Search results for Insulin, Globin Zinc

1093 hits were found for Insulin, Globin Zinc

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 66 0.818
2
INS024 Insulin-Like Growth Factor I 79 0.749
3
P DBT009 Diabetes Mellitus 64 0.719
4
HYP060 Hyperinsulinism 54 0.588
5
HYP066 Hyperglycemia 61 0.571
6
c DBT099 Diabetes Mellitus, Type I 65 0.568
7
P THL005 Thalassemia 60 0.551
8
c BTT014 Beta-Thalassemia 74 0.380
9
P PLY011 Polycystic Ovary Syndrome 56 0.352
10
FTT001 Fatty Liver Disease 61 0.323
11
ERY051 Erythroleukemia, Familial 56 0.313
12
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.309
13
P LVR013 Liver Disease 68 0.308
14
INS001 Insulinoma 60 0.291
15
P SCK005 Sickle Cell Disease 50 0.280
16
P KDN018 Kidney Disease 72 0.279
17
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.277
18
P DRR001 Diarrhea 55 0.272
19
LVR012 Liver Cirrhosis 62 0.271
20
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.266
21
IRN002 Iron Metabolism Disease 57 0.266
22
SCK003 Sickle Cell Anemia 74 0.252
23
c HYP595 Hypertension, Essential 84 0.249
24
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.248
25
48X005 48,xyyy 39 0.242
26
DFC004 Deficiency Anemia 70 0.242
27
ATH013 Atherosclerosis Susceptibility 65 0.241
28
P ALZ034 Alzheimer Disease 88 0.240
29
P HYP750 Hypertriglyceridemia, Familial 62 0.237
30
HLX001 Helix Syndrome 47 0.237
31
ALL026 Allergic Hypersensitivity Disease 62 0.236
32
HMG005 Hemoglobinopathy 56 0.231
33
c ALP101 Alpha-Thalassemia 62 0.228
34
OCL069 Ocular Motor Apraxia 51 0.223
35
P CRN300 Coronary Heart Disease 1 63 0.220
36
P VSC007 Vascular Disease 63 0.220
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.213
38
NTR005 Nutritional Deficiency Disease 62 0.210
39
ATM095 Autoimmune Disease 62 0.210
40
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.209
41
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.209
42
P PRS040 Prostate Cancer 97 0.208
43
ACT088 Acute Insulin Response 41 0.208
44
P CLR023 Colorectal Cancer 99 0.207
45
ISC004 Ischemia 58 0.199
46
ACN002 Acanthosis Nigricans 60 0.198
47
P HYP086 Hypothyroidism 69 0.197
48
P NRB001 Neuroblastoma 72 0.192
49
PRT037 Pertussis 65 0.190
50
c CHR684 Chronic Kidney Disease 70 0.190
51
c PRC016 Pre-Eclampsia 63 0.189
52
HYP043 Hyperandrogenism 48 0.185
53
LPP008 Lipoprotein Quantitative Trait Locus 62 0.183
54
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.182
55
CYT002 Cytokine Deficiency 42 0.180
56
c NRF023 Neurofibromatosis, Type Ii 80 0.180
57
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.176
58
END086 End Stage Renal Disease 51 0.176
59
P LTR001 Lateral Sclerosis 54 0.176
60
CYS001 Cystic Fibrosis 81 0.174
61
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.173
62
RCK004 Rickets 68 0.172
63
ACR007 Acromegaly 71 0.171
64
HYP080 Hypogonadism 50 0.170
65
P HRT032 Heart Disease 75 0.170
66
DWN001 Down Syndrome 70 0.169
67
BNR002 Bone Resorption Disease 48 0.168
68
P HPT023 Hepatocellular Carcinoma 100 0.168
69
c ACT075 Acute Myocardial Infarction 57 0.167
70
c HYP836 Hypercholesterolemia, Familial, 1 73 0.166
71
ADN018 Adenoma 59 0.164
72
CHL079 Children's Interstitial Lung Disease 26 0.164
73
HRW001 Hair Whorl 36 0.164
74
HYP266 Hypoxia 57 0.163
75
P HYP076 Hyperthyroidism 55 0.163
76
ART140 Arteries, Anomalies of 52 0.162
77
PPL052 Papillomatosis, Confluent and Reticulated 33 0.162
78
P PNC035 Pancreatic Cancer 84 0.161
79
P ALP008 Alopecia 54 0.160
80
AGN016 Aging 56 0.160
81
DRM006 Dermatitis 61 0.159
82
47X002 47,xyy 49 0.159
83
ANR007 Anorexia Nervosa 63 0.157
84
URM002 Uremia 49 0.154
85
P TRN020 Turner Syndrome 67 0.153
86
OST159 Osteogenic Sarcoma 66 0.152
87
P INF032 Infertility 57 0.151
88
HMS001 Hemosiderosis 54 0.151
89
P RRH023 Rare Hereditary Hemochromatosis 41 0.150
90
IRN001 Iron Deficiency Anemia 59 0.150
91
P LNG032 Lung Cancer 98 0.148
92
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.148
93
P LKM002 Leukemia 68 0.148
94
ATX019 Ataxia with Vitamin E Deficiency 42 0.148
95
P OST002 Osteoporosis 74 0.146
96
P HML002 Hemolytic Anemia 63 0.145
97
P HRP006 Herpes Simplex 65 0.144
98
GRW007 Growth Hormone Deficiency 46 0.144
99
P PNC044 Pancreatitis 61 0.144
100
HMN044 Human Immunodeficiency Virus Type 1 71 0.143
101
P PRP019 Peripheral Nervous System Disease 58 0.143
102
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.142
103
HYP005 Hypokalemia 55 0.142
104
DPR016 Depression 63 0.139
105
P ENC018 Encephalopathy 61 0.136
106
P PSR002 Psoriasis 62 0.136
107
PST011 Pustulosis of Palm and Sole 52 0.136
108
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.136
109
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.136
110
CRB039 Cerebrovascular Disease 67 0.134
111
P RTN024 Retinoblastoma 73 0.134
112
P CTR002 Cataract 60 0.133
113
ATS010 Autosomal Recessive Disease 48 0.133
114
MLR004 Malaria 81 0.133
115
ATN004 Autonomic Neuropathy 45 0.132
116
P OVR042 Ovarian Cancer 88 0.132
117
P PRD008 Periodontitis 64 0.131
118
P ADN016 Adenocarcinoma 64 0.131
119
DNH001 Donohue Syndrome 62 0.130
120
P PNM007 Pneumonia 68 0.130
121
DBT010 Diabetic Neuropathy 54 0.129
122
c DRR009 Diarrhea 6 46 0.129
124
c FML008 Familial Retinoblastoma 53 0.128
125
c ACT027 Acute Pancreatitis 60 0.128
126
P SLP006 Sleep Apnea 69 0.128
127
STR067 Stroke, Ischemic 81 0.127
128
ALC007 Alcohol Dependence 66 0.126
129
ADL002 Adult Syndrome 70 0.126
130
P AMY004 Amyloidosis 70 0.125
131
P GLM045 Glioma 63 0.125
132
END057 Endometrial Cancer 74 0.125
133
MNT002 Mental Depression 58 0.124
134
GLL048 Glial Tumor 45 0.124
135
P RHM011 Rheumatoid Arthritis 80 0.124
136
P MTR004 Maturity-Onset Diabetes of the Young 65 0.123
137
P GRV001 Graves' Disease 55 0.123
138
CRH001 Crohn's Disease 74 0.123
139
SVR004 Severe Combined Immunodeficiency 73 0.122
140
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.121
141
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.120
142
TRM010 Traumatic Brain Injury 51 0.120
143
SKN016 Skin Disease 63 0.120
144
IMM167 Immune Deficiency Disease 78 0.120
145
P OVR082 Overgrowth Syndrome 50 0.119
146
c PRM038 Primary Agammaglobulinemia 44 0.119
147
MTB004 Metabolic Acidosis 50 0.119
148
PRP027 Peripheral Vascular Disease 71 0.118
149
c WLM018 Wilms Tumor 5 61 0.118
150
BRN071 Brain Injury 49 0.118
151
P ART021 Arteriosclerosis 54 0.117
152
c MCR129 Microvascular Complications of Diabetes 1 66 0.117
153
c ACT071 Acute Kidney Failure 60 0.117
154
GLB015 Glioblastoma Multiforme 75 0.115
155
TXC005 Toxic Shock Syndrome 62 0.114
156
ESP021 Esophageal Cancer 90 0.114
157
P MSC003 Muscular Atrophy 52 0.114
158
P SZR006 Seizure Disorder 56 0.113
159
SPL018 Splenomegaly 48 0.113
160
BLR008 Bilirubin Metabolic Disorder 57 0.113
161
P BCL017 B-Cell Lymphoma 58 0.113
162
P THY032 Thyroiditis 52 0.113
163
P INF037 Inflammatory Bowel Disease 54 0.113
164
P DMN002 Dementia 66 0.112
165
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.112
166
SQM006 Squamous Cell Carcinoma 60 0.112
167
LNG099 Lung Disease 60 0.112
168
P ECL001 Eclampsia 50 0.111
169
ANV001 Anovulation 47 0.111
170
P PHC003 Pheochromocytoma 71 0.111
171
HYP014 Hyperuricemia 52 0.110
172
OST012 Osteoarthritis 78 0.109
173
P HYP069 Hyperparathyroidism 63 0.109
174
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.109
175
CRV035 Cervical Cancer 76 0.109
176
ADR040 Adrenal Gland Pheochromocytoma 46 0.109
177
P MYT002 Myotonic Dystrophy 49 0.108
178
P ALC033 Alcohol Use Disorder 58 0.108
179
VSL002 Visual Epilepsy 59 0.108
180
HPT004 Hepatic Coma 45 0.108
181
ETN001 Eating Disorder 60 0.108
182
PLM001 Pulmonary Tuberculosis 69 0.107
183
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.107
184
P EXN002 Exanthem 57 0.106
185
P ATS364 Autism 70 0.106
186
P MLN007 Male Infertility 55 0.106
187
P MSC005 Muscular Dystrophy 66 0.106
188
ACD008 Acid-Labile Subunit Deficiency 54 0.105
189
IMP005 Impotence 52 0.105
190
P CLC063 Celiac Disease 1 66 0.105
191
ANG054 Angina Pectoris 66 0.105
192
P SCH015 Schizophrenia 74 0.105
193
c HPT016 Hepatitis B 59 0.105
194
MSC007 Muscle Hypertrophy 64 0.104
195
ANX010 Anxiety 73 0.104
196
GNG013 Gingivitis 59 0.104
197
THY029 Thyroid Carcinoma 59 0.103
198
ARG004 Argyria 27 0.103
199
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.103
200
HPT019 Hepatic Encephalopathy 60 0.103
201
c HNT004 Huntington Disease-Like 2 50 0.102
202
PLY150 Polykaryocytosis Inducer 31 0.102
203
MYL069 Myeloma, Multiple 85 0.102
204
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.102
205
ACQ007 Acquired Immunodeficiency Syndrome 60 0.101
206
P NPH012 Nephrotic Syndrome 60 0.101
207
P PLY019 Polyneuropathy 56 0.101
208
TTN003 Tetanus 65 0.101
209
PPT005 Peptic Ulcer Disease 59 0.101
210
P ART022 Arthritis 69 0.100
211
MDD011 Mood Disorder 62 0.100
212
P RHB003 Rhabdomyosarcoma 63 0.100
213
P MJR001 Major Depressive Disorder 68 0.099
214
c SYS001 Systemic Lupus Erythematosus 86 0.098
215
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 57 0.098
216
PLC008 Placenta Disease 50 0.098
217
c FML035 Familial Hyperlipidemia 55 0.097
218
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.097
219
c GRV008 Graves Disease 1 56 0.097
220
PTT037 Pituitary Tumors 44 0.096
221
EYD002 Eye Disease 58 0.096
222
P LNG064 Lung Cancer Susceptibility 3 78 0.096
223
P MYL006 Myeloid Leukemia 60 0.096
224
LRN002 Laron Syndrome 62 0.096
225
P HYP083 Hypopituitarism 53 0.096
226
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 39 0.095
227
P MYP004 Myopathy 70 0.095
228
c VRL010 Viral Hepatitis 52 0.095
229
P CRD119 Cardiac Arrest 67 0.095
230
GST023 Gastric Ulcer 53 0.095
231
P GLM007 Glomerulonephritis 57 0.095
232
P BPL003 Bipolar Disorder 56 0.095
233
NRL016 Neural Tube Defects 82 0.095
234
P MLN008 Melanoma 69 0.094
235
c MJR024 Major Affective Disorder 9 41 0.094
236
c MJR022 Major Affective Disorder 8 38 0.094
237
ATN005 Autonomic Dysfunction 46 0.094
238
c ATS007 Autism Spectrum Disorder 67 0.094
239
c LKM061 Leukemia, Acute Myeloid 84 0.094
240
P LPS004 Lupus Erythematosus 61 0.094
241
AMN001 Amenorrhea 54 0.093
242
P HMG032 Hemoglobin H Disease 52 0.093
243
SRC014 Sarcoma 65 0.093
244
c HNT011 Huntington Disease-Like 3 38 0.093
245
c HMC039 Hemochromatosis, Type 1 74 0.093
246
P ATX030 Ataxia-Telangiectasia 82 0.092
247
BCT022 Bacterial Infectious Disease 56 0.092
248
P OVR049 Ovarian Disease 52 0.092
249
c PLY105 Polycystic Ovary Syndrome 1 38 0.092
250
P LYM118 Lymphoma 68 0.092
251
c SVR001 Severe Acute Respiratory Syndrome 62 0.091
252
P NTR004 Neutropenia 63 0.091
253
MYL009 Myelodysplastic Syndrome 70 0.091
254
CLR108 Colorectal Adenoma 64 0.091
255
AST005 Asthma 76 0.090
256
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.090
257
STM007 Stomatitis 50 0.089
258
GST045 Gastroenteritis 59 0.089
259
BRT037 Brittle Diabetes 25 0.089
260
FST010 Fasting Hypoglycemia 35 0.088
261
HYP781 Hypoascorbemia 51 0.088
262
c HMG003 Hemoglobin E Disease 45 0.088
263
P BND020 Bone Disease 59 0.087
264
ISL001 Islet Cell Tumor 56 0.087
265
TLN003 Telangiectasis 52 0.086
266
PRT036 Peritonitis 64 0.086
267
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.086
268
DYS015 Dysentery 52 0.086
269
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.086
270
HYP020 Hyperprolactinemia 64 0.086
271
CLT003 Colitis 62 0.085
272
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.085
273
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.085
274
CLN015 Colon Adenocarcinoma 65 0.085
275
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.085
276
c BRN108 Branchiootic Syndrome 1 62 0.084
277
CHR178 Chromosomal Triplication 35 0.084
278
PNC129 Pancreatic Adenocarcinoma 68 0.084
279
P TRC086 Trichohepatoenteric Syndrome 1 62 0.084
280
MCS002 Mucositis 56 0.084
281
P NNT009 Neonatal Diabetes Mellitus 50 0.084
282
MCR018 Microcytic Anemia 47 0.083
283
P DRM053 Dermatitis, Atopic 66 0.083
284
P ANR048 Aniridia 1 63 0.083
285
THY030 Thyroid Gland Disease 52 0.083
286
c ACT068 Acute Cystitis 63 0.083
288
SPN035 Spindle Cell Sarcoma 53 0.083
289
c PRM005 Primary Hyperparathyroidism 58 0.082
290
OVR094 Ovarian Epithelial Cancer 38 0.082
291
EMB004 Embryonal Carcinoma 56 0.082
292
ORL015 Oral Squamous Cell Carcinoma 43 0.082
293
P LCT001 Lactic Acidosis 51 0.082
294
P SPP010 Suppressor of Tumorigenicity 3 51 0.082
295
P GST044 Gastritis 56 0.082
296
P SKN015 Skin Carcinoma 66 0.081
297
GT001 Gout 64 0.081
298
P END044 Endometriosis 63 0.081
299
BRK010 Burkitt Lymphoma 67 0.081
300
P ALP009 Alopecia Areata 60 0.080
301
FTL021 Fetal Macrosomia 42 0.080
302
ORL011 Oral Cancer 60 0.080
303
ANX004 Anoxia 40 0.079
304
P TRM003 Tremor 54 0.079
305
P PLY014 Polycystic Kidney Disease 62 0.079
306
c SPN225 Spondyloarthropathy 1 73 0.079
307
RTN023 Retinitis 46 0.079
308
NRR001 Neuroretinitis 42 0.079
309
HMC014 Homocysteinemia 53 0.079
310
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.079
311
PPL022 Papilloma 54 0.078
312
P URT039 Urticaria 58 0.078
313
VSC002 Vascular Dementia 57 0.078
314
DPH001 Diphtheria 60 0.078
315
BRS051 Breast Disease 58 0.077
316
c FNC043 Fanconi Anemia, Complementation Group E 62 0.077
317
P HYP730 Hypogonadotropic Hypogonadism 52 0.077
318
P MLT020 Multiple Sclerosis 72 0.077
319
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.077
320
GLC008 Glucose Metabolism Disease 40 0.077
321
PLM010 Pulmonary Edema 54 0.077
322
HYD038 Hydrops Fetalis, Nonimmune 62 0.076
323
c WLM013 Wilms Tumor 1 65 0.076
324
SXL003 Sexual Disorder 47 0.076
325
P GND004 Gonadal Dysgenesis 48 0.076
326
c CHR682 Chronic Bilirubin Encephalopathy 39 0.076
327
P PLM037 Pulmonary Hypertension 67 0.076
328
P PLM036 Pulmonary Fibrosis 65 0.076
329
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.075
330
P PRK057 Parkinson Disease, Late-Onset 78 0.075
331
EWN003 Ewing Sarcoma 69 0.075
332
HSH003 Hashimoto Thyroiditis 62 0.075
333
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.075
334
P ADL010 Adult Respiratory Distress Syndrome 65 0.075
335
VRL011 Viral Infectious Disease 61 0.075
336
CHG001 Chagas Disease 66 0.075
337
PRT013 Portal Hypertension 59 0.075
338
CVD001 Covid-19 44 0.075
339
P MDL005 Medulloblastoma 77 0.075
340
P MTR014 Motor Neuron Disease 65 0.074
341
c ACT073 Acute Leukemia 58 0.074
342
c EXD008 Exudative Vitreoretinopathy 1 71 0.074
343
c SCN007 Secondary Hyperparathyroidism 51 0.074
344
ISL003 Isolated Growth Hormone Deficiency 49 0.074
345
P KDN017 Kidney Cancer 60 0.074
346
c PRD040 Periodontitis, Chronic 53 0.074
347
INT007 Intermediate Coronary Syndrome 55 0.074
348
P PRD006 Prader-Willi Syndrome 59 0.074
349
P CHN012 Chondrosarcoma 56 0.074
350
HYP001 Hypochromic Microcytic Anemia 38 0.074
351
P MCR010 Microcephaly 59 0.074
352
P BNG032 Benign Mesothelioma 46 0.073
353
NPH009 Nephrolithiasis 55 0.073
354
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.073
355
P PTT006 Pituitary Adenoma 55 0.073
356
49X006 49, Xxxxy Syndrome 41 0.073
357
KHL003 Kohlschutter-Tonz Syndrome 65 0.073
358
c DBT103 Diabetes Mellitus, Permanent Neonatal 4 46 0.072
359
BRR012 Berardinelli-Seip Congenital Lipodystrophy 49 0.072
360
MSL001 Measles 62 0.072
361
ART016 Aortic Aneurysm 69 0.072
362
CRD137 Cardiogenic Shock 47 0.071
363
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.071
364
P RTN018 Retinal Disease 53 0.071
365
P END084 Endocrine System Disease 45 0.071
366
WRN001 Werner Syndrome 69 0.071
367
TRN015 Transient Cerebral Ischemia 63 0.071
368
P RSP003 Respiratory Failure 74 0.071
369
P SYS005 Systemic Scleroderma 68 0.071
370
CHR100 Chronic Ulcer of Skin 55 0.070
371
APN008 Apnea, Obstructive Sleep 64 0.070
372
P EPL164 Epilepsy 71 0.070
373
THR013 Thoracic Outlet Syndrome 54 0.069
374
FBR047 Fibromyalgia 58 0.069
375
P NSP012 Nasopharyngeal Carcinoma 66 0.069
376
c LKM063 Leukemia, Chronic Myeloid 72 0.069
377
VCC001 Vaccinia 49 0.069
378
SQM002 Squamous Cell Papilloma 46 0.069
379
GST020 Gastric Antral Vascular Ectasia 41 0.068
380
P AST007 Astrocytoma 51 0.068
381
INT002 Intermittent Claudication 61 0.068
382
TRT001 Teratocarcinoma 45 0.068
383
ALC006 Alcoholic Hepatitis 61 0.068
384
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.068
385
c CNG012 Congenital Generalized Lipodystrophy 52 0.068
386
P MMP001 Mumps 58 0.068
387
BLM002 Bulimia Nervosa 57 0.068
388
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.067
389
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.067
390
P RTN008 Retinitis Pigmentosa 79 0.067
391
P HYP061 Hypertrophic Cardiomyopathy 70 0.067
392
c DWL002 Dowling-Degos Disease 1 58 0.067
393
RST023 Resting Heart Rate, Variation in 41 0.067
394
P PRN023 Prion Disease 57 0.067
395
P SBR004 Seborrheic Dermatitis 45 0.067
396
CNN003 Conn's Syndrome 79 0.066
397
DSS008 Disease of Mental Health 58 0.066
398
HDN002 Head Injury 46 0.066
399
LYM133 Lymphoma, Hodgkin, Classic 69 0.066
400
NWB001 Newborn Respiratory Distress Syndrome 58 0.066
401
P ATR011 Atrial Fibrillation 66 0.066
402
PRP080 Peripheral Artery Disease 53 0.066
403
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 0.066
404
BRN024 Bronchitis 68 0.066
405
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.066
406
END040 Endogenous Depression 55 0.066
407
MSC157 Muscular Dystrophy, Duchenne Type 72 0.066
408
P PLY018 Polycythemia 56 0.066
409
P GLM040 Glioma Susceptibility 1 81 0.065
410
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.065
411
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.065
412
CHL123 Chlamydia 59 0.065
413
GST050 Gastrointestinal System Disease 56 0.065
414
PST021 Postpartum Depression 50 0.065
415
P RHN004 Rhinitis 57 0.065
416
P RCT021 Rectum Cancer 52 0.065
417
GST092 Gastroesophageal Reflux 67 0.065
418
c MGR028 Migraine with or Without Aura 1 67 0.064
419
MNG006 Monogenic Diabetes 46 0.064
420
PSY004 Psychotic Disorder 67 0.064
421
BRN056 Bronchopulmonary Dysplasia 57 0.064
422
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.064
423
ACT064 Acute Necrotizing Encephalitis 33 0.064
424
ATX010 Ataxia Neuropathy Spectrum 34 0.064
425
BLD137 Blood Group--Ahonen 16 0.064
426
P INS002 in Situ Carcinoma 53 0.064
427
c PNC106 Pancreatic Agenesis 1 51 0.064
428
HYP784 Hypogonadism, Male 40 0.064
429
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.064
430
DBT008 Diabetic Angiopathy 44 0.064
431
c GLL024 Gallbladder Disease 1 53 0.064
432
P MYC084 Mycobacterium Tuberculosis 1 68 0.064
433
P LCH002 Lichen Planus 53 0.064
434
ANR040 Aneurysm 59 0.064
435
ATM052 Autoimmune Disease 1 37 0.063
436
P THR014 Thrombocytopenia 67 0.063
437
MCL006 Macular Retinal Edema 55 0.063
438
PTT009 Pituitary Gland Disease 54 0.063
439
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.063
440
CHC001 Chickenpox 60 0.063
441
DMP001 Dumping Syndrome 44 0.063
442
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.063
443
P CHR345 Chronic Pain 44 0.063
444
SBC016 Subacute Delirium 44 0.063
445
P RBL001 Rubella 59 0.063
446
c MLG068 Malignant Glioma 46 0.063
447
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.063
448
PRT058 Pure Autonomic Failure 59 0.063
449
AZS001 Azoospermia 50 0.062
450
P RTT002 Rett Syndrome 80 0.062
451
OLG001 Oligospermia 45 0.062
452
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.062
453
THR024 Thrombosis 57 0.062
454
CHR074 Choriocarcinoma 47 0.062
455
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.062
456
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.061
457
P SBS003 Substance Abuse 55 0.061
458
c WLF013 Wolfram Syndrome 1 60 0.061
459
RTN020 Retinal Vascular Disease 46 0.061
460
CNN005 Connective Tissue Disease 68 0.061
461
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.061
462
LMB062 Limb Ischemia 55 0.061
463
PRP030 Purpura 54 0.061
464
P MLT074 Multiple Endocrine Neoplasia 56 0.061
465
BCK003 Background Diabetic Retinopathy 46 0.061
466
c SCL052 Scleroderma, Familial Progressive 61 0.061
467
P HYP024 Hypoparathyroidism 56 0.060
468
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.060
469
P OPT006 Optic Nerve Disease 60 0.060
470
PNC034 Pancreas Disease 48 0.060
471
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.060
472
EXC002 Exocrine Pancreatic Insufficiency 42 0.060
473
P SLP005 Sleep Disorder 59 0.059
474
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 57 0.059
475
CHL004 Cholelithiasis 49 0.059
476
RDN001 Reading Disorder 40 0.059
477
CHR066 Chronic Fatigue Syndrome 61 0.059
478
c INS009 Insulin-Resistance Type B 24 0.059
479
DMY004 Demyelinating Disease 52 0.059
480
P DYS154 Dystonia 65 0.059
481
c HYP272 Hypercholesterolemia, Familial, 3 44 0.059
482
IDP033 Idiopathic Edema 44 0.059
483
PHL006 Phelan-Mcdermid Syndrome 62 0.059
484
P SCL018 Scoliosis 60 0.058
485
P PRC019 Precocious Puberty 46 0.058
486
P ANG001 Angelman Syndrome 69 0.058
487
SNS003 Sensory Peripheral Neuropathy 54 0.058
488
AND002 Androgen Insensitivity Syndrome 66 0.058
489
P HYP265 Hypotonia 43 0.058
490
NRT001 Neurotic Disorder 53 0.058
491
CRT013 Carotid Stenosis 50 0.058
492
ADR016 Adrenal Cortical Carcinoma 48 0.057
493
ADR004 Adrenal Cortical Adenocarcinoma 39 0.057
494
HYP835 Hypothalamic Obesity 38 0.057
495
P INT068 Intestinal Disease 53 0.057
496
ORL013 Oral Lichen Planus 45 0.057
497
P VSC011 Vasculitis 62 0.057
498
AMN003 Amnestic Disorder 54 0.057
499
P AXN002 Axenfeld-Rieger Syndrome 59 0.057
500
ALR002 Al-Raqad Syndrome 33 0.057
501
c MYT021 Myotonic Dystrophy 1 69 0.057
502
SFT003 Soft Tissue Sarcoma 56 0.057
503
P OVR046 Ovarian Cyst 47 0.057
504
P DBT005 Diabetes Insipidus 55 0.056
505
MMM006 Mammographic Density 41 0.056
506
P APL001 Aplastic Anemia 74 0.056
508
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.056
509
NRM005 Neuromuscular Disease 64 0.056
510
P HDC001 Headache 57 0.056
511
HRT012 Heart Valve Disease 53 0.056
512
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.056
513
P INF038 Influenza 68 0.056
514
SKN019 Skin Melanoma 68 0.056
515
MTY003 Mutyh Polyposis 30 0.056
516
PHN003 Phenylketonuria 75 0.056
517
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.056
518
CLL003 Cellulitis 54 0.056
519
ACT003 Acute Kidney Tubular Necrosis 45 0.056
520
P ART023 Arthropathy 62 0.056
521
P PRP029 Porphyria 62 0.056
522
RTN003 Retinal Ischemia 50 0.055
523
ART001 Arterial Tortuosity Syndrome 66 0.055
524
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.055
525
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.055
526
P ALP106 Alport Syndrome 1, X-Linked 55 0.055
527
MDD018 Middle East Respiratory Syndrome 43 0.055
528
CRP001 Carpal Tunnel Syndrome 67 0.055
529
KPS004 Kaposi Sarcoma 75 0.055
530
GST040 Gastric Adenocarcinoma 70 0.055
531
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.055
532
BRN028 Brain Cancer 74 0.055
533
CRD223 Cardiac Arrhythmia 60 0.055
534
c MST023 Mesothelioma, Malignant 57 0.055
535
c FNC027 Fanconi Anemia, Complementation Group a 81 0.055
536
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.055
537
DBT004 Diabetic Polyneuropathy 49 0.054
538
P WLF004 Wolfram Syndrome 60 0.054
539
DBT006 Diabetic Macular Edema 48 0.054
540
OST011 Osteomalacia 52 0.054
541
c FML021 Familial Hypercholesterolemia 66 0.054
542
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.054
543
PSR001 Psoriatic Arthritis 61 0.054
544
SPR126 Superior Semicircular Canal Dehiscence 40 0.054
545
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.054
546
P MJR007 Major Affective Disorder 1 43 0.054
547
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.053
548
OVR029 Ovarian Hyperstimulation Syndrome 64 0.053
549
c TYP030 Type 1 Diabetes Mellitus 4 20 0.053
550
c PSR017 Psoriasis 2 53 0.053
551
TBC004 Tobacco Addiction 64 0.053
552
DYS073 Dysphagia 50 0.053
553
LYM019 Lymphosarcoma 46 0.053
554
TRP009 Triple X Syndrome 42 0.053
555
THY111 Thyroid Carcinoma, Familial Medullary 67 0.053
556
P ENC004 Encephalitis 61 0.053
557
END041 Endometrial Adenocarcinoma 63 0.053
558
P LMY004 Leiomyosarcoma 63 0.053
559
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.053
560
SCH012 Schizoaffective Disorder 50 0.053
561
ANG005 Anogenital Venereal Wart 55 0.052
562
CRN036 Craniopharyngioma 65 0.052
563
ANT039 Antisynthetase Syndrome 46 0.052
564
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.052
565
IMM064 Immunodeficiency, Common Variable, 10 44 0.052
566
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.052
567
P LPS002 Liposarcoma 65 0.052
568
IGG001 Iga Glomerulonephritis 48 0.052
569
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.052
570
c MJR003 Major Affective Disorder 6 33 0.052
571
c MJR006 Major Affective Disorder 5 33 0.052
572
HYP068 Hyperostosis 48 0.052
573
c PSR023 Psoriasis 1 52 0.051
574
c PSR032 Psoriasis 11 47 0.051
575
c PSR028 Psoriasis 7 42 0.051
576
c PSR018 Psoriasis 13 41 0.051
577
PLS011 Plasmacytoma 56 0.051
578
P ACR001 Aicardi-Goutieres Syndrome 62 0.051
579
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.051
580
THY125 Thyroid Gland Medullary Carcinoma 50 0.051
581
JVN026 Jeavons Syndrome 24 0.051
582
P BRD002 Bardet-Biedl Syndrome 66 0.051
583
OST017 Osteomyelitis 64 0.051
584
c PNC108 Pancreatitis, Hereditary 70 0.051
585
CMM004 Common Variable Immunodeficiency 68 0.051
586
PLM033 Pulmonary Embolism 59 0.051
587
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.050
588
PCK003 Pick Disease of Brain 68 0.050
589
c BLD140 Blood Group, I System 32 0.050
590
c BSL007 Basal Cell Carcinoma 68 0.050
591
MLT157 Multiple System Atrophy 1 70 0.050
592
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.050
593
RNL024 Renal Glucosuria 58 0.050
594
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.050
595
c MJR008 Major Affective Disorder 2 35 0.050
596
c TYP032 Type 1 Diabetes Mellitus 6 20 0.050
597
CRH005 Crohn's Colitis 53 0.050
598
c HYP768 Hyperlipoproteinemia, Type I 67 0.050
599
CRB037 Cerebral Palsy 69 0.050
600
TST014 Testicular Cancer 46 0.050
601
CHL067 Cholecystitis 57 0.050
602
PRL032 Perlman Syndrome 57 0.050
603
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.050
604
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.049
605
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.049
606
LPT006 Leptin Receptor Deficiency 48 0.049
607
c FML001 Familial Atrial Fibrillation 65 0.049
608
c LPM012 Lipomatosis, Multiple 60 0.049
609
SCH003 Schizophreniform Disorder 56 0.049
610
c MJR023 Major Affective Disorder 7 33 0.049
611
c MJR004 Major Affective Disorder 4 28 0.049
612
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.049
613
c OVR114 Ovarian Cancer 1 38 0.049
614
OBS002 Obsessive-Compulsive Disorder 68 0.049
615
APH002 Aphasia 57 0.049
616
PPL001 Papillary Adenoma 44 0.049
617
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.049
618
P FRN006 Frontotemporal Dementia 68 0.049
619
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.049
620
P PLY006 Polydactyly 59 0.049
621
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.049
622
P SDR002 Siderosis 44 0.049
623
ACR006 Aceruloplasminemia 65 0.048
624
P BNC003 Bone Cancer 58 0.048
625
P OCL013 Oculodentodigital Dysplasia 69 0.048
626
TND005 Tendinitis 54 0.048
627
NRN001 Neuroendocrine Carcinoma 47 0.048
628
HMR039 Hemorrhage, Intracerebral 57 0.048
629
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.048
630
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.048
631
YLL002 Yellow Fever 61 0.048
632
GST049 Gastrointestinal System Cancer 49 0.048
633
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.048
634
c PNS012 Paine Syndrome 61 0.048
635
P RNL015 Renal Hypertension 47 0.047
636
HST010 Histiocytosis 48 0.047
637
GST071 Gastrointestinal Carcinoma 47 0.047
638
ALD013 Aldosterone-Producing Adenoma 39 0.047
639
CRY036 Cryptogenic Cirrhosis 36 0.047
640
ANL018 Analbuminemia 54 0.047
641
CRN322 Coronavirus Infectious Disease 40 0.047
642
PNC001 Pancytopenia 54 0.047
643
IMM136 Immune System Disease 45 0.047
644
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.047
645
AYM001 Ayme-Gripp Syndrome 57 0.047
646
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.047
647
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.047
648
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.047
649
END062 Endometrial Hyperplasia 48 0.047
650
SCH036 Scheie Syndrome 72 0.046
651
SPT006 Septooptic Dysplasia 64 0.046
652
P ANG015 Angioedema 57 0.046
653
P MTC069 Mitochondrial Disorders 56 0.046
654
P CHL066 Cholangitis 51 0.046
655
P MLG074 Malignant Mesenchymoma 40 0.046
656
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.046
657
SRC027 Sarcoma, Synovial 58 0.046
658
P GLL020 Gallbladder Disease 57 0.046
659
CYT008 Cytomegalovirus Infection 57 0.046
660
P OPN001 Open-Angle Glaucoma 49 0.046
661
LRN003 Learning Disability 49 0.046
662
ADR041 Adrenal Cortical Adenoma 43 0.046
663
c HMG001 Hemoglobin C Disease 40 0.046
664
IGR001 Ige Responsiveness, Atopic 59 0.046
665
PLY001 Polycythemia Vera 69 0.045
666
PLS007 Plasmodium Falciparum Malaria 52 0.045
667
DSM007 Desmoplastic Small Round Cell Tumor 52 0.045
668
c LRG001 Large Cell Carcinoma 50 0.045
669
MTC005 Mitochondrial Metabolism Disease 49 0.045
670
FCL012 Facial Paralysis 46 0.045
671
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.045
672
INT067 Interstitial Nephritis 48 0.045
673
PLS009 Plasma Cell Neoplasm 51 0.045
674
P FRG001 Fragile X Syndrome 70 0.045
675
ADR008 Adrenal Adenoma 55 0.045
676
P ANT006 Antiphospholipid Syndrome 55 0.045
677
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.045
678
c MCL013 Mucolipidosis Iv 66 0.045
679
P LCT002 Lactose Intolerance 53 0.045
680
ILS001 Ileus 51 0.045
681
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.045
682
URT049 Urate Oxidase, Pseudogene 25 0.045
683
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.045
684
DCT002 Ductal Carcinoma in Situ 59 0.045
685
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 52 0.045
686
AND005 Androgen Insensitivity Syndrome, Mild 19 0.045
687
BLL003 Bell's Palsy 51 0.045
688
P SYP003 Syphilis 58 0.044
689
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.044
690
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.044
691
BRS099 Breast Ductal Carcinoma 62 0.044
692
TXC002 Toxic Encephalopathy 53 0.044
693
CRT016 Carotid Artery Disease 52 0.044
694
HYP025 Hyperphosphatemia 48 0.044
695
P HMN032 Human Herpesvirus 8 47 0.044
696
P DYS021 Dysautonomia 39 0.044
697
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.044
698
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.044
699
TND004 Tendinopathy 43 0.044
700
NRV004 Nerve Compression Syndrome 40 0.044
701
c RNL113 Renal Failure, Progressive, with Hypertension 34 0.044
702
PST028 Post-Traumatic Stress Disorder 58 0.044
703
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.044
704
ENT004 Enthesopathy 49 0.044
705
c BRD010 Bardet-Biedl Syndrome 1 62 0.044
706
PRP016 Paraplegia 52 0.044
707
BRC012 Brucellosis 64 0.043
708
P INT070 Intestinal Obstruction 58 0.043
709
P PRV006 Pervasive Developmental Disorder 57 0.043
710
CMR002 Coumarin Resistance 56 0.043
711
c INH020 Inherited Metabolic Disorder 47 0.043
712
KRT013 Keratolytic Winter Erythema 46 0.043
713
P NJM001 Nijmegen Breakage Syndrome 74 0.043
714
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.043
715
TRY001 Trypanosomiasis 50 0.043
716
c DRM054 Dermatitis, Atopic, 2 44 0.043
717
HYP457 Hypertrophic Scars 42 0.043
718
CYT018 Cytochrome P450 2d6 Variant 27 0.043
719
P RTN022 Retinal Vein Occlusion 53 0.043
720
c THR092 Thrombophilia Due to Thrombin Defect 73 0.043
721
FML063 Familial Glucocorticoid Deficiency 58 0.043
722
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 54 0.043
723
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.043
724
SYS003 Systolic Heart Failure 49 0.043
725
c BRD013 Bardet-Biedl Syndrome 12 45 0.043
726
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.043
727
P PRS038 Personality Disorder 65 0.043
728
P FNC004 Fanconi Syndrome 50 0.043
729
P PRC031 Preeclampsia/eclampsia 1 38 0.043
730
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.043
731
CHY002 Chylomicron Retention Disease 65 0.042
732
P KLL001 Kallmann Syndrome 61 0.042
733
EXP004 Exophthalmos 52 0.042
734
GNT003 Genital Herpes 54 0.042
735
P NNN008 Noonan Syndrome 1 76 0.041
736
c OPT053 Optic Atrophy 1 63 0.041
737
ALV005 Alveolar Soft Part Sarcoma 61 0.041
738
CRC006 Carcinoid Syndrome 55 0.041
739
c BRD011 Bardet-Biedl Syndrome 10 53 0.041
740
c BRD014 Bardet-Biedl Syndrome 2 52 0.041
741
c BRD012 Bardet-Biedl Syndrome 11 51 0.041
742
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
743
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.041
744
LWC001 Low Compliance Bladder 43 0.041
745
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.041
746
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.041
747
FNT004 Fainting 30 0.041
748
INS034 Insulinomatosis and Diabetes Mellitus 27 0.041
749
SLC006 Silicosis 56 0.041
750
c INF071 Inflammatory Bowel Disease 1 67 0.041
751
PRP001 Propionic Acidemia 65 0.041
752
CRT017 Cartilage Disease 54 0.041
753
c BCT013 Bacterial Pneumonia 48 0.041
754
c PRM196 Premature Ovarian Failure 1 67 0.041
755
ERY029 Erythermalgia, Primary 58 0.041
756
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
757
CRN027 Corneal Neovascularization 47 0.041
758
GLC022 Glucose/galactose Malabsorption 45 0.041
759
PRS063 Paresthesia 41 0.041
760
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.041
761
BHR001 Behr Syndrome 51 0.041
762
CRB090 Cerebral Hypoxia 44 0.041
763
CMM003 Common Wart 32 0.041
764
MYX005 Myxoid Liposarcoma 66 0.041
765
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.041
766
PNM008 Pneumothorax 56 0.041
767
P PTS002 Ptosis 53 0.041
768
VTM033 Vitamin K Deficiency Bleeding 48 0.041
769
P CRN028 Corneal Ulcer 47 0.041
770
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.041
771
RSP007 Respiratory Distress Syndrome, Infant 30 0.041
772
HYP780 Hypoadrenocorticism, Familial 63 0.040
773
THY122 Thyroid Gland Cancer 57 0.040
774
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.040
775
P EMB005 Embryonal Rhabdomyosarcoma 53 0.040
776
MDS022 Mediastinitis 46 0.040
777
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.040
778
PNC008 Pancreatic Endocrine Carcinoma 39 0.040
779
PTT003 Pituitary-Dependent Cushing's Disease 39 0.040
780
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.040
781
c PSD047 Pseudo-Turner Syndrome 21 0.040
782
P TXP001 Toxoplasmosis 60 0.040
783
P PRG092 Pregnancy Loss, Recurrent 1 40 0.040
784
ADR007 Adrenoleukodystrophy 75 0.040
785
P MPL001 Maple Syrup Urine Disease 69 0.040
786
HRL003 Hurler Syndrome 65 0.040
787
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.040
788
AND020 Androgen Insensitivity, Partial 56 0.040
789
ATR057 Atrioventricular Block 55 0.040
791
OCL006 Ocular Hypertension 53 0.040
792
P PNC025 Panic Disorder 53 0.040
793
BWN001 Bowen-Conradi Syndrome 52 0.040
794
QDR001 Quadriplegia 48 0.040
795
ACT084 Acute Stress Disorder 47 0.040
796
RYN005 Raynaud Phenomenon 47 0.040
797
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.040
798
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.040
799
MXD026 Mixed Glioma 45 0.040
801
SPS057 Spasticity 45 0.040
802
PHY002 Physical Disorder 42 0.040
803
GLC096 Galactorrhea 42 0.040
804
ADS004 Aids Dementia Complex 40 0.040
805
MCP033 Mucopolysaccharidoses 38 0.040
806
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.040
807
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.039
808
MYL031 Myeloproliferative Neoplasm 66 0.039
809
DGR001 Digeorge Syndrome 64 0.039
810
c DNG003 Dengue Disease 59 0.039
811
P HYP040 Hypospadias 51 0.039
812
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.039
813
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.039
814
NVS001 Neovascular Glaucoma 53 0.039
815
P SCL009 Sclerosing Cholangitis 48 0.039
816
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.039
817
FNC007 Functioning Pituitary Adenoma 43 0.039
818
CRB025 Carbohydrate Metabolic Disorder 41 0.039
819
HYP344 Hyperthyroidism, Familial Gestational 39 0.039
820
P FML018 Familial Mediterranean Fever 73 0.039
821
FCT007 Factor Vii Deficiency 67 0.039
822
RHM001 Rheumatic Fever 60 0.039
823
FND002 Fundus Dystrophy 55 0.039
824
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.039
825
c INH030 Inherited Retinal Disorder 51 0.039
826
SPS003 Spastic Diplegia 51 0.039
827
c HRD202 Hereditary Lymphedema I 50 0.039
828
RFR010 Refractory Anemia 48 0.039
829
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.039
830
MCC013 Mucocutaneous Ulceration, Chronic 39 0.039
831
HRP008 Herpes Simiae 25 0.039
832
DNG002 Dengue Hemorrhagic Fever 60 0.038
833
PPL049 Papillon-Lefevre Syndrome 65 0.038
834
P CHR071 Charcot-Marie-Tooth Disease 65 0.038
835
OST003 Osteonecrosis 61 0.038
836
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.038
837
HRL004 Hurler-Scheie Syndrome 55 0.038
838
P CYS039 Cystic Kidney Disease 54 0.038
839
ACR041 Acromelic Frontonasal Dysostosis 52 0.038
840
APR001 Apraxia 52 0.038
841
SRS001 Serous Cystadenocarcinoma 52 0.038
842
c ACT150 Acute Adrenal Insufficiency 48 0.038
843
GRM005 Germ Cell Cancer 47 0.038
844
SMN008 Semantic Dementia 47 0.038
845
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.038
846
c CLR017 Clear Cell Sarcoma 45 0.038
847
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.038
848
MYF002 Myofascial Pain Syndrome 42 0.038
849
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.038
850
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.038
851
MSM014 Mismatch Repair Cancer Syndrome 65 0.038
852
PRM126 Primary Peritoneal Carcinoma 62 0.038
853
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.038
854
P HYP726 Hypercalcemia, Infantile, 1 58 0.038
855
ADR005 Adrenal Carcinoma 58 0.038
856
c CHL119 Cholangitis, Primary Sclerosing 57 0.038
857
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.038
858
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.038
859
P TCD001 Tic Disorder 53 0.038
860
P MYC033 Myoclonus 46 0.038
861
CMP004 Complement Factor I Deficiency 44 0.038
862
CRN020 Coronary Restenosis 39 0.038
863
c SYS043 Systemic Lupus Erythematosus 1 38 0.038
864
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.038
865
CLC008 Colchicine Resistance 34 0.038
866
RTN004 Retinal Microaneurysm 33 0.038
867
ADR057 Adrenogenital Syndrome 32 0.038
868
PRP083 Porphyria, Acute Intermittent 64 0.037
869
c DSB006 Desbuquois Dysplasia 1 48 0.037
870
CRV043 Cervical Dystonia 42 0.037
871
HYP748 Hypertelorism 50 0.036
872
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.036
873
BHC003 Behcet Syndrome 71 0.036
874
CRT072 Creutzfeldt-Jakob Disease 70 0.036
875
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.036
876
P PRP003 Porphyria Cutanea Tarda 67 0.036
877
c LCL006 Localized Scleroderma 62 0.036
878
GNR004 Generalized Anxiety Disorder 56 0.036
879
URC002 Urea Cycle Disorder 51 0.036
880
RYN001 Raynaud Disease 48 0.036
881
TTH006 Tooth Disease 46 0.036
882
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.036
883
CRD005 Cardia Cancer 40 0.036
884
P CTN015 Cutaneous T Cell Lymphoma 49 0.036
885
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.036
886
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.036
887
MYC079 Myoclonic Epilepsy of Lafora 64 0.036
888
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.036
889
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.036
890
ADR038 Adermatoglyphia 49 0.036
891
TTR011 Tetraploidy 47 0.036
892
P OCY003 Oocyte Maturation Defect 1 45 0.036
893
CYS009 Cystadenoma 44 0.036
894
BCK006 Back Pain 42 0.036
896
MTR007 Motor Peripheral Neuropathy 39 0.036
897
HYP264 Hypertonia 38 0.036
898
c SCH085 Schizophrenia 2 33 0.036
899
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.036
900
c ART101 Aortic Valve Disease 2 65 0.035
901
P INT143 Interstitial Cystitis 61 0.035
902
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.035
903
LNG108 Langerhans Cell Histiocytosis 58 0.035
904
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.035
905
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.035
906
TRD006 Tardive Dyskinesia 54 0.035
907
c CNT035 Central Nervous System Disease 52 0.035
908
P ATN002 Autonomic Nervous System Disease 52 0.035
909
c INF023 Inflammatory Breast Carcinoma 50 0.035
910
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.035
911
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.035
912
ADN009 Adenosquamous Carcinoma 47 0.035
913
CRC014 Carcinoid Tumors, Intestinal 47 0.035
914
P UTR058 Uterine Anomalies 47 0.035
915
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.035
916
PLY068 Polysubstance Abuse 43 0.035
917
TND006 Tendinosis 42 0.035
918
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.035
919
GRM004 Germinoma 40 0.035
920
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.035
921
P INT260 Intracranial Berry Aneurysm 39 0.035
922
HYP008 Hypertensive Retinopathy 39 0.035
923
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.035
924
P MYC026 Myoclonus Epilepsy 35 0.035
925
c CNG562 Congenital Hypogonadotropic Hypogonadism 34 0.035
926
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.035
927
ATR076 Atrophic Muscular Disease 30 0.035
928
MLG164 Malignant Epithelial Tumor of Ovary 26 0.035
929
c CHR464 Chronic Intestinal Failure 22 0.035
930
LYM053 Lymphomatous Thyroiditis 22 0.035
931
HYP705 Hyperadrenalism 20 0.035
932
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.034
933
P HYP097 Hyperekplexia 61 0.034
934
P LFT003 Left Ventricular Noncompaction 54 0.034
935
LYS002 Lysosomal Storage Disease 52 0.034
936
c DYS119 Dystonia 9 50 0.034
937
OPP004 Oppositional Defiant Disorder 49 0.034
938
CLC006 Calcinosis 48 0.034
939
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.034
940
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.034
941
SCT002 Scotoma 44 0.034
942
c ERL056 Early-Onset Parkinson's Disease 39 0.034
943
CNT060 Central Serous Chorioretinopathy 38 0.034
944
LTT002 Letterer-Siwe Disease 33 0.034
945
CRN311 Coronary Ostial Stenosis or Atresia 20 0.034
946
PHS025 Phosphatase, Acid, of Tissues 28 0.034
947
MYL005 Myelofibrosis 70 0.033
948
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.033
949
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.033
950
MSC152 Muscular Dystrophy, Becker Type 63 0.033
951
MSS001 Masa Syndrome 62 0.033
952
c MCP043 Mucopolysaccharidosis, Type Iiia 61 0.033
953
P CHR285 Chronic Myelomonocytic Leukemia 60 0.033
954
c LTN004 Late-Onset Retinal Degeneration 59 0.033
955
THY022 Thymic Carcinoma 57 0.033
956
HMT008 Hematuria, Benign Familial 56 0.033
957
P DYS193 Dystonia 11, Myoclonic 55 0.033
958
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.033
959
P STS003 Sitosterolemia 54 0.033
960
P RST001 Restless Legs Syndrome 54 0.033
961
c CNT016 Central Retinal Vein Occlusion 53 0.033
962
IMM102 Immunodeficiency 14 53 0.033
963
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.033
964
c ALB020 Albinism, Oculocutaneous, Type Iii 51 0.033
965
ECT026 Ectopic Pregnancy 50 0.033
966
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.033
967
PCT003 Pectus Excavatum 49 0.033
968
END021 Endomyocardial Fibrosis 49 0.033
969
c ALZ054 Alzheimer Disease 4 49 0.033
970
ASP007 Aspiration Pneumonia 48 0.033
971
CLS016 Clostridium Difficile Colitis 48 0.033
972
CLN019 Colonic Disease 47 0.033
973
RTN001 Retinal Vasculitis 47 0.033
974
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.033
975
CHN056 Chondrosarcoma, Extraskeletal Myxoid 46 0.033
976
BRN032 Brain Glioma 45 0.033
977
CNN002 Cannabis Abuse 44 0.033
978
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.033
979
c HYP210 Hypomagnesemia 2, Renal 43 0.033
980
MCR103 Microtia 43 0.033
981
c HYP057 Hypervitaminosis D 42 0.033
982
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 41 0.033
983
PPL007 Papillary Serous Adenocarcinoma 40 0.033
984
HYP030 Hypoactive Sexual Desire Disorder 40 0.033
985
CNN001 Cannabis Dependence 40 0.033
987
P PRM327 Primary Lymphedema 38 0.033
988
FLL029 Fallopian Tube Disease 38 0.033
989
FRN014 Fournier Gangrene 37 0.033
990
CMB081 Combined Immunodeficiency, X-Linked 36 0.033
991
PSD088 Pseudobulbar Affect 36 0.033
992
c PRM340 Primary Adrenal Insufficiency 36 0.033
993
ACL001 Acalculous Cholecystitis 35 0.033
994
P EXT030 Extraosseous Chondrosarcoma 35 0.033
995
FCL011 Facial Nerve Disease 35 0.033
996
DGT005 Digital Arthropathy-Brachydactyly, Familial 34 0.033
997
MYC069 Myoclonic-Astastic Epilepsy 33 0.033
998
P MYX008 Myxoid Chondrosarcoma 32 0.033
999
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.033
1000
PNT003 Pinta Disease 31 0.033
1001
c SCH064 Schizophrenia 10 31 0.033
1002
CRD220 Cardiac Valvular Defect, Developmental 29 0.033
1003
END015 Endometrial Adenosquamous Carcinoma 27 0.033
1004
PGM030 Pigmentation Anomaly of the Skin 26 0.033
1005
ACT094 Acute Articular Rheumatism 26 0.033
1006
IDN001 Iodine Hypothyroidism 26 0.033
1007
FTL073 Fetal Anticonvulsant Syndrome 26 0.033
1008
BTM003 Beta-Aminoisobutyric Aciduria 20 0.033
1009
BLD145 Blood Group--Newfoundland 15 0.033
1010
ALB002 Albinism 46 0.031
1011
NRN002 Neuronitis 32 0.031
1012
c ART115 Aortic Valve Disease 1 75 0.031
1013
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.031
1014
DMN031 Dementia, Lewy Body 65 0.031
1015
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 0.031
1016
c MCP001 Mucopolysaccharidosis Iii 65 0.031
1017
KND001 Kindler Syndrome 64 0.031
1018
c EPS035 Episodic Ataxia, Type 2 63 0.031
1019
c DYS056 Dystonia 12 62 0.031
1020
PNM010 Pneumothorax, Primary Spontaneous 60 0.031
1021
LBR030 Leber Optic Atrophy 60 0.031
1022
IDP011 Idiopathic Interstitial Pneumonia 59 0.031
1023
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 59 0.031
1024
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.031
1025
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.031
1026
P STR022 Stargardt Disease 58 0.031
1027
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.031
1028
c BSL024 Basal Cell Carcinoma 1 56 0.031
1029
P LBR014 Leber Congenital Amaurosis 4 56 0.031
1030
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.031
1031
P FNG006 Feingold Syndrome 1 55 0.031
1032
FCT004 Factor Xii Deficiency 55 0.031
1033
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.031
1034
MCN017 Meconium Ileus 52 0.031
1035
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.031
1036
BRX001 Bruxism 50 0.031
1037
RSP006 Respiratory System Disease 50 0.031
1038
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.031
1039
P IGN003 Iga Nephropathy 1 49 0.031
1040
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.031
1041
CCN002 Cocaine Abuse 49 0.031
1042
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.031
1043
CCN001 Cocaine Dependence 48 0.031
1044
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.031
1045
c PNT034 Pontocerebellar Hypoplasia, Type 2e 48 0.031
1046
P BLR006 Biliary Tract Disease 47 0.031
1047
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 47 0.031
1048
PLC003 Placental Site Trophoblastic Tumor 47 0.031
1049
LCK001 Locked-in Syndrome 46 0.031
1050
HMF009 Hemifacial Hyperplasia 45 0.031
1051
LRN001 Laurence-Moon Syndrome 45 0.031
1052
ASP008 Aspiration Pneumonitis 45 0.031
1053
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.031
1054
c HYP699 Hyperekplexia 1 44 0.031
1055
P EPN001 Ependymoblastoma 44 0.031
1056
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 44 0.031
1057
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 0.031
1058
DFF003 Diffuse Scleroderma 41 0.031
1059
FCL022 Focal Dystonia 41 0.031
1060
c FML363 Familial Adult Myoclonic Epilepsy 41 0.031
1061