Search results for Clotrimazole

1355 hits were found for Clotrimazole

# Family MCID Name MIFTS Score
1
P CND004 Candidiasis 58 0.250
2
ORL005 Oral Candidiasis 56 0.151
3
VLV011 Vulvovaginal Candidiasis 49 0.143
4
DRM011 Dermatophytosis 52 0.131
5
FNG017 Fungal Infectious Disease 53 0.114
6
VGN023 Vaginitis 54 0.113
7
TNP001 Tinea Pedis 46 0.085
8
DRM006 Dermatitis 61 0.077
9
OTM001 Otomycosis 27 0.077
10
P ASP006 Aspergillosis 69 0.074
11
VGN019 Vaginal Discharge 46 0.074
12
PTY002 Pityriasis Versicolor 38 0.072
13
CNT047 Contact Dermatitis 58 0.069
14
ATX019 Ataxia with Vitamin E Deficiency 42 0.069
15
DRM009 Dermatomycosis 36 0.069
16
P SCK005 Sickle Cell Disease 50 0.067
17
VLV010 Vulvovaginitis 41 0.067
18
TRC003 Trichomoniasis 53 0.064
19
SCK003 Sickle Cell Anemia 74 0.059
20
CTN033 Cutaneous Candidiasis 38 0.059
21
BCT002 Bacterial Vaginosis 53 0.053
22
STM007 Stomatitis 50 0.053
23
TNC003 Tinea Corporis 39 0.053
24
CND006 Candida Glabrata 32 0.053
25
CHR063 Chronic Mucocutaneous Candidiasis 63 0.049
26
ACQ007 Acquired Immunodeficiency Syndrome 60 0.049
27
ALL010 Allergic Contact Dermatitis 56 0.049
28
P OTT001 Otitis Externa 39 0.049
29
TNC001 Tinea Cruris 36 0.049
30
DNT008 Denture Stomatitis 35 0.049
31
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.049
32
KRT019 Keratitis, Hereditary 65 0.045
33
P EXN002 Exanthem 57 0.045
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.042
35
P RHM011 Rheumatoid Arthritis 80 0.042
36
c NRF023 Neurofibromatosis, Type Ii 80 0.042
37
P ART022 Arthritis 69 0.042
38
SKN016 Skin Disease 63 0.042
39
CRY005 Cryptococcosis 58 0.042
40
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.042
41
SPR010 Sporotrichosis 46 0.042
42
ESP018 Esophageal Candidiasis 44 0.042
43
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.042
44
SPR126 Superior Semicircular Canal Dehiscence 40 0.042
45
48X005 48,xyyy 39 0.042
46
c HMG029 Hemoglobin Se Disease 39 0.042
47
IMM167 Immune Deficiency Disease 78 0.037
48
GLB015 Glioblastoma Multiforme 75 0.037
49
HMN044 Human Immunodeficiency Virus Type 1 71 0.037
50
DFC004 Deficiency Anemia 70 0.037
51
P MLN008 Melanoma 69 0.037
52
P TRN020 Turner Syndrome 67 0.037
53
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.037
54
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.037
55
CLT003 Colitis 62 0.037
56
NTR005 Nutritional Deficiency Disease 62 0.037
57
P TXP001 Toxoplasmosis 60 0.037
58
ISC004 Ischemia 58 0.037
59
CCC001 Coccidioidomycosis 58 0.037
60
P RHN004 Rhinitis 57 0.037
61
ERY051 Erythroleukemia, Familial 56 0.037
62
BCT022 Bacterial Infectious Disease 56 0.037
63
KRT009 Keratosis 51 0.037
64
VGN020 Vaginal Disease 49 0.037
65
CRY014 Cryptococcal Meningitis 48 0.037
66
FLL008 Folliculitis 46 0.037
67
P SBR004 Seborrheic Dermatitis 45 0.037
68
FNG016 Fungal Keratitis 40 0.037
69
SPR020 Superficial Mycosis 35 0.037
70
MLR004 Malaria 81 0.032
71
ULC004 Ulcerative Colitis 73 0.032
72
P KDN018 Kidney Disease 72 0.032
73
DWN001 Down Syndrome 70 0.032
74
SKN019 Skin Melanoma 68 0.032
75
c INF071 Inflammatory Bowel Disease 1 67 0.032
76
P MNN013 Meningitis 66 0.032
77
P DRM053 Dermatitis, Atopic 66 0.032
78
CLN015 Colon Adenocarcinoma 65 0.032
79
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.032
80
LSH001 Leishmaniasis 63 0.032
81
P END044 Endometriosis 63 0.032
82
P ESP024 Esophagitis 62 0.032
83
CTN007 Cutaneous Leishmaniasis 62 0.032
84
SQM006 Squamous Cell Carcinoma 60 0.032
85
c ACT073 Acute Leukemia 58 0.032
86
HST011 Histoplasmosis 55 0.032
87
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.032
88
P INF037 Inflammatory Bowel Disease 54 0.032
89
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.032
90
ILT001 Ileitis 50 0.032
91
c DRM054 Dermatitis, Atopic, 2 44 0.032
92
ORL015 Oral Squamous Cell Carcinoma 43 0.032
93
P KLZ004 Kala-Azar 1 41 0.032
94
PCH007 Pouchitis 39 0.032
95
ERY010 Erythrasma 25 0.032
96
P CLR023 Colorectal Cancer 99 0.026
98
c LKM061 Leukemia, Acute Myeloid 84 0.026
99
END057 Endometrial Cancer 74 0.026
100
c BTT014 Beta-Thalassemia 74 0.026
101
CRH001 Crohn's Disease 74 0.026
102
P GRF003 Graft-Versus-Host Disease 72 0.026
103
c CHR684 Chronic Kidney Disease 70 0.026
104
P LKM002 Leukemia 68 0.026
105
c RHB024 Rhabdomyosarcoma 2 67 0.026
106
P MCR115 Microvascular Complications of Diabetes 5 66 0.026
107
c MCR129 Microvascular Complications of Diabetes 1 66 0.026
108
CHG001 Chagas Disease 66 0.026
109
c DBT099 Diabetes Mellitus, Type I 65 0.026
110
P DBT009 Diabetes Mellitus 64 0.026
111
P ADN016 Adenocarcinoma 64 0.026
112
P PNC044 Pancreatitis 61 0.026
113
c ACT027 Acute Pancreatitis 60 0.026
114
INS001 Insulinoma 60 0.026
115
P THL005 Thalassemia 60 0.026
116
PNM001 Pneumocystosis 59 0.026
117
P CYS018 Cystitis 59 0.026
118
BRN002 Bronchiolitis 59 0.026
119
EYD002 Eye Disease 58 0.026
120
c DWL002 Dowling-Degos Disease 1 58 0.026
121
P HDC001 Headache 57 0.026
122
CYT008 Cytomegalovirus Infection 57 0.026
123
PHR003 Pharyngitis 57 0.026
124
BRN012 Bronchiolitis Obliterans 55 0.026
125
P DRR001 Diarrhea 55 0.026
126
P NLD001 Nail Disease 54 0.026
127
P ALP008 Alopecia 54 0.026
128
P LCH002 Lichen Planus 53 0.026
129
c MCR113 Microvascular Complications of Diabetes 3 52 0.026
130
P OVR082 Overgrowth Syndrome 50 0.026
131
P CRN028 Corneal Ulcer 47 0.026
132
c MCR120 Microvascular Complications of Diabetes 7 47 0.026
133
KRT013 Keratolytic Winter Erythema 46 0.026
134
ORL013 Oral Lichen Planus 45 0.026
135
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.026
136
MLN073 Melanosis, Neurocutaneous 45 0.026
137
HYP084 Hypopyon 43 0.026
138
PHH001 Phaeohyphomycosis 42 0.026
139
c MCR130 Microvascular Complications of Diabetes 6 41 0.026
140
c MCR133 Microvascular Complications of Diabetes 4 41 0.026
141
OPS001 Opisthorchiasis 41 0.026
142
c MCR112 Microvascular Complications of Diabetes 2 41 0.026
143
PST029 Postmenopausal Atrophic Vaginitis 38 0.026
144
PMP010 Pompholyx 37 0.026
145
BLN010 Balanitis 37 0.026
146
CYT004 Cytomegalic Inclusion Disease 31 0.026
147
BLN009 Balanoposthitis 31 0.026
148
CYT018 Cytochrome P450 2d6 Variant 27 0.026
149
TRC121 Trichomonas Vaginalis Trichomoniasis 23 0.026
150
P HPT023 Hepatocellular Carcinoma 100 0.019
151
P BRS047 Breast Cancer 97 0.019
152
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.019
153
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.019
154
c SYS001 Systemic Lupus Erythematosus 86 0.019
155
MYL069 Myeloma, Multiple 85 0.019
156
c HYP595 Hypertension, Essential 84 0.019
157
P PNC035 Pancreatic Cancer 84 0.019
158
NRL016 Neural Tube Defects 82 0.019
159
P ATX030 Ataxia-Telangiectasia 82 0.019
160
c FNC027 Fanconi Anemia, Complementation Group a 81 0.019
161
CYS001 Cystic Fibrosis 81 0.019
162
STR067 Stroke, Ischemic 81 0.019
163
P BLD134 Bladder Cancer 79 0.019
164
c DLT002 Dilated Cardiomyopathy 79 0.019
165
P RTN008 Retinitis Pigmentosa 79 0.019
166
P LKM071 Leukemia, Chronic Lymphocytic 79 0.019
167
c CWD006 Cowden Syndrome 1 78 0.019
168
GST019 Gastrointestinal Stromal Tumor 78 0.019
169
OST012 Osteoarthritis 78 0.019
170
P LNG064 Lung Cancer Susceptibility 3 78 0.019
171
P PRK057 Parkinson Disease, Late-Onset 78 0.019
172
P MDL005 Medulloblastoma 77 0.019
173
MRF001 Marfan Syndrome 77 0.019
174
c TBR025 Tuberous Sclerosis 1 77 0.019
175
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.019
176
c NRF024 Neurofibromatosis, Type I 77 0.019
177
AST005 Asthma 76 0.019
178
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.019
179
CRV035 Cervical Cancer 76 0.019
180
KPS004 Kaposi Sarcoma 75 0.019
181
P HRT032 Heart Disease 75 0.019
182
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.019
183
c ATR087 Atrial Standstill 1 75 0.019
184
ADR007 Adrenoleukodystrophy 75 0.019
185
LPT014 Leptin Deficiency or Dysfunction 74 0.019
186
P OST002 Osteoporosis 74 0.019
187
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.019
188
c MNN043 Meningioma, Familial 74 0.019
189
VNH007 Von Hippel-Lindau Syndrome 73 0.019
190
SVR004 Severe Combined Immunodeficiency 73 0.019
191
c HYP836 Hypercholesterolemia, Familial, 1 73 0.019
192
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.019
193
c SPN225 Spondyloarthropathy 1 73 0.019
194
c THR092 Thrombophilia Due to Thrombin Defect 73 0.019
195
BSL036 Basal Cell Nevus Syndrome 73 0.019
196
P CNR004 Cone-Rod Dystrophy 2 73 0.019
197
P RTN024 Retinoblastoma 73 0.019
198
ANX010 Anxiety 73 0.019
199
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.019
200
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.019
201
SCH036 Scheie Syndrome 72 0.019
202
BRT054 Brittle Bone Disorder 72 0.019
203
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.019
204
c TBR026 Tuberous Sclerosis 2 72 0.019
205
P MLT020 Multiple Sclerosis 72 0.019
206
c HPT073 Hepatitis C Virus 72 0.019
207
P HNT016 Huntington Disease 72 0.019
208
P NRB001 Neuroblastoma 72 0.019
209
P FML011 Familial Adenomatous Polyposis 72 0.019
210
OTT002 Otitis Media 72 0.019
211
P WSK001 Wiskott-Aldrich Syndrome 72 0.019
212
AGM019 Agammaglobulinemia, X-Linked 71 0.019
213
P PHC003 Pheochromocytoma 71 0.019
214
PRP027 Peripheral Vascular Disease 71 0.019
215
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.019
216
BHC003 Behcet Syndrome 71 0.019
217
P SRC025 Sarcoidosis 1 70 0.019
218
P ATS364 Autism 70 0.019
219
P MYC007 Myocardial Infarction 70 0.019
220
P MTC003 Metachromatic Leukodystrophy 70 0.019
221
P AMY004 Amyloidosis 70 0.019
222
MYL009 Myelodysplastic Syndrome 70 0.019
223
MLT157 Multiple System Atrophy 1 70 0.019
224
c GLY008 Glycogen Storage Disease Ii 70 0.019
225
MYL005 Myelofibrosis 70 0.019
226
ADN011 Adenoid Cystic Carcinoma 70 0.019
227
PTZ001 Peutz-Jeghers Syndrome 70 0.019
228
P OST001 Osteopetrosis 70 0.019
229
P HYP061 Hypertrophic Cardiomyopathy 70 0.019
230
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.019
231
P MYP004 Myopathy 70 0.019
232
P TBR001 Tuberous Sclerosis 70 0.019
233
CNG034 Congestive Heart Failure 69 0.019
234
P DMN001 Diamond-Blackfan Anemia 69 0.019
235
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.019
236
P KRB001 Krabbe Disease 69 0.019
237
PLY001 Polycythemia Vera 69 0.019
238
SVR097 Severe Cutaneous Adverse Reaction 69 0.019
239
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.019
240
P SLP006 Sleep Apnea 69 0.019
241
P TYS001 Tay-Sachs Disease 69 0.019
242
LYM133 Lymphoma, Hodgkin, Classic 69 0.019
243
P OCL013 Oculodentodigital Dysplasia 69 0.019
244
P HYP086 Hypothyroidism 69 0.019
245
P LPR021 Leprosy 3 69 0.019
246
ART016 Aortic Aneurysm 69 0.019
247
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.019
248
EWN003 Ewing Sarcoma 69 0.019
249
LYM007 Lymphangioleiomyomatosis 69 0.019
250
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.019
251
P LKM062 Leukemia, Acute Lymphoblastic 69 0.019
252
P LYM118 Lymphoma 68 0.019
253
P CRN037 Craniosynostosis 68 0.019
254
P TMP003 Temporal Arteritis 68 0.019
255
P LVR013 Liver Disease 68 0.019
256
P SYS005 Systemic Scleroderma 68 0.019
257
P MYC084 Mycobacterium Tuberculosis 1 68 0.019
258
CHL065 Cholangiocarcinoma 68 0.019
259
SND001 Sandhoff Disease 68 0.019
260
CMM004 Common Variable Immunodeficiency 68 0.019
261
c BSL007 Basal Cell Carcinoma 68 0.019
262
c NMN015 Niemann-Pick Disease, Type C1 68 0.019
263
P MYS003 Myasthenia Gravis 68 0.019
264
P INF038 Influenza 68 0.019
265
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.019
266
P ESS003 Essential Thrombocythemia 68 0.019
267
BRN024 Bronchitis 68 0.019
268
CNN005 Connective Tissue Disease 68 0.019
269
RCK004 Rickets 68 0.019
270
P MJR001 Major Depressive Disorder 68 0.019
271
PNC129 Pancreatic Adenocarcinoma 68 0.019
272
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.019
273
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.019
274
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.019
275
P THR014 Thrombocytopenia 67 0.019
276
HYL004 Hyaline Fibromatosis Syndrome 67 0.019
277
P CWD010 Cowden Syndrome 67 0.019
278
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.019
279
GST092 Gastroesophageal Reflux 67 0.019
280
P HPT021 Hepatitis 67 0.019
281
P DYS007 Dyskeratosis Congenita 67 0.019
282
FCT007 Factor Vii Deficiency 67 0.019
283
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.019
284
CRB039 Cerebrovascular Disease 67 0.019
285
ALL003 Allergic Rhinitis 67 0.019
286
c HMP029 Hemophilia a 67 0.019
287
P SHW006 Shwachman-Diamond Syndrome 1 67 0.019
288
P CHR012 Chronic Granulomatous Disease 67 0.019
289
FLL027 Fallopian Tube Carcinoma 67 0.019
290
P HYP098 Hypereosinophilic Syndrome 67 0.019
291
c ATS007 Autism Spectrum Disorder 67 0.019
292
P PLM037 Pulmonary Hypertension 67 0.019
293
c MGR028 Migraine with or Without Aura 1 67 0.019
294
MYC006 Mycosis Fungoides 66 0.019
295
P LNG028 Long Qt Syndrome 66 0.019
296
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.019
297
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.019
298
ALC007 Alcohol Dependence 66 0.019
299
OST159 Osteogenic Sarcoma 66 0.019
300
ANG054 Angina Pectoris 66 0.019
301
GLL008 Gilles De La Tourette Syndrome 66 0.019
302
CHD001 Chediak-Higashi Syndrome 66 0.019
303
P DMN002 Dementia 66 0.019
304
c FML021 Familial Hypercholesterolemia 66 0.019
305
P SKN015 Skin Carcinoma 66 0.019
306
P NSP012 Nasopharyngeal Carcinoma 66 0.019
307
MYX005 Myxoid Liposarcoma 66 0.019
308
c FML346 Familial Adenomatous Polyposis 1 66 0.019
309
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.019
310
HYP056 Hypoglycemia 66 0.019
311
AND002 Androgen Insensitivity Syndrome 66 0.019
312
P CCK001 Cockayne Syndrome 66 0.019
313
MYL031 Myeloproliferative Neoplasm 66 0.019
314
c MCL013 Mucolipidosis Iv 66 0.019
315
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.019
316
KHL003 Kohlschutter-Tonz Syndrome 65 0.019
317
CRN036 Craniopharyngioma 65 0.019
318
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.019
319
P ART005 Arteriovenous Malformation 65 0.019
320
P AGM001 Agammaglobulinemia 65 0.019
321
P CNJ013 Conjunctivitis 65 0.019
322
SRC014 Sarcoma 65 0.019
323
PPL049 Papillon-Lefevre Syndrome 65 0.019
324
P LPS002 Liposarcoma 65 0.019
325
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.019
326
AFB002 Afibrinogenemia, Congenital 65 0.019
327
P MTR014 Motor Neuron Disease 65 0.019
328
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.019
329
PRT037 Pertussis 65 0.019
330
HRL003 Hurler Syndrome 65 0.019
331
IRR002 Irritable Bowel Syndrome 65 0.019
332
P HRP006 Herpes Simplex 65 0.019
333
GRN037 Granulomatosis with Polyangiitis 65 0.019
334
MRK001 Merkel Cell Carcinoma 65 0.019
335
ATH013 Atherosclerosis Susceptibility 65 0.019
336
c WLM013 Wilms Tumor 1 65 0.019
337
P PLR004 Pleuropulmonary Blastoma 65 0.019
338
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.019
339
P ADL010 Adult Respiratory Distress Syndrome 65 0.019
340
P THY023 Thymoma 65 0.019
341
LYS012 Lysosomal Acid Lipase Deficiency 65 0.019
342
c MCP001 Mucopolysaccharidosis Iii 65 0.019
343
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.019
344
PRT036 Peritonitis 64 0.019
345
APN008 Apnea, Obstructive Sleep 64 0.019
346
ANG020 Angiosarcoma 64 0.019
347
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.019
348
NRF007 Neurofibroma 64 0.019
349
P MST009 Mastocytosis 64 0.019
350
TBC004 Tobacco Addiction 64 0.019
351
CTR172 Citrullinemia, Classic 64 0.019
352
c JVN010 Juvenile Rheumatoid Arthritis 64 0.019
353
GT001 Gout 64 0.019
354
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.019
355
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.019
356
DGR001 Digeorge Syndrome 64 0.019
357
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.019
358
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.019
359
P PRD008 Periodontitis 64 0.019
360
MSC007 Muscle Hypertrophy 64 0.019
361
SPT006 Septooptic Dysplasia 64 0.019
362
DSM004 Desmoid Tumor 64 0.019
363
MGK001 Megakaryocytic Leukemia 64 0.019
364
RBR001 Roberts Syndrome 64 0.019
365
P RHB003 Rhabdomyosarcoma 63 0.019
366
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.019
367
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.019
368
BRT002 Birt-Hogg-Dube Syndrome 63 0.019
369
P GLM045 Glioma 63 0.019
370
P HML002 Hemolytic Anemia 63 0.019
371
c PRC016 Pre-Eclampsia 63 0.019
372
P NTR004 Neutropenia 63 0.019
373
P ANR048 Aniridia 1 63 0.019
374
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.019
375
PLG002 Plague 63 0.019
376
c MLG084 Malignant Fibrous Histiocytoma 63 0.019
377
P CRN300 Coronary Heart Disease 1 63 0.019
378
P DST002 Distal Arthrogryposis 63 0.019
379
ACT119 Acute Promyelocytic Leukemia 63 0.019
380
CHN016 Cohen Syndrome 63 0.019
381
END041 Endometrial Adenocarcinoma 63 0.019
382
P MVM001 Movement Disease 63 0.019
383
c ACT068 Acute Cystitis 63 0.019
384
P LMY004 Leiomyosarcoma 63 0.019
385
TRN015 Transient Cerebral Ischemia 63 0.019
386
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.019
387
DPR016 Depression 63 0.019
388
RHB001 Rhabdoid Cancer 63 0.019
389
c ATM011 Autoimmune Hepatitis 63 0.019
390
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.019
391
c ALP101 Alpha-Thalassemia 62 0.019
392
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.019
393
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.019
394
LPD008 Lipid Metabolism Disorder 62 0.019
395
c HPT001 Hepatitis C 62 0.019
396
P PLY014 Polycystic Kidney Disease 62 0.019
397
P PSR002 Psoriasis 62 0.019
398
c GM1007 Gm1 Gangliosidosis 62 0.019
399
c HPT003 Hepatitis a 62 0.019
400
c BRN108 Branchiootic Syndrome 1 62 0.019
401
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.019
402
TKY002 Takayasu Arteritis 62 0.019
403
P SPN046 Spinal Muscular Atrophy 62 0.019
404
c SVR001 Severe Acute Respiratory Syndrome 62 0.019
405
LPP008 Lipoprotein Quantitative Trait Locus 62 0.019
406
PRM126 Primary Peritoneal Carcinoma 62 0.019
407
P HYP750 Hypertriglyceridemia, Familial 62 0.019
408
P ART023 Arthropathy 62 0.019
409
P VSC011 Vasculitis 62 0.019
410
c ANM038 Anemia, Autoimmune Hemolytic 62 0.019
411
ATM095 Autoimmune Disease 62 0.019
412
ALL026 Allergic Hypersensitivity Disease 62 0.019
413
MNN042 Meningioma, Radiation-Induced 62 0.019
414
CRC021 Carcinosarcoma 62 0.019
415
TXC005 Toxic Shock Syndrome 62 0.019
416
P PRM006 Primary Biliary Cirrhosis 62 0.019
417
LVR012 Liver Cirrhosis 62 0.019
418
BLD131 Bladder Urothelial Carcinoma 62 0.019
419
ASP002 Aspartylglucosaminuria 62 0.019
420
MSL001 Measles 62 0.019
421
P DRM010 Dermatomyositis 61 0.019
422
PSR001 Psoriatic Arthritis 61 0.019
423
c MCP043 Mucopolysaccharidosis, Type Iiia 61 0.019
424
P INT143 Interstitial Cystitis 61 0.019
425
P KLL001 Kallmann Syndrome 61 0.019
426
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.019
427
HYP066 Hyperglycemia 61 0.019
428
INT002 Intermittent Claudication 61 0.019
429
CHR001 Churg-Strauss Syndrome 61 0.019
430
c PNS012 Paine Syndrome 61 0.019
431
c SCL052 Scleroderma, Familial Progressive 61 0.019
432
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.019
433
P ENC018 Encephalopathy 61 0.019
434
P ENC004 Encephalitis 61 0.019
435
ALC006 Alcoholic Hepatitis 61 0.019
436
FCS002 Fucosidosis 61 0.019
437
WLD007 Waldenstroem's Macroglobulinemia 61 0.019
438
ALV005 Alveolar Soft Part Sarcoma 61 0.019
439
c WLM018 Wilms Tumor 5 61 0.019
440
P SJG008 Sjogren Syndrome 61 0.019
441
ARG002 Argininosuccinic Aciduria 61 0.019
442
RTN017 Retinal Detachment 61 0.019
443
VRL011 Viral Infectious Disease 61 0.019
444
APP008 Appendicitis 61 0.019
445
c ART144 Arthrogryposis, Distal, Type 1a 61 0.019
446
P HMN010 Hemangioma 61 0.019
447
DCB001 Decubitus Ulcer 61 0.019
448
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.019
449
BTN003 Biotinidase Deficiency 60 0.019
450
P MYL006 Myeloid Leukemia 60 0.019
451
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.019
452
P KDN017 Kidney Cancer 60 0.019
453
SPN186 Spinal Cord Injury 60 0.019
454
HRP004 Herpes Zoster 60 0.019
455
P NPH012 Nephrotic Syndrome 60 0.019
456
SZR001 Sezary's Disease 60 0.019
457
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.019
458
P TST021 Testicular Germ Cell Tumor 60 0.019
459
c LPM012 Lipomatosis, Multiple 60 0.019
460
TRG002 Trigeminal Neuralgia 60 0.019
461
c JVN061 Juvenile Arthritis 60 0.019
462
P BNG030 Benign Ependymoma 60 0.019
463
INT066 Interstitial Lung Disease 60 0.019
464
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.019
465
HPT019 Hepatic Encephalopathy 60 0.019
466
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.019
467
LNG099 Lung Disease 60 0.019
468
c ORF037 Orofaciodigital Syndrome I 60 0.019
469
P ALP009 Alopecia Areata 60 0.019
470
STR039 Sturge-Weber Syndrome 60 0.019
471
LBR030 Leber Optic Atrophy 60 0.019
472
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.019
473
CHC001 Chickenpox 60 0.019
474
P CTR002 Cataract 60 0.019
475
ORL011 Oral Cancer 60 0.019
476
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.019
477
ETN001 Eating Disorder 60 0.019
478
P GLY013 Glycogen Storage Disease 60 0.019
479
c ACT071 Acute Kidney Failure 60 0.019
480
P CHR285 Chronic Myelomonocytic Leukemia 60 0.019
481
VGN017 Vaginal Cancer 60 0.019
482
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.019
483
DYS164 Dyskeratosis Congenita, X-Linked 60 0.019
484
c HRD002 Hereditary Angioedema 60 0.019
485
P OPT006 Optic Nerve Disease 60 0.019
486
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.019
487
SPP011 Suppression of Tumorigenicity 12 59 0.019
488
P MYC008 Myocarditis 59 0.019
489
PRT013 Portal Hypertension 59 0.019
490
CHL014 Cholera 59 0.019
491
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.019
492
P BND020 Bone Disease 59 0.019
493
c HPT016 Hepatitis B 59 0.019
494
P BRN022 Bronchiectasis 59 0.019
495
c PCH015 Pachyonychia Congenita 1 59 0.019
496
THY029 Thyroid Carcinoma 59 0.019
497
IGR001 Ige Responsiveness, Atopic 59 0.019
498
CHL123 Chlamydia 59 0.019
499
PLM033 Pulmonary Embolism 59 0.019
500
P LYM033 Lymphoproliferative Syndrome 59 0.019
501
VSL002 Visual Epilepsy 59 0.019
502
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.019
503
c LTN004 Late-Onset Retinal Degeneration 59 0.019
504
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.019
505
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.019
506
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.019
507
P BRS044 Breast Adenocarcinoma 59 0.019
508
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.019
509
P HMN036 Hemangiopericytoma, Malignant 59 0.019
510
GNG013 Gingivitis 59 0.019
511
ADN018 Adenoma 59 0.019
512
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.019
513
GST045 Gastroenteritis 59 0.019
514
ANR040 Aneurysm 59 0.019
515
c SVR003 Severe Congenital Neutropenia 59 0.019
516
PPT005 Peptic Ulcer Disease 59 0.019
517
SRC027 Sarcoma, Synovial 58 0.019
518
INC002 Inclusion Body Myositis 58 0.019
519
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.019
520
KRT071 Keratosis, Seborrheic 58 0.019
521
P PLY017 Polyarteritis Nodosa 58 0.019
522
P ANP001 Anaplastic Large Cell Lymphoma 58 0.019
523
PST028 Post-Traumatic Stress Disorder 58 0.019
524
P INT070 Intestinal Obstruction 58 0.019
525
RBS001 Rabies 58 0.019
526
P BCL017 B-Cell Lymphoma 58 0.019
527
CRD132 Cardiac Conduction Defect 58 0.019
528
CHR072 Chordoma 58 0.019
529
MCS006 Macs Syndrome 58 0.019
530
THY025 Thymus Cancer 58 0.019
531
c PRG018 Paragangliomas 1 58 0.019
532
SPT004 Septic Arthritis 58 0.019
533
P ALC033 Alcohol Use Disorder 58 0.019
534
HYP458 Hyper Ige Syndrome 58 0.019
535
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.019
536
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.019
537
ERY003 Erythema Multiforme 58 0.019
538
P URT039 Urticaria 58 0.019
539
NWB001 Newborn Respiratory Distress Syndrome 58 0.019
540
DSS008 Disease of Mental Health 58 0.019
541
P MMP001 Mumps 58 0.019
542
MNT002 Mental Depression 58 0.019
543
P EPD003 Epidermolysis Bullosa Simplex 58 0.019
544
LYM027 Lymphopenia 58 0.019
545
P PRP019 Peripheral Nervous System Disease 58 0.019
546
LNG108 Langerhans Cell Histiocytosis 58 0.019
547
MXD005 Mixed Connective Tissue Disease 58 0.019
548
P INF032 Infertility 57 0.019
549
P UVT001 Uveitis 57 0.019
550
PMP006 Pemphigus Vulgaris, Familial 57 0.019
551
P ESP035 Esophagitis, Eosinophilic, 1 57 0.019
552
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.019
553
P GLM007 Glomerulonephritis 57 0.019
554
GLS018 Glass Syndrome 57 0.019
555
CST005 Castleman Disease 57 0.019
556
c CHR417 Chronic Graft Versus Host Disease 57 0.019
557
IRN002 Iron Metabolism Disease 57 0.019
558
BRN056 Bronchopulmonary Dysplasia 57 0.019
559
P PLY041 Polymyositis 57 0.019
560
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.019
561
THY122 Thyroid Gland Cancer 57 0.019
562
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.019
563
c ACT075 Acute Myocardial Infarction 57 0.019
564
THR024 Thrombosis 57 0.019
565
c MST023 Mesothelioma, Malignant 57 0.019
566
APH001 Aphthous Stomatitis 57 0.019
567
PLY023 Polycystic Liver Disease 57 0.019
568
P END033 Endocarditis 57 0.019
569
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.019
570
P FCL005 Focal Segmental Glomerulosclerosis 57 0.019
571
THY022 Thymic Carcinoma 57 0.019
572
P PRV006 Pervasive Developmental Disorder 57 0.019
573
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.019
574
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.019
575
CMM005 Common Cold 57 0.019
576
c ANG068 Angioedema, Hereditary, Type I 57 0.019
577
c GM1004 Gm1-Gangliosidosis, Type I 57 0.019
578
c LKM070 Leukemia, Acute Monocytic 57 0.019
579
HMR039 Hemorrhage, Intracerebral 57 0.019
580
SCH014 Schistosomiasis 57 0.019
581
SKN022 Skin Squamous Cell Carcinoma 57 0.019
582
HYP266 Hypoxia 57 0.019
583
AYM001 Ayme-Gripp Syndrome 57 0.019
584
P ANG015 Angioedema 57 0.019
585
PGM001 Pigmented Villonodular Synovitis 56 0.019
586
P PYL005 Pyelonephritis 56 0.019
587
c BSL024 Basal Cell Carcinoma 1 56 0.019
588
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.019
589
P MYS005 Myositis 56 0.019
590
P PLY018 Polycythemia 56 0.019
591
P ADL017 Adult T-Cell Leukemia 56 0.019
592
P CHN012 Chondrosarcoma 56 0.019
593
CMR002 Coumarin Resistance 56 0.019
594
P FBR017 Fibrosarcoma 56 0.019
595
P PLY011 Polycystic Ovary Syndrome 56 0.019
596
HPT046 Hepatic Veno-Occlusive Disease 56 0.019
597
TRN018 Transitional Cell Carcinoma 56 0.019
598
PLS011 Plasmacytoma 56 0.019
599
EXF001 Exfoliation Syndrome 56 0.019
600
c ACT134 Acute Liver Failure 56 0.019
601
LMY014 Leiomyoma, Uterine 56 0.019
602
P NRP001 Neuropathy 56 0.019
603
SPN041 Spinal Cord Disease 56 0.019
604
SFT003 Soft Tissue Sarcoma 56 0.019
605
ISL001 Islet Cell Tumor 56 0.019
606
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.019
607
HMG005 Hemoglobinopathy 56 0.019
608
P NRF002 Neurofibromatosis 56 0.019
609
EMB004 Embryonal Carcinoma 56 0.019
610
GST050 Gastrointestinal System Disease 56 0.019
611
P LBR014 Leber Congenital Amaurosis 4 56 0.019
612
MCR141 Mucormycosis 56 0.019
613
INT030 Intracranial Aneurysm 56 0.019
614
SCP002 Scapuloperoneal Spinal Muscular Atrophy 56 0.019
615
P HYP024 Hypoparathyroidism 56 0.019
616
MCS002 Mucositis 56 0.019
617
BRN004 Brain Edema 56 0.019
618
AGN016 Aging 56 0.019
619
P GST044 Gastritis 56 0.019
620
MRD002 Marden-Walker Syndrome 56 0.019
621
HPT022 Hepatoblastoma 56 0.019
622
c FML035 Familial Hyperlipidemia 55 0.019
623
HYP005 Hypokalemia 55 0.019
624
NRN004 Neuroendocrine Tumor 55 0.019
625
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.019
626
MCL006 Macular Retinal Edema 55 0.019
627
LMB062 Limb Ischemia 55 0.019
628
ZLL002 Zollinger-Ellison Syndrome 55 0.019
629
MMB001 Membranoproliferative Glomerulonephritis 55 0.019
630
P MLN007 Male Infertility 55 0.019
631
VSC003 Visceral Leishmaniasis 55 0.019
632
c BCT007 Bacterial Meningitis 55 0.019
633
DFF005 Diffuse Large B-Cell Lymphoma 55 0.019
634
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 55 0.019
635
P ANT006 Antiphospholipid Syndrome 55 0.019
636
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.019
637
HRL004 Hurler-Scheie Syndrome 55 0.019
638
CRC006 Carcinoid Syndrome 55 0.019
639
c INT064 Intermediate Uveitis 55 0.019
640
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.019
641
JVN009 Juvenile Pilocytic Astrocytoma 55 0.019
642
ESN005 Eosinophilic Gastroenteritis 55 0.019
643
HNC001 Henoch-Schoenlein Purpura 55 0.019
644
END040 Endogenous Depression 55 0.019
645
INT007 Intermediate Coronary Syndrome 55 0.019
646
HRY003 Hairy Cell Leukemia 55 0.019
647
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.019
648
SYN007 Synovitis 54 0.019
649
PRP030 Purpura 54 0.019
650
RSC001 Rosacea 54 0.019
651
P PMP001 Pemphigus 54 0.019
652
GLS001 Gliosarcoma 54 0.019
653
ACD008 Acid-Labile Subunit Deficiency 54 0.019
654
MNN032 Meningococcal Meningitis 54 0.019
655
GLC003 Glucose Intolerance 54 0.019
656
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.019
657
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.019
658
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.019
659
VLC001 Velocardiofacial Syndrome 54 0.019
660
P CYS039 Cystic Kidney Disease 54 0.019
661
GST037 Gastroparesis 54 0.019
662
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.019
663
CRY003 Cryptosporidiosis 54 0.019
664
PRT038 Protein-Energy Malnutrition 54 0.019
665
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.019
666
CLL010 Cellular Ependymoma 54 0.019
667
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.019
668
ANL018 Analbuminemia 54 0.019
669
P ART021 Arteriosclerosis 54 0.019
670
RVS001 Revesz Syndrome 54 0.019
671
P LTR001 Lateral Sclerosis 54 0.019
672
HMS001 Hemosiderosis 54 0.019
673
LYM040 Lymphoblastic Lymphoma 54 0.019
674
c PST005 Posterior Uveitis 54 0.019
675
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 54 0.019
676
PPL022 Papilloma 54 0.019
677
SLP001 Sleeping Sickness 54 0.019
678
CLL003 Cellulitis 54 0.019
679
NNL006 Non-Alcoholic Steatohepatitis 54 0.019
680
PNC001 Pancytopenia 54 0.019
681
LYM022 Lymphangioma 54 0.019
682
CLR030 Clear Cell Renal Cell Carcinoma 53 0.019
683
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.019
684
P END047 Endophthalmitis 53 0.019
685
P TCD001 Tic Disorder 53 0.019
686
CRY001 Cryptogenic Organizing Pneumonia 53 0.019
687
PST046 Post-Transplant Lymphoproliferative Disease 53 0.019
688
P EPD016 Epidermolysis Bullosa 53 0.019
689
c DMN023 Diamond-Blackfan Anemia 1 53 0.019
690
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.019
691
PLS016 Plasma Cell Leukemia 53 0.019
692
KRT006 Keratoconjunctivitis 53 0.019
693
IMM102 Immunodeficiency 14 53 0.019
694
P MNC007 Monocytic Leukemia 53 0.019
695
PRP036 Peripheral T-Cell Lymphoma 53 0.019
696
CRH005 Crohn's Colitis 53 0.019
697
BRN038 Bronchial Disease 53 0.019
698
P EMB005 Embryonal Rhabdomyosarcoma 53 0.019
699
P RTN016 Retinal Degeneration 53 0.019
700
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.019
701
c PRD040 Periodontitis, Chronic 53 0.019
702
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.019
703
P CNT005 Central Nervous System Lymphoma 53 0.019
704
INF034 Infective Endocarditis 53 0.019
705
P HMR003 Hemorrhagic Disease 53 0.019
706
HYP063 Hypersplenism 53 0.019
707
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.019
708
INT075 Intracranial Hypertension 53 0.019
709
SPN035 Spindle Cell Sarcoma 53 0.019
710
P ACT008 Actinic Keratosis 53 0.019
711
ERD001 Erdheim-Chester Disease 53 0.019
712
IRD001 Iridocyclitis 53 0.019
713
NRT001 Neurotic Disorder 53 0.019
714
GST023 Gastric Ulcer 53 0.019
715
TXC002 Toxic Encephalopathy 53 0.019
716
DNT012 Dental Caries 53 0.019
717
PRP080 Peripheral Artery Disease 53 0.019
718
c FML008 Familial Retinoblastoma 53 0.019
719
c PSR017 Psoriasis 2 53 0.019
720
P INT068 Intestinal Disease 53 0.019
721
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.019
722
P RTN018 Retinal Disease 53 0.019
723
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.019
724
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.019
725
P PRG013 Paraganglioma 52 0.019
726
ESP023 Esophageal Disease 52 0.019
727
MCN017 Meconium Ileus 52 0.019
728
LYS002 Lysosomal Storage Disease 52 0.019
729
c VRL010 Viral Hepatitis 52 0.019
730
ACR041 Acromelic Frontonasal Dysostosis 52 0.019
731
P SML001 Small Cell Carcinoma 52 0.019
732
SMT003 Somatostatinoma 52 0.019
733
GLM004 Gliomatosis Cerebri 52 0.019
734
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.019
735
PST011 Pustulosis of Palm and Sole 52 0.019
736
P HYP730 Hypogonadotropic Hypogonadism 52 0.019
737
P DDN001 Duodenal Ulcer 52 0.019
738
P RCT021 Rectum Cancer 52 0.019
739
IMP005 Impotence 52 0.019
740
CRT016 Carotid Artery Disease 52 0.019
741
ART140 Arteries, Anomalies of 52 0.019
742
THY030 Thyroid Gland Disease 52 0.019
743
P MSC003 Muscular Atrophy 52 0.019
744
c THY107 Thymoma, Familial 52 0.019
745
c PSR023 Psoriasis 1 52 0.019
746
HYP014 Hyperuricemia 52 0.019
747
ACT200 Acute Monoblastic Leukemia 52 0.019
748
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.019
749
TLN003 Telangiectasis 52 0.019
750
P OVR049 Ovarian Disease 52 0.019
751
DSM007 Desmoplastic Small Round Cell Tumor 52 0.019
752
INV006 Inverted Papilloma 52 0.019
753
c ACT135 Acute Graft Versus Host Disease 52 0.019
754
P BRN035 Brain Stem Glioma 52 0.019
755
SRS001 Serous Cystadenocarcinoma 52 0.019
756
P TRT010 Teratoma 52 0.019
757
LMY002 Leiomyoma 52 0.019
758
PNG002 Pain Agnosia 51 0.019
759
SPN051 Spondylitis 51 0.019
760
P HMP007 Hemophilia 51 0.019
761
THR004 Thrombocytosis 51 0.019
762
c CNG208 Congenital Disorder of Glycosylation, Type Iic 51 0.019
763
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.019
764
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 51 0.019
765
P SPP010 Suppressor of Tumorigenicity 3 51 0.019
766
FCT001 Factor Viii Deficiency 51 0.019
767
c NMN014 Niemann-Pick Disease, Type C2 51 0.019
768
FDL002 Food Allergy 51 0.019
769
ALK024 Alkuraya-Kucinskas Syndrome 51 0.019
770
PLS009 Plasma Cell Neoplasm 51 0.019
771
ILS001 Ileus 51 0.019
772
P LCT001 Lactic Acidosis 51 0.019
773
P CPL006 Capillary Hemangioma 51 0.019
774
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 0.019
775
CYS014 Cystadenocarcinoma 51 0.019
776
INT079 Intrahepatic Cholangiocarcinoma 51 0.019
777
CYS036 Cystinosis, Nephropathic 51 0.019
778
VSC006 Vascular Cancer 51 0.019
779
CCC002 Coccidiosis 51 0.019
780
SPL004 Splenic Marginal Zone Lymphoma 51 0.019
781
BLL003 Bell's Palsy 51 0.019
782
FBR008 Fibrillary Astrocytoma 51 0.019
783
TNG007 Tongue Carcinoma 51 0.019
784
GNG012 Gingival Overgrowth 51 0.019
785
P HYP040 Hypospadias 51 0.019
786
HYP074 Hypersensitivity Vasculitis 51 0.019
787
END086 End Stage Renal Disease 51 0.019
788
CRV040 Cervix Carcinoma 51 0.019
789
SKN013 Skin Benign Neoplasm 51 0.019
790
PNM005 Pneumonic Plague 51 0.019
791
P CHL066 Cholangitis 51 0.019
792
URC002 Urea Cycle Disorder 51 0.019
793
ACT017 Acute Chest Syndrome 51 0.019
794
HYP081 Hypolipoproteinemia 51 0.019
795
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.019
796
CHR005 Chorioamnionitis 51 0.019
797
c ALM001 Al Amyloidosis 50 0.019
798
GNT002 Giant Cell Glioblastoma 50 0.019
799
PTT041 Pituitary Stalk Interruption Syndrome 50 0.019
800
P MMB011 Membranous Nephropathy 50 0.019
801
P HYP077 Hypertrichosis 50 0.019
802
PLR007 Pleural Empyema 50 0.019
803
c PRM012 Primary Polycythemia 50 0.019
804
P FNC004 Fanconi Syndrome 50 0.019
805
BRX001 Bruxism 50 0.019
806
SPN021 Spinal Meningioma 50 0.019
807
ALL009 Allergic Conjunctivitis 50 0.019
808
P ECL001 Eclampsia 50 0.019
809
RSP006 Respiratory System Disease 50 0.019
810
HPT014 Hepatorenal Syndrome 50 0.019
811
CRN030 Coronary Stenosis 50 0.019
812
c HRD202 Hereditary Lymphedema I 50 0.019
813
c INF145 Infantile Liver Failure Syndrome 1 50 0.019
814
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.019
815
MCP006 Mucoepidermoid Carcinoma 50 0.019
816
PYD002 Pyoderma 50 0.019
817
P PNV001 Panuveitis 50 0.019
818
c CPL013 Capillary Malformations, Congenital 50 0.019
819
TRY001 Trypanosomiasis 50 0.019
820
P KRT007 Keratoconus 50 0.019
821
HMG002 Hemoglobinuria 50 0.019
822
TRP002 Tropical Spastic Paraparesis 50 0.019
823
BLS002 Blastomycosis 50 0.019
824
CLR003 Clear Cell Adenocarcinoma 50 0.019
825
c CNG027 Congenital Hemolytic Anemia 50 0.019
826
DYS073 Dysphagia 50 0.019
827
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.019
828
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.019
829
ATY042 Atypical Chronic Myeloid Leukemia 49 0.019
830
c CHR418 Chronic Leukemia 49 0.019
831
c THR090 Thrombocythemia 1 49 0.019
832
VRR004 Verrucous Carcinoma 49 0.019
833
BLD053 Blood Platelet Disease 49 0.019
834
P IGN003 Iga Nephropathy 1 49 0.019
835
KRT001 Keratoconjunctivitis Sicca 49 0.019
836
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.019
837
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.019
838
MYC012 Mycetoma 49 0.019
839
PLP001 Pulpitis 49 0.019
840
PRN014 Paronychia 49 0.019
841
P MST002 Mast-Cell Leukemia 49 0.019
842
47X002 47,xyy 49 0.019
843
P OPN001 Open-Angle Glaucoma 49 0.019
844
MCR004 Macroglobulinemia 49 0.019
845
GST049 Gastrointestinal System Cancer 49 0.019
846
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.019
847
P CRV031 Cervical Adenocarcinoma 49 0.019
848
MNN009 Meningoencephalitis 49 0.019
849
MYL003 Myeloid Sarcoma 49 0.019
850
ACT029 Acute Interstitial Pneumonia 49 0.019
851
P CMP008 Compartment Syndrome 49 0.019
852
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.019
853
P HYP828 Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant 49 0.019
854
SBP001 Subependymal Giant Cell Astrocytoma 49 0.019
855
HST010 Histiocytosis 48 0.019
856
RYN001 Raynaud Disease 48 0.019
857
c BCT013 Bacterial Pneumonia 48 0.019
858
BNR002 Bone Resorption Disease 48 0.019
859
INT054 Intraocular Lymphoma 48 0.019
860
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.019
861
ATS010 Autosomal Recessive Disease 48 0.019
862
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.019
863
EVN001 Evans' Syndrome 48 0.019
864
ASP007 Aspiration Pneumonia 48 0.019
865
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.019
866
CHR563 Chronic Eosinophilic Leukemia 48 0.019
867
CRY004 Cryoglobulinemia 48 0.019
868
OLF005 Olfactory Neuroblastoma 48 0.019
869
RFR010 Refractory Anemia 48 0.019
870
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.019
871
ACT098 Acute Erythroid Leukemia 48 0.019
872
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.019
873
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.019
874
CLS016 Clostridium Difficile Colitis 48 0.019
875
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.019
876
DBT006 Diabetic Macular Edema 48 0.019
877
GNG008 Ganglioneuroblastoma 48 0.019
878
SPL018 Splenomegaly 48 0.019
879
P SCL015 Scleritis 48 0.019
880
IGG001 Iga Glomerulonephritis 48 0.019
881
PRS012 Pars Planitis 48 0.019
882
P MCL001 Mucolipidosis 48 0.019
883
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.019
884
DSM003 Desmoid Disease, Hereditary 48 0.019
885
LPT006 Leptin Receptor Deficiency 48 0.019
886
c PNT034 Pontocerebellar Hypoplasia, Type 2e 48 0.019
887
CHL056 Cheilitis 48 0.019
888
HYP025 Hyperphosphatemia 48 0.019
889
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.019
890
c PRK071 Parkinson Disease 14, Autosomal Recessive 48 0.019
891
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.019
892
c PRM226 Primary Central Nervous System Lymphoma 48 0.019
893
RCT020 Rectum Adenocarcinoma 48 0.019
894
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.019
895
ADN009 Adenosquamous Carcinoma 47 0.019
896
GRM005 Germ Cell Cancer 47 0.019
897
PRL017 Prolymphocytic Leukemia 47 0.019
898
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.019
899
DRY001 Dry Eye Syndrome 47 0.019
900
CRC014 Carcinoid Tumors, Intestinal 47 0.019
901
MCC002 Mucocutaneous Leishmaniasis 47 0.019
902
ADN001 Adenosine Deaminase Deficiency 47 0.019
903
P PRR002 Pure Red-Cell Aplasia 47 0.019
904
VRN004 Vernal Keratoconjunctivitis 47 0.019
905
MLT152 Multiple Self-Healing Squamous Epithelioma 47 0.019
906
SPH010 Sphingolipidosis 47 0.019
907
CRN017 Coronary Thrombosis 47 0.019
908
P HMN032 Human Herpesvirus 8 47 0.019
909
KRT008 Keratopathy 47 0.019
910
NRN001 Neuroendocrine Carcinoma 47 0.019
911
c PSR032 Psoriasis 11 47 0.019
912
RNL077 Renal Fibrosis 47 0.019
913
ACT055 Actinomycosis 47 0.019
914
ACT084 Acute Stress Disorder 47 0.019
915
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.019
916
KRT002 Keratomalacia 47 0.019
917
RTC005 Reticulosarcoma 47 0.019
918
KHN001 Kuhnt-Junius Degeneration 47 0.019
919
LYM012 Lymphoplasmacytic Lymphoma 47 0.019
920
RTN001 Retinal Vasculitis 47 0.019
921
c INH020 Inherited Metabolic Disorder 47 0.019
922
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.019
923
SRT004 Serotonin Syndrome 47 0.019
924
STM006 Stomach Disease 47 0.019
925
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.019
926
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.019
927
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.019
928
MLT113 Multicentric Castleman Disease 47 0.019
929
GST071 Gastrointestinal Carcinoma 47 0.019
930
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.019
931
CNT033 Central Nervous System Cancer 47 0.019
932
NDL013 Nodular Regenerative Hyperplasia 47 0.019
933
STR103 Streptococcus Pneumonia 47 0.019
934
CRD137 Cardiogenic Shock 47 0.019
935
CHR074 Choriocarcinoma 47 0.019
936
P OVR046 Ovarian Cyst 47 0.019
937
c PRM093 Premature Ovarian Failure 7 47 0.019
938
NSS002 Neisseria Meningitidis Infection 47 0.019
939
RYN005 Raynaud Phenomenon 47 0.019
940
P BLD051 Blood Coagulation Disease 46 0.019
941
LYM019 Lymphosarcoma 46 0.019
942
RTN023 Retinitis 46 0.019
943
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.019
944
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.019
945
CD4003 Cd40 Ligand Deficiency 46 0.019
946
TST014 Testicular Cancer 46 0.019
947
HYR002 Hoyeraal Hreidarsson Syndrome 46 0.019
948
PRP017 Periapical Periodontitis 46 0.019
949
MCS004 Mucosal Melanoma 46 0.019
950
MNN020 Meningococcal Infection 46 0.019
951
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.019
952
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.019
953
FCL012 Facial Paralysis 46 0.019
954
CLN045 Colonic Benign Neoplasm 46 0.019
955
P BRB001 Beriberi 46 0.019
956
P CHR573 Choroid Plexus Cancer 46 0.019
957
P BNG032 Benign Mesothelioma 46 0.019
958
ANP006 Anaplastic Ependymoma 46 0.019
959
ADR040 Adrenal Gland Pheochromocytoma 46 0.019
960
SBP004 Subependymoma 46 0.019
961
MYX001 Myxopapillary Ependymoma 46 0.019
962
GST010 Gestational Trophoblastic Neoplasm 46 0.019
963
ANG018 Angiomyolipoma 46 0.019
964
SQM002 Squamous Cell Papilloma 46 0.019
965
SPR005 Superficial Basal Cell Carcinoma 46 0.019
966
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.019
967
c DRR009 Diarrhea 6 46 0.019
968
PRX001 Peroxisomal Disease 46 0.019
969
c MLG068 Malignant Glioma 46 0.019
970
GLL048 Glial Tumor 45 0.019
971
BNS007 Bone Sarcoma 45 0.019
972
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.019
973
GST030 Gastrinoma 45 0.019
974
SYN036 Syncope 45 0.019
975
EXT010 Extramedullary Plasmacytoma 45 0.019
976
RTR008 Root Resorption 45 0.019
977
GLY031 Glycoproteinosis 45 0.019
978
MXD026 Mixed Glioma 45 0.019
979
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.019
980
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 45 0.019
981
PPL018 Papillary Adenocarcinoma 45 0.019
982
INT253 Intestinal Benign Neoplasm 45 0.019
983
HMR023 Hemorrhagic Cystitis 45 0.019
984
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.019
985
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.019
986
HPT004 Hepatic Coma 45 0.019
987
IMM136 Immune System Disease 45 0.019
988
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.019
989
ESP027 Esophagus Squamous Cell Carcinoma 45 0.019
991
ACT003 Acute Kidney Tubular Necrosis 45 0.019
992
LYM051 Lymphomatoid Granulomatosis 45 0.019
993
URT051 Ureter, Cancer of 45 0.019
994
SPP008 Suppurative Otitis Media 45 0.019
995
CLL014 Cll/sll 45 0.019
996
GLC036 Glucagonoma 45 0.019
997
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.019
998
c ACQ014 Acquired Hemophilia 45 0.019
999
END035 Endocrine Gland Cancer 45 0.019
1000
MYF001 Myofibroma 45 0.019
1001
OVR112 Ovarian Germ Cell Cancer 45 0.019
1002
ASP008 Aspiration Pneumonitis 45 0.019
1003
c CLR017 Clear Cell Sarcoma 45 0.019
1004
SPS057 Spasticity 45 0.019
1005
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 45 0.019
1006
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.019
1007
MXD023 Mixed Cell Type Cancer 44 0.019
1009
P CHR345 Chronic Pain 44 0.019
1010
P EPT012 Epithelioid Sarcoma 44 0.019
1011
SBC016 Subacute Delirium 44 0.019
1012
CYS009 Cystadenoma 44 0.019
1013
c MYL058 Myeloproliferative Syndrome, Transient 44 0.019
1014
APP009 Appendix Adenocarcinoma 44 0.019
1015
GRN017 Granulocytopenia 44 0.019
1016
LTH001 Lethal Midline Granuloma 44 0.019
1017
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.019
1018
CNN002 Cannabis Abuse 44 0.019
1019
P END039 Endodermal Sinus Tumor 44 0.019
1020
P GNG009 Gangliosidosis 44 0.019
1021
P FBR003 Fibrous Histiocytoma 44 0.019
1022
PLX002 Plexiform Neurofibroma 44 0.019
1023
OVR063 Overnutrition 44 0.019
1024
ACN001 Acinar Cell Carcinoma 44 0.019
1025
PRT035 Peritoneum Cancer 44 0.019
1026
PPL001 Papillary Adenoma 44 0.019
1027
c HYP272 Hypercholesterolemia, Familial, 3 44 0.019
1028
THR012 Thoracic Cancer 44 0.019
1029
P BCT020 Bacteremia 2 44 0.019
1030
P EPN001 Ependymoblastoma 44 0.019
1031
c HRD173 Hereditary Late-Onset Parkinson Disease 44 0.019
1032
c PRM038 Primary Agammaglobulinemia 44 0.019
1033
MTR010 Mature Teratoma 44 0.019
1034
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.019
1035
c ADL023 Adult Medulloblastoma 44 0.019
1036
CVD001 Covid-19 44 0.019
1037
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.019
1038
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.019
1039
P CRN024 Corneal Disease 44 0.019
1040
FBR054 Fibroma 44 0.019
1041
FNG004 Fungal Meningitis 44 0.019
1042
IDP033 Idiopathic Edema 44 0.019
1043
ANP009 Anaplastic Oligodendroglioma 43 0.019
1044
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.019
1045
SMN007 Seminoma 43 0.019
1046
c HYP847 Hyper Ige Recurrent Infection Syndrome 1 43 0.019
1047
SKN005 Skin Atrophy 43 0.019
1048
P TST026 Testicular Germ Cell Cancer 43 0.019
1049
LMY003 Leiomyomatosis 43 0.019
1050
MRG013 Mirage Syndrome 43 0.019
1051
c MLG081 Malignant Teratoma 43 0.019
1052
P PHR004 Pharynx Cancer 43 0.019
1053
NRF003 Neurofibrosarcoma 43 0.019
1054
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.019
1055
SPC005 Speech Disorder 43 0.019
1056
RDC006 Red Cell Aplasia 43 0.019
1057
KPS002 Kaposiform Hemangioendothelioma 43 0.019
1058
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 0.019
1059
LWC001 Low Compliance Bladder 43 0.019
1060
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 0.019
1061
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.019
1062
OPP002 Opportunistic Mycosis 43 0.019
1063
MXD050 Mixed Phenotype Acute Leukemia 43 0.019
1064
c CHR056 Chronic Tic Disorder 43 0.019
1065
HYP457 Hypertrophic Scars 42 0.019
1066
TRP009 Triple X Syndrome 42 0.019
1067
P AVS003 Avascular Necrosis 42 0.019
1068
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.019
1069
DNT014 Dental Pulp Disease 42 0.019
1070
c PSR028 Psoriasis 7 42 0.019
1071
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.019
1072
P PRT026 Parotitis 42 0.019
1073
CHR286 Chronic Neutrophilic Leukemia 42 0.019
1074