Search results for Glucosamine

1013 hits were found for Glucosamine

# Family MCID Name MIFTS Score
1
OST012 Osteoarthritis 77 20.894
2
QLT026 Qualitative or Quantitative Defects of Glucosamine -2-Epimerase/n-Acetylmannosamine Kinase - 1 20.186
3
c MCP046 Mucopolysaccharidosis, Type Iiid 50 15.350
4
OST062 Osteoarthritis with Mild Chondrodysplasia 46 7.743
5
P ART022 Arthritis 70 5.016
6
HYP066 Hyperglycemia 60 4.777
7
BCK006 Back Pain 43 4.500
8
P RHM011 Rheumatoid Arthritis 81 3.008
9
c TYP009 Type 2 Diabetes Mellitus 91 3.002
10
P DRR001 Diarrhea 55 2.858
11
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.651
12
ENT004 Enthesopathy 51 2.603
13
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.513
14
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.501
15
P PRD008 Periodontitis 63 2.482
16
c HYP836 Hypercholesterolemia, Familial, 1 73 2.382
17
HYP060 Hyperinsulinism 53 2.374
18
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.361
19
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.361
20
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.361
21
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.361
22
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.361
23
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.361
24
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.361
25
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.361
26
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.361
27
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.338
28
ANT039 Antisynthetase Syndrome 55 2.315
29
c PNS012 Paine Syndrome 60 2.299
30
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.299
31
c PRD040 Periodontitis, Chronic 52 2.239
32
RHB024 Rhabdomyosarcoma 2 65 2.221
33
KRT002 Keratomalacia 54 2.132
34
c DRR009 Diarrhea 6 46 2.113
35
IRR002 Irritable Bowel Syndrome 64 2.113
36
PRT037 Pertussis 49 2.049
37
48X005 48,xyyy 39 2.043
38
CYT002 Cytokine Deficiency 43 2.029
39
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.026
40
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.015
41
RHM001 Rheumatic Fever 59 1.985
42
P HRP006 Herpes Simplex 65 1.920
43
c PCH010 Pachyonychia Congenita 3 43 1.915
44
SYN007 Synovitis 54 1.881
45
PLC002 Plica Syndrome 35 1.881
46
P LNG032 Lung Cancer 98 1.876
47
c SPN225 Spondyloarthropathy 1 70 1.852
48
SPN051 Spondylitis 51 1.852
49
INF009 Inflammatory Spondylopathy 30 1.852
50
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.835
51
c TYP008 Type 1 Diabetes Mellitus 77 1.835
52
c DWL002 Dowling-Degos Disease 1 58 1.805
53
P BRS047 Breast Cancer 97 1.792
54
BNR002 Bone Resorption Disease 47 1.791
55
ATH013 Atherosclerosis Susceptibility 63 1.757
56
P CLR023 Colorectal Cancer 100 1.755
57
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.736
58
GNG013 Gingivitis 59 1.735
59
P VSC007 Vascular Disease 62 1.716
60
P ART023 Arthropathy 59 1.706
61
P DRM053 Dermatitis, Atopic 65 1.638
62
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.637
63
ADL002 Adult Syndrome 69 1.637
64
NTR005 Nutritional Deficiency Disease 60 1.637
65
P LCH002 Lichen Planus 54 1.637
66
ORL013 Oral Lichen Planus 45 1.637
67
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.628
68
DRM006 Dermatitis 61 1.599
69
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.574
70
SCH014 Schistosomiasis 56 1.574
71
P FBR017 Fibrosarcoma 55 1.567
72
BCT022 Bacterial Infectious Disease 55 1.556
73
GLM045 Glioma 62 1.556
74
GLL048 Glial Tumor 51 1.556
75
ULC004 Ulcerative Colitis 74 1.544
76
P INF037 Inflammatory Bowel Disease 53 1.508
77
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.500
78
ISC004 Ischemia 61 1.495
79
GLC003 Glucose Intolerance 53 1.490
80
STM007 Stomatitis 52 1.487
81
VRC005 Varicose Veins 59 1.479
82
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.469
83
P OST002 Osteoporosis 76 1.469
84
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.469
85
VCC001 Vaccinia 49 1.463
86
P CHN012 Chondrosarcoma 56 1.455
87
HMP009 Haemophilus Influenzae 41 1.455
88
ALL029 Allergic Disease 61 1.448
89
HLX001 Helix Syndrome 47 1.438
90
P CYS018 Cystitis 58 1.425
91
c MCR133 Microvascular Complications of Diabetes 4 41 1.421
92
c MCR113 Microvascular Complications of Diabetes 3 52 1.421
93
c MCR130 Microvascular Complications of Diabetes 6 41 1.421
94
c MCR120 Microvascular Complications of Diabetes 7 47 1.421
95
c SML038 Small Cell Cancer of the Lung 68 1.397
96
TND005 Tendinitis 53 1.397
97
c MCR115 Microvascular Complications of Diabetes 5 65 1.374
98
47X002 47,xyy 47 1.374
99
P VNS003 Venous Insufficiency 54 1.353
100
CVD001 Covid-19 59 1.353
101
CYS001 Cystic Fibrosis 77 1.350
102
KRT019 Keratitis, Hereditary 66 1.349
103
PRP027 Peripheral Vascular Disease 71 1.333
104
DNT012 Dental Caries 53 1.332
105
c MCL062 Mucolipidosis Ii Alpha/beta 69 1.319
106
SKN016 Skin Disease 63 1.313
107
P MYC084 Mycobacterium Tuberculosis 1 68 1.278
108
DGN001 Degenerative Disc Disease 48 1.278
109
INS024 Insulin-Like Growth Factor I 77 1.269
110
HYP266 Hypoxia 56 1.266
111
INS001 Insulinoma 59 1.254
112
P LNG064 Lung Cancer Susceptibility 3 69 1.241
113
TTN003 Tetanus 64 1.241
114
CLT003 Colitis 63 1.233
115
MCP033 Mucopolysaccharidoses 44 1.227
116
MST004 Mast Cell Neoplasm 41 1.227
117
EXT007 Extracutaneous Mastocytoma 38 1.227
118
SHW001 Shwartzman Phenomenon 36 1.214
119
P KDN017 Kidney Cancer 60 1.214
120
AGN016 Aging 53 1.212
121
CHL014 Cholera 62 1.207
122
PLM010 Pulmonary Edema 54 1.199
123
CRH001 Crohn's Disease 80 1.199
124
c MCP001 Mucopolysaccharidosis Iii 69 1.195
125
RCK004 Rickets 64 1.192
126
DRM011 Dermatophytosis 52 1.192
127
P NSP012 Nasopharyngeal Carcinoma 60 1.168
128
P CND004 Candidiasis 57 1.151
129
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.151
130
PRT036 Peritonitis 65 1.118
131
c MCL046 Mucolipidosis Iii Alpha/beta 61 1.114
132
c MCL016 Mucolipidosis Iii Gamma 49 1.114
133
FNG017 Fungal Infectious Disease 54 1.114
134
OST159 Osteogenic Sarcoma 66 1.106
135
KSH004 Kashin-Beck Disease 37 1.106
136
P TYS001 Tay-Sachs Disease 69 1.106
137
P ASP006 Aspergillosis 71 1.094
138
SCR011 Scrapie 39 1.094
139
PLM001 Pulmonary Tuberculosis 69 1.092
140
EXS001 Exostosis 49 1.081
141
ORL011 Oral Cancer 60 1.069
142
ARG004 Argyria 26 1.069
143
P ANR048 Aniridia 1 66 1.053
144
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.053
145
TNP001 Tinea Pedis 48 1.053
146
HYP005 Hypokalemia 55 1.053
147
CHL123 Chlamydia 58 1.052
148
PST011 Pustulosis of Palm and Sole 52 1.043
149
P PSR002 Psoriasis 63 1.043
150
P EXN002 Exanthem 58 1.039
151
P ADN016 Adenocarcinoma 63 1.039
152
CRH005 Crohn's Colitis 53 1.024
153
P MCL001 Mucolipidosis 49 1.024
154
DBT010 Diabetic Neuropathy 54 1.024
155
P MLT020 Multiple Sclerosis 79 1.008
156
LPD008 Lipid Metabolism Disorder 61 1.008
157
P CHR345 Chronic Pain 50 1.008
158
P PLM036 Pulmonary Fibrosis 65 0.991
159
GLB002 Glioblastoma 67 0.973
160
P HPT021 Hepatitis 68 0.973
161
P NRP001 Neuropathy 59 0.973
162
DPH001 Diphtheria 59 0.954
163
P THR014 Thrombocytopenia 66 0.944
164
P PHC003 Pheochromocytoma 70 0.933
165
ADR040 Adrenal Gland Pheochromocytoma 45 0.933
167
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.933
168
SPN035 Spindle Cell Sarcoma 51 0.933
169
SRC014 Sarcoma 64 0.933
170
SKN019 Skin Melanoma 70 0.933
171
P VTR007 Vitreoretinopathy 45 0.933
173
P MYP004 Myopathy 67 0.917
174
P BRS044 Breast Adenocarcinoma 58 0.910
175
P PRS040 Prostate Cancer 95 0.909
176
CRB004 Cerebral Artery Occlusion 45 0.909
177
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.885
178
CHR073 Choreatic Disease 53 0.885
179
ALL014 Allergic Encephalomyelitis 34 0.885
180
P HPT023 Hepatocellular Carcinoma 95 0.883
181
NWC001 Newcastle Disease 47 0.872
182
P ENC004 Encephalitis 61 0.872
183
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.859
184
PLY150 Polykaryocytosis Inducer 29 0.859
185
PRS064 Persistent Vegetative State 33 0.859
186
HPR003 Heparin-Induced Thrombocytopenia 47 0.859
187
MCR141 Mucormycosis 59 0.852
188
P RTN024 Retinoblastoma 72 0.845
189
MDD018 Middle East Respiratory Syndrome 44 0.845
190
P SYS005 Systemic Scleroderma 73 0.845
191
NNK001 Nonaka Myopathy 58 0.842
192
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.830
193
ADN018 Adenoma 58 0.830
194
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.815
195
PRT013 Portal Hypertension 59 0.815
196
c LSS005 Lissencephaly 1 57 0.811
197
ACT088 Acute Insulin Response 39 0.799
198
HRW001 Hair Whorl 35 0.799
199
GST023 Gastric Ulcer 52 0.799
200
P ADL010 Adult Respiratory Distress Syndrome 70 0.799
201
CHG001 Chagas Disease 65 0.799
202
PPT005 Peptic Ulcer Disease 58 0.799
203
MSL001 Measles 61 0.799
204
c THR092 Thrombophilia Due to Thrombin Defect 74 0.788
205
P PST095 Post-Thrombotic Syndrome 51 0.788
206
P RTN018 Retinal Disease 53 0.788
207
c CHR684 Chronic Kidney Disease 73 0.788
208
END072 Endotheliitis 36 0.788
209
P HNT016 Huntington Disease 73 0.782
210
P BNG032 Benign Mesothelioma 53 0.782
211
CNG034 Congestive Heart Failure 69 0.782
212
FBR047 Fibromyalgia 57 0.782
213
P LVR013 Liver Disease 68 0.782
214
P ANG015 Angioedema 56 0.782
215
P TRM003 Tremor 50 0.782
216
P OVR082 Overgrowth Syndrome 41 0.782
217
P DBT009 Diabetes Mellitus 67 0.766
218
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.764
219
P CRN300 Coronary Heart Disease 1 73 0.764
220
RNL077 Renal Fibrosis 46 0.764
221
c MGR028 Migraine with or Without Aura 1 63 0.764
222
P OVR042 Ovarian Cancer 88 0.764
223
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.764
224
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.764
225
SHR118 Shrimp Allergy 28 0.764
226
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.764
227
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.764
228
P ART021 Arteriosclerosis 53 0.764
229
VLK001 Volkmann Contracture 23 0.764
230
P LTR001 Lateral Sclerosis 57 0.764
231
P CHR012 Chronic Granulomatous Disease 69 0.764
232
PLS011 Plasmacytoma 56 0.764
233
P FRS004 Free Sialic Acid Storage Disorders 42 0.764
235
ESP002 Esophageal Varix 51 0.745
236
CLR108 Colorectal Adenoma 63 0.745
237
LYM011 Lymphogranuloma Venereum 32 0.745
238
RHM028 Rheumatic Heart Disease 55 0.745
239
P KDN018 Kidney Disease 71 0.745
240
ACT003 Acute Kidney Tubular Necrosis 46 0.745
241
CND006 Candida Glabrata 29 0.745
242
HYP781 Hypoascorbemia 52 0.729
243
PNG002 Pain Agnosia 51 0.724
244
c SCL052 Scleroderma, Familial Progressive 60 0.724
245
MYL013 Myeloperoxidase Deficiency 44 0.724
246
IGR001 Ige Responsiveness, Atopic 58 0.724
247
OBS082 Obstructive Nephropathy 41 0.724
248
SPN020 Spondylosis 46 0.724
249
P LRY044 Larynx Cancer 53 0.724
250
URT010 Ureteral Obstruction 44 0.724
251
P PRP019 Peripheral Nervous System Disease 57 0.724
252
P GLM007 Glomerulonephritis 59 0.724
253
c HPT016 Hepatitis B 62 0.724
254
P RHN004 Rhinitis 56 0.724
255
SPR010 Sporotrichosis 45 0.724
256
VNZ002 Venezuelan Equine Encephalitis 45 0.724
257
PRS037 Periostitis 40 0.724
258
c ACT134 Acute Liver Failure 57 0.724
259
P AML002 Amelogenesis Imperfecta 56 0.713
260
CRN311 Coronary Ostial Stenosis or Atresia 18 0.713
261
SVR001 Severe Acute Respiratory Syndrome 68 0.708
262
LNG099 Lung Disease 62 0.708
263
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.701
264
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.701
265
P GST053 Gastric Cancer 82 0.701
266
c THY107 Thymoma, Familial 42 0.701
267
P MMB011 Membranous Nephropathy 50 0.701
268
PRS119 Persistent Genital Arousal Disorder 18 0.701
269
c ATM011 Autoimmune Hepatitis 62 0.701
270
c HPT015 Hepatitis D 49 0.701
271
P THY023 Thymoma 64 0.701
272
CNS004 Constipation 56 0.701
273
GNG012 Gingival Overgrowth 49 0.701
274
ART016 Aortic Aneurysm 68 0.701
275
AMN003 Amnestic Disorder 53 0.701
276
HST011 Histoplasmosis 54 0.701
277
P URT039 Urticaria 57 0.701
278
P BCL017 B-Cell Lymphoma 57 0.701
279
FTT001 Fatty Liver Disease 61 0.701
280
RDT001 Radiation Cystitis 31 0.701
281
P HRT017 Heart Tumor 22 0.701
282
P MNN013 Meningitis 65 0.701
283
HRT006 Heart Aneurysm 36 0.701
284
HYP056 Hypoglycemia 65 0.701
285
DWN001 Down Syndrome 70 0.690
286
P NJM001 Nijmegen Breakage Syndrome 75 0.690
287
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.690
288
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.690
289
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.690
290
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.674
291
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.674
292
TND004 Tendinopathy 45 0.674
293
c CNG006 Congenital Hypothyroidism 63 0.674
294
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.674
295
LGG001 Legg-Calve-Perthes Disease 59 0.674
296
MYL069 Myeloma, Multiple 76 0.674
297
MST021 Meester-Loeys Syndrome 37 0.674
298
c HMP004 Hemophilia B 68 0.674
299
SPN392 Spondylosis, Cervical 30 0.674
300
P ANP001 Anaplastic Large Cell Lymphoma 59 0.674
301
IMP005 Impotence 52 0.674
302
CCC001 Coccidioidomycosis 57 0.674
303
CHL068 Cholestasis 61 0.674
304
SVR004 Severe Combined Immunodeficiency 70 0.674
305
P URN019 Urinary Tract Infection 48 0.674
306
MST005 Mastitis 52 0.674
307
SLP001 Sleeping Sickness 56 0.674
308
HMG002 Hemoglobinuria 50 0.674
309
ALL006 Allergic Asthma 55 0.674
310
P MYC008 Myocarditis 59 0.674
311
P HMP007 Hemophilia 52 0.674
312
P MSC005 Muscular Dystrophy 66 0.674
313
ACT181 Acute Motor Axonal Neuropathy 25 0.674
314
P DYS021 Dysautonomia 38 0.674
315
P MYS079 Miyoshi Muscular Dystrophy 53 0.658
316
P BLD134 Bladder Cancer 79 0.643
317
PNC005 Penicilliosis 30 0.643
318
P CRP001 Carpal Tunnel Syndrome 65 0.643
319
INF159 Infantile Sialic Acid Storage Disease 42 0.643
320
P AST005 Asthma 75 0.643
321
NST002 Nestor-Guillermo Progeria Syndrome 35 0.643
322
END057 Endometrial Cancer 76 0.643
323
DYS018 Dysostosis 43 0.643
324
P SKN015 Skin Carcinoma 71 0.643
325
P CHR071 Charcot-Marie-Tooth Disease 64 0.643
326
BLS002 Blastomycosis 47 0.643
327
P UVT001 Uveitis 57 0.643
328
CRY005 Cryptococcosis 61 0.643
329
DYS015 Dysentery 49 0.643
330
END086 End Stage Renal Disease 54 0.643
331
UTR043 Uterine Sarcoma 40 0.643
332
LYS030 Lysosomal Storage Disease with Skeletal Involvement 15 0.643
333
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.643
334
P MLN007 Male Infertility 56 0.627
335
CRT017 Cartilage Disease 52 0.627
336
BRS102 Breast Abscess 25 0.602
337
ORL015 Oral Squamous Cell Carcinoma 43 0.602
338
WLK001 Walker-Warburg Syndrome 62 0.602
339
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 28 0.602
340
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.602
341
TRN074 Turnpenny-Fry Syndrome 33 0.602
342
c MST023 Mesothelioma, Malignant 56 0.602
343
c INF067 Inflammatory Bowel Disease 10 25 0.602
344
VLV011 Vulvovaginal Candidiasis 49 0.602
345
PRC003 Proctitis 49 0.602
346
CHL067 Cholecystitis 59 0.602
347
c CNT035 Central Nervous System Disease 53 0.602
348
RCT015 Reactive Arthritis 60 0.602
349
TNG007 Tongue Carcinoma 55 0.602
350
P RTN016 Retinal Degeneration 52 0.602
351
LYM019 Lymphosarcoma 46 0.602
352
P NRV007 Nervous System Disease 65 0.602
353
PNC060 Punctate Porokeratosis 28 0.602
354
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.602
355
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.602
356
CHR431 Chronic Venous Insufficiency 48 0.586
357
P INF032 Infertility 60 0.586
358
LNG031 Lung Benign Neoplasm 51 0.586
359
P NRB001 Neuroblastoma 66 0.582
360
P MCR129 Microvascular Complications of Diabetes 1 67 0.565
361
c MCP045 Mucopolysaccharidosis, Type Iiic 58 0.530
362
UMB002 Umbilical Hernia 46 0.504
363
c GLC092 Glaucoma, Primary Open Angle 60 0.504
364
c MCP047 Mucopolysaccharidosis, Type Iva 62 0.504
365
P LSS002 Lissencephaly 52 0.504
366
c ALB016 Albinism, Oculocutaneous, Type Vii 38 0.504
367
INT067 Interstitial Nephritis 46 0.504
368
c CHR087 Chronic Cystitis 37 0.504
369
PLM031 Poliomyelitis 62 0.504
370
CRC021 Carcinosarcoma 62 0.504
371
P OPN001 Open-Angle Glaucoma 55 0.504
372
TRC023 Trichinosis 53 0.504
373
TBR011 Tuberculous Meningitis 48 0.504
374
c CRN243 Carney Complex, Type 1 53 0.488
375
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.488
376
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.488
377
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.488
378
P PLR004 Pleuropulmonary Blastoma 65 0.488
379
GLS018 Glass Syndrome 60 0.488
380
HYP458 Hyper Ige Syndrome 60 0.488
381
AGG012 Aggressive Nk-Cell Leukemia 47 0.488
382
CNT017 Central Nervous System Origin Vertigo 44 0.488
383
P BRN120 Bronchus Cancer 42 0.488
384
TBL009 Tibial Muscular Dystrophy 51 0.488
385
P TRN020 Turner Syndrome 67 0.488
386
THR012 Thoracic Cancer 44 0.488
387
P CRV039 Cervicitis 52 0.488
388
PLP001 Pulpitis 48 0.488
389
FSC004 Fasciitis 49 0.488
390
PLN007 Plantar Fasciitis 37 0.488
391
c PRM038 Primary Agammaglobulinemia 47 0.488
392
P PRN023 Prion Disease 60 0.418
393
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.394
394
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.380
395
CHR020 Chronic Interstitial Cystitis 36 0.380
396
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.380
397
IMM167 Immune Deficiency Disease 76 0.368
398
CSY001 C Syndrome 61 0.341
399
SLR001 Sialuria 48 0.341
400
TRT001 Teratocarcinoma 41 0.326
401
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.326
402
c LKM005 Leukemia, T-Cell, Chronic 33 0.326
403
P ALZ034 Alzheimer Disease 87 0.311
404
HMN044 Human Immunodeficiency Virus Type 1 76 0.311
405
P CRN025 Corneal Dystrophy 49 0.311
406
LYS002 Lysosomal Storage Disease 51 0.311
407
CHR074 Choriocarcinoma 46 0.311
408
INF034 Infective Endocarditis 53 0.295
409
MCL075 Macular Dystrophy, Corneal 55 0.295
410
c GLC079 Glaucoma 1, Open Angle, P 23 0.295
411
MYP120 Myopathy, Distal, with Rimmed Vacuoles 34 0.295
412
P GLM040 Glioma Susceptibility 1 70 0.295
413
MLG169 Malignant Astrocytoma 57 0.295
414
P END033 Endocarditis 58 0.295
415
PNC129 Pancreatic Adenocarcinoma 64 0.295
416
PLG002 Plague 58 0.295
417
BRN024 Bronchitis 67 0.295
418
NRL016 Neural Tube Defects 80 0.278
419
c MCP043 Mucopolysaccharidosis, Type Iiia 60 0.278
420
RBS001 Rabies 57 0.278
421
P INT143 Interstitial Cystitis 59 0.278
422
P HYP086 Hypothyroidism 68 0.278
423
IGG001 Iga Glomerulonephritis 50 0.278
424
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.278
425
CHC001 Chickenpox 56 0.278
426
MYX011 Myxozoa 18 0.278
427
OTT002 Otitis Media 70 0.260
428
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 38 0.260
429
ATS010 Autosomal Recessive Disease 42 0.260
430
c GLL024 Gallbladder Disease 1 53 0.260
431
P KLZ004 Kala-Azar 1 41 0.260
432
CLN015 Colon Adenocarcinoma 64 0.260
433
GST045 Gastroenteritis 58 0.260
434
P HRT032 Heart Disease 84 0.260
435
LSH001 Leishmaniasis 63 0.260
436
P AMY004 Amyloidosis 69 0.260
437
MLR004 Malaria 77 0.241
438
PRT251 Proteinuria, Chronic Benign 58 0.241
439
FCS014 Fucosidase Regulator 15 0.241
440
VLV047 Volvulus of Midgut 55 0.241
441
P RTN008 Retinitis Pigmentosa 79 0.241
442
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.241
443
P DNG005 Dengue Virus 55 0.241
444
CLF027 Cleft Palate, Isolated 64 0.241
445
c EXS019 Exostoses, Multiple, Type I 54 0.241
446
LYM027 Lymphopenia 56 0.241
447
URM002 Uremia 47 0.241
448
GTR002 Goiter 52 0.241
449
P GRV001 Graves' Disease 54 0.241
450
PLR005 Pleuropneumonia 33 0.241
451
P KRT007 Keratoconus 49 0.241
452
YLL002 Yellow Fever 61 0.241
453
P GNG009 Gangliosidosis 44 0.241
454
BRT054 Brittle Bone Disorder 74 0.220
455
SND001 Sandhoff Disease 66 0.220
456
P PNC035 Pancreatic Cancer 87 0.220
457
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.220
458
CHL065 Cholangiocarcinoma 57 0.220
459
MLN071 Melanoma Tumor Antigen Gp90 17 0.220
460
BLN006 Blind Loop Syndrome 35 0.220
461
OST015 Osteochondrodysplasia 60 0.220
462
SMN007 Seminoma 42 0.220
463
LYM017 Lyme Disease 63 0.220
464
AVN001 Avian Influenza 61 0.220
465
P GST044 Gastritis 55 0.220
466
P RHB003 Rhabdomyosarcoma 66 0.220
467
EMB004 Embryonal Carcinoma 55 0.220
468
INT079 Intrahepatic Cholangiocarcinoma 51 0.220
469
P PNC044 Pancreatitis 61 0.220
470
c ACT027 Acute Pancreatitis 60 0.220
471
c ACT068 Acute Cystitis 60 0.220
472
JPN002 Japanese Encephalitis 61 0.220
473
c HRD002 Hereditary Angioedema 61 0.220
474
P MLN008 Melanoma 75 0.220
475
P RBL001 Rubella 58 0.220
476
P INF038 Influenza 68 0.220
477
P INS002 in Situ Carcinoma 52 0.220
478
c BCT007 Bacterial Meningitis 55 0.220
479
STN013 Stenotrophomonas Maltophilia Infection 26 0.220
480
P ENC018 Encephalopathy 62 0.220
481
DSR072 Disorder of Energy Metabolism 10 0.220
482
CLS016 Clostridium Difficile Colitis 49 0.197
483
P CLC063 Celiac Disease 1 65 0.197
484
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.197
485
FCS002 Fucosidosis 61 0.197
486
c LKM061 Leukemia, Acute Myeloid 83 0.197
487
c RTN177 Retinitis Pigmentosa 73 37 0.197
488
CHR100 Chronic Ulcer of Skin 57 0.197
489
DSS032 Disease by Infectious Agent 55 0.197
490
P PLM037 Pulmonary Hypertension 69 0.197
491
ASP002 Aspartylglucosaminuria 57 0.197
492
HXS001 Hexosaminidase C 11 0.197
493
WRN001 Werner Syndrome 69 0.197
494
P LKM062 Leukemia, Acute Lymphoblastic 69 0.197
495
IMM080 Immunodeficiency 23 51 0.197
496
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.197
497
ATM095 Autoimmune Disease 61 0.197
498
EPD015 Epidemic Typhus 44 0.197
499
P ACH011 Achondrogenesis 53 0.197
500
INV001 Invasive Aspergillosis 48 0.197
501
CMB007 Combined Immunodeficiency 56 0.197
502
OST017 Osteomyelitis 63 0.197
503
P NPH012 Nephrotic Syndrome 61 0.197
504
P DDN001 Duodenal Ulcer 52 0.197
505
HPT019 Hepatic Encephalopathy 59 0.197
506
P LKM002 Leukemia 65 0.197
507
P GCH001 Gaucher's Disease 69 0.197
508
LVR012 Liver Cirrhosis 62 0.197
509
FLL031 Follicular Adenoma 40 0.197
510
ACT098 Acute Erythroid Leukemia 55 0.197
511
P CRN026 Corneal Edema 42 0.197
512
CHN011 Chondromalacia 38 0.197
513
END041 Endometrial Adenocarcinoma 63 0.197
514
TXC005 Toxic Shock Syndrome 61 0.197
515
ECH003 Echinococcosis 52 0.197
516
NDL007 Nodular Goiter 48 0.197
517
HPT004 Hepatic Coma 43 0.197
518
c JVN010 Juvenile Rheumatoid Arthritis 52 0.197
519
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.197
520
ANX004 Anoxia 40 0.197
521
P HYP265 Hypotonia 42 0.197
522
PST092 Posttransplant Acute Limbic Encephalitis 29 0.197
523
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.170
524
PPL052 Papillomatosis, Confluent and Reticulated 34 0.170
525
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.170
526
ALC007 Alcohol Dependence 65 0.170
527
INT146 Intervertebral Disc Disease 61 0.170
528
HYP457 Hypertrophic Scars 42 0.170
529
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.170
530
P SPP010 Suppressor of Tumorigenicity 3 50 0.170
531
DST005 Diastrophic Dysplasia 57 0.170
532
ENT011 Enterocolitis 55 0.170
533
c ATL015 Atelosteogenesis, Type Ii 40 0.170
534
P MJR001 Major Depressive Disorder 68 0.170
535
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.170
536
BRK010 Burkitt Lymphoma 65 0.170
537
P LKM071 Leukemia, Chronic Lymphocytic 74 0.170
538
MRF001 Marfan Syndrome 76 0.170
539
c ACH042 Achondrogenesis, Type Ib 50 0.170
540
WST005 West Nile Virus 55 0.170
541
P ADL017 Adult T-Cell Leukemia 53 0.170
542
P DSB002 Desbuquois Dysplasia 33 0.170
543
GST071 Gastrointestinal Carcinoma 46 0.170
544
TST018 Testicular Yolk Sac Tumor 38 0.170
545
c HPT001 Hepatitis C 61 0.170
546
P EHL001 Ehlers-Danlos Syndrome 57 0.170
547
INT066 Interstitial Lung Disease 60 0.170
548
P PTT006 Pituitary Adenoma 55 0.170
549
HGH043 High Grade Glioma 46 0.170
550
c GM2006 Gm2 Gangliosidosis 46 0.170
551
c GM1007 Gm1 Gangliosidosis 65 0.170
552
c HPT003 Hepatitis a 63 0.170
553
GRD001 Giardiasis 46 0.170
554
MRR003 Murray Valley Encephalitis 28 0.170
555
P GLL022 Guillain-Barre Syndrome 59 0.170
556
URL001 Urolithiasis 45 0.170
557
PMP014 Pemphigoid 48 0.170
558
c PRC016 Pre-Eclampsia 64 0.170
559
FRM003 Farmer's Lung 41 0.170
560
MNT002 Mental Depression 56 0.170
561
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.170
562
P HML001 Hemolytic-Uremic Syndrome 52 0.170
563
SHG001 Shigellosis 61 0.170
564
GT001 Gout 63 0.170
565
P END039 Endodermal Sinus Tumor 42 0.170
566
P CTR002 Cataract 59 0.170
567
P ART018 Aortic Valve Insufficiency 52 0.170
568
ACQ007 Acquired Immunodeficiency Syndrome 58 0.170
569
P MYL006 Myeloid Leukemia 60 0.170
570
P PMP001 Pemphigus 54 0.170
571
OST016 Osteochondrosis 52 0.170
572
P OVR046 Ovarian Cyst 43 0.170
573
c MLT031 Multiple Epiphyseal Dysplasia, Recessive 18 0.170
574
BBS001 Babesiosis 48 0.170
575
VSC003 Visceral Leishmaniasis 54 0.170
576
AMB001 Amebiasis 56 0.170
577
CLF001 Cleft Lip 54 0.170
578
P MSC003 Muscular Atrophy 52 0.170
579
P OST009 Osteochondritis Dissecans 61 0.170
580
HNS001 Hansen's Disease 32 0.170
581
P LPS004 Lupus Erythematosus 61 0.170
582
TST043 Testicular Seminoma 31 0.170
583
PTT037 Pituitary Tumors 44 0.170
584
FNG016 Fungal Keratitis 40 0.170
585
P STR035 Streptococcal Group a Invasive Disease 24 0.170
586
IDP069 Idiopathic Avascular Necrosis 23 0.170
587
DPR016 Depression 64 0.170
588
PSR001 Psoriatic Arthritis 61 0.139
589
c HNT011 Huntington Disease-Like 3 33 0.139
590
c HNT004 Huntington Disease-Like 2 51 0.139
591
P LYM118 Lymphoma 66 0.139
592
ING001 Inguinal Hernia 59 0.139
593
DCT002 Ductal Carcinoma in Situ 58 0.139
594
TCK001 Tick-Borne Encephalitis 58 0.139
595
RTN017 Retinal Detachment 60 0.139
596
c ALZ049 Alzheimer Disease 2 48 0.139
597
ART140 Arteries, Anomalies of 52 0.139
598
P OST135 Osteogenesis Imperfecta, Type I 60 0.139
599
P SRC025 Sarcoidosis 1 70 0.139
600
DRM046 Dermal Ridges-off-the-End 20 0.139
601
MYX004 Myxedema 43 0.139
602
P GLC113 Galactosemia I 65 0.139
603
RTC012 Reticuloendotheliosis, X-Linked 35 0.139
604
STR067 Stroke, Ischemic 79 0.139
605
SBC001 Subacute Sclerosing Panencephalitis 53 0.139
606
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 39 0.139
607
LPP008 Lipoprotein Quantitative Trait Locus 65 0.139
608
P SML001 Small Cell Carcinoma 52 0.139
609
SYD002 Sydenham Chorea 34 0.139
610
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.139
611
PCK003 Pick Disease of Brain 70 0.139
612
P LPR021 Leprosy 3 71 0.139
613
PHN003 Phenylketonuria 76 0.139
614
THY039 Thyrotropin-Releasing Hormone Deficiency 28 0.139
615
MNN043 Meningioma, Familial 79 0.139
616
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.139
617
c LKM063 Leukemia, Chronic Myeloid 70 0.139
618
LGN006 Legionnaire Disease 52 0.139
619
P MYS005 Myositis 55 0.139
620
PTL009 Patella, Chondromalacia of 40 0.139
621
FRC013 Fructose Utilization 15 0.139
622
P ATL001 Atelosteogenesis 34 0.139
623
DRG013 Drug-Induced Lupus Erythematosus 49 0.139
624
c ATM098 Autoimmune Peripheral Neuropathy 31 0.139
625
TRY001 Trypanosomiasis 50 0.139
626
THR024 Thrombosis 56 0.139
627
P SPN052 Spondyloarthropathy 54 0.139
628
DSS009 Disseminated Intravascular Coagulation 56 0.139
629
P PLY014 Polycystic Kidney Disease 71 0.139
630
c CHR418 Chronic Leukemia 48 0.139
631
P TMP001 Temporal Lobe Epilepsy 49 0.139
632
P OLG002 Oligodendroglioma 66 0.139
633
OVR048 Ovarian Cystadenoma 30 0.139
634
PRP030 Purpura 54 0.139
635
CYS009 Cystadenoma 42 0.139
636
HMS001 Hemosiderosis 48 0.139
637
P PLM006 Pulmonary Alveolar Proteinosis 53 0.139
638
P OTS001 Otosclerosis 49 0.139
639
BRN014 Bronchopneumonia 52 0.139
640
ATR003 Atrophic Rhinitis 40 0.139
641
P MVM001 Movement Disease 61 0.139
642
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.139
643
P CNJ013 Conjunctivitis 66 0.139
644
P ACN011 Acne 55 0.139
645
LPT001 Leptospirosis 65 0.139
646
NRR001 Neuroretinitis 42 0.139
647
MYM001 Myoma 54 0.139
648
P END044 Endometriosis 62 0.139
649
SCR001 Secretory Meningioma 40 0.139
650
HRT012 Heart Valve Disease 53 0.139
651
DFF012 Differentiating Neuroblastoma 27 0.139
652
P SYP003 Syphilis 59 0.139
653
P TRT010 Teratoma 50 0.139
654
GST033 Gestational Diabetes 60 0.139
655
BBN001 Bubonic Plague 40 0.139
656
PRC002 Paracoccidioidomycosis 53 0.139
657
NWB001 Newborn Respiratory Distress Syndrome 56 0.139
658
INT395 Intracranial Meningioma 47 0.139
659
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.139
660
PTL002 Patellofemoral Pain Syndrome 34 0.139
661
P NMN002 Niemann-Pick Disease 60 0.139
662
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.139
663
P INT070 Intestinal Obstruction 57 0.139
664
P SLP005 Sleep Disorder 61 0.139
665
P HML002 Hemolytic Anemia 62 0.139
666
RTN023 Retinitis 45 0.139
667
GST040 Gastric Adenocarcinoma 66 0.139
668
SPN027 Spinal Stenosis 58 0.139
669
P VSC011 Vasculitis 61 0.139
670
OCL006 Ocular Hypertension 53 0.139
671
P MNC007 Monocytic Leukemia 48 0.139
672
FND002 Fundus Dystrophy 54 0.139
673
MNN020 Meningococcal Infection 44 0.139
674
NRF007 Neurofibroma 63 0.139
675
INT007 Intermediate Coronary Syndrome 53 0.139
676
P HYP098 Hypereosinophilic Syndrome 66 0.139
677
STT071 Stat3 Hyper Ige Syndrome 19 0.139
678
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.139
679
P THL005 Thalassemia 56 0.139
680
CTN007 Cutaneous Leishmaniasis 61 0.139
681
KRT006 Keratoconjunctivitis 53 0.139
682
P GNR008 Generalized Resistance to Thyroid Hormone 23 0.139
683
P RRH023 Rare Hereditary Hemochromatosis 52 0.139
684
P LTH050 Lethal Chondrodysplasia 14 0.139
685
DWR001 Dwarfism 44 0.139
686
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.139
687
LKP003 Leukoplakia 39 0.139
688
MST020 Mast Cell Activation Syndrome 27 0.139
689
FTD001 Foot Drop 36 0.139
690
SPS057 Spasticity 43 0.139
691
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.139
692
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.139
693
c ATS007 Autism Spectrum Disorder 71 0.098
694
P HVY001 Heavy Chain Disease 32 0.098
695
P SCL018 Scoliosis 57 0.098
696
ACT119 Acute Promyelocytic Leukemia 62 0.098
697
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.098
698
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.098
699
DFC004 Deficiency Anemia 74 0.098
700
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.098
701
3MC003 3mc Syndrome 49 0.098
702
MTB004 Metabolic Acidosis 48 0.098
703
ALV005 Alveolar Soft Part Sarcoma 61 0.098
704
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.098
705
ILT001 Ileitis 49 0.098
706
FBR054 Fibroma 44 0.098
707
PFF001 Pfeiffer Syndrome 77 0.098
708
c VSC019 Vesicoureteral Reflux 1 56 0.098
709
P ATS364 Autism 72 0.098
710
ALK013 Alkaptonuria 58 0.098
711
c SYS001 Systemic Lupus Erythematosus 85 0.098
712
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.098
713
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.098
714
HYD038 Hydrops Fetalis, Nonimmune 57 0.098
715
P KRB001 Krabbe Disease 69 0.098
716
c MCL013 Mucolipidosis Iv 64 0.098
717
MYP106 Myopathy, Myosin Storage, Autosomal Recessive 33 0.098
718
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.098
719
CLC008 Colchicine Resistance 34 0.098
720
GLL008 Gilles De La Tourette Syndrome 64 0.098
721
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.098
722
P MNN019 Mannosidosis, Beta a, Lysosomal 49 0.098
723
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 0.098
724
c EPP014 Epiphyseal Dysplasia, Multiple, 4 45 0.098
725
c GM1004 Gm1-Gangliosidosis, Type I 59 0.098
726
c GLY008 Glycogen Storage Disease Ii 72 0.098
727
c ANG068 Angioedema, Hereditary, Type I 58 0.098
728
P PSD087 Pseudoxanthoma Elasticum 66 0.098
729
CFF002 Coffin-Lowry Syndrome 59 0.098
730
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.098
731
SPP011 Suppression of Tumorigenicity 12 61 0.098
732
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.098
733
c SCH081 Schizophrenia 6 27 0.098
734
LKR002 Leukoregulin 28 0.098
735
HMC014 Homocysteinemia 52 0.098
736
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 54 0.098
737
ART002 Arts Syndrome 66 0.098
738
c LYM150 Lymphatic Malformation 7 43 0.098
739
HYP025 Hyperphosphatemia 47 0.098
740
VRL003 Variola Major 43 0.098
741
P BRC006 Brachydactyly 52 0.098
742
c RTN036 Retinal Cone Dystrophy 4 35 0.098
743
EWN003 Ewing Sarcoma 69 0.098
744
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.098
745
MSC007 Muscle Hypertrophy 64 0.098
746
c CNG497 Congenital Disorder of Glycosylation, Type Iio 40 0.098
747
CRP037 Carpal Tunnel Syndrome 2 21 0.098
748
SBC019 Subcutaneous Mycosis 34 0.098
749
LRY004 Laryngotracheitis 32 0.098
750
3MC001 3mc Syndrome 2 37 0.098
751
MLT135 Multiple Sulfatase Deficiency 53 0.098
752
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 30 0.098
753
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.098
754
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.098
755
CRN264 Craniosynostosis with Fibular Aplasia 29 0.098
756
c ACH041 Achondrogenesis, Type Ii 54 0.098
757
P HYP750 Hypertriglyceridemia, Familial 61 0.098
758
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.098
759
KPS004 Kaposi Sarcoma 76 0.098
760
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.098
761
c HMC039 Hemochromatosis, Type 1 73 0.098
762
c NMN015 Niemann-Pick Disease, Type C1 68 0.098
763
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 59 0.098
764
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.098
765
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.098
767
P MYC007 Myocardial Infarction 69 0.098
768
c CNG192 Congenital Disorder of Glycosylation, Type Ik 37 0.098
769
c MSC167 Muscular Dystrophy-Dystroglycanopathy , Type a, 11 32 0.098
770
c DWL004 Dowling-Degos Disease 4 20 0.098
771
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.098
772
P HMN032 Human Herpesvirus 8 47 0.098
773
LPT014 Leptin Deficiency or Dysfunction 77 0.098
774
c CNG383 Congenital Disorder of Glycosylation, Type Iik 43 0.098
775
c MSC102 Muscular Dystrophy-Dystroglycanopathy , Type a, 12 29 0.098
776
EPD055 Epidermolysis Bullosa, Nonspecific, Autosomal Recessive 27 0.098
777
MLD001 Melioidosis 67 0.098
778
c ATR087 Atrial Standstill 1 74 0.098
779
BCL014 B-Cell Growth Factor 32 0.098
781
c LKM070 Leukemia, Acute Monocytic 56 0.098
782
MYP126 Myopathy with Storage of Glycoproteins and Glycosaminoglycans 9 0.098
783
c OST080 Osteogenesis Imperfecta, Type Ii 55 0.098
785
INC002 Inclusion Body Myositis 56 0.098
786
CRT072 Creutzfeldt-Jakob Disease 67 0.098
787
ESP021 Esophageal Cancer 84 0.098
788
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.098
789
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.098
790
PMP006 Pemphigus Vulgaris, Familial 57 0.098
791
LNT004 Lentigines 45 0.098
792
CHD004 Chudley-Mccullough Syndrome 47 0.098
793
RFL001 Reflex Sympathetic Dystrophy 51 0.098
794
P ORT004 Orthostatic Intolerance 61 0.098
795
PRS129 Prostatic Hyperplasia, Benign 48 0.098
796
c CNG205 Congenital Disorder of Glycosylation, Type Ij 36 0.098
797
HLC007 Helicobacter Pylori Infection 67 0.098
798
CHR005 Chorioamnionitis 50 0.098
799
P BND020 Bone Disease 60 0.098
800
FBR009 Fibrous Dysplasia 48 0.098
801
LYM040 Lymphoblastic Lymphoma 53 0.098
802
DFF005 Diffuse Large B-Cell Lymphoma 55 0.098
803
RSP021 Respiratory Allergy 41 0.098
804
PLL012 Pollen Allergy 44 0.098
805
LTX001 Latex Allergy 41 0.098
806
c ATM099 Autoimmune Uveitis 44 0.098
807
BCT021 Bacterial Sepsis 43 0.098
808
AML029 Ameloblastoma 46 0.098
809
c CNG547 Congenital Muscular Dystrophy-Dystroglycanopathy Type A11 25 0.098
810
P CRN024 Corneal Disease 43 0.098
811
OST003 Osteonecrosis 60 0.098
812
P MMP001 Mumps 56 0.098
813
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.098
814
VLL003 Villonodular Synovitis 41 0.098
815
HMN047 Human Cytomegalovirus Infection 59 0.098
816
LWG006 Low Grade Glioma 41 0.098
817
MLD018 Mild Cognitive Impairment 48 0.098
818
P CHN059 Chondrocalcinosis 51 0.098
819
PMP004 Pemphigus Foliaceus 43 0.098
820
HMR023 Hemorrhagic Cystitis 43 0.098
821
CLR109 Colorectal Adenocarcinoma 50 0.098
822
BYS001 Byssinosis 27 0.098
823
SLC006 Silicosis 55 0.098
824
ANT018 Anthracosis 50 0.098
825
QFV001 Q Fever 61 0.098
826
MNN032 Meningococcal Meningitis 52 0.098
827
BRR014 Barrett Esophagus 66 0.098
828
P MGR003 Migraine with Aura 51 0.098
829
P PNM006 Pneumoconiosis 55 0.098
830
P HYP069 Hyperparathyroidism 62 0.098
831
VLV032 Vulva Cancer 60 0.098
832
PNC001 Pancytopenia 52 0.098
833
THR004 Thrombocytosis 52 0.098
834
TLR001 Tularemia 56 0.098
835
HYP080 Hypogonadism 49 0.098
836
SKN013 Skin Benign Neoplasm 49 0.098
837
NRL005 Neurilemmoma 60 0.098
838
BLR008 Bilirubin Metabolic Disorder 57 0.098
839
c BSL007 Basal Cell Carcinoma 67 0.098
840
P HMN010 Hemangioma 61 0.098
841
P CYS039 Cystic Kidney Disease 52 0.098
842
BRS099 Breast Ductal Carcinoma 61 0.098
843
c ACT071 Acute Kidney Failure 60 0.098
844
PPL022 Papilloma 53 0.098
845
P EPD016 Epidermolysis Bullosa 53 0.098
846
NRM004 Neuroma 49 0.098
847
RTN020 Retinal Vascular Disease 45 0.098
848
VGN023 Vaginitis 56 0.098
849
P KRN004 Kernicterus 47 0.098
850
NNT012 Neonatal Jaundice 53 0.098
851
CHN002 Chancroid 36 0.098
852
P BRS053 Breast Fibroadenoma 48 0.098
853
CRN022 Corneal Degeneration 33 0.098
854
P HYP730 Hypogonadotropic Hypogonadism 57 0.098
855
CLN044 Colon Adenoma 44 0.098
856
FLN001 Flinders Island Spotted Fever 18 0.098
857
JPN001 Japanese Spotted Fever 21 0.098
858
ALT003 Alternating Exotropia 33 0.098
859
EXT022 Exotropia 42 0.098
860
P PYL005 Pyelonephritis 56 0.098
861
CHR031 Chromoblastomycosis 48 0.098
862
CRD003 Cardiac Sarcoidosis 44 0.098
863
GLN002 Glanders 38 0.098
864
P ECL001 Eclampsia 52 0.098
865
ELP001 Elephantiasis 43 0.098
866
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.098
867
CLL003 Cellulitis 53 0.098
868
P CRV031 Cervical Adenocarcinoma 48 0.098
869
P EYD002 Eye Disease 57 0.098
870
EPD006 Epidermolysis Bullosa Acquisita 48 0.098
871
P GLL018 Gallbladder Cancer 59 0.098
872
SCL002 Scleredema Adultorum 45 0.098
873
NPH009 Nephrolithiasis 54 0.098
874
CNN005 Connective Tissue Disease 66 0.098
875
P INT068 Intestinal Disease 53 0.098
876
CLN019 Colonic Disease 47 0.098
877
P PGT001 Paget's Disease of Bone 60 0.098
878
P DYS154 Dystonia 64 0.098
879
P PNM007 Pneumonia 64 0.098
880
TRN015 Transient Cerebral Ischemia 62 0.098
881
P MTR014 Motor Neuron Disease 65 0.098
882
IRN002 Iron Metabolism Disease 56 0.098
883
FRZ001 Frozen Shoulder 54 0.098
884
c ATM022 Autoimmune Myocarditis 35 0.098
885
P EPL164 Epilepsy 70 0.098
886
c VRL010 Viral Hepatitis 52 0.098
887
c FML021 Familial Hypercholesterolemia 71 0.098
888
KLB003 Klebsiella Pneumonia 49 0.098
889
RFT001 Rift Valley Fever 50 0.098
890
P PRR002 Pure Red-Cell Aplasia 46 0.098
891
SQM002 Squamous Cell Papilloma 45 0.098
892
MMB001 Membranoproliferative Glomerulonephritis 56 0.098
893
P ANT006 Antiphospholipid Syndrome 55 0.098
894
OPT003 Opiate Dependence 49 0.098
895
P AGM001 Agammaglobulinemia 67 0.098
896
P CPL006 Capillary Hemangioma 53 0.098
897
CRV040 Cervix Carcinoma 50 0.098
898
SBC003 Subacute Bacterial Endocarditis 33 0.098
899
PRS042 Prostate Disease 42 0.098
900
CVR006 Cavernous Hemangioma 51 0.098
901
PYD002 Pyoderma 49 0.098
902
NRM005 Neuromuscular Disease 62 0.098
903
PRS021 Prostatic Adenoma 43 0.098
904
MRK001 Merkel Cell Carcinoma 64 0.098
905
SNS003 Sensory Peripheral Neuropathy 51 0.098
906
ORC001 Orchitis 43 0.098
907
CYS014 Cystadenocarcinoma 51 0.098
908
DMY004 Demyelinating Disease 50 0.098
909
OST004 Osteitis Fibrosa 38 0.098
910
BNN003 Bone Inflammation Disease 47 0.098
911
MCP006 Mucoepidermoid Carcinoma 48 0.098
912
PRR001 Periarthritis 33 0.098
913
BLD019 Bile Duct Cystadenocarcinoma 34 0.098
914
PRM236 Primary Biliary Cholangitis 62 0.098
915
LST001 Listeriosis 59 0.098
916
DBT008 Diabetic Angiopathy 47 0.098
917
MNN009 Meningoencephalitis 47 0.098
918
OST011 Osteomalacia 52 0.098
919
P LKD001 Leukodystrophy 58 0.098
920
P FNC004 Fanconi Syndrome 60 0.098
921
MCR013 Microphthalmia 59 0.098
922
c ACT073 Acute Leukemia 59 0.098
923
QDR001 Quadriplegia 49 0.098
924
FLR002 Filariasis 55 0.098
925
SPT005 Spotted Fever 49 0.098
926
PRS045 Prostatic Hypertrophy 53 0.098
927
TNN002 Tinea Unguium 34 0.098
928
END028 Endemic Goiter 36 0.098
929
TTH008 Tooth Resorption 38 0.098
930
END062 Endometrial Hyperplasia 47 0.098
931
MCR011 Microinvasive Gastric Cancer 41 0.098
932
P MCR010 Microcephaly 59 0.098
933
CHL122 Cholesteatoma of Middle Ear 51 0.098
934
P NTR004 Neutropenia 62 0.098
935
P AGG001 Aggressive Periodontitis 55 0.098
936
CRY003 Cryptosporidiosis 55 0.098
937
ALG001 Algoneurodystrophy 37 0.098
938
PLS007 Plasmodium Falciparum Malaria 52 0.098
939
P RNL007 Renal Tubular Acidosis 52 0.098
940
OCH001 Ochronosis 40 0.098
941
PYL006 Pyloric Stenosis 48 0.098
942
HNC001 Henoch-Schoenlein Purpura 56 0.098
943
CYS005 Cysticercosis 60 0.098
944
CHL004 Cholelithiasis 48 0.098
945
LYM009 Lymphocytic Choriomeningitis 46 0.098
946
c PST005 Posterior Uveitis 54 0.098
947
HLL004 Hellp Syndrome 53 0.098
948
BLL006 Bullous Pemphigoid 61 0.098
949
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.098
950
MYS001 Myositis Ossificans 44 0