Search results for Sulfide

955 hits were found for Sulfide

# Family MCID Name MIFTS Score
1
ISC004 Ischemia 61 6.391
2
RPD005 Rapidly Involuting Congenital Hemangioma 48 6.161
3
MTH071 Methane Production 24 4.455
4
HYP266 Hypoxia 56 4.412
5
HMC014 Homocysteinemia 52 4.363
6
HYP066 Hyperglycemia 60 4.360
7
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.165
8
P MYC007 Myocardial Infarction 69 3.970
9
ANX004 Anoxia 40 3.958
10
DRM011 Dermatophytosis 52 3.754
11
ENC055 Encephalopathy, Ethylmalonic 51 3.638
12
c CHR684 Chronic Kidney Disease 73 3.573
13
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.570
14
ULC004 Ulcerative Colitis 74 3.569
15
P PLM037 Pulmonary Hypertension 69 3.499
16
CLT003 Colitis 63 3.496
17
PLM010 Pulmonary Edema 54 3.224
18
c ACT027 Acute Pancreatitis 60 3.192
19
PTY002 Pityriasis Versicolor 38 3.189
20
P PRD008 Periodontitis 63 3.176
21
AGN016 Aging 53 3.108
22
P VSC007 Vascular Disease 62 3.038
23
FTT001 Fatty Liver Disease 61 3.024
24
P HRT032 Heart Disease 84 2.998
25
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.956
26
P CRD119 Cardiac Arrest 68 2.895
27
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.893
28
ATH013 Atherosclerosis Susceptibility 63 2.874
29
END086 End Stage Renal Disease 54 2.807
30
TNC002 Tinea Capitis 42 2.720
31
CNG034 Congestive Heart Failure 69 2.692
32
IMP005 Impotence 52 2.661
33
P PNC044 Pancreatitis 61 2.649
34
P NRB001 Neuroblastoma 66 2.630
35
DWN001 Down Syndrome 70 2.576
36
P KDN018 Kidney Disease 71 2.572
37
ACT119 Acute Promyelocytic Leukemia 62 2.572
38
c MCR133 Microvascular Complications of Diabetes 4 41 2.486
39
c MCR113 Microvascular Complications of Diabetes 3 52 2.486
40
c MCR130 Microvascular Complications of Diabetes 6 41 2.486
41
c MCR120 Microvascular Complications of Diabetes 7 47 2.486
42
48X005 48,xyyy 39 2.478
43
HRW001 Hair Whorl 35 2.464
44
CRB004 Cerebral Artery Occlusion 45 2.425
45
P FML011 Familial Adenomatous Polyposis 70 2.386
46
BRN004 Brain Edema 54 2.380
47
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.341
48
c PRC016 Pre-Eclampsia 64 2.338
49
c ACT075 Acute Myocardial Infarction 55 2.336
50
P ENC018 Encephalopathy 62 2.287
51
BRN071 Brain Injury 50 2.277
52
P AST005 Asthma 75 2.215
53
P ALZ034 Alzheimer Disease 87 2.185
54
PRP027 Peripheral Vascular Disease 71 2.183
55
P CLR023 Colorectal Cancer 100 2.160
56
OCL069 Ocular Motor Apraxia 57 2.155
57
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.141
58
LMB062 Limb Ischemia 55 2.137
59
c ATR087 Atrial Standstill 1 74 2.130
60
P MYC008 Myocarditis 59 2.118
61
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.113
62
c HYP595 Hypertension, Essential 84 2.108
63
P LVR013 Liver Disease 68 2.062
64
P PLM036 Pulmonary Fibrosis 65 2.058
65
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.057
66
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.027
67
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.027
68
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.027
69
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.027
70
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.027
71
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.027
72
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.027
73
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.027
74
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.027
75
P GST053 Gastric Cancer 82 2.011
76
ART140 Arteries, Anomalies of 52 2.010
77
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.995
78
TXC005 Toxic Shock Syndrome 61 1.969
79
LVR012 Liver Cirrhosis 62 1.963
80
PRP080 Peripheral Artery Disease 54 1.951
81
PRT013 Portal Hypertension 59 1.914
82
TRM010 Traumatic Brain Injury 50 1.912
83
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.894
84
P MTH007 Methemoglobinemia 46 1.887
85
ARG004 Argyria 26 1.863
86
THR024 Thrombosis 56 1.852
87
KRT009 Keratosis 52 1.852
88
URT010 Ureteral Obstruction 44 1.850
89
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.837
90
RNL077 Renal Fibrosis 46 1.820
91
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.798
92
PST092 Posttransplant Acute Limbic Encephalitis 29 1.781
93
P RHN004 Rhinitis 56 1.740
94
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.689
95
LNG099 Lung Disease 62 1.672
96
ESP021 Esophageal Cancer 84 1.651
97
VSC002 Vascular Dementia 59 1.640
98
IRR002 Irritable Bowel Syndrome 64 1.640
99
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.638
100
P LTR001 Lateral Sclerosis 57 1.638
101
P MLN008 Melanoma 75 1.638
102
P INF037 Inflammatory Bowel Disease 53 1.623
103
c PRD040 Periodontitis, Chronic 52 1.622
104
P BRS047 Breast Cancer 97 1.606
105
SKN016 Skin Disease 63 1.606
106
MTB004 Metabolic Acidosis 48 1.594
107
P ART022 Arthritis 70 1.581
108
P HPT023 Hepatocellular Carcinoma 95 1.580
109
CYT002 Cytokine Deficiency 43 1.563
110
47X002 47,xyy 47 1.555
111
SYN007 Synovitis 54 1.541
112
PLC002 Plica Syndrome 35 1.541
113
P LNG064 Lung Cancer Susceptibility 3 69 1.527
114
ALL003 Allergic Rhinitis 66 1.514
115
LPD008 Lipid Metabolism Disorder 61 1.506
116
P BND020 Bone Disease 60 1.498
117
P HNT016 Huntington Disease 73 1.494
118
P OVR082 Overgrowth Syndrome 41 1.488
119
PST011 Pustulosis of Palm and Sole 52 1.488
120
P PSR002 Psoriasis 63 1.488
121
c MCR115 Microvascular Complications of Diabetes 5 65 1.482
122
P BCL017 B-Cell Lymphoma 57 1.481
123
HLX001 Helix Syndrome 47 1.478
124
P SZR006 Seizure Disorder 69 1.465
125
P KLZ004 Kala-Azar 1 41 1.455
126
P RSP003 Respiratory Failure 73 1.455
127
LSH001 Leishmaniasis 63 1.455
128
NNL006 Non-Alcoholic Steatohepatitis 54 1.441
129
PPL022 Papilloma 53 1.441
130
KWS002 Kawasaki Disease 65 1.434
131
CLN019 Colonic Disease 47 1.424
132
CHL014 Cholera 62 1.411
133
P PRP019 Peripheral Nervous System Disease 57 1.411
134
ANP008 Anaplastic Oligoastrocytoma 31 1.403
135
SPN186 Spinal Cord Injury 60 1.399
136
ATM095 Autoimmune Disease 61 1.394
137
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.377
138
P ANR048 Aniridia 1 66 1.373
139
TNM001 Tinea Imbricata 41 1.373
140
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.359
141
P RNV001 Renovascular Hypertension 48 1.359
142
BCT022 Bacterial Infectious Disease 55 1.351
143
c TYP009 Type 2 Diabetes Mellitus 91 1.345
144
P ADL010 Adult Respiratory Distress Syndrome 70 1.345
145
P SBR004 Seborrheic Dermatitis 44 1.345
146
P PRK057 Parkinson Disease, Late-Onset 79 1.339
147
P FBR031 Febrile Seizures 52 1.339
148
URM002 Uremia 47 1.330
149
GNG013 Gingivitis 59 1.302
150
STR067 Stroke, Ischemic 79 1.299
151
ENT011 Enterocolitis 55 1.299
152
P DBT009 Diabetes Mellitus 67 1.299
153
P HPT021 Hepatitis 68 1.294
154
HVY002 Heavy Metal Poisoning 22 1.293
155
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.292
156
CRB039 Cerebrovascular Disease 65 1.282
157
PRT251 Proteinuria, Chronic Benign 58 1.280
158
OST159 Osteogenic Sarcoma 66 1.280
159
GLB002 Glioblastoma 67 1.280
160
ALL029 Allergic Disease 61 1.267
161
CYS001 Cystic Fibrosis 77 1.254
162
VSC003 Visceral Leishmaniasis 54 1.254
163
PRT036 Peritonitis 65 1.254
164
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.240
165
GST023 Gastric Ulcer 52 1.240
166
c LKM061 Leukemia, Acute Myeloid 83 1.225
167
OST012 Osteoarthritis 77 1.223
168
P SLP006 Sleep Apnea 69 1.210
169
WLS001 Wilson Disease 70 1.199
170
DRM006 Dermatitis 61 1.199
171
CHR066 Chronic Fatigue Syndrome 59 1.194
172
P PRS040 Prostate Cancer 95 1.193
173
c TYP008 Type 1 Diabetes Mellitus 77 1.193
174
P URN019 Urinary Tract Infection 48 1.186
175
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 1.178
176
CRT013 Carotid Stenosis 51 1.178
177
P CRD246 Cardiovascular System Disease 55 1.178
178
P CYS018 Cystitis 58 1.176
179
ACH005 Achalasia 54 1.176
180
PRN019 Perinatal Necrotizing Enterocolitis 60 1.176
181
P ADN016 Adenocarcinoma 63 1.173
182
CYN003 Cyanide Poisoning 22 1.173
183
MYL069 Myeloma, Multiple 76 1.161
184
SKN019 Skin Melanoma 70 1.161
185
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.160
186
P ART021 Arteriosclerosis 53 1.158
187
GLM045 Glioma 62 1.158
188
GLL048 Glial Tumor 51 1.158
189
OBS082 Obstructive Nephropathy 41 1.147
190
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.138
191
P OST002 Osteoporosis 76 1.138
192
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.138
193
CLN015 Colon Adenocarcinoma 64 1.134
194
CNT047 Contact Dermatitis 56 1.134
195
IRN002 Iron Metabolism Disease 56 1.134
196
ALC007 Alcohol Dependence 65 1.120
197
HYP006 Hypertensive Heart Disease 48 1.120
198
P LCT001 Lactic Acidosis 50 1.120
199
P MRC003 Mercury Poisoning 48 1.120
200
PRS129 Prostatic Hyperplasia, Benign 48 1.117
201
RTN020 Retinal Vascular Disease 45 1.117
202
PRS021 Prostatic Adenoma 43 1.117
203
PRS045 Prostatic Hypertrophy 53 1.117
204
P LKM002 Leukemia 65 1.105
205
c SCL052 Scleroderma, Familial Progressive 60 1.094
206
c OPT053 Optic Atrophy 1 62 1.094
207
P BRB001 Beriberi 44 1.090
208
P GST044 Gastritis 55 1.074
209
GST050 Gastrointestinal System Disease 55 1.074
210
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 1.067
212
P ANP001 Anaplastic Large Cell Lymphoma 59 1.056
213
CNS004 Constipation 56 1.056
214
MTC005 Mitochondrial Metabolism Disease 44 1.056
215
P NRP001 Neuropathy 59 1.056
216
ANX010 Anxiety 70 1.038
217
CRV035 Cervical Cancer 72 1.038
218
SQM002 Squamous Cell Papilloma 45 1.038
219
BRN056 Bronchopulmonary Dysplasia 57 1.038
220
c ACT134 Acute Liver Failure 57 1.038
221
THY029 Thyroid Carcinoma 55 1.038
222
P ACN011 Acne 55 1.035
223
ANT024 Anthrax Disease 57 1.035
224
ADN018 Adenoma 58 1.031
225
P SCH015 Schizophrenia 74 1.019
227
P PHC003 Pheochromocytoma 70 1.019
228
ADR040 Adrenal Gland Pheochromocytoma 45 1.019
229
SVR001 Severe Acute Respiratory Syndrome 68 1.019
230
DNT012 Dental Caries 53 1.018
231
P HML002 Hemolytic Anemia 62 1.018
232
c ACT071 Acute Kidney Failure 60 0.997
233
P SKN015 Skin Carcinoma 71 0.997
234
CND006 Candida Glabrata 29 0.978
235
c MGR028 Migraine with or Without Aura 1 63 0.974
236
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.974
237
P MYP004 Myopathy 67 0.974
238
GLC003 Glucose Intolerance 53 0.974
239
HPT004 Hepatic Coma 43 0.974
240
DBT010 Diabetic Neuropathy 54 0.974
241
P LPS004 Lupus Erythematosus 61 0.974
242
P MSC005 Muscular Dystrophy 66 0.974
243
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.974
244
CYN002 Cyanosis, Transient Neonatal 43 0.963
245
P MYC084 Mycobacterium Tuberculosis 1 68 0.963
246
P HMC002 Homocystinuria 52 0.963
247
P RTN024 Retinoblastoma 72 0.948
248
PHN003 Phenylketonuria 76 0.948
249
P MYL006 Myeloid Leukemia 60 0.948
250
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.948
251
MLR004 Malaria 77 0.947
252
KRT019 Keratitis, Hereditary 66 0.947
253
c ACT249 Acute Asthma 40 0.947
254
SQM006 Squamous Cell Carcinoma 59 0.947
255
RTN003 Retinal Ischemia 48 0.947
256
c DLT002 Dilated Cardiomyopathy 79 0.947
257
OCL006 Ocular Hypertension 53 0.947
258
P HDC001 Headache 56 0.947
259
BNR002 Bone Resorption Disease 47 0.931
260
HMS001 Hemosiderosis 48 0.931
261
BRN002 Bronchiolitis 57 0.931
262
P RRH023 Rare Hereditary Hemochromatosis 52 0.931
263
P TRN020 Turner Syndrome 67 0.915
264
P ATX030 Ataxia-Telangiectasia 80 0.914
265
c THR092 Thrombophilia Due to Thrombin Defect 74 0.914
266
CRV040 Cervix Carcinoma 50 0.914
267
TLN003 Telangiectasis 51 0.914
268
ORL011 Oral Cancer 60 0.914
269
P ATR011 Atrial Fibrillation 66 0.896
270
ACT003 Acute Kidney Tubular Necrosis 46 0.896
271
ENT004 Enthesopathy 51 0.894
272
P ALC033 Alcohol Use Disorder 67 0.888
273
c HPT003 Hepatitis a 63 0.888
274
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.877
275
P BLD134 Bladder Cancer 79 0.877
276
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.877
277
c LKM063 Leukemia, Chronic Myeloid 70 0.877
278
c PCH010 Pachyonychia Congenita 3 43 0.877
279
OST017 Osteomyelitis 63 0.877
280
P MLG056 Malignant Hyperthermia 65 0.877
281
P MTC069 Mitochondrial Disorders 57 0.877
282
P PNM007 Pneumonia 64 0.874
283
c ART115 Aortic Valve Disease 1 72 0.855
284
CYS019 Cystathioninuria 46 0.855
285
HLC007 Helicobacter Pylori Infection 67 0.855
286
P SLM003 Salmonellosis 54 0.855
287
c BSL007 Basal Cell Carcinoma 67 0.855
288
URL001 Urolithiasis 45 0.855
289
FTL064 Fetal Methylmercury Syndrome 26 0.855
290
KRT006 Keratoconjunctivitis 53 0.855
291
P OVR042 Ovarian Cancer 88 0.846
292
MSC157 Muscular Dystrophy, Duchenne Type 78 0.832
293
LPP008 Lipoprotein Quantitative Trait Locus 65 0.832
294
P EXN002 Exanthem 58 0.832
295
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.832
296
DSS009 Disseminated Intravascular Coagulation 56 0.832
297
HPT019 Hepatic Encephalopathy 59 0.832
298
P EPD016 Epidermolysis Bullosa 53 0.832
299
P EYD002 Eye Disease 57 0.832
300
GST045 Gastroenteritis 58 0.832
301
P RHB003 Rhabdomyosarcoma 66 0.832
302
CNT018 Central Nervous System Leukemia 36 0.832
303
P VSC011 Vasculitis 61 0.832
304
PPT005 Peptic Ulcer Disease 58 0.832
305
PTT037 Pituitary Tumors 44 0.832
306
PCH007 Pouchitis 42 0.820
307
PPL052 Papillomatosis, Confluent and Reticulated 34 0.807
308
ORL015 Oral Squamous Cell Carcinoma 43 0.805
309
PLY150 Polykaryocytosis Inducer 29 0.805
310
P MCR129 Microvascular Complications of Diabetes 1 67 0.805
311
ANG054 Angina Pectoris 65 0.805
312
c MCR112 Microvascular Complications of Diabetes 2 42 0.805
313
P LKM062 Leukemia, Acute Lymphoblastic 69 0.805
314
HYP060 Hyperinsulinism 53 0.805
315
P MTR014 Motor Neuron Disease 65 0.805
316
P CND004 Candidiasis 57 0.805
317
P ESP024 Esophagitis 60 0.805
318
HYP005 Hypokalemia 55 0.805
319
SKN020 Skin Papilloma 40 0.805
320
GT001 Gout 63 0.805
321
P RTN018 Retinal Disease 53 0.805
322
OST016 Osteochondrosis 52 0.805
323
SPL018 Splenomegaly 47 0.805
324
LPT014 Leptin Deficiency or Dysfunction 77 0.792
325
BRN024 Bronchitis 67 0.792
326
P RCT021 Rectum Cancer 54 0.778
327
CRH001 Crohn's Disease 80 0.778
328
SXL003 Sexual Disorder 49 0.773
329
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.773
330
P MLT020 Multiple Sclerosis 79 0.773
331
P HYP750 Hypertriglyceridemia, Familial 61 0.773
332
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.773
333
MLD018 Mild Cognitive Impairment 48 0.773
334
CLR109 Colorectal Adenocarcinoma 50 0.773
335
P HMR003 Hemorrhagic Disease 59 0.773
336
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.773
337
EPD006 Epidermolysis Bullosa Acquisita 48 0.773
338
TST015 Testicular Disease 42 0.773
339
P ART023 Arthropathy 59 0.773
340
PMP014 Pemphigoid 48 0.773
341
SCH014 Schistosomiasis 56 0.773
342
BLL006 Bullous Pemphigoid 61 0.773
343
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.773
344
DGN001 Degenerative Disc Disease 48 0.773
345
SYN036 Syncope 44 0.773
346
PRQ002 Paraquat Poisoning 28 0.773
347
ALL010 Allergic Contact Dermatitis 55 0.762
348
c CRN243 Carney Complex, Type 1 53 0.747
349
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.747
350
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.747
351
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.747
352
ALC006 Alcoholic Hepatitis 61 0.747
353
CYT018 Cytochrome P450 2d6 Variant 26 0.747
354
P ACT008 Actinic Keratosis 53 0.747
355
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.747
356
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.747
357
P PNC035 Pancreatic Cancer 87 0.746
358
c HYP836 Hypercholesterolemia, Familial, 1 73 0.746
359
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.746
360
P AMY004 Amyloidosis 69 0.746
361
CRN045 Corneal Dystrophy and Perceptive Deafness 44 0.732
362
ADN011 Adenoid Cystic Carcinoma 68 0.732
363
URN010 Urinary Tract Obstruction 55 0.732
364
PRS047 Prostatitis 57 0.732
365
c SVR005 Severe Pre-Eclampsia 49 0.732
366
PYR009 Pyridoxine Deficiency Anemia 35 0.732
367
P HYP098 Hypereosinophilic Syndrome 66 0.732
368
P RRT020 Rare Tumor 39 0.732
369
IFP003 Ifap Syndrome 2 41 0.729
370
CRB027 Cerebellar Disease 47 0.729
371
PRP016 Paraplegia 52 0.729
372
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.723
373
c FML346 Familial Adenomatous Polyposis 1 65 0.711
374
SCT005 Scott Syndrome 51 0.711
375
VTM002 Vitamin B12 Deficiency 48 0.711
376
FLL008 Folliculitis 45 0.711
377
MRP001 Morphine Dependence 41 0.711
378
CHG001 Chagas Disease 65 0.711
379
DMP001 Dumping Syndrome 43 0.711
380
BRN028 Brain Cancer 73 0.711
381
P EPS003 Episodic Ataxia 59 0.711
382
P RHM011 Rheumatoid Arthritis 81 0.691
383
HND015 Hand Skill, Relative 29 0.691
384
CVT001 Cavitary Optic Disc Anomalies 38 0.691
385
c FML021 Familial Hypercholesterolemia 71 0.691
386
MXL017 Maxillary Cancer 31 0.691
387
P NSL008 Nasal Cavity Cancer 35 0.691
388
ACT162 Acute Sensory Ataxic Neuropathy 24 0.691
389
P CHR345 Chronic Pain 50 0.691
390
LGH007 Leigh Syndrome 70 0.670
391
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.670
392
TNP004 Tn Polyagglutination Syndrome 42 0.670
393
CLR108 Colorectal Adenoma 63 0.670
394
P FBR017 Fibrosarcoma 55 0.670
395
P DRR001 Diarrhea 55 0.670
396
c CNT035 Central Nervous System Disease 53 0.670
397
CMP034 Complete Androgen Insensitivity Syndrome 55 0.670
398
TXC002 Toxic Encephalopathy 51 0.670
399
ACT058 Active Peptic Ulcer Disease 55 0.670
400
HDN002 Head Injury 44 0.670
401
DFC004 Deficiency Anemia 74 0.647
402
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.647
403
LTH043 Lithium Transport 17 0.647
404
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.647
405
MYC006 Mycosis Fungoides 64 0.647
406
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.647
407
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.647
408
CHL068 Cholestasis 61 0.647
409
P CNJ013 Conjunctivitis 66 0.647
410
P INT068 Intestinal Disease 53 0.647
411
P GLM007 Glomerulonephritis 59 0.647
412
ACQ008 Acquired Hyperkeratosis 21 0.647
413
ALC010 Alcoholic Cardiomyopathy 42 0.647
414
P DMN002 Dementia 65 0.647
415
SLP001 Sleeping Sickness 56 0.647
416
PLG002 Plague 58 0.647
417
P RTN016 Retinal Degeneration 52 0.647
418
CHR178 Chromosomal Triplication 33 0.647
419
NRD001 Neurodermatitis 39 0.632
420
BLP005 Blepharitis 50 0.632
421
PNG002 Pain Agnosia 51 0.628
422
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.620
423
c DWL002 Dowling-Degos Disease 1 58 0.620
424
c GLC092 Glaucoma, Primary Open Angle 60 0.620
425
STV003 Stuve-Wiedemann Syndrome 52 0.620
426
P FRG001 Fragile X Syndrome 70 0.620
427
c TRC073 Treacher Collins Syndrome 2 28 0.620
428
HRN029 Hearing Loss, Noise-Induced 37 0.620
429
P GLM040 Glioma Susceptibility 1 70 0.620
430
c HRD202 Hereditary Lymphedema I 54 0.620
431
P PRK039 Parkinsonism 55 0.620
432
CMP002 Campylobacteriosis 50 0.620
433
MLG169 Malignant Astrocytoma 57 0.620
434
TRN018 Transitional Cell Carcinoma 56 0.620
435
P SLF001 Sulfhemoglobinemia 23 0.620
436
P ECL001 Eclampsia 52 0.620
437
NWC001 Newcastle Disease 47 0.620
438
P OPN001 Open-Angle Glaucoma 55 0.620
439
c ACT073 Acute Leukemia 59 0.620
440
MST005 Mastitis 52 0.620
441
DSM004 Desmoid Tumor 65 0.620
442
c INH020 Inherited Metabolic Disorder 47 0.620
443
ALL006 Allergic Asthma 55 0.620
444
TRC023 Trichinosis 53 0.620
445
P HYP265 Hypotonia 42 0.620
446
CRB090 Cerebral Hypoxia 42 0.620
447
APR001 Apraxia 51 0.588
448
APH002 Aphasia 55 0.588
449
ASP007 Aspiration Pneumonia 49 0.588
450
RTN017 Retinal Detachment 60 0.588
451
c SML038 Small Cell Cancer of the Lung 68 0.588
452
P DRM053 Dermatitis, Atopic 65 0.588
453
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.588
454
HYP114 Hypertensive Nephropathy 35 0.588
455
MWT001 Mowat-Wilson Syndrome 57 0.588
456
P LPR021 Leprosy 3 71 0.588
457
WRN001 Werner Syndrome 69 0.588
458
TST044 Testicular Torsion 45 0.588
459
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.588
460
ACR002 Acrocapitofemoral Dysplasia 49 0.588
461
OST003 Osteonecrosis 60 0.588
462
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.588
463
HMR023 Hemorrhagic Cystitis 43 0.588
464
MYL031 Myeloproliferative Neoplasm 66 0.588
465
CHL067 Cholecystitis 59 0.588
466
P LMY004 Leiomyosarcoma 62 0.588
467
PST106 Post-Cardiac Arrest Syndrome 31 0.588
468
BLD044 Bladder Disease 48 0.588
469
LYM027 Lymphopenia 56 0.588
470
STT001 Status Epilepticus 58 0.588
471
CLC001 Calciphylaxis 50 0.588
472
P BRS044 Breast Adenocarcinoma 58 0.588
473
AMN003 Amnestic Disorder 53 0.588
474
RCK004 Rickets 64 0.588
475
P RNL015 Renal Hypertension 45 0.588
476
P HYD006 Hydrocephalus 62 0.588
477
TNG007 Tongue Carcinoma 55 0.588
478
GNG011 Gingival Disease 53 0.588
479
P INF032 Infertility 60 0.588
480
CHR074 Choriocarcinoma 46 0.588
481
MCC002 Mucocutaneous Leishmaniasis 47 0.588
482
P INF038 Influenza 68 0.588
483
HNS001 Hansen's Disease 32 0.588
484
P HMP007 Hemophilia 52 0.588
485
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.588
486
P HYP076 Hyperthyroidism 53 0.588
487
c LKM005 Leukemia, T-Cell, Chronic 33 0.588
488
BCK006 Back Pain 43 0.588
489
P MNN013 Meningitis 65 0.588
490
ATN005 Autonomic Dysfunction 45 0.588
491
WLL004 Wallerian Degeneration 38 0.588
492
CTN007 Cutaneous Leishmaniasis 61 0.588
493
HYP056 Hypoglycemia 65 0.588
494
DWR001 Dwarfism 44 0.588
495
PRM329 Premature Aging 36 0.588
496
WTH001 Withdrawal Disorder 47 0.547
497
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.547
498
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.547
499
PSR001 Psoriatic Arthritis 61 0.547
500
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.547
501
ATR057 Atrioventricular Block 54 0.547
502
HYP003 Hypermethioninemia 51 0.547
503
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.547
504
c SYS001 Systemic Lupus Erythematosus 85 0.547
505
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.547
506
LYM133 Lymphoma, Hodgkin, Classic 69 0.547
507
P CRC039 Coarctation of Aorta 46 0.547
508
FCT001 Factor Viii Deficiency 61 0.547
509
P HRS035 Hirschsprung Disease 1 66 0.547
510
CRD223 Cardiac Arrhythmia 63 0.547
511
LRY022 Laryngoonychocutaneous Syndrome 43 0.547
512
GST092 Gastroesophageal Reflux 59 0.547
513
c CRN256 Craniosynostosis 6 24 0.547
514
c SPR162 Spermatogenic Failure 50 42 0.547
515
FTL006 Fetal Alcohol Spectrum Disorder 43 0.547
516
c THY107 Thymoma, Familial 42 0.547
517
c HMP029 Hemophilia a 69 0.547
518
P LNG032 Lung Cancer 98 0.547
519
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.547
520
c CRN217 Craniosynostosis 3 26 0.547
521
c MGL029 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 22 0.547
522
P FTL001 Fetal Alcohol Syndrome 55 0.547
523
VRT001 Vertebral Artery Occlusion 29 0.547
524
DBT081 Diabetic Encephalopathy 36 0.547
525
BRR014 Barrett Esophagus 66 0.547
526
c VRL005 Viral Pneumonia 52 0.547
527
P THY023 Thymoma 64 0.547
528
ADT003 Auditory System Disease 48 0.547
529
P MLN007 Male Infertility 56 0.547
530
STR103 Streptococcus Pneumonia 47 0.547
531
HMP001 Hemopericardium 47 0.547
532
CLR030 Clear Cell Renal Cell Carcinoma 53 0.547
533
c INF023 Inflammatory Breast Carcinoma 48 0.547
534
RTR008 Root Resorption 44 0.547
535
P HYP086 Hypothyroidism 68 0.547
536
OPT003 Opiate Dependence 49 0.547
537
PLM001 Pulmonary Tuberculosis 69 0.547
538
MCP006 Mucoepidermoid Carcinoma 48 0.547
539
ALC005 Alcoholic Pancreatitis 38 0.547
540
CDQ001 Cauda Equina Syndrome 37 0.547
541
NPH010 Nephrosclerosis 50 0.547
542
DBT008 Diabetic Angiopathy 47 0.547
543
P PRC012 Pericardial Effusion 50 0.547
544
MCR013 Microphthalmia 59 0.547
545
FLR002 Filariasis 55 0.547
546
CVD001 Covid-19 59 0.547
547
MCR011 Microinvasive Gastric Cancer 41 0.547
548
P AGG001 Aggressive Periodontitis 55 0.547
549
PLR005 Pleuropneumonia 33 0.547
550
AZS001 Azoospermia 45 0.547
551
BCK003 Background Diabetic Retinopathy 46 0.547
552
PLP001 Pulpitis 48 0.547
553
DYS015 Dysentery 49 0.547
554
P CTR002 Cataract 59 0.547
555
P INT070 Intestinal Obstruction 57 0.547
556
P SLP005 Sleep Disorder 61 0.547
557
ACT049 Acute Disseminated Encephalomyelitis 53 0.547
558
PLC008 Placenta Disease 48 0.547
559
DYS011 Dyskinesia of Esophagus 41 0.547
560
P PLY018 Polycythemia 56 0.547
561
BRK012 Broken Heart Syndrome 42 0.547
562
P ENC008 Encephalocele 46 0.547
563
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.547
564
P DBT005 Diabetes Insipidus 54 0.547
565
GRV012 Grover's Disease 30 0.547
566
SYS071 Systemic Autoimmune Disease 35 0.547
567
P CRB088 Cerebral Atrophy 32 0.547
568
SPS057 Spasticity 43 0.547
569
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.547
570
c INF071 Inflammatory Bowel Disease 1 65 0.528
571
RHB024 Rhabdomyosarcoma 2 65 0.528
572
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.528
573
MCS002 Mucositis 55 0.528
574
SDD004 Sudden Arrhythmia Death Syndrome 22 0.528
575
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.447
576
c LYM144 Lymphatic Malformation 1 47 0.447
577
c HRD007 Hereditary Lymphedema 34 0.447
578
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.447
579
LGN006 Legionnaire Disease 52 0.447
580
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.447
581
c HRD204 Hereditary Lymphedema Ia 18 0.447
582
THY128 Thyroid Tumor 33 0.447
583
P BNC003 Bone Cancer 58 0.447
584
c MLG084 Malignant Fibrous Histiocytoma 62 0.447
585
ART008 Arteriosclerosis Obliterans 40 0.447
586
MSN004 Mesenchymal Cell Neoplasm 42 0.447
587
P PRP021 Peripheral Nervous System Neoplasm 39 0.447
588
ART006 Arthus Reaction 40 0.447
589
FLR001 Filarial Elephantiasis 59 0.447
590
c JVN010 Juvenile Rheumatoid Arthritis 52 0.447
591
DCB001 Decubitus Ulcer 61 0.447
592
STM006 Stomach Disease 47 0.447
593
P FBR003 Fibrous Histiocytoma 43 0.447
594
PTY001 Pityriasis Rosea 44 0.447
595
LYM019 Lymphosarcoma 46 0.447
596
PLY100 Polyploidy 36 0.447
597
c CNG439 Congenital Lymphedema 31 0.447
598
PRS063 Paresthesia 39 0.447
599
BNG077 Benign Idiopathic Neonatal Seizures 23 0.373
600
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.345
601
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.345
602
CRD137 Cardiogenic Shock 56 0.331
603
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.299
604
SVR004 Severe Combined Immunodeficiency 70 0.299
605
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.264
606
c HLP024 Holoprosencephaly 2 49 0.264
607
VLL003 Villonodular Synovitis 41 0.264
608
PGM001 Pigmented Villonodular Synovitis 55 0.264
609
TNS005 Tonsillitis 57 0.264
610
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.244
611
c SPH014 Spherocytosis, Type 2 38 0.244
612
P NPH012 Nephrotic Syndrome 61 0.244
613
P DDN001 Duodenal Ulcer 52 0.244
614
c VRL010 Viral Hepatitis 52 0.244
615
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.244
616
STN013 Stenotrophomonas Maltophilia Infection 26 0.244
617
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.223
618
CMB007 Combined Immunodeficiency 56 0.223
619
PMP004 Pemphigus Foliaceus 43 0.223
620
SLC006 Silicosis 55 0.223
621
ANT018 Anthracosis 50 0.223
622
P PNM006 Pneumoconiosis 55 0.223
623
PRP030 Purpura 54 0.223
624
BRN012 Bronchiolitis Obliterans 56 0.223
625
c HPT016 Hepatitis B 62 0.223
626
TNC003 Tinea Corporis 40 0.223
627
P PMP001 Pemphigus 54 0.223
628
P CRN300 Coronary Heart Disease 1 73 0.199
629
ILT001 Ileitis 49 0.199
630
MRC009 Mercaptolactate-Cysteine Disulfiduria 20 0.199
631
CRD132 Cardiac Conduction Defect 59 0.199
632
ATS010 Autosomal Recessive Disease 42 0.199
633
SLF020 Sulfide:quinone Oxidoreductase Deficiency 14 0.199
634
SDD001 Sudden Infant Death Syndrome 60 0.199
635
CLL003 Cellulitis 53 0.199
636
TNC001 Tinea Cruris 35 0.199
637
P KDN017 Kidney Cancer 60 0.199
638
P SYP003 Syphilis 59 0.199
639
P TRC031 Trichorhinophalangeal Syndrome 37 0.199
640
P MSC003 Muscular Atrophy 52 0.199
641
P ALP008 Alopecia 53 0.199
642
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.199
643
FNT004 Fainting 29 0.199
644
c WLM013 Wilms Tumor 1 65 0.173
645
P SRC025 Sarcoidosis 1 70 0.173
646
DSS032 Disease by Infectious Agent 55 0.173
647
KPS004 Kaposi Sarcoma 76 0.173
648
IMM167 Immune Deficiency Disease 76 0.173
649
c THY056 Thyroid Dyshormonogenesis 3 32 0.173
650
ACN002 Acanthosis Nigricans 56 0.173
651
IGR001 Ige Responsiveness, Atopic 58 0.173
652
HMN044 Human Immunodeficiency Virus Type 1 76 0.173
653
P FRD001 Friedreich Ataxia 62 0.173
654
TNP001 Tinea Pedis 48 0.173
655
HYP014 Hyperuricemia 51 0.173
656
PNM003 Pneumatosis Cystoides Intestinalis 32 0.173
657
P CRV031 Cervical Adenocarcinoma 48 0.173
658
P INT143 Interstitial Cystitis 59 0.173
659
ACT098 Acute Erythroid Leukemia 55 0.173
660
P OPT006 Optic Nerve Disease 57 0.173
661
BRC012 Brucellosis 66 0.173
662
PHT004 Photoallergic Dermatitis 27 0.173
663
EXT034 Extrinsic Allergic Alveolitis 56 0.173
664
P NRF002 Neurofibromatosis 60 0.173
665
P BRN022 Bronchiectasis 59 0.173
666
INT007 Intermediate Coronary Syndrome 53 0.173
667
HMP009 Haemophilus Influenzae 41 0.173
669
P TRM003 Tremor 50 0.173
670
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.173
671
c ATS007 Autism Spectrum Disorder 71 0.141
672
c MJR022 Major Affective Disorder 8 37 0.141
673
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.141
674
ADN067 Adenoid Hypertrophy 38 0.141
675
P BLR024 Biliary Cirrhosis, Primary, 1 27 0.141
676
DMN031 Dementia, Lewy Body 65 0.141
677
P MPL001 Maple Syrup Urine Disease 69 0.141
678
MNK001 Menkes Disease 64 0.141
679
c SPN225 Spondyloarthropathy 1 70 0.141
680
c BRN108 Branchiootic Syndrome 1 63 0.141
681
P TRM004 Trimethylaminuria 45 0.141
682
PRT112 Portal Hypertension, Noncirrhotic 29 0.141
683
c MJR024 Major Affective Disorder 9 40 0.141
684
c ACT004 Acute Diarrhea 40 0.141
685
P SPP010 Suppressor of Tumorigenicity 3 50 0.141
686
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.141
687
c HMC039 Hemochromatosis, Type 1 73 0.141
688
c GLL024 Gallbladder Disease 1 53 0.141
689
c BLR016 Biliary Cirrhosis, Primary, 2 15 0.141
690
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.141
691
P LKM071 Leukemia, Chronic Lymphocytic 74 0.141
692
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.141
693
MLT157 Multiple System Atrophy 1 69 0.141
694
AMN014 Aminopterin Syndrome Sine Aminopterin 31 0.141
695
KSH001 Keshan Disease 31 0.141
696
MLG157 Malignant Pheochromocytoma 37 0.141
697
ANT017 Anthracosilicosis 24 0.141
698
INT067 Interstitial Nephritis 46 0.141
699
P HYP069 Hyperparathyroidism 62 0.141
700
P TMP001 Temporal Lobe Epilepsy 49 0.141
701
SCK001 Sick Building Syndrome 33 0.141
702
P TCD001 Tic Disorder 50 0.141
703
HRM002 Hermaphroditism 35 0.141
704
ASP008 Aspiration Pneumonitis 43 0.141
705
P BPL003 Bipolar Disorder 56 0.141
706
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.141
707
SPN051 Spondylitis 51 0.141
708
IRN001 Iron Deficiency Anemia 58 0.141
709
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.141
710
HMP005 Hemiplegia 53 0.141
711
P CRN026 Corneal Edema 42 0.141
712
TYP007 Typhoid Fever 63 0.141
713
c SCN006 Secondary Syphilis 36 0.141
714
LNG039 Lung Squamous Cell Carcinoma 57 0.141
715
c SCN007 Secondary Hyperparathyroidism 50 0.141
716
ART016 Aortic Aneurysm 68 0.141
717
P PSD003 Pseudohypoaldosteronism 45 0.141
718
GTR002 Goiter 52 0.141
719
PRM236 Primary Biliary Cholangitis 62 0.141
720
GST033 Gestational Diabetes 60 0.141
721
GRD001 Giardiasis 46 0.141
722
OCC016 Occupational Asthma 33 0.141
723
BCT004 Bacteriuria 48 0.141
724
INF009 Inflammatory Spondylopathy 30 0.141
725
NRN001 Neuroendocrine Carcinoma 47 0.141
726
TXC007 Toxic Pneumonitis 22 0.141
727
ILS001 Ileus 49 0.141
728
CLF001 Cleft Lip 54 0.141
729
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.141
730
MYC017 Mycobacterium Kansasii 36 0.141
731
PRS115 Prosthetic Joint Infection 42 0.141
732
SFT003 Soft Tissue Sarcoma 43 0.141
733
DSC009 Discoid Lupus Erythematosus 42 0.141
734
GLM044 Glomerular Disease 34 0.141
735
LNG095 Lung Abscess 50 0.100
736
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.100
737
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.100
738
AGR018 Agraphia 37 0.100
739
c WLF009 Wolfram Syndrome 2 43 0.100
740
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.100
741
CLS016 Clostridium Difficile Colitis 49 0.100
742
TRC097 Tracheomalacia 43 0.100
743
TNG009 Tongue Squamous Cell Carcinoma 43 0.100
744
HPT067 Hepatocellular Adenoma 42 0.100
745
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.100
746
P PNC113 Punctate Palmoplantar Keratoderma 24 0.100
747
ADN002 Adenoiditis 36 0.100
748
ERY003 Erythema Multiforme 56 0.100
749
ACT149 Acetaminophen Metabolism 37 0.100
750
PFF001 Pfeiffer Syndrome 77 0.100
751
c VSC019 Vesicoureteral Reflux 1 56 0.100
752
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.100
753
P CLC063 Celiac Disease 1 65 0.100
754
VRC005 Varicose Veins 59 0.100
755
OTT002 Otitis Media 70 0.100
756
c FBR073 Febrile Seizures, Familial, 1 40 0.100
757
CYS041 Cystic Angiomatosis of Bone, Diffuse 32 0.100
758
DNB001 Danubian Endemic Familial Nephropathy 42 0.100
759
DSC013 Discrimination, Two-Point, Reduction in 21 0.100
760
PRR015 Preauricular Fistulae, Congenital 20 0.100
761
c CLR131 Ciliary Dyskinesia, Primary, 1 62 0.100
762
P PTY003 Pityriasis Rubra Pilaris 57 0.100
763
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.100
764
HNZ004 Heinz Body Anemias 40 0.100
765
HYP765 Hyperbilirubinemia, Shunt, Primary 17 0.100
766
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.100
767
P MCH002 Machado-Joseph Disease 62 0.100
768
BSL036 Basal Cell Nevus Syndrome 73 0.100
769
SHR107 Short Stature-Obesity Syndrome 25 0.100
770
INS024 Insulin-Like Growth Factor I 77 0.100
771
c FBR075 Febrile Seizures, Familial, 2 32 0.100
772
SCK003 Sickle Cell Anemia 74 0.100
773
c SYS043 Systemic Lupus Erythematosus 1 38 0.100
774
c CRB094 Cerebral Cavernous Malformations 3 41 0.100
775
ART002 Arts Syndrome 66 0.100
776
c SLV028 Silver-Russell Syndrome 3 33 0.100
777
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 31 0.100
778
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.100
779
CRB204 Cerebellar, Ocular, Craniofacial, and Genital Syndrome 27 0.100
780
CRR001 Carrion's Disease 31 0.100
781
P RST001 Restless Legs Syndrome 52 0.100
782
c HPT073 Hepatitis C Virus 70 0.100
783
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.100
784
KSH004 Kashin-Beck Disease 37 0.100
785
c PRM093 Premature Ovarian Failure 7 47 0.100
786
BLC012 Bile Acid Malabsorption, Primary 45 0.100
787
c CHL119 Cholangitis, Primary Sclerosing 57 0.100
788
LYM007 Lymphangioleiomyomatosis 68 0.100
789
ANG020 Angiosarcoma 63 0.100
790
TNB001 Tinea Barbae 27 0.100
791
KRN001 Korean Hemorrhagic Fever 34 0.100
792
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.100
793
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.100
794
URT049 Urate Oxidase, Pseudogene 24 0.100
795
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.100
796
P CRB048 Cerebral Cavernous Malformations 63 0.100
797
P LRY029 Laryngomalacia 47 0.100
798
MYL013 Myeloperoxidase Deficiency 44 0.100
799
c GRV008 Graves Disease 1 54 0.100
800
MST021 Meester-Loeys Syndrome 37 0.100
801
c LSS010 Lissencephaly 4 38 0.100
802
P MJR001 Major Depressive Disorder 68 0.100
803
GST019 Gastrointestinal Stromal Tumor 78 0.100
804
P GRF003 Graft-Versus-Host Disease 71 0.100
805
c EPS028 Episodic Pain Syndrome, Familial, 3 41 0.100
806
HYP020 Hyperprolactinemia 63 0.100
807
SVR097 Severe Cutaneous Adverse Reaction 68 0.100
808
MCN017 Meconium Ileus 52 0.100
809
c ACR091 Aicardi-Goutieres Syndrome 4 35 0.100
810
P DNG005 Dengue Virus 55 0.100
811
CHL065 Cholangiocarcinoma 57 0.100
812
APN008 Apnea, Obstructive Sleep 66 0.100
813
INT051 Intussusception 53 0.100
814
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.100
815
c NNP008 Nanophthalmos 3 14 0.100
816
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.100
817
PGM003 Pigmentation Disease 45 0.100
818
P SML016 Small Intestine Cancer 48 0.100
819
ACQ070 Acquired Laryngomalacia 10 0.100
820
ONC002 Onchocerciasis 50 0.100
821
P PLY014 Polycystic Kidney Disease 71 0.100
822
QFV001 Q Fever 61 0.100
823
ASB001 Asbestosis 47 0.100
824
P SHR001 Short Bowel Syndrome 53 0.100
825
P WLF004 Wolfram Syndrome 61 0.100
826
HDR002 Hidradenitis Suppurativa 54 0.100
827
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.100
828
PST028 Post-Traumatic Stress Disorder 58 0.100
829
HDR003 Hidradenitis 49 0.100
830
KRT008 Keratopathy 46 0.100
831
BLD053 Blood Platelet Disease 51 0.100
832
P ECT006 Ectodermal Dysplasia 62 0.100
833
TLR001 Tularemia 56 0.100
834
BLR008 Bilirubin Metabolic Disorder 57 0.100
835
P BNG032 Benign Mesothelioma 53 0.100
836
P END084 Endocrine System Disease 44 0.100
837
ACL001 Acalculous Cholecystitis 34 0.100
838
BCT002 Bacterial Vaginosis 52 0.100
839
PLM029 Palmoplantar Keratosis 48 0.100
840
HNT019 Hantavirus Hemorrhagic Fever with Renal Syndrome 44 0.100
841
ENM001 Enamel Caries 28 0.100
842
CRB037 Cerebral Palsy 66 0.100
843
P BRS053 Breast Fibroadenoma 48 0.100
844
CLN044 Colon Adenoma 44 0.100
845
CTN033 Cutaneous Candidiasis 38 0.100
846
DYS003 Dysgraphia 35 0.100
847
P EPD003 Epidermolysis Bullosa Simplex 56 0.100
848
WHT017 Wheat Allergy 30 0.100
849
MST004 Mast Cell Neoplasm 41 0.100
850
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.100
851
CPP004 Copper Deficiency Myelopathy 28 0.100
852
ANL017 Anal Squamous Cell Carcinoma 44 0.100
853
LPT001 Leptospirosis 65 0.100
854
P SCL009 Sclerosing Cholangitis 46 0.100
855
P PLY011 Polycystic Ovary Syndrome 57 0.100
856
P END033 Endocarditis 58 0.100
857
P OBS001 Obstructive Jaundice 49 0.100
858
P PRP029 Porphyria 60 0.100
859
TNM002 Tinea Manuum 26 0.100
860
MGL001 Megaloblastic Anemia 59 0.100
861
P PRR002 Pure Red-Cell Aplasia 46 0.100
862
P PLY019 Polyneuropathy 52 0.100
863
IGG001 Iga Glomerulonephritis 50 0.100
864
P END044 Endometriosis 62 0.100
865
AVN001 Avian Influenza 61 0.100
866
PNC129 Pancreatic Adenocarcinoma 64 0.100
867
PLR007 Pleural Empyema 50 0.100
868
P PTT006 Pituitary Adenoma 55 0.100
869
HGH043 High Grade Glioma 46 0.100
870
GLS001 Gliosarcoma 63 0.100
871
P JNC001 Junctional Epidermolysis Bullosa 54 0.100
872
DMY004 Demyelinating Disease 50 0.100
873
EXT007 Extracutaneous Mastocytoma 38 0.100
874
P PRL003 Proliferative Glomerulonephritis 43 0.100
875
INT079 Intrahepatic Cholangiocarcinoma 51 0.100
876
GLC008 Glucose Metabolism Disease 40 0.100
877
PRT018 Portal Vein Thrombosis 50 0.100
878
PRT038 Protein-Energy Malnutrition 53 0.100
879
OST011 Osteomalacia 52 0.100
880
THY001 Thyroid Crisis 30 0.100
881
RNL011 Renal Osteodystrophy 48 0.100
882
c ACT068 Acute Cystitis 60 0.100
883
SPT005 Spotted Fever 49 0.100
884
P HYP024 Hypoparathyroidism 55 0.100
885
PLM011 Plummer's Disease 34 0.100
886
P ART005 Arteriovenous Malformation 64 0.100
887
DBT004 Diabetic Polyneuropathy 50 0.100
888
CYS010 Cystinosis 61 0.100
889
P THR014 Thrombocytopenia 66 0.100
890
MNT002 Mental Depression 56 0.100
891
LYM022 Lymphangioma 54 0.100
892
P HML001 Hemolytic-Uremic Syndrome 52 0.100
893
NDL007 Nodular Goiter 48 0.100
894
P FML340 Familial Episodic Pain Syndrome 50 0.100
895
PLR008 Pleurisy 49 0.100
896
VRC001 Varicocele 48 0.100
897
SCB001 Scabies 49 0.100
898
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.100
899
GST040 Gastric Adenocarcinoma 66 0.100
900
LNG031 Lung Benign Neoplasm 51 0.100
901
ACQ007 Acquired Immunodeficiency Syndrome 58 0.100
902
HPT022 Hepatoblastoma 54 0.100
903
RSC001 Rosacea 55 0.100
904
ART010 Arteriolosclerosis 37 0.100
905
PRM209 Primary Trimethylaminuria 19 0.100
906
BWN006 Bowen's Disease 32 0.100
907
AMB001 Amebiasis 56 0.100
908
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.100
909
APP008 Appendicitis 62 0.100
910
P HYP120 Hypoaldosteronism 33 0.100
911
NPH018 Nephrogenic Systemic Fibrosis 48 0.100
912
P CHL066 Cholangitis 51 0.100
913
STM007 Stomatitis 52 0.100
914
PTH003 Pathologic Nystagmus 52 0.100
915
MSL001 Measles 61 0.100
916
P NRV007 Nervous System Disease 65 0.100
917
P ORL007 Oral Cavity Cancer 51 0.100
918
STR019 Steroid-Induced Glaucoma 30 0.100
919
P TXP001 Toxoplasmosis 59 0.100
920
ALL014 Allergic Encephalomyelitis 34 0.100
921
PLM052 Pulmonary Arteriovenous Malformation 43 0.100
922
PRT058 Pure Autonomic Failure 58 0.100
923
P THL005 Thalassemia 56 0.100
924
ANR040 Aneurysm 60 0.100
925
STC004 Stachybotrys Chartarum 33 0.100
926
ASB003 Asbestos Intoxication 32 0.100
927
OVR094 Ovarian Epithelial Cancer 39 0.100
928
MYC005 Myocardial Stunning 45 0.100
929
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.100
930
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.100
931
FRN014 Fournier Gangrene 26 0.100
932
LYM035 Lymphangiectasis 30 0.100
933
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.100
934
LMB050 Limbal Stem Cell Deficiency 51 0.100
935
INV015 Invasive Non-Typhoidal Salmonellosis 13 0.100
936
P PRM327 Primary Lymphedema 36 0.100
937
SNG003 Single Ventricular Heart 30 0.100
938
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.100
939
HST016 Histiocytic Sarcoma 38 0.100
940
PLS031 Plastic Bronchitis 26 0.100
941
ERY066 Erythema Multiforme Major 29 0.100
942
MST020 Mast Cell Activation Syndrome 27 0.100
943
MYC015 Mycobacterium Fortuitum 28 0.100
944
CVR010 Cavernous Malformation 29 0.100
945
ADG002 Audiogenic Seizures 25 0.100
946
SLN002 Selenium Poisoning 10 0.100
947
SPS019 Spastic Paraparesis 38 0.100
948
WHT007 White Platelet Syndrome 11 0.100
949
DPR016 Depression 64 0.100
950
CRB086 Cerebral Aneurysms 40 0.100
951
CLF004 Cleft Lip/palate 56 0.100
952
P RRL003 Rare Lymphatic Malformation 31 0.100
953
MTH047 Methanol Poisoning 37 0.100
954
CRC033 Circumscribed Palmoplantar Hypokeratosis 11 0.100
955
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.100