Search results for Cysteine

1352 hits were found for Cysteine

# Family MCID Name MIFTS Score
1
MRC009 Mercaptolactate-Cysteine Disulfiduria 22 5.022
2
CYS043 Cysteine Peptiduria 7 3.545
3
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 26 3.537
4
AMP011 Ampola Syndrome 4 2.506
5
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.706
6
HLX001 Helix Syndrome 47 0.227
7
CHG001 Chagas Disease 66 0.160
8
LSH001 Leishmaniasis 63 0.158
9
P KLZ004 Kala-Azar 1 41 0.158
10
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.140
11
P PRD008 Periodontitis 62 0.139
12
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 32 0.124
13
P KDN018 Kidney Disease 70 0.120
14
P NRB001 Neuroblastoma 71 0.119
15
BNR002 Bone Resorption Disease 48 0.119
16
P CLR023 Colorectal Cancer 98 0.115
17
HMN044 Human Immunodeficiency Virus Type 1 71 0.114
18
HMC014 Homocysteinemia 53 0.114
19
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.110
20
BRT054 Brittle Bone Disorder 70 0.108
21
CYS001 Cystic Fibrosis 80 0.105
22
AMB001 Amebiasis 49 0.103
23
c ACT071 Acute Kidney Failure 59 0.101
24
P BRS047 Breast Cancer 96 0.099
25
P LVR013 Liver Disease 68 0.099
26
VSC003 Visceral Leishmaniasis 55 0.099
27
P PLY011 Polycystic Ovary Syndrome 56 0.097
28
TRY001 Trypanosomiasis 50 0.097
29
SLP001 Sleeping Sickness 48 0.097
30
CYT002 Cytokine Deficiency 44 0.097
31
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.095
32
P MSC005 Muscular Dystrophy 66 0.095
33
P ADN016 Adenocarcinoma 64 0.095
34
P CTR002 Cataract 60 0.095
35
P LTR001 Lateral Sclerosis 53 0.095
36
47X002 47,xyy 49 0.095
37
CYS013 Cystinuria 62 0.093
38
SQM006 Squamous Cell Carcinoma 60 0.093
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.093
40
P HMC002 Homocystinuria 54 0.093
41
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.093
42
GLB015 Glioblastoma Multiforme 75 0.091
43
P LKM002 Leukemia 66 0.091
44
IDP011 Idiopathic Interstitial Pneumonia 63 0.091
45
P PLM036 Pulmonary Fibrosis 61 0.091
46
ISC004 Ischemia 60 0.091
47
48X005 48,xyyy 39 0.091
48
P PNC035 Pancreatic Cancer 84 0.089
49
SVR004 Severe Combined Immunodeficiency 73 0.089
50
BRN024 Bronchitis 68 0.089
51
ALL026 Allergic Hypersensitivity Disease 64 0.089
52
CHL123 Chlamydia 59 0.089
53
P LNG032 Lung Cancer 97 0.086
54
P PHC003 Pheochromocytoma 71 0.086
55
PRT037 Pertussis 65 0.086
56
P GLM045 Glioma 63 0.086
57
LNG099 Lung Disease 61 0.086
58
ATM095 Autoimmune Disease 61 0.086
59
P BPL003 Bipolar Disorder 56 0.086
60
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.086
61
BCT022 Bacterial Infectious Disease 56 0.086
62
ADR040 Adrenal Gland Pheochromocytoma 46 0.086
63
GLL048 Glial Tumor 45 0.086
64
c MJR024 Major Affective Disorder 9 41 0.086
65
c MJR022 Major Affective Disorder 8 38 0.086
66
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.084
67
P VSC007 Vascular Disease 63 0.084
68
CTN007 Cutaneous Leishmaniasis 61 0.084
69
CYS010 Cystinosis 60 0.084
70
THY029 Thyroid Carcinoma 59 0.084
71
P INF032 Infertility 57 0.084
72
TRC003 Trichomoniasis 52 0.084
73
BRN071 Brain Injury 49 0.084
74
P OVR042 Ovarian Cancer 89 0.082
75
ATH013 Atherosclerosis Susceptibility 66 0.082
76
LVR012 Liver Cirrhosis 63 0.082
77
HYP066 Hyperglycemia 61 0.082
78
SCH014 Schistosomiasis 56 0.082
79
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.082
80
P GST053 Gastric Cancer 83 0.079
81
IMM167 Immune Deficiency Disease 78 0.079
82
c HYP836 Hypercholesterolemia, Familial, 1 72 0.079
83
MLN008 Melanoma 69 0.079
84
c SVR001 Severe Acute Respiratory Syndrome 55 0.079
85
PRG008 Paragonimiasis 38 0.079
86
PPL052 Papillomatosis, Confluent and Reticulated 34 0.079
87
P HPT023 Hepatocellular Carcinoma 100 0.077
88
OST012 Osteoarthritis 78 0.077
89
P PRK057 Parkinson Disease, Late-Onset 76 0.077
90
c CHR684 Chronic Kidney Disease 66 0.077
91
DPR016 Depression 63 0.077
92
TXC005 Toxic Shock Syndrome 61 0.077
93
TRM010 Traumatic Brain Injury 53 0.077
94
VCC001 Vaccinia 49 0.077
95
c MCR120 Microvascular Complications of Diabetes 7 47 0.077
96
P ALZ034 Alzheimer Disease 88 0.074
97
MLR004 Malaria 80 0.074
98
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.074
99
OST159 Osteogenic Sarcoma 66 0.074
100
P ATS364 Autism 65 0.074
101
P HRP006 Herpes Simplex 65 0.074
102
HYP266 Hypoxia 56 0.074
103
CLN003 Clonorchiasis 43 0.074
104
FSC002 Fascioliasis 41 0.074
105
P RHM011 Rheumatoid Arthritis 80 0.071
106
P AMY004 Amyloidosis 70 0.071
107
FTT001 Fatty Liver Disease 61 0.071
108
P SZR006 Seizure Disorder 58 0.071
109
MNT002 Mental Depression 57 0.071
110
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
111
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.071
112
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
113
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
114
c FML021 Familial Hypercholesterolemia 68 0.069
115
P THR014 Thrombocytopenia 68 0.069
116
HYP056 Hypoglycemia 66 0.069
117
c HPT003 Hepatitis a 63 0.069
118
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.069
119
ACQ007 Acquired Immunodeficiency Syndrome 60 0.069
120
P ALC033 Alcohol Use Disorder 58 0.069
121
P LYM031 Lymphocytic Leukemia 55 0.069
122
CYS005 Cysticercosis 54 0.069
123
P AST007 Astrocytoma 50 0.069
124
INS024 Insulin-Like Growth Factor I 79 0.066
125
P BLD134 Bladder Cancer 78 0.066
126
MRF001 Marfan Syndrome 75 0.066
127
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.066
128
P MYC007 Myocardial Infarction 70 0.066
129
THY111 Thyroid Carcinoma, Familial Medullary 67 0.066
130
c SML038 Small Cell Cancer of the Lung 65 0.066
131
P MYP004 Myopathy 64 0.066
132
NTR005 Nutritional Deficiency Disease 61 0.066
133
P MLT074 Multiple Endocrine Neoplasia 55 0.066
134
THY125 Thyroid Gland Medullary Carcinoma 51 0.066
135
c ACT134 Acute Liver Failure 51 0.066
136
OBS002 Obsessive-Compulsive Disorder 68 0.063
137
P INF038 Influenza 68 0.063
138
c RHB024 Rhabdomyosarcoma 2 65 0.063
139
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.063
140
c WLM013 Wilms Tumor 1 65 0.063
141
c ACT027 Acute Pancreatitis 59 0.063
142
P BCL017 B-Cell Lymphoma 58 0.063
143
END030 End Stage Renal Failure 58 0.063
144
P MLN007 Male Infertility 56 0.063
145
P GST044 Gastritis 55 0.063
146
c OST080 Osteogenesis Imperfecta, Type Ii 55 0.063
147
P CHR345 Chronic Pain 50 0.063
148
FSC004 Fasciitis 50 0.063
149
NCR007 Necrotizing Fasciitis 49 0.063
150
CRB004 Cerebral Artery Occlusion 44 0.063
151
c PLY105 Polycystic Ovary Syndrome 1 38 0.063
152
HRN029 Hearing Loss, Noise-Induced 37 0.063
153
SPR006 Sparganosis 32 0.063
154
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.063
155
c SYS001 Systemic Lupus Erythematosus 86 0.059
156
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.059
157
P SCH015 Schizophrenia 75 0.059
158
MSC157 Muscular Dystrophy, Duchenne Type 71 0.059
159
c HPT073 Hepatitis C Virus 70 0.059
160
P LKM062 Leukemia, Acute Lymphoblastic 68 0.059
161
ALC007 Alcohol Dependence 66 0.059
162
P MCR115 Microvascular Complications of Diabetes 5 66 0.059
163
P TRN020 Turner Syndrome 65 0.059
164
c PRC016 Pre-Eclampsia 63 0.059
165
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.059
166
P CRN300 Coronary Heart Disease 1 63 0.059
167
P ADL010 Adult Respiratory Distress Syndrome 63 0.059
168
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.059
169
HMS001 Hemosiderosis 54 0.059
170
c PRD040 Periodontitis, Chronic 54 0.059
171
P MSC003 Muscular Atrophy 52 0.059
172
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.059
173
VLV047 Volvulus of Midgut 50 0.059
174
ANX004 Anoxia 42 0.059
175
P RRH023 Rare Hereditary Hemochromatosis 41 0.059
176
PLY150 Polykaryocytosis Inducer 31 0.059
178
c LKM061 Leukemia, Acute Myeloid 83 0.056
179
P RTN008 Retinitis Pigmentosa 77 0.056
180
P HRT032 Heart Disease 75 0.056
181
ADR007 Adrenoleukodystrophy 74 0.056
182
P OST002 Osteoporosis 73 0.056
183
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.056
184
P HNT016 Huntington Disease 71 0.056
185
CNG034 Congestive Heart Failure 70 0.056
186
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.056
187
P PLM037 Pulmonary Hypertension 68 0.056
188
PSY004 Psychotic Disorder 67 0.056
189
c HPT001 Hepatitis C 63 0.056
190
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.056
191
P PNC044 Pancreatitis 61 0.056
192
SPN186 Spinal Cord Injury 60 0.056
193
VSL002 Visual Epilepsy 58 0.056
194
BRN056 Bronchopulmonary Dysplasia 57 0.056
195
P NRP001 Neuropathy 56 0.056
196
AGN016 Aging 56 0.056
197
c OST135 Osteogenesis Imperfecta, Type I 55 0.056
198
CHK001 Chikungunya 53 0.056
199
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 51 0.056
200
NNL006 Non-Alcoholic Steatohepatitis 51 0.056
201
MTB004 Metabolic Acidosis 50 0.056
202
PTH002 Pathological Gambling 48 0.056
203
RTN023 Retinitis 46 0.056
204
NRR001 Neuroretinitis 43 0.056
205
ALL014 Allergic Encephalomyelitis 39 0.056
206
ADR022 Adrenomyeloneuropathy 38 0.056
207
PRC051 Paracetamol Poisoning 30 0.056
208
ESP021 Esophageal Cancer 90 0.052
209
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.052
210
P LNG064 Lung Cancer Susceptibility 3 77 0.052
211
DFC004 Deficiency Anemia 75 0.052
212
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
213
P RTN024 Retinoblastoma 72 0.052
214
ANX010 Anxiety 72 0.052
215
P GRF003 Graft-Versus-Host Disease 71 0.052
216
PLM001 Pulmonary Tuberculosis 70 0.052
217
c MGR028 Migraine with or Without Aura 1 69 0.052
218
CRB039 Cerebrovascular Disease 69 0.052
219
P LYM118 Lymphoma 68 0.052
220
P PNM007 Pneumonia 68 0.052
221
BRK010 Burkitt Lymphoma 67 0.052
222
P HPT021 Hepatitis 67 0.052
223
P VNW001 Von Willebrand's Disease 64 0.052
224
TBC004 Tobacco Addiction 64 0.052
225
P END044 Endometriosis 62 0.052
226
P PRP029 Porphyria 62 0.052
227
ALC006 Alcoholic Hepatitis 61 0.052
228
c HPT016 Hepatitis B 59 0.052
229
ADN018 Adenoma 58 0.052
230
IRN002 Iron Metabolism Disease 57 0.052
231
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.052
232
DSS008 Disease of Mental Health 57 0.052
233
P TRM003 Tremor 53 0.052
234
c FML008 Familial Retinoblastoma 53 0.052
235
TRC010 Trichotillomania 50 0.052
236
STM007 Stomatitis 49 0.052
237
MNN009 Meningoencephalitis 49 0.052
238
BBS001 Babesiosis 48 0.052
239
CYS019 Cystathioninuria 45 0.052
240
DWR001 Dwarfism 44 0.052
241
c PCH010 Pachyonychia Congenita 3 43 0.052
242
P MJR007 Major Affective Disorder 1 43 0.052
243
HMP009 Haemophilus Influenzae 42 0.052
244
STR077 Streptococcal Toxic-Shock Syndrome 37 0.052
245
c MJR008 Major Affective Disorder 2 34 0.052
246
c MJR003 Major Affective Disorder 6 33 0.052
247
c MJR006 Major Affective Disorder 5 33 0.052
248
c MJR023 Major Affective Disorder 7 33 0.052
249
c MJR004 Major Affective Disorder 4 28 0.052
250
P PRS040 Prostate Cancer 97 0.048
251
c DLT002 Dilated Cardiomyopathy 79 0.048
252
AST005 Asthma 77 0.048
253
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.048
254
ULC004 Ulcerative Colitis 73 0.048
255
ADL002 Adult Syndrome 69 0.048
256
c EXD008 Exudative Vitreoretinopathy 1 69 0.048
257
P HYP086 Hypothyroidism 68 0.048
258
c NMN015 Niemann-Pick Disease, Type C1 68 0.048
259
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.048
260
P CRN018 Coronary Artery Anomaly 63 0.048
261
P NTR004 Neutropenia 63 0.048
262
c ACT068 Acute Cystitis 63 0.048
263
LPD008 Lipid Metabolism Disorder 62 0.048
264
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.048
265
P HML002 Hemolytic Anemia 62 0.048
266
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.048
267
P ENC018 Encephalopathy 61 0.048
268
P LPS004 Lupus Erythematosus 61 0.048
269
MSL001 Measles 61 0.048
270
P MYL006 Myeloid Leukemia 60 0.048
271
P BND020 Bone Disease 59 0.048
272
P BRS044 Breast Adenocarcinoma 59 0.048
273
ANR040 Aneurysm 58 0.048
274
c ACT073 Acute Leukemia 58 0.048
275
NWB001 Newborn Respiratory Distress Syndrome 58 0.048
276
P EXN002 Exanthem 57 0.048
277
P DRR001 Diarrhea 57 0.048
278
P FBR017 Fibrosarcoma 56 0.048
279
P INF037 Inflammatory Bowel Disease 56 0.048
280
ALL006 Allergic Asthma 56 0.048
281
PRP030 Purpura 55 0.048
282
MCS002 Mucositis 55 0.048
283
PPL022 Papilloma 54 0.048
284
P RTN016 Retinal Degeneration 53 0.048
285
ART140 Arteries, Anomalies of 53 0.048
286
c HPT007 Hepatitis E 52 0.048
287
BCT002 Bacterial Vaginosis 52 0.048
288
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.048
289
CYS036 Cystinosis, Nephropathic 51 0.048
290
HYP781 Hypoascorbemia 50 0.048
291
P TMP001 Temporal Lobe Epilepsy 50 0.048
292
SPL018 Splenomegaly 48 0.048
293
ANV001 Anovulation 47 0.048
294
LYM019 Lymphosarcoma 47 0.048
295
c INH020 Inherited Metabolic Disorder 46 0.048
296
CHL147 Chlamydia Pneumonia 45 0.048
297
ACT003 Acute Kidney Tubular Necrosis 45 0.048
298
NWC001 Newcastle Disease 44 0.048
299
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.048
300
SQM002 Squamous Cell Papilloma 42 0.048
301
THR035 Thrombasthenia 41 0.048
302
c HYP595 Hypertension, Essential 84 0.044
303
c ATR087 Atrial Standstill 1 74 0.044
304
P EPL164 Epilepsy 71 0.044
305
PRP027 Peripheral Vascular Disease 71 0.044
306
OTT002 Otitis Media 71 0.044
307
P FRN006 Frontotemporal Dementia 70 0.044
308
P MJR001 Major Depressive Disorder 68 0.044
309
P DMN002 Dementia 67 0.044
310
P DRM053 Dermatitis, Atopic 66 0.044
311
ACH004 Achondroplasia 66 0.044
312
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.044
313
c MCR129 Microvascular Complications of Diabetes 1 66 0.044
314
P DBT009 Diabetes Mellitus 64 0.044
315
PPL049 Papillon-Lefevre Syndrome 63 0.044
316
CLT003 Colitis 62 0.044
317
P THN009 Thanatophoric Dysplasia, Type I 62 0.044
318
MDD011 Mood Disorder 62 0.044
319
c PNS012 Paine Syndrome 61 0.044
320
DPH001 Diphtheria 60 0.044
321
INS001 Insulinoma 60 0.044
322
GNG013 Gingivitis 59 0.044
323
GST045 Gastroenteritis 59 0.044
324
BRN002 Bronchiolitis 59 0.044
325
P PRV006 Pervasive Developmental Disorder 57 0.044
326
P HDC001 Headache 57 0.044
327
P PRP019 Peripheral Nervous System Disease 57 0.044
328
VSC002 Vascular Dementia 57 0.044
329
BRN004 Brain Edema 55 0.044
330
PRT038 Protein-Energy Malnutrition 54 0.044
331
END040 Endogenous Depression 54 0.044
332
HYP060 Hyperinsulinism 54 0.044
333
TRC008 Trachoma 53 0.044
334
NRT001 Neurotic Disorder 52 0.044
335
LYS002 Lysosomal Storage Disease 52 0.044
336
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
337
VNZ002 Venezuelan Equine Encephalitis 46 0.044
338
HDN002 Head Injury 45 0.044
339
GRD001 Giardiasis 45 0.044
340
P SPR086 Spermatogenic Failure 3 44 0.044
341
P PHT010 Photoparoxysmal Response 1 42 0.044
342
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.044
343
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.044
344
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
345
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.044
346
PRM004 Primary Amebic Meningoencephalitis 31 0.044
347
ARG004 Argyria 28 0.044
348
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.040
349
P ATX030 Ataxia-Telangiectasia 83 0.040
350
NRL016 Neural Tube Defects 82 0.040
351
P GLM040 Glioma Susceptibility 1 81 0.040
352
STR067 Stroke, Ischemic 80 0.040
353
P NRF023 Neurofibromatosis, Type Ii 76 0.040
354
PHN003 Phenylketonuria 75 0.040
355
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.040
356
P RSP003 Respiratory Failure 74 0.040
357
CRH001 Crohn's Disease 74 0.040
358
P MLT020 Multiple Sclerosis 72 0.040
359
P CNR004 Cone-Rod Dystrophy 2 71 0.040
360
P SLP006 Sleep Apnea 69 0.040
361
P CLC063 Celiac Disease 1 68 0.040
362
c ATS007 Autism Spectrum Disorder 67 0.040
363
CHL065 Cholangiocarcinoma 67 0.040
364
ALL003 Allergic Rhinitis 67 0.040
365
P NSP012 Nasopharyngeal Carcinoma 67 0.040
366
P SKN015 Skin Carcinoma 67 0.040
367
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.040
368
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.040
369
c HMP029 Hemophilia a 65 0.040
370
P MNN013 Meningitis 65 0.040
371
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.040
372
KHL003 Kohlschutter-Tonz Syndrome 64 0.040
373
c SCL052 Scleroderma, Familial Progressive 62 0.040
374
BRS099 Breast Ductal Carcinoma 62 0.040
375
c NMN013 Niemann-Pick Disease, Type a 62 0.040
376
c FNC043 Fanconi Anemia, Complementation Group E 62 0.040
377
CHR066 Chronic Fatigue Syndrome 61 0.040
378
c BRN108 Branchiootic Syndrome 1 61 0.040
379
P SNS001 Sensorineural Hearing Loss 61 0.040
380
CRD223 Cardiac Arrhythmia 60 0.040
381
P NMN002 Niemann-Pick Disease 60 0.040
382
ORL011 Oral Cancer 60 0.040
383
CHC001 Chickenpox 60 0.040
384
P THL005 Thalassemia 60 0.040
385
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.040
386
P BRN022 Bronchiectasis 59 0.040
387
HLC007 Helicobacter Pylori Infection 59 0.040
388
PPT005 Peptic Ulcer Disease 58 0.040
389
CMP010 Complex Regional Pain Syndrome 58 0.040
390
EYD002 Eye Disease 58 0.040
391
P RHN004 Rhinitis 57 0.040
392
PLG002 Plague 57 0.040
393
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.040
394
APH002 Aphasia 57 0.040
395
SCH003 Schizophreniform Disorder 56 0.040
396
LMB062 Limb Ischemia 55 0.040
397
CHL014 Cholera 55 0.040
398
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.040
399
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.040
400
FCT001 Factor Viii Deficiency 55 0.040
401
PRN019 Perinatal Necrotizing Enterocolitis 54 0.040
402
CLL003 Cellulitis 54 0.040
403
P LRY044 Larynx Cancer 54 0.040
404
BRN038 Bronchial Disease 53 0.040
405
KRT009 Keratosis 53 0.040
406
GLS018 Glass Syndrome 53 0.040
407
SPN008 Spondyloepiphyseal Dysplasia Congenita 52 0.040
408
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.040
409
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.040
410
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.040
412
c ACT135 Acute Graft Versus Host Disease 51 0.040
413
TLN003 Telangiectasis 51 0.040
414
DNT012 Dental Caries 51 0.040
415
GLC004 Galactokinase Deficiency 51 0.040
416
P ATR005 Atrophic Gastritis 50 0.040
417
ENT011 Enterocolitis 50 0.040
418
CCC002 Coccidiosis 50 0.040
419
INT079 Intrahepatic Cholangiocarcinoma 50 0.040
420
VGN020 Vaginal Disease 50 0.040
421
CCN001 Cocaine Dependence 48 0.040
422
ATS010 Autosomal Recessive Disease 48 0.040
423
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.040
424
P TCL004 T-Cell Leukemia 47 0.040
425
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.040
426
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.040
427
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.040
428
ANR004 Anuria 46 0.040
429
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.040
430
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.040
431
CWP001 Cowpox 45 0.040
432
ACT029 Acute Interstitial Pneumonia 44 0.040
433
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.040
434
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.040
435
SLF014 Sulfite Oxidase Deficiency, Isolated 40 0.040
436
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.040
437
PRM329 Premature Aging 39 0.040
438
ACT228 Acute Radiation Syndrome 29 0.040
439
PLY028 Polycystic Bone Disease 17 0.040
440
P MDL005 Medulloblastoma 77 0.034
441
CRV035 Cervical Cancer 76 0.034
442
END057 Endometrial Cancer 74 0.034
443
c MNN043 Meningioma, Familial 74 0.034
444
BRN028 Brain Cancer 73 0.034
445
c BTT014 Beta-Thalassemia 72 0.034
446
P SRC025 Sarcoidosis 1 70 0.034
447
DWN001 Down Syndrome 70 0.034
448
ART016 Aortic Aneurysm 68 0.034
449
P MYC084 Mycobacterium Tuberculosis 1 68 0.034
450
PCK003 Pick Disease of Brain 68 0.034
451
CNN005 Connective Tissue Disease 66 0.034
452
GLN010 Glanzmann Thrombasthenia 66 0.034
453
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.034
454
ANG054 Angina Pectoris 66 0.034
455
SRC014 Sarcoma 65 0.034
456
LNG039 Lung Squamous Cell Carcinoma 65 0.034
458
P LPS002 Liposarcoma 65 0.034
459
P TRC102 Trichothiodystrophy 1, Photosensitive 65 0.034
460
P THY023 Thymoma 65 0.034
461
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.034
462
TTN003 Tetanus 64 0.034
463
P GCH001 Gaucher's Disease 64 0.034
464
CLN015 Colon Adenocarcinoma 63 0.034
465
LYM017 Lyme Disease 63 0.034
466
SKN016 Skin Disease 63 0.034
467
P FRD001 Friedreich Ataxia 63 0.034
468
ACT119 Acute Promyelocytic Leukemia 63 0.034
469
ANR007 Anorexia Nervosa 63 0.034
470
P RHB003 Rhabdomyosarcoma 62 0.034
472
c WLM018 Wilms Tumor 5 62 0.034
473
MNN042 Meningioma, Radiation-Induced 62 0.034
474
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.034
475
P PRM006 Primary Biliary Cirrhosis 61 0.034
476
P KDN017 Kidney Cancer 61 0.034
477
CHL068 Cholestasis 60 0.034
478
ACN002 Acanthosis Nigricans 60 0.034
479
RTN017 Retinal Detachment 60 0.034
480
DNG002 Dengue Hemorrhagic Fever 60 0.034
481
ANT009 Antithrombin Iii Deficiency 59 0.034
482
P CYS018 Cystitis 59 0.034
483
PLM033 Pulmonary Embolism 59 0.034
484
c NMN016 Niemann-Pick Disease, Type B 58 0.034
485
CNS004 Constipation 57 0.034
486
DSS009 Disseminated Intravascular Coagulation 57 0.034
487
P DNG005 Dengue Virus 57 0.034
488
P EHL001 Ehlers-Danlos Syndrome 57 0.034
489
P GLM007 Glomerulonephritis 57 0.034
490
THR024 Thrombosis 56 0.034
491
P ISL078 Isolated Ectopia Lentis 56 0.034
492
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.034
493
P CHN012 Chondrosarcoma 56 0.034
494
c ACT075 Acute Myocardial Infarction 56 0.034
495
P CRD246 Cardiovascular System Disease 56 0.034
496
P PLY019 Polyneuropathy 56 0.034
497
SLC006 Silicosis 56 0.034
498
HPT022 Hepatoblastoma 56 0.034
499
MCL006 Macular Retinal Edema 55 0.034
500
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.034
501
PYC001 Pycnodysostosis 55 0.034
502
P DBT005 Diabetes Insipidus 55 0.034
503
PLM010 Pulmonary Edema 55 0.034
504
AMN003 Amnestic Disorder 54 0.034
506
P ART021 Arteriosclerosis 54 0.034
507
FCL014 Focal Epilepsy 54 0.034
508
c THY107 Thymoma, Familial 54 0.034
509
PLM012 Pulmonary Sarcoidosis 53 0.034
510
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.034
511
ECH003 Echinococcosis 53 0.034
512
NNT012 Neonatal Jaundice 53 0.034
513
PRP080 Peripheral Artery Disease 53 0.034
514
PLS007 Plasmodium Falciparum Malaria 52 0.034
515
c LTN004 Late-Onset Retinal Degeneration 52 0.034
516
P HMR003 Hemorrhagic Disease 52 0.034
517
DMY004 Demyelinating Disease 52 0.034
518
PRS045 Prostatic Hypertrophy 52 0.034
519
P HMP007 Hemophilia 51 0.034
520
c VRL010 Viral Hepatitis 51 0.034
521
PRS021 Prostatic Adenoma 51 0.034
522
P ECL001 Eclampsia 51 0.034
523
PNG002 Pain Agnosia 51 0.034
524
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.034
525
SPN035 Spindle Cell Sarcoma 51 0.034
526
HPT014 Hepatorenal Syndrome 50 0.034
527
LNG031 Lung Benign Neoplasm 50 0.034
528
CLR109 Colorectal Adenocarcinoma 50 0.034
529
P SCK005 Sickle Cell Disease 50 0.034
530
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
531
P OVR082 Overgrowth Syndrome 50 0.034
532
IMP004 Impetigo 49 0.034
533
PRS129 Prostatic Hyperplasia, Benign 49 0.034
534
URM002 Uremia 49 0.034
535
DBT006 Diabetic Macular Edema 48 0.034
536
HYP043 Hyperandrogenism 48 0.034
537
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.034
538
CCN002 Cocaine Abuse 48 0.034
539
c SCH079 Schizophrenia 1 48 0.034
540
SPN021 Spinal Meningioma 47 0.034
541
P VTR007 Vitreoretinopathy 46 0.034
542
GLT007 Glutathione Synthetase Deficiency 46 0.034
543
P OCY003 Oocyte Maturation Defect 1 45 0.034
544
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.034
545
IMP006 Impulse Control Disorder 45 0.034
546
P GNT008 Giant Cell Tumor 44 0.034
547
HYP003 Hypermethioninemia 44 0.034
548
CNN002 Cannabis Abuse 44 0.034
549
LMY003 Leiomyomatosis 43 0.034
550
DNT014 Dental Pulp Disease 43 0.034
551
SNL007 Senile Cataract 42 0.034
552
c ADL066 Adult Neuronal Ceroid Lipofuscinosis 42 0.034
553
DNT006 Dental Pulp Necrosis 40 0.034
555
ANC001 Ancylostomiasis 39 0.034
556
CNN001 Cannabis Dependence 38 0.034
557
SCR001 Secretory Meningioma 37 0.034
558
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.034
559
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.034
560
HRW001 Hair Whorl 36 0.034
561
INT020 Intravenous Leiomyomatosis 36 0.034
562
c SCH073 Schizophrenia 9 33 0.034
563
c SCH083 Schizophrenia 7 33 0.034
564
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.034
565
ACD003 Acid Sphingomyelinase Deficiency 32 0.034
566
CNJ001 Conjugate Gaze Palsy 30 0.034
567
RSP007 Respiratory Distress Syndrome, Infant 30 0.034
568
MYC021 Mycobacterium Xenopi 25 0.034
569
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.034
570
CYN003 Cyanide Poisoning 24 0.034
571
P STR035 Streptococcal Group a Invasive Disease 23 0.034
572
c TRC125 Trichothiodystrophy 7, Nonphotosensitive 17 0.034
573
P RTT002 Rett Syndrome 80 0.028
574
c LKM071 Leukemia, Chronic Lymphocytic 79 0.028
575
PFF001 Pfeiffer Syndrome 79 0.028
576
GST019 Gastrointestinal Stromal Tumor 76 0.028
577
KPS004 Kaposi Sarcoma 75 0.028
578
c SPN225 Spondyloarthropathy 1 73 0.028
579
c GCH015 Gaucher Disease, Type I 70 0.028
580
P ART022 Arthritis 70 0.028
581
GST040 Gastric Adenocarcinoma 70 0.028
582
RCK004 Rickets 69 0.028
583
c PNC108 Pancreatitis, Hereditary 69 0.028
584
P ALP004 Alport Syndrome 68 0.028
585
CRB037 Cerebral Palsy 68 0.028
586
c HMP004 Hemophilia B 67 0.028
587
P MLG056 Malignant Hyperthermia 67 0.028
588
P CRD119 Cardiac Arrest 67 0.028
589
KRT019 Keratitis, Hereditary 67 0.028
590
PNC129 Pancreatic Adenocarcinoma 67 0.028
591
P ATR011 Atrial Fibrillation 66 0.028
592
P HYP098 Hypereosinophilic Syndrome 66 0.028
593
P NRV007 Nervous System Disease 66 0.028
594
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.028
595
P LNG028 Long Qt Syndrome 65 0.028
596
GST092 Gastroesophageal Reflux 65 0.028
597
PRT036 Peritonitis 65 0.028
598
P PRS038 Personality Disorder 65 0.028
599
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 64 0.028
600
CLF027 Cleft Palate, Isolated 64 0.028
601
P MTR014 Motor Neuron Disease 64 0.028
602
GT001 Gout 63 0.028
603
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.028
604
MSC152 Muscular Dystrophy, Becker Type 63 0.028
605
OVR029 Ovarian Hyperstimulation Syndrome 63 0.028
606
P HYP069 Hyperparathyroidism 62 0.028
607
P LMY004 Leiomyosarcoma 62 0.028
608
P ART023 Arthropathy 62 0.028
609
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.028
610
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.028
611
WLL001 Williams-Beuren Syndrome 62 0.028
612
c ALP101 Alpha-Thalassemia 62 0.028
613
TRN015 Transient Cerebral Ischemia 62 0.028
614
P PLZ001 Pelizaeus-Merzbacher Disease 62 0.028
615
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.028
616
P MVM001 Movement Disease 61 0.028
617
P ENC004 Encephalitis 61 0.028
618
BRC012 Brucellosis 61 0.028
619
SDD001 Sudden Infant Death Syndrome 61 0.028
620
VRL011 Viral Infectious Disease 61 0.028
621
ING001 Inguinal Hernia 60 0.028
622
HPT019 Hepatic Encephalopathy 60 0.028
623
P TXP001 Toxoplasmosis 60 0.028
624
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.028
625
DCB001 Decubitus Ulcer 60 0.028
626
P HRD011 Hereditary Spherocytosis 60 0.028
627
ETN001 Eating Disorder 59 0.028
628
P SLP005 Sleep Disorder 59 0.028
629
P MYC008 Myocarditis 59 0.028
630
STT001 Status Epilepticus 59 0.028
631
P RBL001 Rubella 58 0.028
632
IRN001 Iron Deficiency Anemia 58 0.028
633
PRL032 Perlman Syndrome 58 0.028
634
CRV038 Cervical Squamous Cell Carcinoma 58 0.028
635
c DWL002 Dowling-Degos Disease 1 58 0.028
636
CNT047 Contact Dermatitis 57 0.028
637
SPT004 Septic Arthritis 57 0.028
638
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.028
639
BLM002 Bulimia Nervosa 57 0.028
640
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.028
641
P PRN023 Prion Disease 57 0.028
642
TNS005 Tonsillitis 57 0.028
643
ERY051 Erythroleukemia, Familial 56 0.028
644
PHR003 Pharyngitis 56 0.028
645
PLS011 Plasmacytoma 56 0.028
646
SFT003 Soft Tissue Sarcoma 56 0.028
647
P ALP008 Alopecia 56 0.028
648
GLL018 Gallbladder Cancer 56 0.028
649
P MTC069 Mitochondrial Disorders 56 0.028
650
MTH009 Mouth Disease 56 0.028
651
FNC009 Fanconi-Bickel Syndrome 56 0.028
652
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.028
653
HYP005 Hypokalemia 55 0.028
654
P PLY018 Polycythemia 55 0.028
655
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
656
c MYP132 Myopathy, Congenital 55 0.028
657
FLR002 Filariasis 55 0.028
658
INT007 Intermediate Coronary Syndrome 55 0.028
659
P MYP006 Myopia 55 0.028
660
DBT010 Diabetic Neuropathy 55 0.028
661
VGN023 Vaginitis 55 0.028
662
P ANG015 Angioedema 54 0.028
663
ANL018 Analbuminemia 54 0.028
664
ACR058 Acrofacial Dysostosis 1, Nager Type 54 0.028
665
GLC003 Glucose Intolerance 54 0.028
666
CRY003 Cryptosporidiosis 54 0.028
667
P SPN052 Spondyloarthropathy 54 0.028
668
PRT082 Preterm Premature Rupture of the Membranes 54 0.028
669
c CNT035 Central Nervous System Disease 54 0.028
670
CHR100 Chronic Ulcer of Skin 53 0.028
671
RFL001 Reflex Sympathetic Dystrophy 53 0.028
672
CCC001 Coccidioidomycosis 53 0.028
673
P EPD016 Epidermolysis Bullosa 53 0.028
674
c LBR014 Leber Congenital Amaurosis 4 53 0.028
675
HRT012 Heart Valve Disease 53 0.028
676
P BRC006 Brachydactyly 53 0.028
677
MST005 Mastitis 53 0.028
678
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.028
679
P RTN018 Retinal Disease 52 0.028
680
c HYP768 Hyperlipoproteinemia, Type I 52 0.028
681
P SHR001 Short Bowel Syndrome 52 0.028
682
MCN007 Meconium Aspiration Syndrome 52 0.028
683
SPN051 Spondylitis 52 0.028
684
DYS165 Dysfibrinogenemia, Congenital 52 0.028
685
IMP005 Impotence 52 0.028
686
PRV004 Periventricular Leukomalacia 51 0.028
687
HYP014 Hyperuricemia 51 0.028
688
CHL122 Cholesteatoma of Middle Ear 51 0.028
689
c VNW010 Von Willebrand Disease, Type 2 51 0.028
690
PRT129 Prothrombin Deficiency, Congenital 51 0.028
691
ONC002 Onchocerciasis 51 0.028
692
HYP081 Hypolipoproteinemia 50 0.028
693
P PST095 Post-Thrombotic Syndrome 50 0.028
694
RTN003 Retinal Ischemia 50 0.028
695
LMY002 Leiomyoma 50 0.028
696
DYS015 Dysentery 50 0.028
697
c AMY009 Amyloidosis Aa 50 0.028
698
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.028
699
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.028
700
NTR046 Neutrophil Migration 50 0.028
701
BLR001 Biliary Atresia 50 0.028
702
c HYP843 Hypoalphalipoproteinemia, Primary, 2 50 0.028
703
PLC008 Placenta Disease 49 0.028
704
P OPN001 Open-Angle Glaucoma 49 0.028
705
P GND004 Gonadal Dysgenesis 49 0.028
706
c LRG001 Large Cell Carcinoma 49 0.028
707
GYN001 Gynecomastia 49 0.028
708
c SPN330 Spondylocostal Dysostosis 5 49 0.028
709
URT001 Urethritis 48 0.028
710
MTC005 Mitochondrial Metabolism Disease 48 0.028
711
KHN001 Kuhnt-Junius Degeneration 48 0.028
712
P MRC003 Mercury Poisoning 48 0.028
713
BNG036 Bone Giant Cell Tumor 48 0.028
714
RTN020 Retinal Vascular Disease 48 0.028
715
ATX019 Ataxia with Vitamin E Deficiency 48 0.028
716
STM006 Stomach Disease 48 0.028
717
P CRN028 Corneal Ulcer 47 0.028
718
RFT001 Rift Valley Fever 47 0.028
719
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.028
720
RNL077 Renal Fibrosis 47 0.028
721
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.028
722
CLS016 Clostridium Difficile Colitis 46 0.028
723
TST014 Testicular Cancer 46 0.028
724
ALB002 Albinism 46 0.028
725
c SPN312 Spinocerebellar Ataxia 14 45 0.028
726
SYN036 Syncope 45 0.028
727
c MLG068 Malignant Glioma 45 0.028
728
P PSD003 Pseudohypoaldosteronism 45 0.028
729
P BNG032 Benign Mesothelioma 45 0.028
730
KWS001 Kwashiorkor 45 0.028
731
P END084 Endocrine System Disease 44 0.028
732
CRB025 Carbohydrate Metabolic Disorder 44 0.028
733
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.028
734
BRN032 Brain Glioma 43 0.028
735
PNM013 Pneumococcal Meningitis 43 0.028
736
HPT004 Hepatic Coma 43 0.028
737
TST015 Testicular Disease 43 0.028
738
c PRM038 Primary Agammaglobulinemia 43 0.028
739
BSL008 Basal Ganglia Disease 43 0.028
740
c SRC023 Sarcoidosis 2 43 0.028
741
P CLS010 Cluster Headache 43 0.028
742
c CHR576 Chronic Beryllium Disease 42 0.028
743
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.028
744
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.028
745
GST020 Gastric Antral Vascular Ectasia 41 0.028
746
49X006 49, Xxxxy Syndrome 41 0.028
747
RDN001 Reading Disorder 40 0.028
748
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.028
749
TXC011 Toxocariasis 40 0.028
750
P BRY005 Beryllium Disease 40 0.028
751
C1N001 C1 Inhibitor Deficiency 40 0.028
753
ANS003 Anisakiasis 39 0.028
754
ENT001 Enterocele 39 0.028
755
c MLG074 Malignant Mesenchymoma 39 0.028
756
FLT009 Folate Malabsorption, Hereditary 39 0.028
757
AML001 Amelanotic Melanoma 39 0.028
758
c CHR682 Chronic Bilirubin Encephalopathy 38 0.028
759
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 38 0.028
760
SCR011 Scrapie 38 0.028
761
ENC005 Encephalomalacia 38 0.028
762
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.028
763
OVR094 Ovarian Epithelial Cancer 38 0.028
764
BLR028 Biliary Atresia, Extrahepatic 37 0.028
765
c CHR020 Chronic Interstitial Cystitis 37 0.028
766
c WLM011 Wilms Tumor 6 37 0.028
767
P MXL015 Maxillary Sinusitis 37 0.028
768
LYM011 Lymphogranuloma Venereum 36 0.028
769
PSD088 Pseudobulbar Affect 36 0.028
770
FXD003 Fixed Drug Eruption 35 0.028
771
ACT149 Acetaminophen Metabolism 35 0.028
772
c ACR088 Aicardi-Goutieres Syndrome 3 35 0.028
773
HWK001 Hawkinsinuria 35 0.028
774
PYR009 Pyridoxine Deficiency Anemia 34 0.028
775
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.028
776
c PRS136 Prostate Cancer, Hereditary, 6 33 0.028
777
c PRS130 Prostate Cancer, Hereditary, 8 32 0.028
778
HPT085 Hepatitis, Fulminant Viral 32 0.028
779
MTC108 Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency 32 0.028
780
INF009 Inflammatory Spondylopathy 32 0.028
781
P HRD084 Hereditary Cerebral Amyloid Angiopathy 31 0.028
782
INF021 Infant Gynecomastia 31 0.028
783
FNT004 Fainting 31 0.028
784
PYR016 Pyridoxine Deficiency 30 0.028
785
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 30 0.028
786
P SKL032 Skeletal Muscle Disease 29 0.028
787
c ALC016 Alcohol Sensitivity, Acute 29 0.028
788
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.028
789
GRN004 Granulomatous Amebic Encephalitis 29 0.028
790
PST092 Posttransplant Acute Limbic Encephalitis 29 0.028
791
TBL029 Tubulin, Beta 28 0.028
792
TCK004 Tick Infestation 27 0.028
793
c CRN110 Cranioectodermal Dysplasia 3 27 0.028
794
CHL079 Children's Interstitial Lung Disease 27 0.028
795
MST020 Mast Cell Activation Syndrome 27 0.028
796
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.028
797
c HYP819 Hyperlipoproteinemia, Type Id 24 0.028
798
HVY002 Heavy Metal Poisoning 22 0.028
799
EXT009 Extratemporal Epilepsy 21 0.028
800
LTH004 Lathyrism 16 0.028
801
FCS014 Fucosidase Regulator 15 0.028
802
MYL069 Myeloma, Multiple 85 0.020
803
P LYN001 Lynch Syndrome 77 0.020
804
c TBR025 Tuberous Sclerosis 1 76 0.020
805
P APL001 Aplastic Anemia 74 0.020
806
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.020
807
c HMC039 Hemochromatosis, Type 1 74 0.020
808
ACR006 Aceruloplasminemia 73 0.020
809
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.020
810
LPT014 Leptin Deficiency or Dysfunction 73 0.020
811
P ALG028 Alagille Syndrome 1 73 0.020
812
AGM019 Agammaglobulinemia, X-Linked 72 0.020
813
P FML011 Familial Adenomatous Polyposis 72 0.020
814
c LKM063 Leukemia, Chronic Myeloid 71 0.020
815
FBR012 Fabry Disease 71 0.020
816
MLT157 Multiple System Atrophy 1 70 0.020
817
WLS001 Wilson Disease 70 0.020
818
P TBR001 Tuberous Sclerosis 70 0.020
819
P MTC003 Metachromatic Leukodystrophy 70 0.020
820
MYL009 Myelodysplastic Syndrome 70 0.020
821
P SYS005 Systemic Scleroderma 70 0.020
822
P TTR001 Tetralogy of Fallot 69 0.020
823
CRT072 Creutzfeldt-Jakob Disease 69 0.020
824
P OCL013 Oculodentodigital Dysplasia 69 0.020
825
c BSL007 Basal Cell Carcinoma 68 0.020
826
NVS017 Nevus, Epidermal 68 0.020
827
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.020
828
P CRN037 Craniosynostosis 68 0.020
829
CRZ001 Crouzon Syndrome 68 0.020
830
SKN019 Skin Melanoma 67 0.020
831
P LBR001 Leber Congenital Amaurosis 67 0.020
832
P PRP003 Porphyria Cutanea Tarda 67 0.020
833
P LPR021 Leprosy 3 67 0.020
834
P PSD087 Pseudoxanthoma Elasticum 67 0.020
835
MLD001 Melioidosis 67 0.020
836
P ANG001 Angelman Syndrome 67 0.020
837
c FML001 Familial Atrial Fibrillation 66 0.020
838
P HYP061 Hypertrophic Cardiomyopathy 66 0.020
839
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.020
840
AND002 Androgen Insensitivity Syndrome 66 0.020
841
LPT001 Leptospirosis 66 0.020
842
P ASP006 Aspergillosis 66 0.020
843
P LYS001 Loeys-Dietz Syndrome 66 0.020
844
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.020
845
P HYD006 Hydrocephalus 65 0.020
846
GLC006 Galactosemia 65 0.020
847
c CNG006 Congenital Hypothyroidism 65 0.020
848
P AGM001 Agammaglobulinemia 65 0.020
849
P HRS035 Hirschsprung Disease 1 65 0.020
850
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.020
851
DMN031 Dementia, Lewy Body 65 0.020
852
P DYS154 Dystonia 65 0.020
853
BRR014 Barrett Esophagus 64 0.020
854
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.020
855
INC002 Inclusion Body Myositis 64 0.020
856
KWS002 Kawasaki Disease 64 0.020
857
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.020
858
CLR108 Colorectal Adenoma 64 0.020
859
MYC079 Myoclonic Epilepsy of Lafora 64 0.020
860
P KLL001 Kallmann Syndrome 64 0.020
861
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.020
862
PRP083 Porphyria, Acute Intermittent 63 0.020
863
IRR002 Irritable Bowel Syndrome 63 0.020
864
MSC007 Muscle Hypertrophy 63 0.020
865
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.020
866
NRM005 Neuromuscular Disease 63 0.020
867
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.020
868
P ANR048 Aniridia 1 63 0.020
869
P MCH002 Machado-Joseph Disease 63 0.020
870
P PRM002 Primary Hyperoxaluria 62 0.020
871
c GLC092 Glaucoma, Primary Open Angle 62 0.020
872
P VSC011 Vasculitis 62 0.020
873
P ESP024 Esophagitis 62 0.020
874
HMT002 Hematologic Cancer 62 0.020
875
c ATM011 Autoimmune Hepatitis 62 0.020
876
HYD038 Hydrops Fetalis, Nonimmune 61 0.020
877
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.020
878
INT002 Intermittent Claudication 61 0.020
879
CRC021 Carcinosarcoma 61 0.020
880
P HYP750 Hypertriglyceridemia, Familial 61 0.020
881
DRM006 Dermatitis 61 0.020
882
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.020
883
c HRD002 Hereditary Angioedema 61 0.020
884
P TST021 Testicular Germ Cell Tumor 61 0.020
885
OST003 Osteonecrosis 61 0.020
886
RHM001 Rheumatic Fever 61 0.020
887
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 61 0.020
888
P ACH003 Achromatopsia 60 0.020
889
PRT013 Portal Hypertension 60 0.020
890
P BRN019 Bernard-Soulier Syndrome 60 0.020
891
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.020
892
RCT015 Reactive Arthritis 60 0.020
893
P VNT002 Ventricular Septal Defect 60 0.020
894
STF001 Stiff-Person Syndrome 60 0.020
895
P HYP035 Hypophosphatasia 60 0.020
896
HRP004 Herpes Zoster 60 0.020
897
P SCL018 Scoliosis 60 0.020
898
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.020
899
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.020
900
CHR072 Chordoma 59 0.020
901
P GLL022 Guillain-Barre Syndrome 59 0.020
902
P ECT006 Ectodermal Dysplasia 59 0.020
903
SPP011 Suppression of Tumorigenicity 12 59 0.020
904
CLS005 Clouston Syndrome 59 0.020
905
P LKD001 Leukodystrophy 59 0.020
906
P PLY014 Polycystic Kidney Disease 59 0.020
907
P TRC086 Trichohepatoenteric Syndrome 1 59 0.020
908
GRD007 Grade Iii Astrocytoma 59 0.020
909
c MLT159 Multiple Endocrine Neoplasia, Type Iib 59 0.020
910
P SYP003 Syphilis 59 0.020
911
DCT002 Ductal Carcinoma in Situ 59 0.020
912
HYP042 Hypochondroplasia 59 0.020
913
c BNG091 Benign Chronic Pemphigus 59 0.020
914
P PLV020 Pelvic Organ Prolapse 59 0.020
915
CRD132 Cardiac Conduction Defect 59 0.020
916
CHL067 Cholecystitis 58 0.020
917
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.020
918
BRS051 Breast Disease 58 0.020
919
P GLL020 Gallbladder Disease 58 0.020
920
RBS001 Rabies 58 0.020
921
ADL030 Adult-Onset Still's Disease 58 0.020
922
PLM070 Pulmonic Stenosis 57 0.020
923
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.020
924
P MMP001 Mumps 57 0.020
925
THY022 Thymic Carcinoma 57 0.020
926
LYM027 Lymphopenia 57 0.020
927
P END033 Endocarditis 57 0.020
928
P PLY041 Polymyositis 57 0.020
929
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.020
930
c ADL017 Adult T-Cell Leukemia 57 0.020
931
P STC001 Stickler Syndrome 57 0.020
932
P EPD003 Epidermolysis Bullosa Simplex 56 0.020
933
PRS047 Prostatitis 56 0.020
934
c ANG068 Angioedema, Hereditary, Type I 56 0.020
935
TRN018 Transitional Cell Carcinoma 56 0.020
936
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.020
937
P EXD001 Exudative Vitreoretinopathy 56 0.020
938
LMY014 Leiomyoma, Uterine 56 0.020
939
AVN001 Avian Influenza 56 0.020
940
SKN022 Skin Squamous Cell Carcinoma 56 0.020
941
KRT071 Keratosis, Seborrheic 56 0.020
942
CMM005 Common Cold 56 0.020
943
P MYS005 Myositis 56 0.020
944
RHM027 Rheumatic Disease 56 0.020
945
CHR177 Chromophobe Renal Cell Carcinoma 56 0.020
946
GST050 Gastrointestinal System Disease 56 0.020
947
BRN012 Bronchiolitis Obliterans 56 0.020
948
DFF005 Diffuse Large B-Cell Lymphoma 56 0.020
949
P PLM034 Pulmonary Emphysema 56 0.020
950
HMG005 Hemoglobinopathy 55 0.020
951
P PNM006 Pneumoconiosis 55 0.020
952
SYN007 Synovitis 55 0.020
953
GRN034 Grange Syndrome 55 0.020
954
c FML035 Familial Hyperlipidemia 55 0.020
955
P GRV001 Graves' Disease 55 0.020
956
c BCT007 Bacterial Meningitis 55 0.020
957
ATR057 Atrioventricular Block 55 0.020
958
ALL010 Allergic Contact Dermatitis 55 0.020
959
PLV003 Pelvic Inflammatory Disease 55 0.020
960
ACT058 Active Peptic Ulcer Disease 55 0.020
961
GNG005 Gangliocytoma 55 0.020
962
P HYP076 Hyperthyroidism 55 0.020
963
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.020
964
SHG001 Shigellosis 55 0.020
965
NRN004 Neuroendocrine Tumor 55 0.020
966
AND020 Androgen Insensitivity, Partial 55 0.020
967
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.020
968
P PMP001 Pemphigus 55 0.020
969
END002 Endometrioid Ovary Carcinoma 55 0.020
970
P SBS003 Substance Abuse 54 0.020
971
CFF003 Caffey Disease 54 0.020
972
FCT004 Factor Xii Deficiency 54 0.020
973
P PTT006 Pituitary Adenoma 54 0.020
974
HMP005 Hemiplegia 54 0.020
975
P CNG010 Congenital Stationary Night Blindness 54 0.020
976
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.020
977
LYM040 Lymphoblastic Lymphoma 54 0.020
978
P CLS054 Classic Ehlers-Danlos Syndrome 54 0.020
979
P NLD001 Nail Disease 54 0.020
980
P MNC007 Monocytic Leukemia 54 0.020
981
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.020
982
PRP016 Paraplegia 53 0.020
983
MLT135 Multiple Sulfatase Deficiency 53 0.020
984
MYM001 Myoma 53 0.020
985
RST011 Restrictive Dermopathy, Lethal 53 0.020
986
OCL006 Ocular Hypertension 53 0.020
987
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.020
988
P RCT021 Rectum Cancer 53 0.020
989
OST016 Osteochondrosis 53 0.020
990
PRP036 Peripheral T-Cell Lymphoma 53 0.020
991
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.020
992
GST023 Gastric Ulcer 53 0.020
993
P HST010 Histiocytosis 53 0.020
994
P THY032 Thyroiditis 53 0.020
995
GNG002 Ganglioneuroma 53 0.020
996
THR013 Thoracic Outlet Syndrome 53 0.020
997
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.020
998
P INT068 Intestinal Disease 52 0.020
999
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.020
1000
ACR041 Acromelic Frontonasal Dysostosis 52 0.020
1001
P PTS002 Ptosis 52 0.020
1002
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.020
1003
ABL002 Ablepharon-Macrostomia Syndrome 52 0.020
1004
MCN017 Meconium Ileus 52 0.020
1005
DRM011 Dermatophytosis 52 0.020
1006
P END047 Endophthalmitis 52 0.020
1007
GTR002 Goiter 52 0.020
1008
P ACT105 Acute Mountain Sickness 52 0.020
1009
P INS002 in Situ Carcinoma 52 0.020
1010
c GLL024 Gallbladder Disease 1 52 0.020
1011
ESN005 Eosinophilic Gastroenteritis 52 0.020
1012
CHR073 Choreatic Disease 52 0.020
1013
P RTN022 Retinal Vein Occlusion 52 0.020
1014
P ACT008 Actinic Keratosis 52 0.020
1015
THY124 Thyroid Gland Papillary Carcinoma 52 0.020
1016
INF034 Infective Endocarditis 52 0.020
1017
OCL069 Ocular Motor Apraxia 51 0.020
1018
P LRY019 Laryngitis 51 0.020
1019
CHR005 Chorioamnionitis 51 0.020
1020
MSC190 Muscular Disease 51 0.020
1021
THR016 Thrombophlebitis 51 0.020
1022
ILS001 Ileus 51 0.020
1023
SPP010 Suppressor of Tumorigenicity 3 51 0.020
1024
ADR049 Adrenal Hypoplasia, Congenital 51 0.020
1025
PLR008 Pleurisy 51 0.020
1026
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 51 0.020
1027
SCB001 Scabies 51 0.020
1028
GSG001 Gas Gangrene 50 0.020
1029
SCH012 Schizoaffective Disorder 50 0.020
1030
c SCN007 Secondary Hyperparathyroidism 50 0.020
1031
AZS001 Azoospermia 50 0.020
1032
HRT011 Heart Septal Defect 50 0.020
1033
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 50 0.020
1034
P FNC004 Fanconi Syndrome 50 0.020
1035
P CHL066 Cholangitis 50 0.020
1036
P AGG001 Aggressive Periodontitis 50 0.020
1037
FLR001 Filarial Elephantiasis 50 0.020
1038
CRT013 Carotid Stenosis 50 0.020
1039
ILT001 Ileitis 50 0.020
1040
MCR004 Macroglobulinemia 50 0.020
1041
CRV040 Cervix Carcinoma 50 0.020
1042
CRN030 Coronary Stenosis 50 0.020
1043
c ALZ049 Alzheimer Disease 2 50 0.020
1044
PRS034 Parasitic Helminthiasis Infectious Disease 49 0.020
1045
TLR001 Tularemia 49 0.020
1046
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 49 0.020
1047
VRC001 Varicocele 49 0.020
1048
c CRD187 Cardiomyopathy, Dilated, 3b 49 0.020
1049
HYP017 Hypophosphatemia 49 0.020
1050
FDL002 Food Allergy 49 0.020
1051
P MTC133 Mitochondrial Myopathy 49 0.020
1052
MLL001 Molluscum Contagiosum 49 0.020
1053
c CNT016 Central Retinal Vein Occlusion 49 0.020
1054
BLP005 Blepharitis 49 0.020
1055
CHL004 Cholelithiasis 49 0.020
1056
LRN003 Learning Disability 49 0.020
1057
ART017 Aortic Disease 49 0.020
1058
c OST121 Osteogenesis Imperfecta, Type Iv 49 0.020
1059
HMG002 Hemoglobinuria 49 0.020
1060
ECT026 Ectopic Pregnancy 49 0.020
1061
PLY024 Polymicrogyria 49 0.020
1062
ALN001 Aland Island Eye Disease 49 0.020
1063
c VNW005 Von Willebrand Disease, Type 1 49 0.020
1064
c HPT015 Hepatitis D 49 0.020
1065
P CMP008 Compartment Syndrome 48 0.020
1066
c OST119 Osteogenesis Imperfecta, Type Vii 48 0.020
1067
VTM033 Vitamin K Deficiency Bleeding 48 0.020
1068
c OST132 Osteogenesis Imperfecta, Type Vi 48 0.020
1069
SBP001 Subependymal Giant Cell Astrocytoma 48 0.020
1070
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.020
1071
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.020
1072
P CLR019 Color Blindness 48 0.020
1073
CRD137 Cardiogenic Shock 48 0.020
1074
ASP007 Aspiration Pneumonia 48 0.020
1075
IGG001 Iga Glomerulonephritis 48 0.020
1076
P MYF003 Myofibrillar Myopathy 48 0.020
1077
SXL003 Sexual Disorder 48 0.020
1078
ERY004 Erysipelas 48 0.020
1079