Search results for Arginine

1518 hits were found for Arginine

# Family MCID Name MIFTS Score
1
CRB148 Cerebral Creatine Deficiency Syndrome 3 43 8.178
2
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 12 4.511
3
URC002 Urea Cycle Disorder 51 2.618
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.461
5
P DBT005 Diabetes Insipidus 55 0.256
6
P KDN018 Kidney Disease 70 0.199
7
c PRC016 Pre-Eclampsia 63 0.190
8
c HYP595 Hypertension, Essential 84 0.181
9
c HYP836 Hypercholesterolemia, Familial, 1 72 0.181
10
TXC005 Toxic Shock Syndrome 61 0.180
11
P PLM037 Pulmonary Hypertension 68 0.178
12
HLX001 Helix Syndrome 47 0.176
13
HYP056 Hypoglycemia 66 0.169
14
ISC004 Ischemia 60 0.165
15
c ACT027 Acute Pancreatitis 59 0.165
16
CNG034 Congestive Heart Failure 70 0.154
17
ALL026 Allergic Hypersensitivity Disease 64 0.149
18
P PNC044 Pancreatitis 61 0.149
19
HYP066 Hyperglycemia 61 0.146
20
P SCK005 Sickle Cell Disease 50 0.146
21
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.140
22
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.138
23
P VSC007 Vascular Disease 63 0.131
24
ATH013 Atherosclerosis Susceptibility 66 0.124
25
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.120
26
P HRT032 Heart Disease 75 0.120
27
CYS001 Cystic Fibrosis 80 0.118
28
IMP005 Impotence 52 0.118
29
P ECL001 Eclampsia 51 0.118
30
P LVR013 Liver Disease 68 0.117
31
c CHR684 Chronic Kidney Disease 66 0.117
32
P CRN018 Coronary Artery Anomaly 63 0.117
33
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.115
34
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.114
35
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.114
36
c ACT071 Acute Kidney Failure 59 0.114
37
P VNW001 Von Willebrand's Disease 64 0.112
38
48X005 48,xyyy 39 0.112
39
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.112
40
END030 End Stage Renal Failure 58 0.111
41
GRW007 Growth Hormone Deficiency 43 0.111
42
ARG007 Argininemia 57 0.109
43
P HPT023 Hepatocellular Carcinoma 100 0.108
44
GLB015 Glioblastoma Multiforme 75 0.108
45
LVR012 Liver Cirrhosis 63 0.108
46
P HRP006 Herpes Simplex 65 0.106
47
BRN004 Brain Edema 55 0.106
48
ENT011 Enterocolitis 50 0.106
49
HMN044 Human Immunodeficiency Virus Type 1 71 0.105
50
P MSC005 Muscular Dystrophy 66 0.105
51
P DBT009 Diabetes Mellitus 64 0.105
52
P ENC018 Encephalopathy 61 0.105
53
ART140 Arteries, Anomalies of 53 0.105
54
INS024 Insulin-Like Growth Factor I 79 0.103
55
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.103
56
P CLR023 Colorectal Cancer 98 0.101
57
PRP027 Peripheral Vascular Disease 71 0.101
58
P PRD008 Periodontitis 62 0.101
59
HYP266 Hypoxia 56 0.101
60
GLC003 Glucose Intolerance 54 0.101
61
URM002 Uremia 49 0.101
62
P NRB001 Neuroblastoma 71 0.100
63
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.100
64
DNT012 Dental Caries 51 0.100
65
DFC004 Deficiency Anemia 75 0.098
66
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.098
67
CRB004 Cerebral Artery Occlusion 44 0.098
68
P BRS047 Breast Cancer 96 0.096
69
SCK003 Sickle Cell Anemia 72 0.096
70
MLN008 Melanoma 69 0.096
71
P SZR006 Seizure Disorder 58 0.096
72
VSL002 Visual Epilepsy 58 0.096
73
P GLM007 Glomerulonephritis 57 0.096
74
CHL014 Cholera 55 0.096
75
PRN019 Perinatal Necrotizing Enterocolitis 54 0.096
76
P LCT001 Lactic Acidosis 51 0.096
77
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.094
78
ANG054 Angina Pectoris 66 0.094
79
PRT037 Pertussis 65 0.094
80
PRT036 Peritonitis 65 0.094
81
P MYP004 Myopathy 64 0.094
82
CYT002 Cytokine Deficiency 44 0.094
83
AST005 Asthma 77 0.092
84
HYP060 Hyperinsulinism 54 0.092
85
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.091
86
P LTR001 Lateral Sclerosis 53 0.091
87
TRM010 Traumatic Brain Injury 53 0.091
88
OCL069 Ocular Motor Apraxia 51 0.091
89
PNG002 Pain Agnosia 51 0.091
90
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.091
91
ARG002 Argininosuccinic Aciduria 60 0.089
92
P CRD246 Cardiovascular System Disease 56 0.089
93
BRN071 Brain Injury 49 0.089
94
c HMG029 Hemoglobin Se Disease 38 0.089
95
P PNC035 Pancreatic Cancer 84 0.087
96
MSC157 Muscular Dystrophy, Duchenne Type 71 0.087
97
CRB039 Cerebrovascular Disease 69 0.087
98
P CRD119 Cardiac Arrest 67 0.087
99
HPT004 Hepatic Coma 43 0.087
100
SPR126 Superior Semicircular Canal Dehiscence 40 0.087
101
P CRN300 Coronary Heart Disease 1 63 0.085
102
P THL005 Thalassemia 60 0.085
103
P HYP086 Hypothyroidism 68 0.083
104
P HMP007 Hemophilia 51 0.083
105
47X002 47,xyy 49 0.083
106
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 33 0.083
107
P GST053 Gastric Cancer 83 0.081
108
MLR004 Malaria 80 0.081
109
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.081
110
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.081
111
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.081
112
CYS013 Cystinuria 62 0.081
113
CLT003 Colitis 62 0.081
114
ATM095 Autoimmune Disease 61 0.081
115
ORT008 Orotic Aciduria 54 0.081
116
P ALZ034 Alzheimer Disease 88 0.078
117
STR067 Stroke, Ischemic 80 0.078
118
ADL002 Adult Syndrome 69 0.078
119
DPR016 Depression 63 0.078
120
LNG099 Lung Disease 61 0.078
121
SPN186 Spinal Cord Injury 60 0.078
122
LYS003 Lysinuric Protein Intolerance 56 0.078
123
HMC014 Homocysteinemia 53 0.078
124
P MSC003 Muscular Atrophy 52 0.078
125
INP001 Inappropriate Adh Syndrome 49 0.078
126
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.078
127
P PRS040 Prostate Cancer 97 0.076
128
P RHM011 Rheumatoid Arthritis 80 0.076
129
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.076
130
P RTN024 Retinoblastoma 72 0.076
131
P MYC007 Myocardial Infarction 70 0.076
132
P ATS364 Autism 65 0.076
133
P GLM045 Glioma 63 0.076
134
P MYL006 Myeloid Leukemia 60 0.076
135
c FML008 Familial Retinoblastoma 53 0.076
136
ATX019 Ataxia with Vitamin E Deficiency 48 0.076
137
GLL048 Glial Tumor 45 0.076
138
ACT088 Acute Insulin Response 41 0.076
139
P LKM002 Leukemia 66 0.074
140
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.074
141
P DRR001 Diarrhea 57 0.074
142
GYR004 Gyrate Atrophy of Choroid and Retina 56 0.074
143
c MCR113 Microvascular Complications of Diabetes 3 52 0.074
144
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.074
145
P LNG032 Lung Cancer 97 0.072
146
BRT054 Brittle Bone Disorder 70 0.072
147
P MCR115 Microvascular Complications of Diabetes 5 66 0.072
148
LSH001 Leishmaniasis 63 0.072
149
LPD008 Lipid Metabolism Disorder 62 0.072
150
P BRS044 Breast Adenocarcinoma 59 0.072
151
MNT002 Mental Depression 57 0.072
152
c ACT075 Acute Myocardial Infarction 56 0.072
153
AGN016 Aging 56 0.072
154
FCT001 Factor Viii Deficiency 55 0.072
155
c MCR120 Microvascular Complications of Diabetes 7 47 0.072
156
P KLZ004 Kala-Azar 1 41 0.072
157
c MCR130 Microvascular Complications of Diabetes 6 41 0.072
158
c MCR133 Microvascular Complications of Diabetes 4 41 0.072
159
CRT055 Creatine Deficiency Syndromes 38 0.072
160
c LKM061 Leukemia, Acute Myeloid 83 0.069
161
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.069
162
IMM167 Immune Deficiency Disease 78 0.069
163
ULC004 Ulcerative Colitis 73 0.069
164
c BTT014 Beta-Thalassemia 72 0.069
165
MLT157 Multiple System Atrophy 1 70 0.069
166
P FRN006 Frontotemporal Dementia 70 0.069
167
P LYM118 Lymphoma 68 0.069
168
c HMP029 Hemophilia a 65 0.069
169
CTR172 Citrullinemia, Classic 64 0.069
170
c PNS012 Paine Syndrome 61 0.069
171
GST033 Gestational Diabetes 57 0.069
172
P NRP001 Neuropathy 56 0.069
173
P HYP076 Hyperthyroidism 55 0.069
174
P BNG032 Benign Mesothelioma 45 0.069
175
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.069
176
PPL052 Papillomatosis, Confluent and Reticulated 34 0.069
177
P OVR042 Ovarian Cancer 89 0.067
178
ACR007 Acromegaly 71 0.067
179
DWN001 Down Syndrome 70 0.067
180
c MGR028 Migraine with or Without Aura 1 69 0.067
181
c ATS007 Autism Spectrum Disorder 67 0.067
182
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.067
183
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.067
184
c SML038 Small Cell Cancer of the Lung 65 0.067
185
HPT019 Hepatic Encephalopathy 60 0.067
186
P CYS018 Cystitis 59 0.067
187
ADN018 Adenoma 58 0.067
188
P PLY011 Polycystic Ovary Syndrome 56 0.067
189
P MTC069 Mitochondrial Disorders 56 0.067
190
LMB062 Limb Ischemia 55 0.067
191
P HYP083 Hypopituitarism 53 0.067
192
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.067
193
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.067
194
P MTC133 Mitochondrial Myopathy 49 0.067
195
VCC001 Vaccinia 49 0.067
196
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.067
197
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.067
198
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.067
199
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.067
200
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.067
201
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.067
202
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.067
203
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.067
204
c SYS001 Systemic Lupus Erythematosus 86 0.064
205
OST012 Osteoarthritis 78 0.064
206
P SCH015 Schizophrenia 75 0.064
207
P MNN013 Meningitis 65 0.064
208
NTR005 Nutritional Deficiency Disease 61 0.064
209
P INT143 Interstitial Cystitis 61 0.064
210
P CTR002 Cataract 60 0.064
211
P PLY014 Polycystic Kidney Disease 59 0.064
212
P INF032 Infertility 57 0.064
213
P MLN007 Male Infertility 56 0.064
214
P SHR001 Short Bowel Syndrome 52 0.064
215
MTB004 Metabolic Acidosis 50 0.064
216
ORN004 Ornithinemia 17 0.064
217
P MJR001 Major Depressive Disorder 68 0.061
218
CHG001 Chagas Disease 66 0.061
219
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.061
220
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.061
221
DCB001 Decubitus Ulcer 60 0.061
222
P BCL017 B-Cell Lymphoma 58 0.061
223
P HDC001 Headache 57 0.061
224
BCT022 Bacterial Infectious Disease 56 0.061
225
ALL006 Allergic Asthma 56 0.061
226
PRP080 Peripheral Artery Disease 53 0.061
227
BNR002 Bone Resorption Disease 48 0.061
228
HRW001 Hair Whorl 36 0.061
229
c DLT002 Dilated Cardiomyopathy 79 0.058
230
c ATR087 Atrial Standstill 1 74 0.058
231
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.058
232
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.058
233
c ALP101 Alpha-Thalassemia 62 0.058
234
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.058
235
INT002 Intermittent Claudication 61 0.058
236
FTT001 Fatty Liver Disease 61 0.058
237
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.058
238
c HPT016 Hepatitis B 59 0.058
239
CHL123 Chlamydia 59 0.058
240
PLM033 Pulmonary Embolism 59 0.058
241
ISL003 Isolated Growth Hormone Deficiency 52 0.058
242
HPT014 Hepatorenal Syndrome 50 0.058
243
HYP781 Hypoascorbemia 50 0.058
244
P RNV001 Renovascular Hypertension 49 0.058
245
URT010 Ureteral Obstruction 46 0.058
246
DWR001 Dwarfism 44 0.058
247
c MLG079 Malignant Pleural Mesothelioma 42 0.058
248
P PRC031 Preeclampsia/eclampsia 1 37 0.058
249
P BLD134 Bladder Cancer 78 0.055
250
OST159 Osteogenic Sarcoma 66 0.055
251
SRC014 Sarcoma 65 0.055
252
c RHB024 Rhabdomyosarcoma 2 65 0.055
253
P ADN016 Adenocarcinoma 64 0.055
254
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.055
255
MDD011 Mood Disorder 62 0.055
256
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.055
257
P BPL003 Bipolar Disorder 56 0.055
258
P FBR017 Fibrosarcoma 56 0.055
259
P INF037 Inflammatory Bowel Disease 56 0.055
260
P LYM031 Lymphocytic Leukemia 55 0.055
261
c PRD040 Periodontitis, Chronic 54 0.055
262
PTT009 Pituitary Gland Disease 54 0.055
263
INT075 Intracranial Hypertension 53 0.055
264
SPN035 Spindle Cell Sarcoma 51 0.055
265
P RNL015 Renal Hypertension 48 0.055
266
c MJR024 Major Affective Disorder 9 41 0.055
267
c MJR022 Major Affective Disorder 8 38 0.055
268
BRN028 Brain Cancer 73 0.052
269
SVR004 Severe Combined Immunodeficiency 73 0.052
270
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
271
P HNT016 Huntington Disease 71 0.052
272
c HPT073 Hepatitis C Virus 70 0.052
273
PLM001 Pulmonary Tuberculosis 70 0.052
274
RCK004 Rickets 69 0.052
275
P PNM007 Pneumonia 68 0.052
276
c HMP004 Hemophilia B 67 0.052
277
MNT001 Mantle Cell Lymphoma 66 0.052
278
ALC007 Alcohol Dependence 66 0.052
279
P LPS002 Liposarcoma 65 0.052
280
P TRN020 Turner Syndrome 65 0.052
281
IDP011 Idiopathic Interstitial Pneumonia 63 0.052
282
c HPT001 Hepatitis C 63 0.052
283
ANR007 Anorexia Nervosa 63 0.052
284
c SCL052 Scleroderma, Familial Progressive 62 0.052
285
P PLM036 Pulmonary Fibrosis 61 0.052
286
c BRN108 Branchiootic Syndrome 1 61 0.052
287
CHL068 Cholestasis 60 0.052
288
ACQ007 Acquired Immunodeficiency Syndrome 60 0.052
289
GNG013 Gingivitis 59 0.052
290
GST045 Gastroenteritis 59 0.052
291
P PRD006 Prader-Willi Syndrome 59 0.052
292
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.052
293
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.052
294
P PRP019 Peripheral Nervous System Disease 57 0.052
295
VSC002 Vascular Dementia 57 0.052
296
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.052
297
HYP005 Hypokalemia 55 0.052
298
PLM010 Pulmonary Edema 55 0.052
299
P ART021 Arteriosclerosis 54 0.052
300
c ACT134 Acute Liver Failure 51 0.052
301
NNL006 Non-Alcoholic Steatohepatitis 51 0.052
302
P OBS001 Obstructive Jaundice 48 0.052
303
P TCL004 T-Cell Leukemia 47 0.052
304
c INH020 Inherited Metabolic Disorder 46 0.052
305
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.052
306
c PCH010 Pachyonychia Congenita 3 43 0.052
307
P MTC004 Mitochondrial Encephalomyopathy 43 0.052
308
P HYP265 Hypotonia 42 0.052
309
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.052
310
CRV035 Cervical Cancer 76 0.049
311
P OST002 Osteoporosis 73 0.049
312
ANX010 Anxiety 72 0.049
313
P CNR004 Cone-Rod Dystrophy 2 71 0.049
314
BRN024 Bronchitis 68 0.049
315
BRK010 Burkitt Lymphoma 67 0.049
316
P HPT021 Hepatitis 67 0.049
317
P SPN046 Spinal Muscular Atrophy 64 0.049
318
CLN015 Colon Adenocarcinoma 63 0.049
319
P HYP750 Hypertriglyceridemia, Familial 61 0.049
320
INS001 Insulinoma 60 0.049
321
SQM006 Squamous Cell Carcinoma 60 0.049
322
PRT058 Pure Autonomic Failure 59 0.049
323
P INT070 Intestinal Obstruction 58 0.049
324
DSS009 Disseminated Intravascular Coagulation 57 0.049
325
THR024 Thrombosis 56 0.049
326
c BCT007 Bacterial Meningitis 55 0.049
327
DBT010 Diabetic Neuropathy 55 0.049
328
CHR100 Chronic Ulcer of Skin 53 0.049
329
P EPD016 Epidermolysis Bullosa 53 0.049
330
GLS018 Glass Syndrome 53 0.049
331
PLS007 Plasmodium Falciparum Malaria 52 0.049
332
PRS045 Prostatic Hypertrophy 52 0.049
333
P CHR345 Chronic Pain 50 0.049
334
ATS010 Autosomal Recessive Disease 48 0.049
335
CRD137 Cardiogenic Shock 48 0.049
336
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.049
337
LYM019 Lymphosarcoma 47 0.049
338
RNL077 Renal Fibrosis 47 0.049
339
HDN002 Head Injury 45 0.049
340
OLG001 Oligospermia 45 0.049
341
NWC001 Newcastle Disease 44 0.049
342
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.049
343
SNG003 Single Ventricular Heart 30 0.049
344
CHL079 Children's Interstitial Lung Disease 27 0.049
345
c HRD156 Hereditary Central Diabetes Insipidus 22 0.049
346
ESP021 Esophageal Cancer 90 0.045
347
c LKM071 Leukemia, Chronic Lymphocytic 79 0.045
348
P MLT020 Multiple Sclerosis 72 0.045
349
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.045
350
P PHC003 Pheochromocytoma 71 0.045
351
LYM133 Lymphoma, Hodgkin, Classic 69 0.045
352
P SLP006 Sleep Apnea 69 0.045
353
ART016 Aortic Aneurysm 68 0.045
354
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
355
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.045
356
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.045
357
P ATR011 Atrial Fibrillation 66 0.045
358
HYP020 Hyperprolactinemia 64 0.045
359
ART002 Arts Syndrome 63 0.045
360
P NTR004 Neutropenia 63 0.045
361
c ACT068 Acute Cystitis 63 0.045
362
c HPT003 Hepatitis a 63 0.045
363
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.045
364
P LYM033 Lymphoproliferative Syndrome 60 0.045
365
ANT009 Antithrombin Iii Deficiency 59 0.045
366
PPT005 Peptic Ulcer Disease 58 0.045
367
P OPT006 Optic Nerve Disease 57 0.045
368
INT030 Intracranial Aneurysm 56 0.045
369
HMG005 Hemoglobinopathy 55 0.045
370
PRP030 Purpura 55 0.045
371
INT007 Intermediate Coronary Syndrome 55 0.045
372
P PTT006 Pituitary Adenoma 54 0.045
373
PRS021 Prostatic Adenoma 51 0.045
374
SPP010 Suppressor of Tumorigenicity 3 51 0.045
375
BWN001 Bowen-Conradi Syndrome 51 0.045
376
ACT017 Acute Chest Syndrome 50 0.045
377
SYS003 Systolic Heart Failure 50 0.045
378
PRS129 Prostatic Hyperplasia, Benign 49 0.045
379
MTC005 Mitochondrial Metabolism Disease 48 0.045
380
RYN005 Raynaud Phenomenon 46 0.045
381
ADR040 Adrenal Gland Pheochromocytoma 46 0.045
382
PTT037 Pituitary Tumors 44 0.045
383
OBS082 Obstructive Nephropathy 43 0.045
384
IDP033 Idiopathic Edema 43 0.045
385
HMP009 Haemophilus Influenzae 42 0.045
386
ALL014 Allergic Encephalomyelitis 39 0.045
387
DPS001 Dipsogenic Diabetes Insipidus 23 0.045
388
P ATX030 Ataxia-Telangiectasia 83 0.041
389
P EPL164 Epilepsy 71 0.041
390
P ART022 Arthritis 70 0.041
391
EWN003 Ewing Sarcoma 68 0.041
392
P LKM062 Leukemia, Acute Lymphoblastic 68 0.041
393
P THR014 Thrombocytopenia 68 0.041
394
PSY004 Psychotic Disorder 67 0.041
395
c MCR129 Microvascular Complications of Diabetes 1 66 0.041
396
GLC006 Galactosemia 65 0.041
397
APN008 Apnea, Obstructive Sleep 65 0.041
398
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.041
399
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.041
400
SKN016 Skin Disease 63 0.041
401
P NPH012 Nephrotic Syndrome 63 0.041
402
TRN015 Transient Cerebral Ischemia 62 0.041
403
P ESP024 Esophagitis 62 0.041
404
P LPS004 Lupus Erythematosus 61 0.041
405
P KDN017 Kidney Cancer 61 0.041
406
PRT013 Portal Hypertension 60 0.041
407
P SCL018 Scoliosis 60 0.041
408
P MYC008 Myocarditis 59 0.041
409
STT001 Status Epilepticus 59 0.041
410
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.041
411
CRD132 Cardiac Conduction Defect 59 0.041
412
ANR040 Aneurysm 58 0.041
413
P ALC033 Alcohol Use Disorder 58 0.041
414
P DNG005 Dengue Virus 57 0.041
415
HMR039 Hemorrhage, Intracerebral 57 0.041
416
PLC005 Placental Insufficiency 57 0.041
417
c ADL017 Adult T-Cell Leukemia 57 0.041
418
SCH003 Schizophreniform Disorder 56 0.041
419
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.041
420
P GST044 Gastritis 55 0.041
421
MCS002 Mucositis 55 0.041
422
P BRT004 Bartter Disease 55 0.041
423
P GRV001 Graves' Disease 55 0.041
424
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.041
425
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.041
426
c OST080 Osteogenesis Imperfecta, Type Ii 55 0.041
427
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 0.041
428
AMN003 Amnestic Disorder 54 0.041
429
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.041
430
P TRM003 Tremor 53 0.041
431
GST023 Gastric Ulcer 53 0.041
432
c VRL010 Viral Hepatitis 51 0.041
433
c VNW010 Von Willebrand Disease, Type 2 51 0.041
434
TLN003 Telangiectasis 51 0.041
435
P FBR031 Febrile Seizures 51 0.041
436
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.041
437
SCH012 Schizoaffective Disorder 50 0.041
438
TRY001 Trypanosomiasis 50 0.041
439
P OVR082 Overgrowth Syndrome 50 0.041
440
CRN030 Coronary Stenosis 50 0.041
441
NPH010 Nephrosclerosis 49 0.041
442
c SVR005 Severe Pre-Eclampsia 49 0.041
443
WTH001 Withdrawal Disorder 48 0.041
444
SXL003 Sexual Disorder 48 0.041
445
SPL018 Splenomegaly 48 0.041
446
PRD004 Prediabetes Syndrome 47 0.041
447
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.041
448
CHL147 Chlamydia Pneumonia 45 0.041
449
SYN036 Syncope 45 0.041
450
ANX004 Anoxia 42 0.041
451
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.041
452
P DNT007 Dentin Sensitivity 35 0.041
453
c PRS136 Prostate Cancer, Hereditary, 6 33 0.041
454
c PRS130 Prostate Cancer, Hereditary, 8 32 0.041
455
RRS014 Rare Surgical Neurologic Disease 32 0.041
456
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.041
457
P GLM040 Glioma Susceptibility 1 81 0.037
458
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.037
459
P LNG064 Lung Cancer Susceptibility 3 77 0.037
460
P RTN008 Retinitis Pigmentosa 77 0.037
461
P PRK057 Parkinson Disease, Late-Onset 76 0.037
462
KPS004 Kaposi Sarcoma 75 0.037
463
P RSP003 Respiratory Failure 74 0.037
464
ACR006 Aceruloplasminemia 73 0.037
465
OTT002 Otitis Media 71 0.037
466
P SRC025 Sarcoidosis 1 70 0.037
467
GST040 Gastric Adenocarcinoma 70 0.037
468
P FRG001 Fragile X Syndrome 68 0.037
469
CRB037 Cerebral Palsy 68 0.037
470
SKN019 Skin Melanoma 67 0.037
471
KRT019 Keratitis, Hereditary 67 0.037
472
CRP001 Carpal Tunnel Syndrome 67 0.037
473
P NSP012 Nasopharyngeal Carcinoma 67 0.037
474
P SKN015 Skin Carcinoma 67 0.037
475
CNN005 Connective Tissue Disease 66 0.037
476
P HYP061 Hypertrophic Cardiomyopathy 66 0.037
477
P HYD006 Hydrocephalus 65 0.037
478
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.037
479
P DYS154 Dystonia 65 0.037
480
P PRS038 Personality Disorder 65 0.037
481
c MCL013 Mucolipidosis Iv 64 0.037
482
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.037
483
PRP083 Porphyria, Acute Intermittent 63 0.037
484
c ART101 Aortic Valve Disease 2 63 0.037
485
P THR117 Three M Syndrome 1 63 0.037
486
MSC152 Muscular Dystrophy, Becker Type 63 0.037
487
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.037
488
P HYP055 Hypoplastic Left Heart Syndrome 62 0.037
489
P HML002 Hemolytic Anemia 62 0.037
490
c FNC043 Fanconi Anemia, Complementation Group E 62 0.037
491
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.037
492
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.037
493
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.037
494
EYD002 Eye Disease 58 0.037
495
P MLN069 Melanoma, Uveal 58 0.037
496
URN010 Urinary Tract Obstruction 57 0.037
497
RNL024 Renal Glucosuria 57 0.037
498
c MST023 Mesothelioma, Malignant 57 0.037
499
SCH014 Schistosomiasis 56 0.037
500
PLS011 Plasmacytoma 56 0.037
501
MTH009 Mouth Disease 56 0.037
502
GST050 Gastrointestinal System Disease 56 0.037
503
VSC003 Visceral Leishmaniasis 55 0.037
504
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.037
505
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.037
506
END040 Endogenous Depression 54 0.037
507
LYM040 Lymphoblastic Lymphoma 54 0.037
508
AMN001 Amenorrhea 54 0.037
509
P CNT005 Central Nervous System Lymphoma 53 0.037
510
SPN008 Spondyloepiphyseal Dysplasia Congenita 52 0.037
511
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.037
512
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.037
513
CRB150 Cerebral Creatine Deficiency Syndrome 2 52 0.037
514
BCT002 Bacterial Vaginosis 52 0.037
515
RYS001 Reye Syndrome 51 0.037
516
BLD053 Blood Platelet Disease 51 0.037
517
FML063 Familial Glucocorticoid Deficiency 51 0.037
518
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
519
HYP081 Hypolipoproteinemia 50 0.037
520
CCC002 Coccidiosis 50 0.037
521
P DDN001 Duodenal Ulcer 50 0.037
522
NTR046 Neutrophil Migration 50 0.037
523
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.037
524
OLF005 Olfactory Neuroblastoma 49 0.037
525
c HPT015 Hepatitis D 49 0.037
526
SLP001 Sleeping Sickness 48 0.037
527
TBR011 Tuberculous Meningitis 48 0.037
528
ART004 Aortic Atherosclerosis 48 0.037
529
ATN005 Autonomic Dysfunction 47 0.037
530
c LRG017 Large Intestine Cancer 47 0.037
531
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.037
532
P BLD051 Blood Coagulation Disease 46 0.037
533
RTN023 Retinitis 46 0.037
534
c MLG068 Malignant Glioma 45 0.037
535
ACT003 Acute Kidney Tubular Necrosis 45 0.037
536
ATN004 Autonomic Neuropathy 44 0.037
537
SBC016 Subacute Delirium 44 0.037
538
CRB090 Cerebral Hypoxia 43 0.037
539
ORL015 Oral Squamous Cell Carcinoma 43 0.037
540
NRR001 Neuroretinitis 43 0.037
541
LWC001 Low Compliance Bladder 42 0.037
542
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.037
543
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.037
544
DYS032 Dystrophinopathies 41 0.037
545
AMN002 Amino Acid Metabolic Disorder 40 0.037
546
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.037
547
CRB086 Cerebral Aneurysms 40 0.037
548
MCC013 Mucocutaneous Ulceration, Chronic 39 0.037
549
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.037
550
HYP110 Hyperproinsulinemia 38 0.037
551
c SCH080 Schizophrenia 3 37 0.037
552
CRB009 Cerebritis 36 0.037
554
RTC003 Root Caries 33 0.037
555
CRB137 Cerebral Creatine Deficiency Syndrome 33 0.037
556
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.037
557
AMN012 Aminoacidopathies 21 0.037
558
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.037
559
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.037
561
MYL069 Myeloma, Multiple 85 0.032
562
GST019 Gastrointestinal Stromal Tumor 76 0.032
563
PHN003 Phenylketonuria 75 0.032
564
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.032
565
CRH001 Crohn's Disease 74 0.032
566
LPT014 Leptin Deficiency or Dysfunction 73 0.032
567
P AMY004 Amyloidosis 70 0.032
568
P TBR001 Tuberous Sclerosis 70 0.032
569
MYL009 Myelodysplastic Syndrome 70 0.032
570
P SYS005 Systemic Scleroderma 70 0.032
571
P PRM011 Primary Ciliary Dyskinesia 69 0.032
572
OBS002 Obsessive-Compulsive Disorder 68 0.032
573
P INF038 Influenza 68 0.032
574
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.032
575
P FLL037 Follicular Lymphoma 66 0.032
576
LPT001 Leptospirosis 66 0.032
577
P HYP098 Hypereosinophilic Syndrome 66 0.032
578
MYC006 Mycosis Fungoides 66 0.032
579
P LNG028 Long Qt Syndrome 65 0.032
580
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.032
581
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.032
582
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.032
583
P MTR014 Motor Neuron Disease 64 0.032
584
MSC007 Muscle Hypertrophy 63 0.032
585
P ADL010 Adult Respiratory Distress Syndrome 63 0.032
586
P ORT004 Orthostatic Intolerance 63 0.032
587
P END044 Endometriosis 62 0.032
588
P ART023 Arthropathy 62 0.032
589
P PSR002 Psoriasis 62 0.032
590
c GLC092 Glaucoma, Primary Open Angle 62 0.032
591
P PRP029 Porphyria 62 0.032
592
CTN007 Cutaneous Leishmaniasis 61 0.032
593
CRC021 Carcinosarcoma 61 0.032
594
P ANP001 Anaplastic Large Cell Lymphoma 61 0.032
595
MSL001 Measles 61 0.032
596
SZR001 Sezary's Disease 60 0.032
597
DPH001 Diphtheria 60 0.032
598
CYS010 Cystinosis 60 0.032
599
P PTN014 Patent Ductus Arteriosus 1 60 0.032
600
P HRD011 Hereditary Spherocytosis 60 0.032
601
CHC001 Chickenpox 60 0.032
602
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.032
603
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.032
604
CHL067 Cholecystitis 58 0.032
605
c ACT073 Acute Leukemia 58 0.032
606
BRS051 Breast Disease 58 0.032
607
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.032
608
MNR012 Meniere Disease 57 0.032
609
BLM002 Bulimia Nervosa 57 0.032
610
P END033 Endocarditis 57 0.032
611
IRN002 Iron Metabolism Disease 57 0.032
612
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.032
613
BRN056 Bronchopulmonary Dysplasia 57 0.032
614
P UVT001 Uveitis 57 0.032
615
P EXN002 Exanthem 57 0.032
616
P EHL001 Ehlers-Danlos Syndrome 57 0.032
617
DSS008 Disease of Mental Health 57 0.032
618
ERY051 Erythroleukemia, Familial 56 0.032
619
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.032
620
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.032
621
SFT003 Soft Tissue Sarcoma 56 0.032
622
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.032
623
ACT058 Active Peptic Ulcer Disease 55 0.032
624
WST005 West Nile Virus 55 0.032
625
P SBS003 Substance Abuse 54 0.032
626
CLL003 Cellulitis 54 0.032
627
P ANG015 Angioedema 54 0.032
628
HMS001 Hemosiderosis 54 0.032
629
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.032
630
OCL022 Ocular Melanoma 53 0.032
631
P RTN016 Retinal Degeneration 53 0.032
632
MRG003 Marginal Zone B-Cell Lymphoma 53 0.032
633
P BRC006 Brachydactyly 53 0.032
634
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.032
635
NRT001 Neurotic Disorder 52 0.032
636
P INT068 Intestinal Disease 52 0.032
637
P HMR003 Hemorrhagic Disease 52 0.032
638
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.032
639
PST011 Pustulosis of Palm and Sole 52 0.032
640
DMY004 Demyelinating Disease 52 0.032
641
P INS002 in Situ Carcinoma 52 0.032
642
OLG003 Oligohydramnios 52 0.032
643
MTN003 Motion Sickness 52 0.032
644
PRV004 Periventricular Leukomalacia 51 0.032
645
HYP014 Hyperuricemia 51 0.032
646
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 51 0.032
647
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 51 0.032
648
GLC004 Galactokinase Deficiency 51 0.032
649
SPL004 Splenic Marginal Zone Lymphoma 51 0.032
650
HRT011 Heart Septal Defect 50 0.032
651
LNG031 Lung Benign Neoplasm 50 0.032
652
CLR109 Colorectal Adenocarcinoma 50 0.032
653
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
654
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.032
655
HYP080 Hypogonadism 50 0.032
656
c ACQ017 Acquired Von Willebrand Syndrome 49 0.032
657
HYP017 Hypophosphatemia 49 0.032
658
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.032
659
P OPN001 Open-Angle Glaucoma 49 0.032
660
P GND004 Gonadal Dysgenesis 49 0.032
661
c FLL041 Follicular Lymphoma 1 49 0.032
662
c OST121 Osteogenesis Imperfecta, Type Iv 49 0.032
663
P CMP008 Compartment Syndrome 48 0.032
664
QDR001 Quadriplegia 48 0.032
665
CRB151 Cerebral Creatine Deficiency Syndrome 1 48 0.032
666
c PRM226 Primary Central Nervous System Lymphoma 47 0.032
667
CMP034 Complete Androgen Insensitivity Syndrome 47 0.032
668
c PRM093 Premature Ovarian Failure 7 47 0.032
669
P CRC039 Coarctation of Aorta 47 0.032
670
c MLG069 Malignant Hypertension 47 0.032
671
P PRC019 Precocious Puberty 47 0.032
672
PLS025 Plasmablastic Lymphoma 47 0.032
673
ANT011 Antisocial Personality Disorder 46 0.032
674
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.032
675
MYC005 Myocardial Stunning 46 0.032
676
PSD009 Pseudohermaphroditism 46 0.032
677
LCK001 Locked-in Syndrome 46 0.032
678
P CTR177 Citrullinemia, Type Ii, Adult-Onset 46 0.032
679
KWS001 Kwashiorkor 45 0.032
680
LYM051 Lymphomatoid Granulomatosis 45 0.032
681
P END084 Endocrine System Disease 44 0.032
683
CRB008 Cerebral Atherosclerosis 44 0.032
684
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.032
685
INT253 Intestinal Benign Neoplasm 44 0.032
686
P GNG009 Gangliosidosis 44 0.032
687
P MJR007 Major Affective Disorder 1 43 0.032
688
c HYP272 Hypercholesterolemia, Familial, 3 43 0.032
689
P CLS010 Cluster Headache 43 0.032
690
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
691
LRG008 Large Granular Lymphocyte Leukemia 41 0.032
692
c MCR112 Microvascular Complications of Diabetes 2 41 0.032
693
HYP064 Hypogonadotropism 40 0.032
694
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.032
695
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 39 0.032
696
c CHR682 Chronic Bilirubin Encephalopathy 38 0.032
697
SCR011 Scrapie 38 0.032
698
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.032
699
IDP070 Idiopathic Scoliosis 37 0.032
700
SML008 Small Intestine Lymphoma 35 0.032
701
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.032
702
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.032
703
HYP114 Hypertensive Nephropathy 34 0.032
704
c MJR003 Major Affective Disorder 6 33 0.032
705
c MJR006 Major Affective Disorder 5 33 0.032
706
PLR005 Pleuropneumonia 32 0.032
707
c RNG008 Ring Chromosome 13 31 0.032
708
INT074 Intracranial Arteriosclerosis 31 0.032
709
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.032
710
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 30 0.032
711
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.032
712
SYN116 Syndromic Obesity 29 0.032
713
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.032
714
CGN007 Cognitive Function 1, Social 28 0.032
715
SHR118 Shrimp Allergy 27 0.032
716
DFC001 Defective Apolipoprotein B-100 27 0.032
717
c RST020 Restless Legs Syndrome 6 25 0.032
718
EXT039 Extrapontine Myelinolysis 18 0.032
719
IDP022 Idiopathic Spinal Cord Herniation 17 0.032
720
c UNP008 Uniparental Disomy of Chromosome 15 15 0.032
721
c FNC027 Fanconi Anemia, Complementation Group a 81 0.026
722
CNN003 Conn's Syndrome 79 0.026
723
P MDL005 Medulloblastoma 77 0.026
724
ADR007 Adrenoleukodystrophy 74 0.026
725
c SPN225 Spondyloarthropathy 1 73 0.026
726
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.026
727
ADN011 Adenoid Cystic Carcinoma 70 0.026
728
P TTR001 Tetralogy of Fallot 69 0.026
729
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.026
730
CRT072 Creutzfeldt-Jakob Disease 69 0.026
731
P TYS001 Tay-Sachs Disease 68 0.026
732
P ALP004 Alport Syndrome 68 0.026
733
c INF071 Inflammatory Bowel Disease 1 68 0.026
734
SND001 Sandhoff Disease 68 0.026
735
P MLG056 Malignant Hyperthermia 67 0.026
736
P DMN002 Dementia 67 0.026
737
c FML001 Familial Atrial Fibrillation 66 0.026
738
AND002 Androgen Insensitivity Syndrome 66 0.026
739
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.026
740
CRN036 Craniopharyngioma 65 0.026
741
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.026
742
CLF027 Cleft Palate, Isolated 64 0.026
743
OST017 Osteomyelitis 64 0.026
744
CLR108 Colorectal Adenoma 64 0.026
745
TBC004 Tobacco Addiction 64 0.026
746
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.026
747
TYP007 Typhoid Fever 63 0.026
748
P ANR048 Aniridia 1 63 0.026
749
PPL049 Papillon-Lefevre Syndrome 63 0.026
750
P HYP069 Hyperparathyroidism 62 0.026
751
DNH001 Donohue Syndrome 62 0.026
752
P VSC011 Vasculitis 62 0.026
753
PSR001 Psoriatic Arthritis 62 0.026
754
HYP780 Hypoadrenocorticism, Familial 62 0.026
755
ALC006 Alcoholic Hepatitis 61 0.026
756
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.026
757
CHR066 Chronic Fatigue Syndrome 61 0.026
758
DRM006 Dermatitis 61 0.026
759
c GM1007 Gm1 Gangliosidosis 61 0.026
760
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.026
761
P SNS001 Sensorineural Hearing Loss 61 0.026
762
VRC005 Varicose Veins 60 0.026
763
P ATR010 Atrial Heart Septal Defect 60 0.026
764
ING001 Inguinal Hernia 60 0.026
765
ACN002 Acanthosis Nigricans 60 0.026
766
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.026
767
CRD223 Cardiac Arrhythmia 60 0.026
768
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.026
769
P VNT002 Ventricular Septal Defect 60 0.026
770
RTN017 Retinal Detachment 60 0.026
771
INT066 Interstitial Lung Disease 59 0.026
772
P ECT006 Ectodermal Dysplasia 59 0.026
773
P WLF004 Wolfram Syndrome 59 0.026
774
HYD002 Hydronephrosis 59 0.026
775
c DNG003 Dengue Disease 59 0.026
776
P BND020 Bone Disease 59 0.026
777
BRN002 Bronchiolitis 59 0.026
778
HLC007 Helicobacter Pylori Infection 59 0.026
779
ANT024 Anthrax Disease 58 0.026
780
PST028 Post-Traumatic Stress Disorder 58 0.026
781
P URT039 Urticaria 58 0.026
782
RBS001 Rabies 58 0.026
783
P FNC044 Fanconi Anemia, Complementation Group C 58 0.026
784
c PRM005 Primary Hyperparathyroidism 58 0.026
785
NWB001 Newborn Respiratory Distress Syndrome 58 0.026
786
c WLF013 Wolfram Syndrome 1 58 0.026
787
CNT047 Contact Dermatitis 57 0.026
788
P CND004 Candidiasis 57 0.026
789
CHR081 Choroideremia 57 0.026
790
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.026
791
P PRV006 Pervasive Developmental Disorder 57 0.026
792
EMB004 Embryonal Carcinoma 57 0.026
793
PLG002 Plague 57 0.026
794
P EPD003 Epidermolysis Bullosa Simplex 56 0.026
795
PRS047 Prostatitis 56 0.026
796
P ALP008 Alopecia 56 0.026
797
LMY014 Leiomyoma, Uterine 56 0.026
798
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 56 0.026
799
CMR002 Coumarin Resistance 56 0.026
800
PTN001 Patent Foramen Ovale 56 0.026
801
PNM008 Pneumothorax 56 0.026
802
ACS001 Acoustic Neuroma 56 0.026
803
P PLY019 Polyneuropathy 56 0.026
804
P PLM034 Pulmonary Emphysema 56 0.026
805
c SVR001 Severe Acute Respiratory Syndrome 55 0.026
806
GRN034 Grange Syndrome 55 0.026
807
c FML035 Familial Hyperlipidemia 55 0.026
808
MCL006 Macular Retinal Edema 55 0.026
809
P PLY018 Polycythemia 55 0.026
810
CPL003 Capillary Leak Syndrome 55 0.026
811
NRN004 Neuroendocrine Tumor 55 0.026
812
P MYP006 Myopia 55 0.026
813
P ANT006 Antiphospholipid Syndrome 54 0.026
814
PRT038 Protein-Energy Malnutrition 54 0.026
815
NRG002 Neurogenic Bladder 54 0.026
816
CRT017 Cartilage Disease 54 0.026
817
PPL022 Papilloma 54 0.026
818
P ICH004 Ichthyosis 54 0.026
819
CRY003 Cryptosporidiosis 54 0.026
820
P LRY044 Larynx Cancer 54 0.026
821
CLR030 Clear Cell Renal Cell Carcinoma 53 0.026
822
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.026
823
MYM001 Myoma 53 0.026
824
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.026
825
P RCT021 Rectum Cancer 53 0.026
826
BRD004 Borderline Personality Disorder 53 0.026
827
KRT009 Keratosis 53 0.026
828
P THY032 Thyroiditis 53 0.026
829
c LTN004 Late-Onset Retinal Degeneration 52 0.026
830
SPN051 Spondylitis 52 0.026
831
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.026
832
P SML001 Small Cell Carcinoma 52 0.026
833
P ACT105 Acute Mountain Sickness 52 0.026
834
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.026
835
PTH003 Pathologic Nystagmus 51 0.026
836
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 51 0.026
837
ILS001 Ileus 51 0.026
838
PRT129 Prothrombin Deficiency, Congenital 51 0.026
839
APR001 Apraxia 51 0.026
840
VSC006 Vascular Cancer 51 0.026
841
GSG001 Gas Gangrene 50 0.026
842
AZS001 Azoospermia 50 0.026
843
RTN003 Retinal Ischemia 50 0.026
844
P FNC004 Fanconi Syndrome 50 0.026
845
SPS003 Spastic Diplegia 50 0.026
846
LMY002 Leiomyoma 50 0.026
847
P AST007 Astrocytoma 50 0.026
848
P MGR003 Migraine with Aura 50 0.026
849
VLV047 Volvulus of Midgut 50 0.026
850
CRT013 Carotid Stenosis 50 0.026
851
P PRT096 Peritoneal Mesothelioma 50 0.026
852
P RNL007 Renal Tubular Acidosis 50 0.026
853
MCP006 Mucoepidermoid Carcinoma 50 0.026
854
STM007 Stomatitis 49 0.026
855
P CTN015 Cutaneous T Cell Lymphoma 49 0.026
856
STT002 Status Asthmaticus 49 0.026
857
FDL002 Food Allergy 49 0.026
858
P MYT002 Myotonic Dystrophy 49 0.026
859
PLC008 Placenta Disease 49 0.026
860
ECT026 Ectopic Pregnancy 49 0.026
861
CLN045 Colonic Benign Neoplasm 49 0.026
862
HPT009 Hepatopulmonary Syndrome 49 0.026
863
KRT002 Keratomalacia 48 0.026
864
GLT035 Glutaric Acidemia I 48 0.026
865
CCN001 Cocaine Dependence 48 0.026
866
IGG001 Iga Glomerulonephritis 48 0.026
867
KHN001 Kuhnt-Junius Degeneration 48 0.026
868
P MGR001 Migraine Without Aura 48 0.026
869
RTN020 Retinal Vascular Disease 48 0.026
870
c HYP837 Hypercholesterolemia, Familial, 2 48 0.026
871
P INN002 Inner Ear Disease 48 0.026
872
ACT084 Acute Stress Disorder 48 0.026
873
GLC106 Glucocorticoid Resistance, Generalized 48 0.026
874
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.026
875
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.026
876
MYL013 Myeloperoxidase Deficiency 46 0.026
877
P PRD021 Periodic Paralysis 46 0.026
878
AYM001 Ayme-Gripp Syndrome 46 0.026
879
ORC001 Orchitis 45 0.026
880
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.026
881
MXD026 Mixed Glioma 45 0.026
882
RSP021 Respiratory Allergy 45 0.026
883
PPL001 Papillary Adenoma 45 0.026
884
CWP001 Cowpox 45 0.026
885
RTR001 Retrograde Amnesia 45 0.026
886
NCT003 N-Acetylglutamate Synthase Deficiency 44 0.026
887
SMN007 Seminoma 44 0.026
888
CRT015 Carotid Artery Occlusion 44 0.026
889
EMP001 Empty Sella Syndrome 44 0.026
890
GNG003 Gingival Recession 44 0.026
891
BCT021 Bacterial Sepsis 44 0.026
892
CNT017 Central Nervous System Origin Vertigo 44 0.026
893
FNC007 Functioning Pituitary Adenoma 44 0.026
894
BRN032 Brain Glioma 43 0.026
895
c PRM038 Primary Agammaglobulinemia 43 0.026
896
LPP002 Lipoprotein Glomerulopathy 43 0.026
897
MRS001 Marasmus 43 0.026
898
TRP009 Triple X Syndrome 42 0.026
899
SQM002 Squamous Cell Papilloma 42 0.026
900
PRS036 Parasitic Protozoa Infectious Disease 42 0.026
901
HYP085 Hypothalamic Disease 42 0.026
902
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.026
903
MYF001 Myofibroma 42 0.026
904
GST020 Gastric Antral Vascular Ectasia 41 0.026
905
MRP001 Morphine Dependence 41 0.026
906
SPS057 Spasticity 41 0.026
907
RDN001 Reading Disorder 40 0.026
908
EXT006 Extrahepatic Cholestasis 40 0.026
909
TXC011 Toxocariasis 40 0.026
910
ISL114 Isolated Growth Hormone Deficiency, Type Ii 40 0.026
911
PTT003 Pituitary-Dependent Cushing's Disease 39 0.026
912
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 39 0.026
913
PRM020 Premenstrual Tension 39 0.026
914
ENT001 Enterocele 39 0.026
915
c MLG074 Malignant Mesenchymoma 39 0.026
916
P HYP111 Hyperprolinemia 39 0.026
917
PRP028 Peripheral Vertigo 39 0.026
918
HMR023 Hemorrhagic Cystitis 38 0.026
919
c ALB024 Albinism, Ocular, Type I 38 0.026
920
THR123 Thrombotic Microangiopathy 38 0.026
921
c OVR114 Ovarian Cancer 1 38 0.026
922
ADR022 Adrenomyeloneuropathy 38 0.026
923
c HNT011 Huntington Disease-Like 3 38 0.026
924
AMN006 Aminoaciduria 38 0.026
925
PLC009 Placenta Praevia 37 0.026
926
ANT019 Anterograde Amnesia 37 0.026
927
SCR003 Secretory Diarrhea 36 0.026
928
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.026
929
MYT011 Myotonia 35 0.026
930
c MJR008 Major Affective Disorder 2 34 0.026
931
ART010 Arteriolosclerosis 34 0.026
932
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.026
933
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.026
934
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.026
935
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.026
936
c MJR023 Major Affective Disorder 7 33 0.026
937
MLC004 Mulchandani-Bhoj-Conlin Syndrome 32 0.026
938
c FBR072 Febrile Seizures, Familial, 11 32 0.026
939
INF009 Inflammatory Spondylopathy 32 0.026
940
MLT116 Multiple System Atrophy, Parkinsonian Type 31 0.026
941
SBM005 Submucous Uterine Fibroid 30 0.026
942
ENM001 Enamel Caries 30 0.026
943
INT082 Intraocular Retinoblastoma 29 0.026
944
THY069 Thyroid Hormone Resistance, Selective Pituitary 29 0.026
945
c MJR004 Major Affective Disorder 4 28 0.026
946
ARG004 Argyria 28 0.026
947
CYT018 Cytochrome P450 2d6 Variant 27 0.026
948
ENM002 Enamel Erosion 27 0.026
949
MST020 Mast Cell Activation Syndrome 27 0.026
950
c RNG015 Ring Chromosome 2 26 0.026
951
HYP144 Hyperacusis 23 0.026
952
c DMN005 Diamond-Blackfan Anemia 2 23 0.026
953
P ART034 Aortopulmonary Window 23 0.026
954
MD2001 Med23 22 0.026
955
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.026
957
c CHR695 Chronic Primary Adrenal Insufficiency 19 0.026
958
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.026
959
PFF001 Pfeiffer Syndrome 79 0.018
960
c TBR025 Tuberous Sclerosis 1 76 0.018
961
P NRF023 Neurofibromatosis, Type Ii 76 0.018
962
MRF001 Marfan Syndrome 75 0.018
963
END057 Endometrial Cancer 74 0.018
964
c MNN043 Meningioma, Familial 74 0.018
965
P GRF003 Graft-Versus-Host Disease 71 0.018
966
c LKM063 Leukemia, Chronic Myeloid 71 0.018
967
P OST001 Osteopetrosis 71 0.018
968
APR006 Apert Syndrome 70 0.018
969
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.018
970
P DMN001 Diamond-Blackfan Anemia 69 0.018
971
P OCL013 Oculodentodigital Dysplasia 69 0.018
972
c BSL007 Basal Cell Carcinoma 68 0.018
973
P CRN037 Craniosynostosis 68 0.018
974
c FML021 Familial Hypercholesterolemia 68 0.018
975
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.018
976
PNC129 Pancreatic Adenocarcinoma 67 0.018
977
CHL065 Cholangiocarcinoma 67 0.018
978
CMM004 Common Variable Immunodeficiency 67 0.018
979
ALL003 Allergic Rhinitis 67 0.018
980
P LPR021 Leprosy 3 67 0.018
981
MLD001 Melioidosis 67 0.018
982
STH001 Saethre-Chotzen Syndrome 67 0.018
983
BLM001 Bloom Syndrome 66 0.018
984
P DRM053 Dermatitis, Atopic 66 0.018
985
P MTR004 Maturity-Onset Diabetes of the Young 66 0.018
986
FCT007 Factor Vii Deficiency 66 0.018
987
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.018
988
PRP001 Propionic Acidemia 66 0.018
989
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.018
990
P ASP006 Aspergillosis 66 0.018
991
P LYS001 Loeys-Dietz Syndrome 66 0.018
992
MRK001 Merkel Cell Carcinoma 66 0.018
993
P CNJ013 Conjunctivitis 65 0.018
994
c CNG006 Congenital Hypothyroidism 65 0.018
995
LNG039 Lung Squamous Cell Carcinoma 65 0.018
996
DRM014 Dermatofibrosarcoma Protuberans 65 0.018
997
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.018
998
P BLD062 Bile Duct Cancer 65 0.018
999
AFB002 Afibrinogenemia, Congenital 65 0.018
1000
GST092 Gastroesophageal Reflux 65 0.018
1001
P THY023 Thymoma 65 0.018
1002
BRR014 Barrett Esophagus 64 0.018
1003
KWS002 Kawasaki Disease 64 0.018
1004
P CHR071 Charcot-Marie-Tooth Disease 64 0.018
1005
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.018
1006
TTN003 Tetanus 64 0.018
1007
KHL003 Kohlschutter-Tonz Syndrome 64 0.018
1008
IRR002 Irritable Bowel Syndrome 63 0.018
1009
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.018
1010
P MST009 Mastocytosis 63 0.018
1011
NRM005 Neuromuscular Disease 63 0.018
1012
NRR002 Norrie Disease 63 0.018
1013
OVR029 Ovarian Hyperstimulation Syndrome 63 0.018
1014
LRN002 Laron Syndrome 63 0.018
1015
P MCH002 Machado-Joseph Disease 63 0.018
1016
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.018
1017
P CTS001 Cutis Laxa 62 0.018
1018
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.018
1019
HSH003 Hashimoto Thyroiditis 62 0.018
1020
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.018
1021
MNN042 Meningioma, Radiation-Induced 62 0.018
1022
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 62 0.018
1023
c ANM038 Anemia, Autoimmune Hemolytic 61 0.018
1024
P MVM001 Movement Disease 61 0.018
1025
P HMN010 Hemangioma 61 0.018
1026
c GLY060 Glycogen Storage Disease Ia 61 0.018
1027
P ENC004 Encephalitis 61 0.018
1028
P HYP097 Hyperekplexia 61 0.018
1029
c HRD002 Hereditary Angioedema 61 0.018
1030
VRL011 Viral Infectious Disease 61 0.018
1031
P OCL002 Oculocutaneous Albinism 60 0.018
1032
P NRM001 Neuromyelitis Optica 60 0.018
1033
P BRN019 Bernard-Soulier Syndrome 60 0.018
1034
YLL002 Yellow Fever 60 0.018
1035
P SLV026 Salivary Gland Carcinoma 60 0.018
1036
P TXP001 Toxoplasmosis 60 0.018
1037
P NMN002 Niemann-Pick Disease 60 0.018
1038
ORL011 Oral Cancer 60 0.018
1039
HRP004 Herpes Zoster 60 0.018
1040
ETN001 Eating Disorder 59 0.018
1041
P GLY013 Glycogen Storage Disease 59 0.018
1042
c VSC019 Vesicoureteral Reflux 1 59 0.018
1043
THY029 Thyroid Carcinoma 59 0.018
1044
MXD005 Mixed Connective Tissue Disease 59 0.018
1045
P BRN022 Bronchiectasis 59 0.018
1046
P TRC086 Trichohepatoenteric Syndrome 1 59 0.018
1047
P SYP003 Syphilis 59 0.018
1048
MNK003 Muenke Syndrome 59 0.018
1049
P WRD001 Waardenburg's Syndrome 59 0.018
1050
HYP052 Hyperkalemic Periodic Paralysis 59 0.018
1051
FBR047 Fibromyalgia 59 0.018
1052
c SPN301 Spinocerebellar Ataxia 2 59 0.018
1053
P RBL001 Rubella 58 0.018
1054
c LNG047 Long Qt Syndrome 2 58 0.018
1055
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.018
1056
CMP010 Complex Regional Pain Syndrome 58 0.018
1057
P FCL005 Focal Segmental Glomerulosclerosis 58 0.018
1058
LNG108 Langerhans Cell Histiocytosis 58 0.018
1059
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.018
1060
c MCP004 Mucopolysaccharidosis Iv 58 0.018
1061
P MCR010 Microcephaly 58 0.018
1062
c NMN016 Niemann-Pick Disease, Type B 58 0.018
1063
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.018
1064
c DWL002 Dowling-Degos Disease 1 58 0.018
1065
CNS004 Constipation 57 0.018
1066
GLB001 Gilbert Syndrome 57 0.018
1067
P EPD083 Epidermodysplasia Verruciformis 1 57 0.018
1068
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.018
1069
CPR004 Coproporphyria, Hereditary 57 0.018
1070
LYM027 Lymphopenia 57 0.018
1071
P RHN004 Rhinitis 57 0.018
1072
BLR008 Bilirubin Metabolic Disorder 57 0.018
1073
P BNC003 Bone Cancer 57 0.018
1074
P PRN023 Prion Disease 57 0.018
1075
DNT005 Dentatorubral-