Search results for diabetes mellitus, type ii, susceptibility to

886 hits were found for diabetes mellitus, type ii, susceptibility to

# Family MCID Name MIFTS Score
1
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 10.357
2
P DBT009 Diabetes Mellitus 72 1.750
3
c BLD140 Blood Group, I System 37 1.256
4
GLC008 Glucose Metabolism Disease 38 0.904
5
P NRP001 Neuropathy 63 0.549
6
ATM095 Autoimmune Disease 66 0.521
7
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.498
8
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.495
9
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.495
10
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.495
11
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.495
12
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.495
13
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.495
14
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.495
15
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.494
16
END072 Endotheliitis 46 0.493
17
IMM136 Immune System Disease 57 0.491
18
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.475
19
GST033 Gestational Diabetes 62 0.462
20
P BRS047 Breast Cancer 100 0.462
21
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.457
22
P HPT021 Hepatitis 75 0.443
23
P KDN018 Kidney Disease 69 0.436
24
P PNC044 Pancreatitis 64 0.434
25
AGN016 Aging 65 0.431
26
P MCR115 Microvascular Complications of Diabetes 5 66 0.426
27
c MCR113 Microvascular Complications of Diabetes 3 55 0.415
28
c MCR120 Microvascular Complications of Diabetes 7 34 0.413
29
c MCR130 Microvascular Complications of Diabetes 6 42 0.412
30
c MCR133 Microvascular Complications of Diabetes 4 32 0.412
31
ART140 Arteries, Anomalies of 51 0.396
32
P CRN018 Coronary Artery Anomaly 69 0.385
33
P HRT032 Heart Disease 80 0.382
34
P LKM002 Leukemia 75 0.378
35
HYP066 Hyperglycemia 64 0.377
36
P ART022 Arthritis 77 0.366
37
P LNG032 Lung Cancer 99 0.339
38
ISC004 Ischemia 66 0.338
39
P MYC007 Myocardial Infarction 81 0.338
40
P THY032 Thyroiditis 56 0.335
41
P CRN300 Coronary Heart Disease 1 57 0.331
42
P LYM118 Lymphoma 71 0.330
43
VSC007 Vascular Disease 71 0.327
44
PRS047 Prostatitis 59 0.322
45
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.316
46
URN009 Urinary System Disease 58 0.313
47
DBT010 Diabetic Neuropathy 60 0.311
48
P PRS040 Prostate Cancer 88 0.305
49
P CLR023 Colorectal Cancer 98 0.297
50
P RHM011 Rheumatoid Arthritis 91 0.296
51
P ADN016 Adenocarcinoma 71 0.293
52
RTN023 Retinitis 52 0.288
53
P LVR013 Liver Disease 76 0.285
54
CRB009 Cerebritis 41 0.281
55
NRN002 Neuronitis 43 0.276
56
P PRD008 Periodontitis 67 0.276
57
ISC006 Ischemic Heart Disease 73 0.270
58
P MYC084 Mycobacterium Tuberculosis 1 69 0.266
59
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.264
60
SPS003 Spastic Diplegia 55 0.259
61
AST005 Asthma 83 0.257
62
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.256
63
MLN008 Melanoma 72 0.253
64
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.251
65
P ALZ034 Alzheimer Disease 95 0.250
66
GST053 Gastric Cancer 84 0.249
67
GLC003 Glucose Intolerance 58 0.247
68
P ART021 Arteriosclerosis 62 0.244
69
P HPT023 Hepatocellular Carcinoma 94 0.242
70
c CHR089 Chronic Kidney Failure 72 0.240
71
DBT062 Diabetic Foot Ulcers 59 0.237
72
P PLY019 Polyneuropathy 58 0.236
73
THR024 Thrombosis 61 0.236
74
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.235
75
P SCH015 Schizophrenia 71 0.234
76
DBT006 Diabetic Macular Edema 49 0.233
77
HYP060 Hyperinsulinism 56 0.229
78
P CRV039 Cervicitis 49 0.227
79
P NRV007 Nervous System Disease 75 0.226
80
P MLT020 Multiple Sclerosis 85 0.225
81
P ENC018 Encephalopathy 58 0.225
82
c HPT001 Hepatitis C 73 0.225
83
c MCR129 Microvascular Complications of Diabetes 1 62 0.223
84
SKN016 Skin Disease 68 0.222
85
INS024 Insulin-Like Growth Factor I 83 0.221
86
P INF038 Influenza 77 0.221
87
CNG034 Congestive Heart Failure 74 0.220
88
DBT008 Diabetic Angiopathy 48 0.219
89
ANX010 Anxiety 72 0.219
90
NRM005 Neuromuscular Disease 60 0.215
91
c MCL042 Macular Degeneration, Age-Related, 1 79 0.215
92
SKN027 Skin Conditions 48 0.213
93
NRT004 Neuritis 55 0.212
94
VRL011 Viral Infectious Disease 64 0.211
95
P LPS004 Lupus Erythematosus 69 0.210
96
DMN002 Dementia 68 0.209
97
ACQ007 Acquired Immunodeficiency Syndrome 65 0.209
98
P HYP086 Hypothyroidism 62 0.207
99
ANR040 Aneurysm 61 0.207
100
P PNC035 Pancreatic Cancer 89 0.205
101
P PNM007 Pneumonia 70 0.205
102
P PSR002 Psoriasis 65 0.203
103
c HYP595 Hypertension, Essential 78 0.203
104
c SYS001 Systemic Lupus Erythematosus 86 0.203
105
P CTR002 Cataract 60 0.201
106
MNT002 Mental Depression 60 0.201
107
P OVR042 Ovarian Cancer 82 0.199
108
P MTR004 Maturity-Onset Diabetes of the Young 62 0.199
109
GST050 Gastrointestinal System Disease 66 0.197
110
P EPL164 Epilepsy 70 0.197
111
PRP019 Peripheral Nervous System Disease 53 0.196
112
P ESP024 Esophagitis 64 0.194
113
c MCR112 Microvascular Complications of Diabetes 2 30 0.194
114
FTT001 Fatty Liver Disease 62 0.192
115
HYP266 Hypoxia 61 0.192
116
c HPT016 Hepatitis B 68 0.191
117
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.190
118
LNG099 Lung Disease 67 0.190
119
c SML038 Small Cell Cancer of the Lung 67 0.190
120
P RTN016 Retinal Degeneration 56 0.190
121
P OST002 Osteoporosis 75 0.189
122
OST012 Osteoarthritis 88 0.188
123
P GLM045 Glioma 61 0.187
124
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.186
125
P INF032 Infertility 59 0.186
126
P CLC063 Celiac Disease 1 65 0.185
127
LPD008 Lipid Metabolism Disorder 59 0.183
128
P GLM007 Glomerulonephritis 61 0.182
129
PRD007 Periodontal Disease 64 0.182
130
SRC014 Sarcoma 68 0.178
131
P ANR048 Aniridia 1 68 0.177
132
P MYL006 Myeloid Leukemia 69 0.177
133
PRD004 Prediabetes Syndrome 46 0.175
134
c HPT073 Hepatitis C Virus 73 0.174
135
P INT068 Intestinal Disease 65 0.173
136
ANR038 Anorexia Nervosa 1 21 0.173
137
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.173
138
c ACT075 Acute Myocardial Infarction 64 0.171
139
BLD137 Blood Group--Ahonen 17 0.171
140
P ART023 Arthropathy 68 0.171
141
PST011 Pustulosis of Palm and Sole 47 0.168
142
ADN018 Adenoma 63 0.168
143
P MYP006 Myopia 56 0.167
144
BRS051 Breast Disease 67 0.167
145
CYS001 Cystic Fibrosis 85 0.165
146
PRP027 Peripheral Vascular Disease 71 0.163
147
DRM006 Dermatitis 67 0.163
148
P MYP004 Myopathy 69 0.162
149
HSH003 Hashimoto Thyroiditis 67 0.162
150
P BLD134 Bladder Cancer 78 0.162
151
RSP006 Respiratory System Disease 63 0.161
152
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.161
153
END030 End Stage Renal Failure 59 0.160
154
P BCL006 B-Cell Lymphomas 70 0.160
155
c TRC078 Trichohepatoenteric Syndrome 2 34 0.160
156
PLM001 Pulmonary Tuberculosis 72 0.158
157
MTH009 Mouth Disease 64 0.158
158
HPT082 Hepatic Adenomas, Familial 52 0.158
159
P LYM026 Lymphoblastic Leukemia 66 0.157
160
PRT036 Peritonitis 67 0.157
161
P GRV001 Graves' Disease 62 0.157
162
ALR002 Al-Raqad Syndrome 30 0.156
163
CRB039 Cerebrovascular Disease 68 0.155
164
P ENC004 Encephalitis 66 0.154
165
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.153
166
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.152
167
CLT003 Colitis 63 0.152
168
P AMY004 Amyloidosis 69 0.152
169
P PLY011 Polycystic Ovary Syndrome 65 0.151
170
P MNN013 Meningitis 71 0.151
171
GNG013 Gingivitis 64 0.150
172
P NRB001 Neuroblastoma 73 0.149
173
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.149
174
PSY004 Psychotic Disorder 72 0.148
175
P DRR001 Diarrhea 60 0.148
176
RHM027 Rheumatic Disease 62 0.146
177
CNN005 Connective Tissue Disease 65 0.145
178
OVR063 Overnutrition 53 0.145
179
P INF037 Inflammatory Bowel Disease 52 0.144
180
PRP080 Peripheral Artery Disease 54 0.144
181
P MLG056 Malignant Hyperthermia 60 0.143
182
PNC034 Pancreas Disease 59 0.143
183
c BRN108 Branchiootic Syndrome 1 47 0.143
184
c LKM061 Leukemia, Acute Myeloid 81 0.142
185
c PRC016 Pre-Eclampsia 65 0.142
186
SLP005 Sleep Disorder 59 0.142
187
c HPT003 Hepatitis a 63 0.142
188
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.142
189
P SLP006 Sleep Apnea 65 0.142
190
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.141
191
P CLL015 Collagen Disease 53 0.141
192
MYL069 Myeloma, Multiple 86 0.140
193
JNT002 Joint Disorders 60 0.139
194
ALP046 Alport Syndrome, X-Linked 74 0.139
195
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.138
196
CRH001 Crohn's Disease 80 0.138
197
ANG054 Angina Pectoris 53 0.138
198
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.137
199
P ATR011 Atrial Fibrillation 68 0.137
200
P CND004 Candidiasis 61 0.137
201
BRN106 Burns 57 0.137
202
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.137
203
BRC012 Brucellosis 71 0.135
204
MDD011 Mood Disorder 64 0.135
205
P BPL003 Bipolar Disorder 61 0.135
206
P ECL001 Eclampsia 57 0.134
207
ATM052 Autoimmune Disease 1 30 0.134
208
P TCL004 T-Cell Leukemia 50 0.133
209
LVR012 Liver Cirrhosis 73 0.132
210
ART016 Aortic Aneurysm 70 0.131
211
P THR014 Thrombocytopenia 65 0.131
212
STR067 Stroke, Ischemic 84 0.130
213
P HYP750 Hypertriglyceridemia, Familial 55 0.130
214
SPN051 Spondylitis 55 0.129
215
ENT004 Enthesopathy 38 0.129
216
P MSC005 Muscular Dystrophy 66 0.128
217
SPS057 Spasticity 41 0.128
218
LMB062 Limb Ischemia 52 0.127
219
P END044 Endometriosis 71 0.127
220
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.127
221
BNF002 Bone Fracture 56 0.127
222
ULC004 Ulcerative Colitis 80 0.125
223
STM006 Stomach Disease 52 0.125
224
P MLT074 Multiple Endocrine Neoplasia 55 0.125
225
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.124
226
c SPN225 Spondyloarthropathy 1 71 0.124
227
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.123
228
P RNG031 Ring Chromosome Y Syndrome 29 0.123
229
P EXN002 Exanthem 62 0.122
230
ALL026 Allergic Hypersensitivity Disease 59 0.122
231
HYP080 Hypogonadism 54 0.121
232
NNL002 Nonalcoholic Steatohepatitis 56 0.121
233
INS001 Insulinoma 66 0.121
234
LYM133 Lymphoma, Hodgkin, Classic 78 0.121
235
P PYL005 Pyelonephritis 56 0.120
236
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.120
237
P AST007 Astrocytoma 66 0.119
238
P MJR001 Major Depressive Disorder 70 0.119
239
APN008 Apnea, Obstructive Sleep 67 0.119
240
P MSC003 Muscular Atrophy 55 0.119
241
DFF005 Diffuse Large B-Cell Lymphoma 64 0.118
242
HMT018 Hematopoietic Stem Cell Transplantation 58 0.118
243
P NPH012 Nephrotic Syndrome 60 0.118
244
GT001 Gout 60 0.117
245
P ALP008 Alopecia 56 0.117
246
P KDN017 Kidney Cancer 66 0.116
247
FTL021 Fetal Macrosomia 46 0.116
248
CHR008 Choroiditis 47 0.115
249
DDN006 Duodenitis 46 0.115
250
MYL009 Myelodysplastic Syndrome 75 0.115
251
P RBL001 Rubella 61 0.115
252
P LCT001 Lactic Acidosis 51 0.115
253
P UVT001 Uveitis 61 0.114
254
c ACT027 Acute Pancreatitis 61 0.114
255
TTH006 Tooth Disease 54 0.114
256
VGN023 Vaginitis 59 0.114
257
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.113
258
HDC001 Headache 55 0.112
259
GND003 Gonadal Disease 32 0.112
260
NRL016 Neural Tube Defects 79 0.112
261
LSH001 Leishmaniasis 71 0.112
262
P LPD010 Lipodystrophy 57 0.112
263
SFT003 Soft Tissue Sarcoma 58 0.112
264
MCS002 Mucositis 61 0.112
265
P OVR049 Ovarian Disease 58 0.112
266
DWR001 Dwarfism 48 0.111
267
OST017 Osteomyelitis 64 0.111
268
c SCL052 Scleroderma, Familial Progressive 60 0.111
269
P THL005 Thalassemia 65 0.110
270
PRP030 Purpura 61 0.110
271
END057 Endometrial Cancer 76 0.110
272
MRB003 Morbid Obesity 61 0.109
273
MSL001 Measles 64 0.109
274
ERY003 Erythema Multiforme 60 0.108
275
P VSC018 Visceral Steatosis 38 0.108
276
P NSP012 Nasopharyngeal Carcinoma 71 0.107
277
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.107
278
P MYT002 Myotonic Dystrophy 50 0.107
279
P PLM037 Pulmonary Hypertension 79 0.107
280
P ATS364 Autism 70 0.107
281
NSP002 Nasopharyngitis 46 0.107
282
P SPN046 Spinal Muscular Atrophy 63 0.107
283
P DRM053 Dermatitis, Atopic 68 0.107
284
GRW007 Growth Hormone Deficiency 52 0.106
285
BRT054 Brittle Bone Disorder 67 0.106
286
PSR001 Psoriatic Arthritis 66 0.106
287
HLC007 Helicobacter Pylori Infection 64 0.106
288
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.106
289
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.106
290
P WLF004 Wolfram Syndrome 61 0.105
291
P EHL001 Ehlers-Danlos Syndrome 61 0.105
292
c ATM011 Autoimmune Hepatitis 63 0.105
293
P CNJ013 Conjunctivitis 67 0.105
294
GST045 Gastroenteritis 65 0.105
295
c MYT020 Myotonic Dystrophy 2 56 0.104
296
P CHR345 Chronic Pain 52 0.104
297
CNN003 Conn's Syndrome 70 0.104
298
BRN071 Brain Injury 54 0.104
299
P PMP001 Pemphigus 55 0.104
300
P GRF003 Graft-Versus-Host Disease 72 0.103
301
HMP009 Haemophilus Influenzae 49 0.103
302
P GST044 Gastritis 61 0.103
303
P PHC003 Pheochromocytoma 72 0.102
304
ACR006 Aceruloplasminemia 65 0.102
305
ACN002 Acanthosis Nigricans 60 0.101
306
VSC011 Vasculitis 66 0.100
307
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.100
308
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.099
309
P DLT002 Dilated Cardiomyopathy 76 0.099
310
P HYD006 Hydrocephalus 68 0.099
311
c LKM063 Leukemia, Chronic Myeloid 80 0.098
312
P KLZ004 Kala-Azar 1 31 0.098
313
KWS002 Kawasaki Disease 72 0.097
314
P PRK057 Parkinson Disease, Late-Onset 78 0.097
315
P RTN008 Retinitis Pigmentosa 81 0.097
316
ETN001 Eating Disorder 61 0.096
317
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.096
318
P MYS003 Myasthenia Gravis 73 0.096
319
BRN024 Bronchitis 67 0.096
320
P DYS154 Dystonia 61 0.095
321
BLD044 Bladder Disease 55 0.095
322
P DYS021 Dysautonomia 47 0.095
323
CRD119 Cardiac Arrest 63 0.094
324
CHL068 Cholestasis 60 0.094
325
P ACT074 Acute Lymphocytic Leukemia 61 0.093
326
P STR035 Streptococcal Group a Invasive Disease 28 0.093
327
P ALP009 Alopecia Areata 64 0.093
328
STM007 Stomatitis 52 0.093
329
CND006 Candida Glabrata 38 0.092
330
P CHL066 Cholangitis 52 0.092
331
NCR002 Necrobiosis Lipoidica 35 0.092
332
P RSP003 Respiratory Failure 71 0.092
333
P HYP607 Hypercholesterolemia, Familial 81 0.092
334
DNT012 Dental Caries 50 0.092
335
P SCL018 Scoliosis 56 0.092
336
P MMB011 Membranous Nephropathy 55 0.092
337
CHL065 Cholangiocarcinoma 70 0.092
338
P NTR004 Neutropenia 60 0.091
339
URM002 Uremia 52 0.091
340
P CHR071 Charcot-Marie-Tooth Disease 67 0.091
341
VSC002 Vascular Dementia 58 0.091
342
P HST010 Histiocytosis 60 0.091
343
WRN001 Werner Syndrome 70 0.091
344
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.091
345
P TXP001 Toxoplasmosis 65 0.090
346
VLV010 Vulvovaginitis 45 0.090
347
c VRL010 Viral Hepatitis 59 0.090
348
c TYP031 Type 1 Diabetes Mellitus 5 26 0.089
349
FSC004 Fasciitis 48 0.089
350
P TRN020 Turner Syndrome 69 0.089
351
BRN038 Bronchial Disease 58 0.089
352
P SNS014 Sinusitis 62 0.089
353
P HYP076 Hyperthyroidism 56 0.088
354
CHL123 Chlamydia 64 0.088
355
EPD016 Epidermolysis Bullosa 57 0.088
356
P ASP006 Aspergillosis 65 0.088
357
P PLM036 Pulmonary Fibrosis 68 0.088
358
P GRM010 Germ Cells Tumors 37 0.088
359
CLR108 Colorectal Adenoma 60 0.088
360
TTN003 Tetanus 65 0.088
361
LYM027 Lymphopenia 56 0.088
362
P ATX030 Ataxia-Telangiectasia 80 0.087
363
P HMR012 Hemorrhagic Fever 60 0.087
364
c MLG074 Malignant Mesenchymoma 51 0.087
365
CYT008 Cytomegalovirus Infection 57 0.087
366
ALC007 Alcohol Dependence 65 0.087
367
PNG002 Pain Agnosia 41 0.087
368
DWN001 Down Syndrome 70 0.087
369
URT001 Urethritis 44 0.087
370
ALB002 Albinism 45 0.086
371
P HMP007 Hemophilia 61 0.086
372
DBT007 Diabetic Cataract 38 0.086
373
P HYP014 Hyperuricemia 54 0.086
374
P CYS018 Cystitis 57 0.086
375
ANX004 Anoxia 49 0.086
376
CRN030 Coronary Stenosis 52 0.086
377
P OPN001 Open-Angle Glaucoma 51 0.085
378
HMS001 Hemosiderosis 50 0.085
379
P MYC008 Myocarditis 58 0.085
380
P PRP029 Porphyria 62 0.085
381
P MMP001 Mumps 61 0.085
382
c ATM024 Autoimmune Pancreatitis 49 0.085
383
BLD163 Blood Group, Dombrock System 23 0.084
384
LYM067 Lymphoid Leukemia 43 0.084
385
P SCL057 Scoliosis, Isolated 1 28 0.084
386
CRN025 Corneal Dystrophy 42 0.083
387
HRP004 Herpes Zoster 61 0.083
388
MNG003 Mungan Syndrome 34 0.083
389
P SML001 Small Cell Carcinoma 58 0.082
390
SCK005 Sickle Cell Disease 54 0.082
391
c MYS011 Myasthenia Gravis Congenital 28 0.082
392
P TRM003 Tremor 54 0.082
393
OTT002 Otitis Media 67 0.082
394
P PRD006 Prader-Willi Syndrome 66 0.082
395
P HYP265 Hypotonia 40 0.081
396
c BLM008 Bulimia Nervosa 2 53 0.081
397
SCK003 Sickle Cell Anemia 73 0.081
398
TRM010 Traumatic Brain Injury 54 0.081
399
P NRF023 Neurofibromatosis, Type Ii 69 0.081
400
MTN003 Motion Sickness 52 0.081
401
P PLY014 Polycystic Kidney Disease 60 0.081
402
c ACT210 Acute Respiratory Distress Syndrome 63 0.081
403
INT007 Intermediate Coronary Syndrome 55 0.081
404
MDS022 Mediastinitis 44 0.081
405
P HYP061 Hypertrophic Cardiomyopathy 65 0.081
406
GST092 Gastroesophageal Reflux 64 0.081
407
APL001 Aplastic Anemia 74 0.081
408
IGR001 Ige Responsiveness, Atopic 56 0.081
409
P HML002 Hemolytic Anemia 62 0.080
410
P LNG028 Long Qt Syndrome 63 0.080
411
P MYS005 Myositis 63 0.080
412
CTN007 Cutaneous Leishmaniasis 66 0.080
413
c CNG124 Congenital Rubella 47 0.080
414
CHR073 Choreatic Disease 40 0.080
415
PRN011 Pernicious Anemia 50 0.080
416
P MCR010 Microcephaly 57 0.080
417
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.080
418
CRT016 Carotid Artery Disease 58 0.080
419
IRN002 Iron Metabolism Disease 45 0.079
420
CNS004 Constipation 57 0.079
421
MST005 Mastitis 56 0.079
422
P BCT020 Bacteremia 2 34 0.079
423
ADG002 Audiogenic Seizures 26 0.079
424
VLV011 Vulvovaginal Candidiasis 53 0.079
425
ACT118 Acute Non Lymphoblastic Leukemia 32 0.079
426
P SZR006 Seizure Disorder 55 0.079
427
P LCH002 Lichen Planus 58 0.079
428
SVR004 Severe Combined Immunodeficiency 71 0.078
429
HYP005 Hypokalemia 53 0.078
430
P END033 Endocarditis 58 0.078
431
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.078
432
P HYP024 Hypoparathyroidism 55 0.078
433
CRN024 Corneal Disease 47 0.078
434
SYS003 Systolic Heart Failure 44 0.078
435
c ADL017 Adult T-Cell Leukemia 63 0.078
436
DMY004 Demyelinating Disease 58 0.078
437
c ACT042 Acute Pyelonephritis 48 0.077
438
CRN036 Craniopharyngioma 63 0.077
439
PLM033 Pulmonary Embolism 62 0.077
440
GRN007 Granuloma Annulare 40 0.077
441
P THY023 Thymoma 65 0.077
442
c HMC039 Hemochromatosis, Type 1 71 0.077
443
SXL003 Sexual Disorder 45 0.077
444
P DMY001 Demyelinating Polyneuropathy 46 0.076
445
DYS014 Dyspepsia 54 0.076
446
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.076
447
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.076
448
P AST055 Asthma-Related Traits 1 18 0.076
449
ART008 Arteriosclerosis Obliterans 45 0.076
450
IRN001 Iron Deficiency Anemia 55 0.076
451
PLM010 Pulmonary Edema 57 0.076
452
KRT006 Keratoconjunctivitis 56 0.075
453
VSC003 Visceral Leishmaniasis 59 0.075
454
P NRC002 Narcolepsy 64 0.075
455
INT002 Intermittent Claudication 61 0.075
456
P FNC004 Fanconi Syndrome 54 0.075
457
SPS019 Spastic Paraparesis 33 0.074
458
SCH012 Schizoaffective Disorder 51 0.074
459
RST001 Restless Legs Syndrome 54 0.074
460
NPH009 Nephrolithiasis 57 0.074
461
P MDL005 Medulloblastoma 76 0.074
462
PNM001 Pneumocystosis 55 0.074
463
c LKM062 Leukemia, Acute Lymphoblastic 64 0.074
464
BLL006 Bullous Pemphigoid 64 0.074
465
LNG108 Langerhans Cell Histiocytosis 63 0.074
466
LYM009 Lymphocytic Choriomeningitis 46 0.074
467
P ACT105 Acute Mountain Sickness 58 0.074
468
ORL005 Oral Candidiasis 51 0.074
469
P PRC031 Preeclampsia/eclampsia 1 41 0.074
470
P ATM019 Autoimmune Polyendocrine Syndrome 47 0.073
471
CLF001 Cleft Lip 54 0.073
472
P ADL010 Adult Respiratory Distress Syndrome 67 0.073
473
KRT001 Keratoconjunctivitis Sicca 63 0.073
474
GLL018 Gallbladder Cancer 67 0.073
475
CCC001 Coccidioidomycosis 60 0.072
476
P CRD132 Cardiac Conduction Defect 53 0.072
477
TRP002 Tropical Spastic Paraparesis 58 0.072
478
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.072
479
P HYP614 Hyperlipidemia, Familial Combined 57 0.072
480
P INT001 Intrahepatic Cholestasis 62 0.072
481
PRP016 Paraplegia 53 0.072
482
P DDN001 Duodenal Ulcer 53 0.072
483
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.072
484
HYD002 Hydronephrosis 49 0.072
485
MLD001 Melioidosis 73 0.072
486
HDN002 Head Injury 48 0.072
487
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.072
488
DFC004 Deficiency Anemia 62 0.071
489
c LBR014 Leber Congenital Amaurosis 4 48 0.071
490
P PMP005 Pemphigus Vulgaris 56 0.071
491
WLL001 Williams-Beuren Syndrome 63 0.071
492
SYN007 Synovitis 61 0.071
493
DRY001 Dry Eye Syndrome 51 0.071
494
P PRP003 Porphyria Cutanea Tarda 67 0.071
495
P LYM025 Lymphedema 63 0.071
496
NCR007 Necrotizing Fasciitis 49 0.070
497
CHL067 Cholecystitis 58 0.070
498
RNL077 Renal Fibrosis 49 0.070
499
CLL003 Cellulitis 53 0.070
500
SNS001 Sensorineural Hearing Loss 59 0.070
501
c GRV008 Graves Disease 1 52 0.070
502
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.070
503
P PLY018 Polycythemia 60 0.070
504
c ATS007 Autism Spectrum Disorder 68 0.069
505
P PRG013 Paraganglioma 57 0.069
506
c HMP029 Hemophilia a 69 0.069
507
P PTS002 Ptosis 50 0.069
508
c JVN010 Juvenile Rheumatoid Arthritis 71 0.069
509
P DRM007 Dermatitis Herpetiformis 56 0.069
510
P THR015 Thrombophilia 58 0.069
511
P FCL005 Focal Segmental Glomerulosclerosis 60 0.069
512
TST014 Testicular Cancer 54 0.068
513
P OCL002 Oculocutaneous Albinism 57 0.068
514
SCH014 Schistosomiasis 62 0.068
515
CLN015 Colon Adenocarcinoma 53 0.068
516
EPD070 Epidermoid Cysts 46 0.068
517
ALL014 Allergic Encephalomyelitis 37 0.068
518
P ANT006 Antiphospholipid Syndrome 59 0.068
519
P LPS002 Liposarcoma 61 0.068
520
P HMN010 Hemangioma 61 0.068
521
OST003 Osteonecrosis 63 0.068
522
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.068
523
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 59 0.068
524
MYC006 Mycosis Fungoides 73 0.068
525
P GLL020 Gallbladder Disease 64 0.067
526
P ALC004 Alcohol Abuse 63 0.067
527
c BTT014 Beta-Thalassemia 70 0.067
528
c ACT135 Acute Graft Versus Host Disease 57 0.067
529
SLM003 Salmonellosis 56 0.067
530
CHG001 Chagas Disease 72 0.067
531
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.067
532
MYC033 Myoclonus 40 0.067
533
ART005 Arteriovenous Malformation 64 0.067
534
PHC013 Phaeochromocytoma 44 0.067
535
P AGG001 Aggressive Periodontitis 55 0.067
536
P SPN052 Spondyloarthropathy 61 0.067
537
PST053 Postherpetic Neuralgia 44 0.067
538
c TYP037 Type 1 Diabetes Mellitus 13 27 0.067
539
FRZ001 Frozen Shoulder 48 0.066
540
MLT006 Multidrug-Resistant Tuberculosis 48 0.066
541
P MYM013 Moyamoya Disease 1 50 0.066
542
c PMP006 Pemphigus Vulgaris, Familial 26 0.066
543
P PRT013 Portal Hypertension 59 0.066
544
ART017 Aortic Disease 57 0.066
545
CYT005 Cytomegalovirus Retinitis 51 0.066
546
c PSR018 Psoriasis 13 39 0.066
547
HRT012 Heart Valve Disease 45 0.066
548
ECH003 Echinococcosis 57 0.066
549
c WLF013 Wolfram Syndrome 1 52 0.066
550
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.065
551
ISC002 Ischemic Optic Neuropathy 48 0.065
552
PLS011 Plasmacytoma 60 0.065
553
P TMP003 Temporal Arteritis 67 0.065
554
c GLL024 Gallbladder Disease 1 39 0.065
555
RHM028 Rheumatic Heart Disease 54 0.065
556
BLD138 Blood Group--Diego System 18 0.065
557
P SYP003 Syphilis 55 0.065
558
P END046 Endometritis 51 0.065
559
c CNG021 Congenital Toxoplasmosis 57 0.065
560
c CHR417 Chronic Graft Versus Host Disease 65 0.065
561
P XRD010 Xeroderma Pigmentosum, Variant Type 62 0.064
562
PRC013 Pericarditis 55 0.064
563
P RNV001 Renovascular Hypertension 48 0.064
564
NPH003 Nephrocalcinosis 49 0.064
565
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.064
566
GST023 Gastric Ulcer 57 0.064
567
PRG023 Progeroid Short Stature with Pigmented Nevi 32 0.064
568
CRT013 Carotid Stenosis 52 0.064
569
P FNC027 Fanconi Anemia, Complementation Group a 78 0.064
570
WST005 West Nile Virus 58 0.064
571
CYS010 Cystinosis 55 0.064
572
RHM001 Rheumatic Fever 59 0.064
573
DNG002 Dengue Hemorrhagic Fever 66 0.064
574
CNT047 Contact Dermatitis 64 0.063
575
c ANT034 Anterior Uveitis 53 0.063
576
FBR019 Fibromatosis 47 0.063
577
P TBR001 Tuberous Sclerosis 69 0.063
578
CRY005 Cryptococcosis 54 0.063
579
IRR002 Irritable Bowel Syndrome 63 0.063
580
OST097 Osteoporotic Fracture 41 0.063
581
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.063
582
P MTH007 Methemoglobinemia 46 0.063
583
c HRD088 Hereditary Neuropathies 40 0.063
584
NWB001 Newborn Respiratory Distress Syndrome 56 0.063
585
P ENC011 Encephalomyopathy 40 0.062
586
c DRM040 Dermatitis Herpetiformis, Familial 32 0.062
587
CRD223 Cardiac Arrhythmia 52 0.062
588
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.062
589
RHM035 Rheumatic Fever-Related Antigen 34 0.062
590
DRM009 Dermatomycosis 39 0.062
591
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.062
592
PYD002 Pyoderma 51 0.061
593
P PNC025 Panic Disorder 57 0.061
594
c CHL119 Cholangitis, Primary Sclerosing 60 0.061
595
BRK010 Burkitt Lymphoma 71 0.061
596
ALP072 Alpha-Fetoprotein Deficiency 32 0.061
597
HPD002 Hepadnavirus Infection 14 0.061
598
VRC005 Varicose Veins 64 0.061
599
TNS005 Tonsillitis 61 0.061
600
CHP002 Chops Syndrome 40 0.061
601
MXD005 Mixed Connective Tissue Disease 66 0.060
602
TRD006 Tardive Dyskinesia 59 0.060
603
P SYS005 Systemic Scleroderma 67 0.060
604
P CCK001 Cockayne Syndrome 64 0.060
605
HPT019 Hepatic Encephalopathy 59 0.060
606
PMP004 Pemphigus Foliaceus 46 0.060
607
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.060
608
DCB001 Decubitus Ulcer 44 0.060
609
EPD001 Epidermodysplasia Verruciformis 52 0.060
610
PLY020 Polyradiculoneuropathy 48 0.060
611
P ESS003 Essential Thrombocythemia 71 0.060
612
CLF027 Cleft Palate, Isolated 61 0.060
613
OCL069 Ocular Motor Apraxia 45 0.060
614
P CRB088 Cerebral Atrophy 38 0.060
615
ALC009 Alcoholic Liver Cirrhosis 53 0.059
616
BLR006 Biliary Tract Disease 55 0.059
617
P FNC043 Fanconi Anemia, Complementation Group E 52 0.059
618
OBS002 Obsessive-Compulsive Disorder 68 0.059
619
c PRM196 Premature Ovarian Failure 1 68 0.059
620
HMN032 Human Herpesvirus 8 50 0.059
621
P BCK002 Beckwith-Wiedemann Syndrome 58 0.059
622
P OTT001 Otitis Externa 51 0.059
623
RLP001 Relapsing Polychondritis 55 0.059
624
P PLM034 Pulmonary Emphysema 59 0.059
625
SNL007 Senile Cataract 41 0.058
626
TXC005 Toxic Shock Syndrome 61 0.058
627
THR004 Thrombocytosis 55 0.058
628
ORL013 Oral Lichen Planus 51 0.058
629
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.058
630
NRM004 Neuroma 51 0.058
631
APP008 Appendicitis 64 0.058
632
LYM040 Lymphoblastic Lymphoma 58 0.058
633
P CRN028 Corneal Ulcer 48 0.058
634
STT001 Status Epilepticus 60 0.058
635
P SRC025 Sarcoidosis 1 63 0.058
636
TYP007 Typhoid Fever 67 0.058
637
c PSR028 Psoriasis 7 37 0.058
638
IMM001 Immune-Complex Glomerulonephritis 39 0.058
639
c PSR032 Psoriasis 11 35 0.058
640
P FML018 Familial Mediterranean Fever 73 0.057
641
APH002 Aphasia 58 0.057
642
P CRN037 Craniosynostosis 68 0.057
643
P HYP040 Hypospadias 60 0.057
644
DSS009 Disseminated Intravascular Coagulation 56 0.057
645
BRN004 Brain Edema 57 0.057
646
LYM017 Lyme Disease 68 0.057
647
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 46 0.057
648
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.057
649
SPL018 Splenomegaly 45 0.057
650
TNP001 Tinea Pedis 43 0.056
651
INS006 Insulin Autoimmune Syndrome 39 0.056
652
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 31 0.056
653
EPD006 Epidermolysis Bullosa Acquisita 50 0.056
654
FLR002 Filariasis 58 0.056
655
ART004 Aortic Atherosclerosis 48 0.056
656
XNT003 Xanthomatosis 53 0.056
657
P THR117 Three M Syndrome 1 52 0.056
658
FBR012 Fabry Disease 72 0.056
659
P OST135 Osteogenesis Imperfecta, Type I 56 0.056
660
PRT038 Protein-Energy Malnutrition 52 0.056
661
INT051 Intussusception 51 0.055
662
TBR011 Tuberculous Meningitis 54 0.055
663
c INF145 Infantile Liver Failure Syndrome 1 33 0.055
664
BRN056 Bronchopulmonary Dysplasia 61 0.055
665
c PSR017 Psoriasis 2 40 0.055
666
P PRK001 Porokeratosis 49 0.055
667
P AXN001 Axonal Neuropathy 38 0.055
668
HMR039 Hemorrhage, Intracerebral 57 0.055
669
P RTT002 Rett Syndrome 82 0.055
670
INT067 Interstitial Nephritis 51 0.055
671
P OBS001 Obstructive Jaundice 53 0.055
672
P BLM007 Bulimia Nervosa 1 53 0.055
673
LKP003 Leukoplakia 42 0.055
674
SPR010 Sporotrichosis 50 0.055
675
GNG003 Gingival Recession 45 0.055
676
TLN003 Telangiectasis 52 0.055
677
c CNG006 Congenital Hypothyroidism 62 0.055
678
PLR008 Pleurisy 52 0.054
679
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 40 0.054
680
MYX004 Myxedema 44 0.054
681
CNT025 Central Pontine Myelinolysis 45 0.054
682
PRM003 Premature Ejaculation 47 0.054
683
TKY002 Takayasu Arteritis 66 0.054
684
CCC002 Coccidiosis 52 0.054
685
MNN020 Meningococcal Infection 47 0.054
686
ALC006 Alcoholic Hepatitis 62 0.054
687
IMM003 Immunoglobulin Alpha Deficiency 37 0.054
688
P MLT007 Multiple Epiphyseal Dysplasia 57 0.054
689
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.054
690
P WSK001 Wiskott-Aldrich Syndrome 76 0.054
691
HYP077 Hypertrichosis 49 0.053
692
HYP780 Hypoadrenocorticism, Familial 59 0.053
693
c PNC108 Pancreatitis, Hereditary 60 0.053
694
FCL014 Focal Epilepsy 56 0.053
695
DNT008 Denture Stomatitis 41 0.053
696
PRV006 Pervasive Developmental Disorder 56 0.053
697
MTC004 Mitochondrial Encephalomyopathy 42 0.053
698
RCR004 Recurrent Respiratory Papillomatosis 47 0.053
699
P CHR012 Chronic Granulomatous Disease 69 0.053
700
OPT009 Optic Neuritis 53 0.053
701
c PYR010 Peyronie's Disease 54 0.052
702
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.052
703
NRL004 Neuroleptic Malignant Syndrome 44 0.052
704
P HML001 Hemolytic-Uremic Syndrome 50 0.052
705
HDR003 Hidradenitis 47 0.052
706
TND004 Tendinopathy 45 0.052
707
P NRM001 Neuromyelitis Optica 67 0.052
708
RDC002 Radiculopathy 55 0.052
709
HYP020 Hyperprolactinemia 64 0.052
710
PRC002 Paracoccidioidomycosis 59 0.052
711
HDR002 Hidradenitis Suppurativa 54 0.052
712
SHW002 Shwachman-Diamond Syndrome 63 0.051
713
SPP008 Suppurative Otitis Media 50 0.051
714
ADN002 Adenoiditis 40 0.051
715
ORL004 Oral Submucous Fibrosis 56 0.051
716
P MTC133 Mitochondrial Myopathy 53 0.051
717
FDL002 Food Allergy 55 0.051
718
INT075 Intracranial Hypertension 53 0.051
719
FML037 Female Breast Cancer 52 0.051
720
TRY001 Trypanosomiasis 55 0.051
721
ORL012 Oral Leukoplakia 45 0.050
722
KRT002 Keratomalacia 55 0.050
723
P OCL001 Ocular Albinism 46 0.050
724
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.050
725
c ALP101 Alpha-Thalassemia 60 0.050
726
HMC014 Homocysteinemia 49 0.050
727
c HYP768 Hyperlipoproteinemia, Type I 44 0.050
728
FSC002 Fascioliasis 45 0.050
729
HLL004 Hellp Syndrome 53 0.050
730
TRG002 Trigeminal Neuralgia 60 0.050
731
WGN006 Wegener Granulomatosis 71 0.050
732
LCH009 Lichen Sclerosus 45 0.049
733
c ALP061 Alopecia, Androgenetic, 1 44 0.049
734
ALL010 Allergic Contact Dermatitis 60 0.049
735
EXF001 Exfoliation Syndrome 55 0.049
736
VGT001 Vogt-Koyanagi-Harada Disease 60 0.049
737
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.049
738
P FML011 Familial Adenomatous Polyposis 71 0.049
739
P ENC008 Encephalocele 48 0.048
740
AND014 Androgenic Alopecia 39 0.048
741
INF034 Infective Endocarditis 56 0.048
742
ADR012 Adrenal Gland Disease 51 0.048
743
HST011 Histoplasmosis 56 0.048
744
PLM014 Pleomorphic Adenoma 55 0.048
745
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.048
746
PLM012 Pulmonary Sarcoidosis 58 0.047
747
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.047
748
P RTN014 Retinal Artery Occlusion 45 0.047
749
HPT009 Hepatopulmonary Syndrome 53 0.047
750
P HYP724 Hyperlipoproteinemia, Type Iii 59 0.047
751
GNG004 Ganglioglioma 51 0.047
752
MTC069 Mitochondrial Disorders 49 0.047
753
HNS001 Hansen's Disease 31 0.047
754
P SCK002 Sick Sinus Syndrome 53 0.047
755
SPT005 Spotted Fever 57 0.046
756
c PST041 Posterior Urethral Valves 51 0.046
757
TCK001 Tick-Borne Encephalitis 55 0.046
758
SCR008 Scrub Typhus 65 0.046
759
P ANG001 Angelman Syndrome 61 0.046
760
RTC003 Root Caries 38 0.046
761
c SVR005 Severe Pre-Eclampsia 53 0.046
762
P HRD001 Hereditary Multiple Exostoses 45 0.046
763
P SCL015 Scleritis 50 0.046
764
TNG002 Tangier Disease 65 0.046
765
c EXS020 Exostoses, Multiple, Type Ii 35 0.046
766
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.046
767
RCT015 Reactive Arthritis 65 0.046
768
ACR008 Acrocallosal Syndrome 56 0.045
769
MNN032 Meningococcal Meningitis 45 0.045
770
P PLC011 Pilocytic Astrocytoma 63 0.045
771
c MNN047 Mannosidosis, Alpha B, Lysosomal 63 0.045
772
LSS003 Lassa Fever 45 0.045
773
BRN014 Bronchopneumonia 45 0.045
774
LYM007 Lymphangioleiomyomatosis 68 0.045
775
QFV001 Q Fever 61 0.045
776
TCD001 Tic Disorder 54 0.045
777
MCC012 Mccune-Albright Syndrome 65 0.045
778
ART031 Aortic Coarctation 48 0.044
779
BRG013 Buerger Disease 62 0.044
780
WST001 West Syndrome 57 0.044
781
LTH045 Lutheran Suppressor, X-Linked 41 0.044
782
ACS001 Acoustic Neuroma 60 0.044
783
ATY016 Atypical Werner Syndrome 31 0.044
784
ADR010 Adrenal Cortical Hypofunction 41 0.044
785
CYS008 Cystic Echinococcosis 47 0.044
786
SPN331 Spondyloocular Syndrome 34 0.044
787
ABT001 Abetalipoproteinemia 64 0.044
788
P PST059 Pustular Psoriasis 40 0.044
789
SPN050 Spinocerebellar Degeneration 41 0.044
790
FBR032 Fibromuscular Dysplasia 53 0.044
791
P AML002 Amelogenesis Imperfecta 46 0.043
792
P OTS001 Otosclerosis 53 0.043
793
c MJR008 Major Affective Disorder 2 33 0.043
794
P SDR002 Siderosis 48 0.043
795
WBR001 Weber Syndrome 40 0.043
796
P CMM008 Communicating Hydrocephalus 35 0.043
797
c HYP740 Hyperlipoproteinemia, Type V 48 0.043
798
PRT018 Portal Vein Thrombosis 50 0.043
799
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.043
800
MCR103 Microtia 39 0.043
801
PRN019 Perinatal Necrotizing Enterocolitis 56 0.043
802
ADR013 Adrenal Gland Hyperfunction 54 0.042
803
IRT001 Iritis 36 0.042
804
PRP083 Porphyria, Acute Intermittent 60 0.042
805
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.042
806
VSC012 Vesiculobullous Skin Disease 32 0.042
807
c ACT036 Acute Cholangitis 35 0.042
808
LYM021 Lymphadenitis 62 0.042
809
SZR001 Sezary's Disease 58 0.042
810
P NNN008 Noonan Syndrome 1 77 0.042
811
FLL008 Folliculitis 50 0.042
812
P PLY017 Polyarteritis Nodosa 51 0.042
813
DDF001 Dedifferentiated Liposarcoma 47 0.041
814
P BRY005 Beryllium Disease 43 0.041
815
ACT049 Acute Disseminated Encephalomyelitis 52 0.041
816
ATM078 Autoimmune Addison Disease 30 0.041
817
MLT134 Multiple Pterygium Syndrome, Lethal Type 48 0.041
818
NNT049 Nontuberculous Mycobacterial Lung Disease 45 0.041
819
CLF004 Cleft Lip/palate 49 0.041
820
c CHR576 Chronic Beryllium Disease 42 0.041
821
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 47 0.041
822
IDP024 Idiopathic Inflammatory Myopathy 49 0.041
823
MCR011 Microinvasive Gastric Cancer 45 0.040
824
HND002 Hand, Foot and Mouth Disease 50 0.040
825
P BRN035 Brain Stem Glioma 42 0.040
826
P ANX007 Anauxetic Dysplasia 1 36 0.040
827
CHR063 Chronic Mucocutaneous Candidiasis 66 0.040
828
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.040
829
CRB008 Cerebral Atherosclerosis 42 0.040
830
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 0.039
831
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.039
832
VLV008 Vulvitis 38 0.039
833
LYM004 Lymphoid Interstitial Pneumonia 47 0.039
834
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.039
835
HYP008 Hypertensive Retinopathy 39 0.039
836
VGN020 Vaginal Disease 44 0.039
837
CRT004 Carotid Artery Thrombosis 37 0.039
838
P FML035 Familial Hyperlipidemia 48 0.038
839
MHR001 Mohr-Tranebjaerg Syndrome 39 0.038
840
HYP081 Hypolipoproteinemia 49 0.038
841
DNG001 Dengue Shock Syndrome 47 0.038
842
HYP213 Hypomelanotic Disorder 25 0.038
843
VGN019 Vaginal Discharge 34 0.038
844
URN003 Urinary Schistosomiasis 50 0.038
845
P ACT010 Acth-Secreting Pituitary Adenoma 58 0.038
846
c ALZ056 Alzheimer Disease 3 41 0.037
847
c DWL002 Dowling-Degos Disease 1 50 0.037
848
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 0.037
849
MLT002 Multiple Symmetrical Lipomatosis 39 0.037
850
APH001 Aphthous Stomatitis 64 0.037
851
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.037
852
c PSR021 Psoriasis 14, Pustular 44 0.036
853
HYP748 Hypertelorism 46 0.036
854
c CNG033 Congenital Syphilis 40 0.036
855
c ATM075 Autoimmune Encephalitis 40 0.035
856
PTY001 Pityriasis Rosea 45 0.035
857
GLC011 Galactose Epimerase Deficiency 46 0.035
858
HMN038 Human Coronavirus Sensitivity 17 0.035
859
DRM013 Dermoid Cyst 43 0.034
860
EPD015 Epidemic Typhus 45 0.034
861
HYP732 Hyperalphalipoproteinemia 1 52 0.034
862
c JVN009 Juvenile Pilocytic Astrocytoma 47 0.034
863
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 29 0.033
864
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 42 0.033
865
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.033
866
DYS022 Dyschromatosis Symmetrica Hereditaria 49 0.033
867
ANC002 Anca-Associated Vasculitis 42 0.033
868
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.033
869
CHN065 Choanal Atresia, Posterior 43 0.033
870
IDP035 Idiopathic Achalasia 47 0.033
871
PST046 Post-Transplant Lymphoproliferative Disease 56 0.032
872
CHR103 Charge Syndrome 59 0.032
873
GLC106 Glucocorticoid Resistance, Generalized 41 0.032
874
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 33 0.032
875
DSS008 Disease of Mental Health 51 0.031
876
CRH005 Crohn's Colitis 53 0.031
877
CRT009 Critical Illness Polyneuropathy 44 0.031
878
PRL019 Prolidase Deficiency 41 0.031
879
c PRM200 Primary Fanconi Syndrome 27 0.031
880
IDP074 Idiopathic Bronchiectasis 37 0.030
881
c CWD006 Cowden Syndrome 1 54 0.030
882
NVS017 Nevus, Epidermal 66 0.030
883
AND001 Anodontia 46 0.029
884
FML330 Familial Lcat Deficiency 37 0.029
885
TRP005 Trophoblastic Neoplasm 37 0.027
886
P RSM001 Rasmussen Encephalitis 46 0.027
Content
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