024
SCH036 Scheie Syndrome 68 0.031
1025
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.031
1026
CHL067 Cholecystitis 60 0.031
1027
P RBL001 Rubella 56 0.031
1028
P MMB011 Membranous Nephropathy 54 0.031
1029
NPH003 Nephrocalcinosis 52 0.031
1030
FND002 Fundus Dystrophy 52 0.031
1031
TRY001 Trypanosomiasis 50 0.031
1032
THR013 Thoracic Outlet Syndrome 49 0.031
1033
VTM033 Vitamin K Deficiency Bleeding 47 0.031
1034
URT010 Ureteral Obstruction 46 0.031
1035
SMN007 Seminoma 43 0.031
1036
P CRB088 Cerebral Atrophy 43 0.031
1037
ACT084 Acute Stress Disorder 42 0.031
1038
ACT088 Acute Insulin Response 42 0.031
1039
PNM005 Pneumonic Plague 40 0.031
1040
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.031
1041
MSM014 Mismatch Repair Cancer Syndrome 65 0.031
1042
LYM017 Lyme Disease 64 0.031
1043
P MVM001 Movement Disease 63 0.031
1044
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.031
1045
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.031
1046
PRT058 Pure Autonomic Failure 60 0.031
1047
P ANT006 Antiphospholipid Syndrome 56 0.031
1048
BRN012 Bronchiolitis Obliterans 55 0.031
1049
P HST010 Histiocytosis 54 0.031
1050
PRC013 Pericarditis 54 0.031
1051
P LRY019 Laryngitis 53 0.031
1052
URC002 Urea Cycle Disorder 51 0.031
1053
RTN020 Retinal Vascular Disease 49 0.031
1054
BWN001 Bowen-Conradi Syndrome 49 0.031
1055
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.031
1056
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.031
1057
SDD008 Sudden Sensorineural Hearing Loss 44 0.031
1058
ATN004 Autonomic Neuropathy 43 0.031
1059
P PRC031 Preeclampsia/eclampsia 1 42 0.031
1060
MCP033 Mucopolysaccharidoses 39 0.031
1061
P HRD144 Hereditary Mixed Polyposis Syndrome 38 0.031
1062
MYT011 Myotonia 37 0.031
1063
FNT004 Fainting 31 0.031
1064
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.031
1065
MNK001 Menkes Disease 62 0.030
1066
P THR117 Three M Syndrome 1 58 0.030
1067
P ORL007 Oral Cavity Cancer 57 0.030
1068
BLM002 Bulimia Nervosa 56 0.030
1069
OST016 Osteochondrosis 55 0.030
1070
RHM028 Rheumatic Heart Disease 54 0.030
1071
CRT013 Carotid Stenosis 50 0.030
1072
BRN014 Bronchopneumonia 47 0.030
1073
IRR003 Irritant Dermatitis 46 0.030
1074
INT052 Intestinal Volvulus 44 0.030
1075
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 39 0.030
1076
HRN029 Hearing Loss, Noise-Induced 38 0.030
1077
c DRM040 Dermatitis Herpetiformis, Familial 36 0.030
1078
ADN011 Adenoid Cystic Carcinoma 71 0.029
1079
c FML021 Familial Hypercholesterolemia 67 0.029