Search results for Miconazole

1354 hits were found for Miconazole

# Family MCID Name MIFTS Score
1
P CND004 Candidiasis 57 12.860
2
ORL005 Oral Candidiasis 55 7.621
3
VLV011 Vulvovaginal Candidiasis 49 7.096
4
DRM011 Dermatophytosis 52 6.805
5
VGN023 Vaginitis 56 6.747
6
STM007 Stomatitis 52 4.828
7
FNG017 Fungal Infectious Disease 54 4.531
8
CTN033 Cutaneous Candidiasis 38 4.380
9
DNT008 Denture Stomatitis 35 4.296
10
DRM006 Dermatitis 61 4.224
11
TNP001 Tinea Pedis 48 3.976
12
VLV010 Vulvovaginitis 42 3.823
13
OTM001 Otomycosis 29 3.601
14
P EXN002 Exanthem 58 3.521
15
P ASP006 Aspergillosis 71 3.429
16
KRT019 Keratitis, Hereditary 66 3.412
17
CCC001 Coccidioidomycosis 57 3.391
18
BCT002 Bacterial Vaginosis 52 3.349
19
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.337
20
TNC001 Tinea Cruris 35 3.178
21
DRM009 Dermatomycosis 36 3.169
22
PTY002 Pityriasis Versicolor 38 3.106
23
CRY005 Cryptococcosis 61 3.046
24
P MNN013 Meningitis 65 2.843
25
P ACN011 Acne 55 2.674
26
BLS002 Blastomycosis 47 2.627
27
CND006 Candida Glabrata 29 2.536
28
TRC003 Trichomoniasis 53 2.443
29
P LCH002 Lichen Planus 54 2.393
30
ORL013 Oral Lichen Planus 45 2.393
31
P OTT001 Otitis Externa 43 2.365
32
FNG016 Fungal Keratitis 40 2.333
33
CNT047 Contact Dermatitis 56 2.326
34
PRC002 Paracoccidioidomycosis 53 2.171
35
CRY014 Cryptococcal Meningitis 48 2.127
36
HST011 Histoplasmosis 54 2.127
37
P END047 Endophthalmitis 53 2.049
38
MCS002 Mucositis 55 2.043
39
SPR020 Superficial Mycosis 34 1.950
40
CHR063 Chronic Mucocutaneous Candidiasis 68 1.926
41
VGN020 Vaginal Disease 49 1.920
42
P KLZ004 Kala-Azar 1 41 1.912
43
FNG004 Fungal Meningitis 46 1.912
44
LSH001 Leishmaniasis 63 1.912
45
AGN016 Aging 53 1.873
46
P SBR004 Seborrheic Dermatitis 44 1.860
47
P CRN028 Corneal Ulcer 47 1.798
48
P BLD134 Bladder Cancer 79 1.756
49
ESP018 Esophageal Candidiasis 47 1.742
50
TNC003 Tinea Corporis 40 1.665
51
THR004 Thrombocytosis 52 1.608
52
P END044 Endometriosis 62 1.590
53
P HYP098 Hypereosinophilic Syndrome 66 1.516
54
MLN073 Melanosis, Neurocutaneous 45 1.486
55
c FNC043 Fanconi Anemia, Complementation Group E 62 1.486
56
HNT002 Hantavirus Pulmonary Syndrome 55 1.486
57
ATX019 Ataxia with Vitamin E Deficiency 44 1.486
58
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.486
59
P NTR004 Neutropenia 62 1.483
60
ACN019 Acanthamoeba Keratitis 31 1.453
61
BCT022 Bacterial Infectious Disease 55 1.444
62
SPR010 Sporotrichosis 45 1.444
63
PPT005 Peptic Ulcer Disease 58 1.404
64
ALL010 Allergic Contact Dermatitis 55 1.380
65
PLM007 Pulmonary Aspergilloma 30 1.358
66
P DRR001 Diarrhea 55 1.358
67
GRN017 Granulocytopenia 42 1.332
68
PYD002 Pyoderma 49 1.312
69
c ACT073 Acute Leukemia 59 1.312
70
P LNG028 Long Qt Syndrome 63 1.306
71
MNN009 Meningoencephalitis 47 1.306
72
CTN007 Cutaneous Leishmaniasis 61 1.304
73
TNC002 Tinea Capitis 42 1.274
74
MYC012 Mycetoma 49 1.274
75
SKN016 Skin Disease 63 1.241
76
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.239
77
P ESP024 Esophagitis 60 1.223
78
OPS001 Opisthorchiasis 41 1.215
79
TNN001 Tinea Nigra 28 1.208
80
BNR002 Bone Resorption Disease 47 1.185
81
P CNJ013 Conjunctivitis 66 1.185
82
48X005 48,xyyy 39 1.185
83
ERY010 Erythrasma 27 1.170
84
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.165
85
OST159 Osteogenic Sarcoma 66 1.165
86
PRT036 Peritonitis 65 1.165
87
IRR003 Irritant Dermatitis 47 1.143
88
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.119
89
OST017 Osteomyelitis 63 1.111
90
P ALZ034 Alzheimer Disease 87 1.093
91
CCC002 Coccidiosis 50 1.093
92
P HYP086 Hypothyroidism 68 1.093
93
P PRD008 Periodontitis 63 1.088
94
ENT011 Enterocolitis 55 1.085
95
P NPH012 Nephrotic Syndrome 61 1.065
96
KRT009 Keratosis 52 1.065
97
GNG013 Gingivitis 59 1.065
98
c ACT068 Acute Cystitis 60 1.065
99
c DWL002 Dowling-Degos Disease 1 58 1.033
100
NRR001 Neuroretinitis 42 1.033
101
PST011 Pustulosis of Palm and Sole 52 1.033
102
ALL029 Allergic Disease 61 1.033
103
RTN023 Retinitis 45 1.033
104
P PSR002 Psoriasis 63 1.033
105
LNG099 Lung Disease 62 1.033
106
P PLY188 Polyendocrinopathy 29 1.033
107
GLB002 Glioblastoma 67 1.011
108
CYS001 Cystic Fibrosis 77 0.994
109
P CYS018 Cystitis 58 0.994
110
P PMP001 Pemphigus 54 0.994
111
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.994
112
c LKM005 Leukemia, T-Cell, Chronic 33 0.994
113
SRT004 Serotonin Syndrome 54 0.994
114
INT071 Intestinal Perforation 49 0.986
115
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.976
116
PRP030 Purpura 54 0.976
117
SCH014 Schistosomiasis 56 0.976
118
47X002 47,xyy 47 0.976
119
P MYS003 Myasthenia Gravis 67 0.945
120
P GRF003 Graft-Versus-Host Disease 71 0.945
121
GRN037 Granulomatosis with Polyangiitis 66 0.945
122
PHR003 Pharyngitis 57 0.945
123
CHR001 Churg-Strauss Syndrome 61 0.945
124
P BND020 Bone Disease 60 0.938
125
VGN019 Vaginal Discharge 33 0.938
126
DYS073 Dysphagia 53 0.938
127
CHR031 Chromoblastomycosis 48 0.918
128
CRB004 Cerebral Artery Occlusion 45 0.918
129
IMP004 Impetigo 48 0.896
130
ANG049 Angioedema Induced by Ace Inhibitors 38 0.893
131
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.872
132
HLC007 Helicobacter Pylori Infection 67 0.872
133
P GST044 Gastritis 55 0.872
134
LNG095 Lung Abscess 50 0.846
135
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.846
136
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.846
137
TNF001 Tinea Favosa 26 0.846
138
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.840
139
TRC121 Trichomonas Vaginalis Trichomoniasis 23 0.840
140
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.840
141
RCK004 Rickets 64 0.840
142
KRT002 Keratomalacia 54 0.840
143
TNN002 Tinea Unguium 34 0.818
144
CHL056 Cheilitis 46 0.818
145
MTB004 Metabolic Acidosis 48 0.786
146
c PSR029 Psoriasis 9 24 0.786
147
GST023 Gastric Ulcer 52 0.786
148
CLL003 Cellulitis 53 0.786
149
ANR004 Anuria 44 0.786
150
PLR008 Pleurisy 49 0.786
151
CHR078 Chorioretinitis 50 0.786
152
ANG061 Angular Cheilitis 27 0.747
153
c EXD008 Exudative Vitreoretinopathy 1 71 0.747
154
P PTN014 Patent Ductus Arteriosus 1 59 0.747
155
ECT004 Ecthyma 26 0.747
156
MST005 Mastitis 52 0.747
157
c SYS038 Systemic Lupus Erythematosus 2 20 0.698
158
P PLY041 Polymyositis 58 0.698
159
MYC087 Mycoplasma Pneumoniae Pneumonia 52 0.698
160
P TRT010 Teratoma 50 0.698
161
P DRM010 Dermatomyositis 61 0.698
162
PRN019 Perinatal Necrotizing Enterocolitis 60 0.698
163
c BCT013 Bacterial Pneumonia 47 0.698
164
MCR141 Mucormycosis 59 0.646
165
ACQ007 Acquired Immunodeficiency Syndrome 58 0.608
166
P DNG005 Dengue Virus 55 0.577
167
VLV008 Vulvitis 31 0.577
168
MRR003 Murray Valley Encephalitis 28 0.577
169
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.577
170
FXD003 Fixed Drug Eruption 34 0.577
171
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.577
172
ART002 Arts Syndrome 66 0.565
173
FSR001 Fusariosis 45 0.542
174
FLL008 Folliculitis 45 0.542
175
P ALP008 Alopecia 53 0.542
176
IMP005 Impotence 52 0.516
177
LVR012 Liver Cirrhosis 62 0.516
178
TXC005 Toxic Shock Syndrome 61 0.516
179
P MLN008 Melanoma 75 0.516
180
P CTR002 Cataract 59 0.516
181
c PRD040 Periodontitis, Chronic 52 0.488
182
IMM167 Immune Deficiency Disease 76 0.488
183
HPT022 Hepatoblastoma 54 0.488
184
P ENC004 Encephalitis 61 0.488
185
NRL016 Neural Tube Defects 80 0.455
186
c LKM061 Leukemia, Acute Myeloid 83 0.455
187
EMY001 Eumycotic Mycetoma 35 0.455
188
P UVT001 Uveitis 57 0.455
189
HYP266 Hypoxia 56 0.455
190
P OVR082 Overgrowth Syndrome 41 0.455
191
ADR007 Adrenoleukodystrophy 73 0.417
192
P BRS047 Breast Cancer 97 0.417
193
DSS032 Disease by Infectious Agent 55 0.417
194
CLN015 Colon Adenocarcinoma 64 0.417
195
c ACT071 Acute Kidney Failure 60 0.417
196
P SCL015 Scleritis 47 0.417
197
MCL006 Macular Retinal Edema 56 0.417
198
P URN019 Urinary Tract Infection 48 0.417
199
CHG001 Chagas Disease 65 0.417
200
RSC001 Rosacea 55 0.417
201
IRD001 Iridocyclitis 54 0.417
202
ADR022 Adrenomyeloneuropathy 38 0.417
203
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.417
204
P END033 Endocarditis 58 0.381
205
CLT003 Colitis 63 0.367
206
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.367
207
CRH005 Crohn's Colitis 53 0.367
208
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.367
209
APH002 Aphasia 55 0.367
210
P INF037 Inflammatory Bowel Disease 53 0.367
211
P SRC025 Sarcoidosis 1 70 0.367
212
LYM133 Lymphoma, Hodgkin, Classic 69 0.367
214
SCK003 Sickle Cell Anemia 74 0.367
215
PRP027 Peripheral Vascular Disease 71 0.367
216
P GST053 Gastric Cancer 82 0.367
217
CRY001 Cryptogenic Organizing Pneumonia 53 0.367
218
c THY107 Thymoma, Familial 42 0.367
219
P SPP010 Suppressor of Tumorigenicity 3 50 0.367
220
KPS004 Kaposi Sarcoma 76 0.367
221
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.367
222
CHL065 Cholangiocarcinoma 57 0.367
223
ATM095 Autoimmune Disease 61 0.367
224
c LKM070 Leukemia, Acute Monocytic 56 0.367
225
P MYS005 Myositis 55 0.367
226
PMP006 Pemphigus Vulgaris, Familial 57 0.367
227
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.367
228
PRS012 Pars Planitis 47 0.367
229
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.367
230
CHR008 Choroiditis 48 0.367
231
LMB062 Limb Ischemia 55 0.367
232
PNC001 Pancytopenia 52 0.367
233
DNT012 Dental Caries 53 0.367
234
P THY023 Thymoma 64 0.367
235
BRN012 Bronchiolitis Obliterans 56 0.367
236
PPL022 Papilloma 53 0.367
237
P VSC007 Vascular Disease 62 0.367
238
ESP023 Esophageal Disease 52 0.367
239
IRN002 Iron Metabolism Disease 56 0.367
240
P DMN001 Diamond-Blackfan Anemia 73 0.367
241
BRN002 Bronchiolitis 57 0.367
242
SVR001 Severe Acute Respiratory Syndrome 68 0.367
243
P AGM001 Agammaglobulinemia 67 0.367
244
P LVR013 Liver Disease 68 0.367
245
P PLM036 Pulmonary Fibrosis 65 0.367
246
P CHR012 Chronic Granulomatous Disease 69 0.367
247
INT079 Intrahepatic Cholangiocarcinoma 51 0.367
248
P ART022 Arthritis 70 0.367
249
P HML002 Hemolytic Anemia 62 0.367
250
BRN024 Bronchitis 67 0.367
251
c JVN010 Juvenile Rheumatoid Arthritis 52 0.367
252
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.367
253
CRH001 Crohn's Disease 80 0.367
254
P SCK005 Sickle Cell Disease 56 0.367
255
c CHR684 Chronic Kidney Disease 73 0.367
256
P PLY017 Polyarteritis Nodosa 59 0.367
257
HYP056 Hypoglycemia 65 0.367
258
LKP003 Leukoplakia 39 0.367
259
PST092 Posttransplant Acute Limbic Encephalitis 29 0.367
260
TNB001 Tinea Barbae 27 0.318
261
TRC006 Trichosporonosis 29 0.318
262
HYP084 Hypopyon 37 0.318
263
PRT013 Portal Hypertension 59 0.295
264
c SYS001 Systemic Lupus Erythematosus 85 0.269
265
P DRM053 Dermatitis, Atopic 65 0.269
266
PRM004 Primary Amebic Meningoencephalitis 27 0.269
267
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.269
268
TNM002 Tinea Manuum 26 0.269
269
P HYD006 Hydrocephalus 62 0.269
270
P HRP006 Herpes Simplex 65 0.269
271
C1N001 C1 Inhibitor Deficiency 43 0.247
272
P PRV006 Pervasive Developmental Disorder 52 0.247
273
c ATS007 Autism Spectrum Disorder 71 0.247
274
P PHR004 Pharynx Cancer 44 0.247
275
CNN010 Connective Tissue Benign Neoplasm 44 0.247
276
GBM001 Gaba Aminotransferase Deficiency 31 0.247
277
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.247
278
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 0.247
279
MLR004 Malaria 77 0.247
280
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.247
281
c MJR022 Major Affective Disorder 8 37 0.247
282
ACT119 Acute Promyelocytic Leukemia 62 0.247
283
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.247
284
ALK024 Alkuraya-Kucinskas Syndrome 46 0.247
285
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.247
286
PRT251 Proteinuria, Chronic Benign 58 0.247
287
DFC004 Deficiency Anemia 74 0.247
288
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.247
289
P CRN300 Coronary Heart Disease 1 73 0.247
291
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.247
292
c LPR022 Leprosy 2 35 0.247
293
CD4003 Cd40 Ligand Deficiency 53 0.247
294
MYL009 Myelodysplastic Syndrome 67 0.247
295
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.247
296
SPL004 Splenic Marginal Zone Lymphoma 50 0.247
297
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.247
298
LNG108 Langerhans Cell Histiocytosis 57 0.247
299
c BSL024 Basal Cell Carcinoma 1 55 0.247
300
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.247
301
LTN004 Late-Onset Retinal Degeneration 59 0.247
302
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 53 0.247
303
P APL001 Aplastic Anemia 72 0.247
304
c ALP101 Alpha-Thalassemia 62 0.247
305
AMG001 Amegakaryocytic Thrombocytopenia, Congenital 55 0.247
306
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 0.247
307
PLY023 Polycystic Liver Disease 62 0.247
308
P PRG013 Paraganglioma 57 0.247
309
ZLL002 Zollinger-Ellison Syndrome 55 0.247
310
c PSR028 Psoriasis 7 42 0.247
311
ALV005 Alveolar Soft Part Sarcoma 61 0.247
312
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.247
313
ILT001 Ileitis 49 0.247
314
P SLP006 Sleep Apnea 69 0.247
315
FBR054 Fibroma 44 0.247
316
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.247
317
PNG002 Pain Agnosia 51 0.247
318
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.247
319
ERY003 Erythema Multiforme 56 0.247
320
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.247
321
c PSR023 Psoriasis 1 52 0.247
322
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.247
323
P RHM011 Rheumatoid Arthritis 81 0.247
324
P SCH015 Schizophrenia 74 0.247
325
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.247
326
c ART144 Arthrogryposis, Distal, Type 1a 61 0.247
327
ART140 Arteries, Anomalies of 52 0.247
328
BHC003 Behcet Syndrome 70 0.247
329
BLR027 Blue Rubber Bleb Nevus 39 0.247
330
P CMP005 Campomelic Dysplasia 65 0.247
331
VLC001 Velocardiofacial Syndrome 57 0.247
332
c WLM013 Wilms Tumor 1 65 0.247
333
IMM166 Immunodeficiency 27a 58 0.247
334
P ATS364 Autism 72 0.247
335
CHR072 Chordoma 56 0.247
336
EHL079 Ehlers-Danlos Syndrome, Dermatosparaxis Type 52 0.247
337
DWN001 Down Syndrome 70 0.247
338
c ANM038 Anemia, Autoimmune Hemolytic 63 0.247
339
TKY002 Takayasu Arteritis 61 0.247
340
CHN019 Chand Syndrome 31 0.247
341
CHD001 Chediak-Higashi Syndrome 66 0.247
342
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.247
343
LPM012 Lipomatosis, Multiple 59 0.247
344
c CRN243 Carney Complex, Type 1 53 0.247
345
P IGN003 Iga Nephropathy 1 39 0.247
346
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 0.247
347
c NRF024 Neurofibromatosis, Type I 76 0.247
348
CPL013 Capillary Malformations, Congenital 53 0.247
349
P FNG006 Feingold Syndrome 1 61 0.247
350
P OST002 Osteoporosis 76 0.247
351
c PCH015 Pachyonychia Congenita 1 60 0.247
352
PPL052 Papillomatosis, Confluent and Reticulated 34 0.247
353
P MDL005 Medulloblastoma 75 0.247
354
c MGR028 Migraine with or Without Aura 1 63 0.247
355
P OST135 Osteogenesis Imperfecta, Type I 60 0.247
356
P OVR042 Ovarian Cancer 88 0.247
357
CMP040 Complement Component 4, Partial Deficiency of 34 0.247
358
P MJR007 Major Affective Disorder 1 42 0.247
359
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.247
360
c TYP009 Type 2 Diabetes Mellitus 91 0.247
361
ERY051 Erythroleukemia, Familial 37 0.247
362
BRT002 Birt-Hogg-Dube Syndrome 64 0.247
363
DSM003 Desmoid Disease, Hereditary 49 0.247
364
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.247
365
P PRS040 Prostate Cancer 95 0.247
366
SCP002 Scapuloperoneal Spinal Muscular Atrophy 54 0.247
367
SPT006 Septooptic Dysplasia 62 0.247
368
c SCL052 Scleroderma, Familial Progressive 60 0.247
369
RYN001 Raynaud Disease 49 0.247
370
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.247
371
P RTN024 Retinoblastoma 72 0.247
372
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 0.247
373
PPL049 Papillon-Lefevre Syndrome 65 0.247
374
P KRB001 Krabbe Disease 69 0.247
375
c MCL046 Mucolipidosis Iii Alpha/beta 61 0.247
376
c MCL013 Mucolipidosis Iv 64 0.247
377
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.247
378
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.247
379
c FML346 Familial Adenomatous Polyposis 1 65 0.247
380
PTZ001 Peutz-Jeghers Syndrome 69 0.247
381
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.247
382
P HMN038 Human Coronavirus Sensitivity 30 0.247
383
P PHT010 Photoparoxysmal Response 1 46 0.247
384
FCT001 Factor Viii Deficiency 61 0.247
385
GLL008 Gilles De La Tourette Syndrome 64 0.247
386
HMN035 Hemangioma-Thrombocytopenia Syndrome 39 0.247
387
CRC014 Carcinoid Tumors, Intestinal 46 0.247
388
LRY022 Laryngoonychocutaneous Syndrome 43 0.247
389
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.247
390
MRD002 Marden-Walker Syndrome 56 0.247
391
c MCP043 Mucopolysaccharidosis, Type Iiia 60 0.247
392
c MCP045 Mucopolysaccharidosis, Type Iiic 58 0.247
393
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.247
394
c MCP049 Mucopolysaccharidosis, Type Vii 62 0.247
395
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.247
396
STR039 Sturge-Weber Syndrome 60 0.247
397
P TMP003 Temporal Arteritis 68 0.247
398
c THR090 Thrombocythemia 1 50 0.247
399
DGR001 Digeorge Syndrome 62 0.247
400
TBC004 Tobacco Addiction 63 0.247
401
c FNC027 Fanconi Anemia, Complementation Group a 80 0.247
402
FCS002 Fucosidosis 61 0.247
403
c GM1004 Gm1-Gangliosidosis, Type I 59 0.247
404
c GCH015 Gaucher Disease, Type I 67 0.247
405
c GCH016 Gaucher Disease, Type Ii 53 0.247
406
c GCH017 Gaucher Disease, Type Iii 52 0.247
407
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.247
408
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.247
409
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.247
410
c GLY008 Glycogen Storage Disease Ii 72 0.247
411
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.247
412
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.247
413
AND020 Androgen Insensitivity, Partial 54 0.247
414
c MJR008 Major Affective Disorder 2 34 0.247
415
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 42 0.247
416
c ORF037 Orofaciodigital Syndrome I 59 0.247
417
c PNS012 Paine Syndrome 60 0.247
418
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.247
419
ALL027 Allergic Bronchopulmonary Aspergillosis, Familial 30 0.247
420
c ANG068 Angioedema, Hereditary, Type I 58 0.247
421
c SPN225 Spondyloarthropathy 1 70 0.247
422
BSL036 Basal Cell Nevus Syndrome 73 0.247
423
BRT059 Bartsocas-Papas Syndrome 55 0.247
424
c INF071 Inflammatory Bowel Disease 1 65 0.247
425
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.247
426
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.247
427
ATX049 Ataxia with Vitamin 3 Deficiency 52 0.247
428
AND002 Androgen Insensitivity Syndrome 63 0.247
429
SVR066 Severe Combined Immunodeficiency, X-Linked 65 0.247
430
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.247
431
P CLR023 Colorectal Cancer 100 0.247
432
P MLT020 Multiple Sclerosis 79 0.247
433
STR067 Stroke, Ischemic 79 0.247
434
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.247
435
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 35 0.247
436
ACR041 Acromelic Frontonasal Dysostosis 53 0.247
437
SPP011 Suppression of Tumorigenicity 12 61 0.247
438
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.247
439
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.247
440
c HYP272 Hypercholesterolemia, Familial, 3 46 0.247
441
P PLR004 Pleuropulmonary Blastoma 65 0.247
442
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 0.247
443
c SYS043 Systemic Lupus Erythematosus 1 38 0.247
444
c PSR017 Psoriasis 2 53 0.247
445
c FCL025 Focal Segmental Glomerulosclerosis 1 49 0.247
446
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.247
447
NRL018 Neural Tube Defects, Folate-Sensitive 46 0.247
448
BRT054 Brittle Bone Disorder 74 0.247
449
SCT005 Scott Syndrome 51 0.247
450
SND001 Sandhoff Disease 66 0.247
451
TNM001 Tinea Imbricata 41 0.247
452
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 0.247
453
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.247
454
AGM019 Agammaglobulinemia, X-Linked 71 0.247
455
SRC027 Sarcoma, Synovial 58 0.247
456
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.247
457
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 0.247
458
SCH036 Scheie Syndrome 73 0.247
459
HRL004 Hurler-Scheie Syndrome 58 0.247
460
P NSP012 Nasopharyngeal Carcinoma 60 0.247
461
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.247
462
ATM052 Autoimmune Disease 1 36 0.247
463
GLB024 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor 32 0.247
464
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.247
465
c JVN061 Juvenile Arthritis 56 0.247
466
LPP008 Lipoprotein Quantitative Trait Locus 65 0.247
467
HYP457 Hypertrophic Scars 42 0.247
468
CHR100 Chronic Ulcer of Skin 57 0.247
469
ANG054 Angina Pectoris 65 0.247
470
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.247
471
P FML011 Familial Adenomatous Polyposis 70 0.247
472
HYP025 Hyperphosphatemia 47 0.247
473
P SML001 Small Cell Carcinoma 52 0.247
474
c HPT073 Hepatitis C Virus 70 0.247
475
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.247
476
c MJR006 Major Affective Disorder 5 32 0.247
477
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.247
478
EWN003 Ewing Sarcoma 69 0.247
479
c MJR023 Major Affective Disorder 7 33 0.247
480
c MJR024 Major Affective Disorder 9 40 0.247
481
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.247
482
CHP002 Chops Syndrome 47 0.247
483
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.247
484
MRG013 Mirage Syndrome 44 0.247
485
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 48 0.247
486
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.247
487
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.247
488
P PLM037 Pulmonary Hypertension 69 0.247
489
c MCR113 Microvascular Complications of Diabetes 3 52 0.247
490
FLL041 Follicular Lymphoma 1 44 0.247
491
MCS006 Macs Syndrome 57 0.247
492
MYX005 Myxoid Liposarcoma 65 0.247
493
MSC007 Muscle Hypertrophy 64 0.247
494
LYM007 Lymphangioleiomyomatosis 68 0.247
495
HRL003 Hurler Syndrome 66 0.247
496
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.247
497
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.247
498
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.247
499
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.247
500
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.247
501
AMD002 Amed Syndrome, Digenic 36 0.247
502
ANG020 Angiosarcoma 63 0.247
503
P PNC035 Pancreatic Cancer 87 0.247
504
PLY001 Polycythemia Vera 69 0.247
505
MLT163 Multiple Pterygium Syndrome, Escobar Variant 62 0.247
506
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.247
507
c RHB023 Rhabdomyosarcoma, Embryonal, 1 44 0.247
508
P TYS001 Tay-Sachs Disease 69 0.247
509
P TST021 Testicular Germ Cell Tumor 61 0.247
510
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 0.247
511
LYS012 Lysosomal Acid Lipase Deficiency 64 0.247
512
DYS164 Dyskeratosis Congenita, X-Linked 56 0.247
513
c HMP029 Hemophilia a 69 0.247
514
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.247
515
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.247
516
ASP002 Aspartylglucosaminuria 57 0.247
517
P ATX030 Ataxia-Telangiectasia 80 0.247
518
P JBR020 Joubert Syndrome 1 74 0.247
519
P CHN012 Chondrosarcoma 56 0.247
520
c TBR025 Tuberous Sclerosis 1 84 0.247
521
URT051 Ureter, Cancer of 46 0.247
522
CYS036 Cystinosis, Nephropathic 51 0.247
523
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.247
524
TRG002 Trigeminal Neuralgia 61 0.247
525
PCK003 Pick Disease of Brain 70 0.247
526
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.247
527
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.247
528
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.247
529
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.247
530
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.247
531
LMY014 Leiomyoma, Uterine 55 0.247
532
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 54 0.247
533
c HYP543 Hypoplastic Left Heart Syndrome 1 46 0.247
534
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 52 0.247
535
P MTC003 Metachromatic Leukodystrophy 71 0.247
536
MYC006 Mycosis Fungoides 64 0.247
537
MYL005 Myelofibrosis 70 0.247
538
ARM010 Arima Syndrome 56 0.247
539
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.247
540
P LPR021 Leprosy 3 71 0.247
541
LTT002 Letterer-Siwe Disease 33 0.247
542
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.247
543
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.247
544
MYL069 Myeloma, Multiple 76 0.247
545
P RTN008 Retinitis Pigmentosa 79 0.247
546
P SJG008 Sjogren Syndrome 60 0.247
547
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.247
548
P WSK001 Wiskott-Aldrich Syndrome 72 0.247
549
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 47 0.247
550
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.247
551
FRN006 Frontotemporal Dementia 68 0.247
552
ABC001 Abcd Syndrome 44 0.247
554
PLY105 Polycystic Ovary Syndrome 1 39 0.247
555
c THR092 Thrombophilia Due to Thrombin Defect 74 0.247
556
P AST005 Asthma 75 0.247
557
c MCR115 Microvascular Complications of Diabetes 5 65 0.247
558
c TBR026 Tuberous Sclerosis 2 71 0.247
559
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.247
560
c PSR018 Psoriasis 13 40 0.247
561
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.247
562
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.247
563
P MYC007 Myocardial Infarction 69 0.247
564
P MJR001 Major Depressive Disorder 68 0.247
565
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.247
566
GST019 Gastrointestinal Stromal Tumor 78 0.247
567
JVN004 Juvenile Myelomonocytic Leukemia 66 0.247
568
c OVR114 Ovarian Cancer 1 60 0.247
569
P BCT020 Bacteremia 2 43 0.247
570
P MMB011 Membranous Nephropathy 50 0.247
572
ERY061 Erythroderma, Congenital, with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-Ige 39 0.247
573
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.247
574
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.247
575
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.247
576
c LKM063 Leukemia, Chronic Myeloid 70 0.247
577
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.247
578
SVR097 Severe Cutaneous Adverse Reaction 68 0.247
579
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.247
580
c DRR009 Diarrhea 6 46 0.247
581
P HMN032 Human Herpesvirus 8 47 0.247
582
LPT014 Leptin Deficiency or Dysfunction 77 0.247
583
LPT006 Leptin Receptor Deficiency 50 0.247
584
IMM240 Immunodeficiency 14a, Autosomal Dominant 52 0.247
585
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 49 0.247
586
HMR039 Hemorrhage, Intracerebral 57 0.247
587
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.247
588
c INF145 Infantile Liver Failure Syndrome 1 44 0.247
589
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.247
590
KWS002 Kawasaki Disease 65 0.247
591
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.247
592
P PRG092 Pregnancy Loss, Recurrent 1 42 0.247
593
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.247
594
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 0.247
595
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 0.247
596
c BTT014 Beta-Thalassemia 72 0.247
597
c NRF023 Neurofibromatosis, Type Ii 70 0.247
598
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.247
599
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.247
600
c ATR087 Atrial Standstill 1 74 0.247
601
BRK010 Burkitt Lymphoma 65 0.247
602
c DMN023 Diamond-Blackfan Anemia 1 68 0.247
603
APN008 Apnea, Obstructive Sleep 66 0.247
604
c BLD140 Blood Group, I System 47 0.247
605
P LKM071 Leukemia, Chronic Lymphocytic 74 0.247
606
MRF001 Marfan Syndrome 76 0.247
607
c CWD006 Cowden Syndrome 1 78 0.247
608
MYL057 Myelopathy, Htlv-1-Associated 39 0.247
609
c MYL058 Myeloproliferative Syndrome, Transient 48 0.247
610
P OCL013 Oculodentodigital Dysplasia 66 0.247
611
P PRK057 Parkinson Disease, Late-Onset 79 0.247
612
P HNT016 Huntington Disease 73 0.247
613
PLM102 Palmoplantar Keratoderma, Epidermolytic 55 0.247
614
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.247
615
P HYP828 Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant 57 0.247
616
IMM162 Immunoglobulin E Concentration, Serum 28 0.247
617
INC002 Inclusion Body Myositis 56 0.247
618
c HYP836 Hypercholesterolemia, Familial, 1 73 0.247
619
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.247
620
c HYP595 Hypertension, Essential 84 0.247
621
P CNR004 Cone-Rod Dystrophy 2 74 0.247
622
c SPN330 Spondylocostal Dysostosis 5 55 0.247
623
CMR002 Coumarin Resistance 59 0.247
624
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 32 0.247
625
ESP021 Esophageal Cancer 84 0.247
626
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.247
627
HRW001 Hair Whorl 35 0.247
628
P HYP733 Hypercalciuria, Absorptive, 2 45 0.247
629
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.247
630
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.247
631
MLT157 Multiple System Atrophy 1 69 0.247
632
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.247
633
c MST023 Mesothelioma, Malignant 56 0.247
634
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 55 0.247
635
CYC010 Cyclic Neutropenia 63 0.247
636
c OST131 Osteopetrosis, Autosomal Dominant 2 52 0.247
637
c PRG018 Paragangliomas 1 59 0.247
638
P PHC003 Pheochromocytoma 70 0.247
639
P HPT023 Hepatocellular Carcinoma 95 0.247
640
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.247
641
c PSR032 Psoriasis 11 47 0.247
642
HYL004 Hyaline Fibromatosis Syndrome 67 0.247
643
FBR089 Fibrosclerosis, Multifocal 35 0.247
644
P PRC031 Preeclampsia/eclampsia 1 43 0.247
645
KRT013 Keratolytic Winter Erythema 45 0.247
646
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 51 0.247
647
AYM001 Ayme-Gripp Syndrome 57 0.247
648
CHD004 Chudley-Mccullough Syndrome 47 0.247
649
P LBR014 Leber Congenital Amaurosis 4 56 0.247
650
P KHL003 Kohlschutter-Tonz Syndrome 57 0.247
651
FCT007 Factor Vii Deficiency 64 0.247
652
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.247
653
CRV035 Cervical Cancer 72 0.247
654
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.247
655
P ESP035 Esophagitis, Eosinophilic, 1 57 0.247
656
P PTT014 Pitt-Hopkins Syndrome 63 0.247
657
c MJR004 Major Affective Disorder 4 28 0.247
658
c MJR003 Major Affective Disorder 6 32 0.247
659
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.247
660
RDD003 Riddle Syndrome 58 0.247
661
GLS018 Glass Syndrome 60 0.247
662
END057 Endometrial Cancer 76 0.247
663
P LNG064 Lung Cancer Susceptibility 3 69 0.247
664
P ADL017 Adult T-Cell Leukemia 53 0.247
665
c SVR003 Severe Congenital Neutropenia 59 0.247
666
P DST002 Distal Arthrogryposis 63 0.247
667
CHL149 Childhood Acute Myeloid Leukemia 42 0.247
668
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 0.247
669
ADL096 Adult Hepatocellular Carcinoma 60 0.247
670
CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 35 0.247
671
P ANP001 Anaplastic Large Cell Lymphoma 59 0.247
672
MNT001 Mantle Cell Lymphoma 65 0.247
673
ATY042 Atypical Chronic Myeloid Leukemia 50 0.247
674
P LYM033 Lymphoproliferative Syndrome 59 0.247
675
WLD007 Waldenstroem's Macroglobulinemia 59 0.247
676
c HRD202 Hereditary Lymphedema I 54 0.247
677
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.247
678
SPR126 Superior Semicircular Canal Dehiscence 41 0.247
679
P SLV026 Salivary Gland Carcinoma 59 0.247
680
ADR040 Adrenal Gland Pheochromocytoma 45 0.247
681
LBR036 Leber Plus Disease 67 0.247
682
IMM102 Immunodeficiency 14 51 0.247
683
TRY001 Trypanosomiasis 50 0.247
684
OST003 Osteonecrosis 60 0.247
685
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.247
686
PLY043 Polyomavirus Allograft Nephropathy 12 0.247
687
THR024 Thrombosis 56 0.247
688
P RSP003 Respiratory Failure 73 0.247
689
P PRK039 Parkinsonism 55 0.247
690
ACT011 Acute Contagious Conjunctivitis 41 0.247
691
CHR563 Chronic Eosinophilic Leukemia 48 0.247
692
HMN047 Human Cytomegalovirus Infection 59 0.247
693
LWG006 Low Grade Glioma 41 0.247
694
MLD018 Mild Cognitive Impairment 48 0.247
695
RTN001 Retinal Vasculitis 46 0.247
696
FML035 Familial Hyperlipidemia 54 0.247
697
P PLY014 Polycystic Kidney Disease 71 0.247
698
P MCL001 Mucolipidosis 49 0.247
699
HYP458 Hyper Ige Syndrome 60 0.247
700
NNL006 Non-Alcoholic Steatohepatitis 54 0.247
701
c CHR708 Chronic Urticaria 42 0.247
702
PRP080 Peripheral Artery Disease 54 0.247
703
HMR023 Hemorrhagic Cystitis 43 0.247
704
P FLL037 Follicular Lymphoma 66 0.247
705
PRL017 Prolymphocytic Leukemia 47 0.247
706
P PRT026 Parotitis 42 0.247
707
AGG012 Aggressive Nk-Cell Leukemia 47 0.247
708
LYM012 Lymphoplasmacytic Lymphoma 50 0.247
709
MRG003 Marginal Zone B-Cell Lymphoma 52 0.247
710
PRP036 Peripheral T-Cell Lymphoma 52 0.247
711
MYC004 Mycotic Corneal Ulcer 14 0.247
712
INT030 Intracranial Aneurysm 55 0.247
713
END040 Endogenous Depression 54 0.247
714
PRT035 Peritoneum Cancer 45 0.247
715
P RCT021 Rectum Cancer 54 0.247
716
HPT019 Hepatic Encephalopathy 59 0.247
717
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.247
718
PST028 Post-Traumatic Stress Disorder 58 0.247
719
CPL002 Capillary Lymphangioma 37 0.247
720
P CRN037 Craniosynostosis 67 0.247
721
P ART021 Arteriosclerosis 53 0.247
722
CLN045 Colonic Benign Neoplasm 48 0.247
723
P ESS003 Essential Thrombocythemia 68 0.247
724
MYL031 Myeloproliferative Neoplasm 66 0.247
725
c ATM011 Autoimmune Hepatitis 62 0.247
726
P GCH001 Gaucher's Disease 69 0.247
727
SPH010 Sphingolipidosis 47 0.247
728
SRS001 Serous Cystadenocarcinoma 51 0.247
729
SKN013 Skin Benign Neoplasm 49 0.247
730
P CNT005 Central Nervous System Lymphoma 51 0.247
731
PPL007 Papillary Serous Adenocarcinoma 42 0.247
732
PRV003 Perivascular Epithelioid Cell Tumor 38 0.247
733
TRN018 Transitional Cell Carcinoma 56 0.247
734
P DYS007 Dyskeratosis Congenita 66 0.247
735
P TCD001 Tic Disorder 50 0.247
736
c BSL007 Basal Cell Carcinoma 67 0.247
737
P HMN010 Hemangioma 61 0.247
738
RNL001 Renal Artery Obstruction 31 0.247
739
ACN001 Acinar Cell Carcinoma 44 0.247
740
FDL002 Food Allergy 47 0.247
741
GNT002 Giant Cell Glioblastoma 57 0.247
742
P GLY013 Glycogen Storage Disease 59 0.247
743
P BNG032 Benign Mesothelioma 53 0.247
744
P EPD016 Epidermolysis Bullosa 53 0.247
745
IDP011 Idiopathic Interstitial Pneumonia 59 0.247
746
ACT029 Acute Interstitial Pneumonia 49 0.247
747
HRY003 Hairy Cell Leukemia 53 0.247
748
P FBR017 Fibrosarcoma 55 0.247
749
CRT016 Carotid Artery Disease 52 0.247
750
P LPS002 Liposarcoma 64 0.247
751
HST010 Histiocytosis 49 0.247
752
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.247
753
BLD051 Blood Coagulation Disease 52 0.247
754
SQM006 Squamous Cell Carcinoma 59 0.247
755
THY122 Thyroid Gland Cancer 59 0.247
756
c MLG084 Malignant Fibrous Histiocytoma 62 0.247
757
HYP014 Hyperuricemia 51 0.247
758
FLL027 Fallopian Tube Carcinoma 66 0.247
759
P LMY004 Leiomyosarcoma 62 0.247
760
P TBR001 Tuberous Sclerosis 69 0.247
761
P OST001 Osteopetrosis 70 0.247
762
PLN001 Plantar Wart 33 0.247
763
END035 Endocrine Gland Cancer 42 0.247
764
P SPN046 Spinal Muscular Atrophy 62 0.247
765
NRN004 Neuroendocrine Tumor 55 0.247
766
GST071 Gastrointestinal Carcinoma 46 0.247
767
MCS004 Mucosal Melanoma 46 0.247
768
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 0.247
769
ACD008 Acid-Labile Subunit Deficiency 52 0.247
770
CST005 Castleman Disease 56 0.247
771
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 0.247
772
MLT113 Multicentric Castleman Disease 46 0.247
773
CHR286 Chronic Neutrophilic Leukemia 42 0.247
774
P CHR285 Chronic Myelomonocytic Leukemia 59 0.247
775
ALL002 Allergic Cutaneous Vasculitis 24 0.247
776
DFF003 Diffuse Scleroderma 41 0.247
777
P ECL001 Eclampsia 52 0.247
778
INT253 Intestinal Benign Neoplasm 46 0.247
779
ADL054 Adult Brain Stem Glioma 30 0.247
780
P BNG030 Benign Ependymoma 51 0.247
781
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.247
782
P EPD003 Epidermolysis Bullosa Simplex 56 0.247
783
BRN004 Brain Edema 54 0.247
784
BNM001 Bone Marrow Cancer 45 0.247
785
NRT001 Neurotic Disorder 56 0.247
786
P TRN020 Turner Syndrome 67 0.247
787
CNT033 Central Nervous System Cancer 47 0.247
788
INT002 Intermittent Claudication 61 0.247
789
P CRV031 Cervical Adenocarcinoma 48 0.247
790
CLR030 Clear Cell Renal Cell Carcinoma 53 0.247
791
SMT003 Somatostatinoma 52 0.247
792
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.247
793
CLL010 Cellular Ependymoma 58 0.247
794
DNT014 Dental Pulp Disease 44 0.247
795
P EYD002 Eye Disease 57 0.247
796
INT020 Intravenous Leiomyomatosis 35 0.247
797
P MLG074 Malignant Mesenchymoma 40 0.247
798
CRN020 Coronary Restenosis 39 0.247
799
PHT003 Phototoxic Dermatitis 27 0.247
800
THR012 Thoracic Cancer 44 0.247
801
NTR005 Nutritional Deficiency Disease 60 0.247
802
LMY003 Leiomyomatosis 43 0.247
803
PLX002 Plexiform Neurofibroma 44 0.247
804
MXD026 Mixed Glioma 45 0.247
805
LPD008 Lipid Metabolism Disorder 61 0.247
806
SPN041 Spinal Cord Disease 54 0.247
807
P EMB005 Embryonal Rhabdomyosarcoma 53 0.247
808
ISC004 Ischemia 61 0.247
809
c HYP847 Hyper Ige Recurrent Infection Syndrome 1 45 0.247
810
c CNT035 Central Nervous System Disease 53 0.247
811
P BPL003 Bipolar Disorder 56 0.247
812
ANG018 Angiomyolipoma 45 0.247
813
NPH009 Nephrolithiasis 54 0.247
814
OVR015 Ovarian Mixed Germ Cell Neoplasm 36 0.247
815
CNG034 Congestive Heart Failure 69 0.247
816
MNN001 Meningeal Melanocytoma 38 0.247
817
CMP009 Complement Deficiency 40 0.247
818
IMM005 Immature Teratoma of Ovary 35 0.247
819
CNN005 Connective Tissue Disease 66 0.247
820
ADN018 Adenoma 58 0.247
821
SPN051 Spondylitis 51 0.247
822
P INT068 Intestinal Disease 53 0.247
823
TST018 Testicular Yolk Sac Tumor 38 0.247
824
OVR051 Ovarian Endodermal Sinus Tumor 36 0.247
825
CHR075 Choriocarcinoma of Ovary 31 0.247
826
CHR076 Choriocarcinoma of the Testis 33 0.247
827
GST030 Gastrinoma 45 0.247
828
P HPT021 Hepatitis 68 0.247
829
FML039 Female Reproductive System Disease 37 0.247
830
P LTR001 Lateral Sclerosis 57 0.247
831
P MTR014 Motor Neuron Disease 65 0.247
832
GST045 Gastroenteritis 58 0.247
833
FCL012 Facial Paralysis 49 0.247
834
P INT143 Interstitial Cystitis 59 0.247
835
SML008 Small Intestine Lymphoma 33 0.247
836
RTR008 Root Resorption 44 0.247
837
FST001 Foster-Kennedy Syndrome 39 0.247
838
P HRT032 Heart Disease 84 0.247
839
P PLY011 Polycystic Ovary Syndrome 57 0.247
840
BTT017 Beta-Thalassemia Major 54 0.247
841
PLS025 Plasmablastic Lymphoma 47 0.247
842
NSL029 Nasal Type Extranodal Nk/t-Cell Lymphoma 41 0.247
843
FCL011 Facial Nerve Disease 38 0.247
844
PNC008 Pancreatic Endocrine Carcinoma 39 0.247
845
P EPL164 Epilepsy 70 0.247
846
P OPT006 Optic Nerve Disease 57 0.247
847
c HPT001 Hepatitis C 61 0.247
848
c VRL010 Viral Hepatitis 52 0.247
849
VGN017 Vaginal Cancer 58 0.247
850
GST037 Gastroparesis 52 0.247
851
P PRP021 Peripheral Nervous System Neoplasm 39 0.247
852
c ANT023 Anterior Scleritis 30 0.247
853
c FML021 Familial Hypercholesterolemia 71 0.247
854
XRP001 Xerophthalmia 42 0.247
855
DRY001 Dry Eye Syndrome 49 0.247
856
P OVR049 Ovarian Disease 50 0.247
857
LCH001 Leech Infestation 37 0.247
858
P PRR002 Pure Red-Cell Aplasia 46 0.247
859
HYP081 Hypolipoproteinemia 49 0.247
860
SQM002 Squamous Cell Papilloma 45 0.247
861
MMB001 Membranoproliferative Glomerulonephritis 56 0.247
862
P GLM007 Glomerulonephritis 59 0.247
863
IGG001 Iga Glomerulonephritis 50 0.247
864
P CRV039 Cervicitis 52 0.247
865
P KDN017 Kidney Cancer 60 0.247
866
P CPL006 Capillary Hemangioma 53 0.247
867
HMG005 Hemoglobinopathy 55 0.247
868
P ADN016 Adenocarcinoma 63 0.247
869
GRM005 Germ Cell Cancer 46 0.247
870
c HPT016 Hepatitis B 62 0.247
871
HYP005 Hypokalemia 55 0.247
872
P MSN005 Mesenchymal Chondrosarcoma 46 0.247
873
P EPN001 Ependymoblastoma 44 0.247
874
ADN009 Adenosquamous Carcinoma 49 0.247
875
ESP025 Esophagus Adenocarcinoma 37 0.247
876
THY030 Thyroid Gland Disease 50 0.247
877
P SYS005 Systemic Scleroderma 73 0.247
878
P BRN035 Brain Stem Glioma 49 0.247
879
P MYP004 Myopathy 67 0.247
880
CLR017 Clear Cell Sarcoma 44 0.247
881
ERD001 Erdheim-Chester Disease 53 0.247
882
GNG008 Ganglioneuroblastoma 46 0.247
883
SPN035 Spindle Cell Sarcoma 51 0.247
884
CRC021 Carcinosarcoma 62 0.247
885
MYF001 Myofibroma 42 0.247
886
END041 Endometrial Adenocarcinoma 63 0.247
887
INS001 Insulinoma 59 0.247
888
MRK001 Merkel Cell Carcinoma 64 0.247
889
BLD131 Bladder Urothelial Carcinoma 59 0.247
890
P NRV006 Nervous System Cancer 47 0.247
891
INT066 Interstitial Lung Disease 60 0.247
892
GST049 Gastrointestinal System Cancer 49 0.247
893
ESN005 Eosinophilic Gastroenteritis 55 0.247
894
PNC129 Pancreatic Adenocarcinoma 64 0.247
895
BRX001 Bruxism 50 0.247
896
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.247
897
FBR002 Fibrosarcoma of Bone 47 0.247
898
P ANG015 Angioedema 56 0.247
899
RSP006 Respiratory System Disease 51 0.247
900
TTH007 Tooth Erosion 30 0.247
901
VRN001 Vernal Conjunctivitis 35 0.247
902
HMT002 Hematologic Cancer 61 0.247
903
CYS014 Cystadenocarcinoma 51 0.247
904
HGH043 High Grade Glioma 46 0.247
905
GLS001 Gliosarcoma 63 0.247
906
PPL018 Papillary Adenocarcinoma 44 0.247
907
P ART023 Arthropathy 59 0.247
908
MLR006 Male Reproductive Organ Cancer 40 0.247
909
ADL023 Adult Medulloblastoma 43 0.247
910
PHT004 Photoallergic Dermatitis 27 0.247
911
BLL003 Bell's Palsy 48 0.247
912
PPL001 Papillary Adenoma 44 0.247
913
ADL008 Adult Oligodendroglioma 35 0.247
914
TRP002 Tropical Spastic Paraparesis 48 0.247
915
LYS002 Lysosomal Storage Disease 51 0.247
916
P RHB003 Rhabdomyosarcoma 66 0.247
917
GRM004 Germinoma 40 0.247
918
c GM1007 Gm1 Gangliosidosis 65 0.247
919
GLY031 Glycoproteinosis 49 0.247
920
P SKN015 Skin Carcinoma 71 0.247
921
P BRS044 Breast Adenocarcinoma 58 0.247
922
BRN036 Brain Stem Infarction 38 0.247
923
ADL018 Adult Choroid Plexus Cancer 15 0.247
924
APP009 Appendix Adenocarcinoma 47 0.247
925
ART016 Aortic Aneurysm 68 0.247
926
PLS011 Plasmacytoma 56 0.247
927
ESP027 Esophagus Squamous Cell Carcinoma 45 0.247
928
FML008 Familial Retinoblastoma 49 0.247
929
INT082 Intraocular Retinoblastoma 30 0.247
930
P PNC044 Pancreatitis 61 0.247
931
c ACT027 Acute Pancreatitis 60 0.247
932
IMM136 Immune System Disease 46 0.247
933
P CCK001 Cockayne Syndrome 67 0.247
934
CRN030 Coronary Stenosis 50 0.247
935
P HYP061 Hypertrophic Cardiomyopathy 68 0.247
936
CNN003 Conn's Syndrome 77 0.247
937
P PNV001 Panuveitis 48 0.247
938
PRM236 Primary Biliary Cholangitis 62 0.247
939
P GRV001 Graves' Disease 54 0.247
940
P ADL010 Adult Respiratory Distress Syndrome 70 0.247
941
DNT006 Dental Pulp Necrosis 43 0.247
942
VSL002 Visual Epilepsy 39 0.247
943
CRN017 Coronary Thrombosis 46 0.247
944
P LKD001 Leukodystrophy 58 0.247
945
c CHR056 Chronic Tic Disorder 36 0.247
946
GLC003 Glucose Intolerance 53 0.247