Search results for "thyroid hormone metabolism"

The MalaCard for "thyroid hormone metabolism" has been retired.
Searching MalaCards for entries containing "thyroid hormone metabolism"

1330 hits were found for 'thyroid hormone metabolism'

# Family MCID Name MIFTS Score
1
THY064 Thyroid Hormone Metabolism, Abnormal 25 5.443
2
P THY032 Thyroiditis 54 1.356
3
THY028 Thyroid Cancer 68 0.473
4
P HYP086 Hypothyroidism 65 0.376
5
P OBS005 Obesity 93 0.332
6
ADN018 Adenoma 59 0.305
7
P BRS047 Breast Cancer 100 0.295
8
GRW007 Growth Hormone Deficiency 48 0.273
9
P HPT021 Hepatitis 70 0.267
10
THY030 Thyroid Gland Disease 51 0.260
11
GTR002 Goiter 54 0.245
12
PRS047 Prostatitis 56 0.239
13
P PRS040 Prostate Cancer 89 0.237
14
P LYM118 Lymphoma 70 0.235
15
P GRV001 Graves' Disease 61 0.230
16
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.224
17
P ADN016 Adenocarcinoma 69 0.221
18
PPL002 Papillary Carcinoma 49 0.217
19
INS024 Insulin-Like Growth Factor I 74 0.215
20
c SBC007 Subacute Thyroiditis 39 0.213
21
GLC008 Glucose Metabolism Disease 47 0.212
22
DFF036 Differentiated Thyroid Carcinoma 47 0.208
23
P HYP076 Hyperthyroidism 56 0.206
24
END035 Endocrine Gland Cancer 52 0.204
25
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.201
26
NTR005 Nutritional Deficiency Disease 39 0.196
27
LPD008 Lipid Metabolism Disorder 58 0.187
28
P THY097 Thyroid Hormone Resistance 54 0.182
29
P PLY011 Polycystic Ovary Syndrome 66 0.181
30
END072 Endotheliitis 42 0.178
31
P HYP060 Hyperinsulinism 59 0.176
32
ACD009 Acid-Labile Subunit, Deficiency of 48 0.171
33
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.170
34
ADL002 Adult Syndrome 53 0.161
35
NRN002 Neuronitis 42 0.161
36
MTB004 Metabolic Acidosis 48 0.160
37
P HRT032 Heart Disease 76 0.159
38
P MLT074 Multiple Endocrine Neoplasia 55 0.158
39
P PNC044 Pancreatitis 60 0.158
40
ACR007 Acromegaly 65 0.156
41
HSH003 Hashimoto Thyroiditis 61 0.156
42
P LKM002 Leukemia 70 0.152
43
PTT006 Pituitary Adenoma 55 0.151
44
P ABD016 Abdominal Obesity-Metabolic Syndrome 26 0.150
45
c CNG006 Congenital Hypothyroidism 59 0.149
46
P INF032 Infertility 61 0.148
47
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.147
48
THY009 Thyroid Lymphoma 47 0.145
49
P HYP069 Hyperparathyroidism 57 0.143
50
CRB009 Cerebritis 38 0.143
51
CRB025 Carbohydrate Metabolic Disorder 47 0.142
52
ISL003 Isolated Growth Hormone Deficiency 44 0.142
53
MRC001 Marchiafava Bignami Disease 50 0.142
54
EYD002 Eye Disease 63 0.141
55
P OST002 Osteoporosis 64 0.141
56
P HYP083 Hypopituitarism 52 0.141
57
ALL026 Allergic Hypersensitivity Disease 53 0.140
58
HDN004 Head and Neck Carcinoma 55 0.140
59
MLR007 Male Reproductive System Disease 37 0.140
60
P ENC018 Encephalopathy 59 0.139
61
P ART022 Arthritis 75 0.138
62
P CRV039 Cervicitis 44 0.137
63
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.136
64
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.136
65
BNS002 Bone Structure Disease 36 0.135
66
P MYP004 Myopathy 67 0.135
67
DWR001 Dwarfism 46 0.132
68
PRS042 Prostate Disease 52 0.131
69
P ORL007 Oral Cavity Cancer 58 0.131
70
ORL011 Oral Cancer 55 0.131
71
PTT009 Pituitary Gland Disease 48 0.131
72
BNC003 Bone Cancer 45 0.130
73
MSC004 Muscle Tissue Disease 36 0.130
74
ATH003 Atherosclerosis 62 0.129
75
P NRV006 Nervous System Cancer 62 0.129
76
P LVR013 Liver Disease 72 0.128
77
THY103 Thyroid Cancer, Monmedullary, 1 54 0.126
78
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.124
79
c HPT001 Hepatitis C 68 0.123
80
HYP085 Hypothalamic Disease 44 0.122
81
P OVR049 Ovarian Disease 55 0.122
82
RPR002 Reproductive System Disease 46 0.122
83
CHL071 Child Syndrome 58 0.122
84
HYP056 Hypoglycemia 61 0.120
85
P LNG032 Lung Cancer 94 0.120
86
KDS001 Kid Syndrome 53 0.118
87
GLT021 Glutaricaciduria, Type I 48 0.118
88
P RHM011 Rheumatoid Arthritis 88 0.117
89
P OVR042 Ovarian Cancer 75 0.117
90
BND014 Bone Development Disease 42 0.117
91
ACR002 Acrocapitofemoral Dysplasia 36 0.117
92
P TRN020 Turner Syndrome 64 0.116
93
CSY001 C Syndrome 49 0.116
94
HYP266 Hypoxia 55 0.116
95
BRT030 Birth Defects 43 0.115
96
OVR063 Overnutrition 49 0.115
97
P MSC033 Muscle Disorders 52 0.115
98
ATM014 Autoimmune Disease of Endocrine System 37 0.114
99
FML039 Female Reproductive System Disease 48 0.114
100
ACR041 Acromelic Frontonasal Dysostosis 46 0.114
101
P CRN211 Coronary Artery Disease 75 0.113
102
NRN004 Neuroendocrine Tumor 54 0.113
103
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.113
104
MDY003 Mody, Type Ii 38 0.113
105
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.113
106
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.112
107
HYP066 Hyperglycemia 60 0.112
108
GNR008 Generalized Resistance to Thyroid Hormone 31 0.112
109
P THY102 Thyroid Cancer, Nonmedullary, 2 60 0.112
110
HYP080 Hypogonadism 54 0.111
111
SXL003 Sexual Disorder 47 0.111
112
P CSH001 Cushing's Syndrome 64 0.111
113
PTT037 Pituitary Tumors 45 0.110
114
BRS051 Breast Disease 62 0.109
115
MYX004 Myxedema 38 0.109
116
NDL007 Nodular Goiter 46 0.108
117
P SCH015 Schizophrenia 76 0.108
118
BLD054 Blood Protein Disease 40 0.108
119
P RNL014 Renal Cell Carcinoma 81 0.107
120
HPT023 Hepatocellular Carcinoma 91 0.106
121
P HYP024 Hypoparathyroidism 52 0.106
122
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.106
123
ETN001 Eating Disorder 60 0.104
124
WTH001 Withdrawal Disorder 41 0.103
125
PCK002 Pick Disease 67 0.103
126
FTT001 Fatty Liver Disease 60 0.102
127
STM006 Stomach Disease 50 0.102
128
P PRC019 Precocious Puberty 51 0.102
129
MDD011 Mood Disorder 61 0.101
130
P MDL005 Medulloblastoma 77 0.101
131
P CLR023 Colorectal Cancer 97 0.101
132
SKN016 Skin Disease 68 0.100
133
P KDN017 Kidney Cancer 67 0.100
134
WLL006 Wells Syndrome 56 0.100
135
MSS002 Mass Syndrome 59 0.100
136
GLC003 Glucose Intolerance 55 0.099
137
P SKN013 Skin Benign Neoplasm 46 0.099
138
P MYC007 Myocardial Infarction 79 0.099
139
PPL018 Papillary Adenocarcinoma 48 0.099
140
ART111 Artery Disease 57 0.099
141
ALR002 Al-Raqad Syndrome 36 0.098
142
P LPS004 Lupus Erythematosus 63 0.098
143
GDS001 Good Syndrome 45 0.098
144
P PRD006 Prader-Willi Syndrome 63 0.097
145
OCL009 Ocular Cancer 62 0.096
146
FML037 Female Breast Cancer 51 0.096
147
P PSD015 Pseudohypoparathyroidism 44 0.096
148
SRC014 Sarcoma 66 0.095
149
ATM053 Autoimmune Disease 2 19 0.095
150
PRT030 Parathyroid Gland Disease 49 0.095
151
ATM052 Autoimmune Disease 1 28 0.094
152
c SYS001 Systemic Lupus Erythematosus 87 0.094
153
P EPL164 Epilepsy 66 0.094
154
TST021 Testicular Germ Cell Tumor 70 0.094
155
c CRN214 Coronary Heart Disease 5 23 0.093
156
CNG034 Congestive Heart Failure 71 0.093
157
P SPS003 Spastic Diplegia 53 0.093
158
VTM003 Vitamin Metabolic Disorder 33 0.093
159
P PHC003 Pheochromocytoma 71 0.093
160
PRT029 Parathyroid Adenoma 47 0.093
161
c INH020 Inherited Metabolic Disorder 49 0.092
162
P NRP001 Neuropathy 60 0.092
163
ALN001 Aland Island Eye Disease 45 0.092
164
CRC006 Carcinoid Syndrome 51 0.091
165
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.091
166
c CRN175 Coronary Heart Disease 4 21 0.091
167
EWN003 Ewing Sarcoma 64 0.091
168
GST033 Gestational Diabetes 56 0.091
169
P ANR007 Anorexia Nervosa 63 0.091
170
c CRN172 Coronary Heart Disease 3 21 0.090
171
P CRV031 Cervical Adenocarcinoma 52 0.090
172
P NRB001 Neuroblastoma 69 0.090
173
P LPD010 Lipodystrophy 52 0.090
174
SKN023 Skin Tag 46 0.090
175
GRM001 Germ Cell and Embryonal Cancer 39 0.089
176
GND003 Gonadal Disease 43 0.089
177
c MLT136 Multiple Endocrine Neoplasia 1 68 0.089
178
DWN001 Down Syndrome 65 0.089
179
ATM054 Autoimmune Disease 3 18 0.088
180
BRN106 Burns 52 0.088
181
HMT002 Hematologic Cancer 64 0.088
182
MNR003 Mineral Metabolism Disease 41 0.088
183
ADR014 Adrenal Medulla Cancer 38 0.087
184
MRB003 Morbid Obesity 58 0.087
185
SXD001 Sex Differentiation Disease 40 0.086
186
P STR021 Struma Ovarii 37 0.086
187
P CRN178 Coronary Heart Disease 6 24 0.086
188
c CRN174 Coronary Heart Disease 2 22 0.086
189
ATM055 Autoimmune Disease 4 18 0.086
190
MLN007 Male Infertility 56 0.086
191
PRP027 Peripheral Vascular Disease 69 0.086
192
C3D001 C3 Deficiency 53 0.085
193
IMM136 Immune System Disease 50 0.085
194
P GLM045 Glioma 58 0.085
195
P PSR002 Psoriasis 63 0.085
196
P CLC005 Celiac Disease 67 0.085
197
AMN001 Amenorrhea 51 0.084
198
GST053 Gastric Cancer 77 0.084
199
DSS008 Disease of Mental Health 55 0.084
200
DMN002 Dementia 64 0.083
201
NNL002 Nonalcoholic Steatohepatitis 53 0.083
202
SKN027 Skin Conditions 45 0.083
203
ALP008 Alopecia 55 0.083
204
ISC006 Ischemic Heart Disease 68 0.083
205
ISC004 Ischemia 59 0.082
206
VND001 Vein Disease 52 0.082
207
ATN002 Autonomic Nervous System Disease 47 0.082
208
PLC008 Placenta Disease 36 0.082
209
P MCR129 Microvascular Complications of Diabetes 1 57 0.081
210
CNN005 Connective Tissue Disease 61 0.081
211
MTH009 Mouth Disease 63 0.081
212
EMB004 Embryonal Carcinoma 56 0.081
213
HV1006 Hiv-1 82 0.081
214
c GRV008 Graves Disease 1 45 0.081
215
P TRT010 Teratoma 52 0.080
216
LVR012 Liver Cirrhosis 67 0.080
217
LYM116 Lymph Node Disease 44 0.080
218
HYP043 Hyperandrogenism 48 0.080
219
GLB003 Globe Disease 35 0.080
220
c ACT053 Acute Thyroiditis 30 0.080
221
ATM012 Autoimmune Disease of Blood 37 0.080
222
CRD118 Cardiovascular Cancer 47 0.080
223
P PRT010 Parathyroid Carcinoma 62 0.080
224
P BCL006 B-Cell Lymphomas 64 0.080
225
PHY002 Physical Disorder 44 0.079
226
P PRM019 Premature Ovarian Failure 64 0.079
227
HRT007 Heart Cancer 50 0.079
228
P HRT017 Heart Tumor 35 0.079
229
SLP005 Sleep Disorder 53 0.079
230
END057 Endometrial Cancer 75 0.079
231
LPD004 Lipoid Nephrosis 48 0.079
232
MNT002 Mental Depression 54 0.079
233
P END044 Endometriosis 53 0.079
234
RSP006 Respiratory System Disease 62 0.079
235
P LRY019 Laryngitis 55 0.079
236
BRN028 Brain Cancer 70 0.079
237
c HYP595 Hypertension, Essential 69 0.078
238
ADJ001 Adjustment Disorder 38 0.078
239
P CRD011 Cardiomyopathy 67 0.078
240
SPC003 Specific Developmental Disorder 40 0.078
241
c ADL079 Adult Heart Tumor 19 0.078
242
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.078
243
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.078
244
c CNT075 Central Precocious Puberty 53 0.078
245
P OCY001 Oocyte Maturation Defect 39 0.078
246
PRD004 Prediabetes Syndrome 43 0.077
247
ETH011 Ethylmalonic Encephalopathy 59 0.077
248
BRN071 Brain Injury 52 0.077
249
P LYM026 Lymphoblastic Leukemia 60 0.077
250
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.077
251
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.077
252
LYM020 Lymph Node Cancer 41 0.077
253
RTN023 Retinitis 49 0.076
254
P OVR046 Ovarian Cyst 50 0.076
255
P AST005 Asthma 82 0.075
256
BNF002 Bone Fracture 47 0.075
257
PPL010 Papillary Follicular Thyroid Adenocarcinoma 17 0.075
258
VSC007 Vascular Disease 67 0.075
259
P ADD001 Addison's Disease 62 0.075
260
ADR012 Adrenal Gland Disease 49 0.075
261
VSC006 Vascular Cancer 54 0.075
262
HYP020 Hyperprolactinemia 57 0.075
263
BNR001 Bone Remodeling Disease 40 0.074
264
P HST010 Histiocytosis 55 0.074
265
MSC072 Muscle Cancer 51 0.074
266
LRN003 Learning Disability 51 0.074
267
P PND002 Pendred Syndrome 56 0.074
268
c TRC078 Trichohepatoenteric Syndrome 2 31 0.073
269
PRP021 Peripheral Nervous System Neoplasm 50 0.073
270
P BPL003 Bipolar Disorder 62 0.073
271
FDL002 Food Allergy 54 0.073
272
LNG099 Lung Disease 62 0.073
273
c HPT073 Hepatitis C Virus 72 0.073
274
P SLP006 Sleep Apnea 61 0.073
275
THY096 Thyroid Carcinoma, Hurthle Cell 28 0.072
276
P AMY004 Amyloidosis 64 0.072
277
URT039 Urticaria 59 0.072
278
END036 Endocrine Organ Benign Neoplasm 37 0.072
279
P THL005 Thalassemia 61 0.072
280
STR067 Stroke, Ischemic 77 0.072
281
FRB001 Farber Lipogranulomatosis 51 0.071
282
P ESP024 Esophagitis 62 0.071
283
P UTR038 Uterine Disease 40 0.071
284
PLS009 Plasma Cell Neoplasm 48 0.071
285
P NRV007 Nervous System Disease 71 0.070
286
P PNC035 Pancreatic Cancer 85 0.070
287
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.070
288
ANX002 Anxiety Disorder 69 0.070
289
P MTC069 Mitochondrial Disorders 52 0.070
290
DRG001 Drug Psychosis 40 0.070
291
PRT036 Peritonitis 62 0.070
292
PLS011 Plasmacytoma 56 0.070
293
NNT010 Nontoxic Goiter 34 0.070
294
CYS001 Cystic Fibrosis 86 0.070
295
ATM059 Autoimmune Disease 6 26 0.069
296
CLT003 Colitis 59 0.069
297
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.069
298
NNT019 Neonatal Hypothyroidism 35 0.069
299
OBS061 Obstructive Sleep Apnea 66 0.069
300
P ATX004 Ataxia 53 0.069
301
P DBT005 Diabetes Insipidus 53 0.069
302
HYP029 Hyperthyroxinemia 25 0.069
303
ADR021 Adrenocorticotropic Hormone Deficiency 45 0.069
304
P MLT019 Multiple Myeloma 80 0.069
305
SML033 Small Cell Cancer of the Lung, Somatic 53 0.069
306
PRT038 Protein-Energy Malnutrition 49 0.069
307
P EST001 Estrogen-Receptor Positive Breast Cancer 48 0.069
308
c HMG001 Hemoglobin C Disease 47 0.068
309
PRM097 Primary Immunodeficiency Disease 61 0.068
310
P RCK004 Rickets 59 0.068
311
P ESN007 Eosinophilia 61 0.068
312
TRM010 Traumatic Brain Injury 52 0.068
313
P PLM037 Pulmonary Hypertension 79 0.068
314
ADR005 Adrenal Carcinoma 56 0.068
315
PTT008 Pituitary Carcinoma 44 0.068
316
CRV034 Cervical Benign Neoplasm 12 0.068
317
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.067
318
PRD011 Proud Syndrome 42 0.067
319
CCN007 Cocoon Syndrome 35 0.067
320
P PRP029 Porphyria 58 0.067
321
LPM004 Lipoma 58 0.067
322
IMP003 Impaired Renal Function Disease 37 0.066
323
OVR029 Ovarian Hyperstimulation Syndrome 60 0.066
324
TNG009 Tongue Squamous Cell Carcinoma 74 0.066
325
END030 End Stage Renal Failure 52 0.066
326
c CRN177 Coronary Heart Disease 7 22 0.066
327
c CRN173 Coronary Heart Disease 8 20 0.066
328
ATR060 Atrial Standstill, Digenic 53 0.066
329
P PRP019 Peripheral Nervous System Disease 54 0.066
330
P PRD008 Periodontitis 46 0.066
331
MTC005 Mitochondrial Metabolism Disease 38 0.065
332
GST050 Gastrointestinal System Disease 54 0.065
333
P CHR084 Chromosomal Disease 37 0.065
334
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.065
335
TBR010 Tuberculosis 69 0.065
336
P GND004 Gonadal Dysgenesis 53 0.065
337
WLS001 Wilson Disease 72 0.065
338
c PND001 Pain Disorder 55 0.065
339
LYM019 Lymphosarcoma 53 0.065
340
P INT063 Intellectual Disability 53 0.065
341
LMY002 Leiomyoma 42 0.065
342
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.064
343
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.064
344
P RSP003 Respiratory Failure 70 0.064
345
DRM006 Dermatitis 61 0.064
346
NRM005 Neuromuscular Disease 57 0.064
347
c HPT016 Hepatitis B 64 0.064
348
RHM027 Rheumatic Disease 57 0.063
349
CHL068 Cholestasis 58 0.063
350
WST001 West Syndrome 61 0.063
351
CLN019 Colonic Disease 50 0.063
352
HDG012 Hodgkin Lymphoma 73 0.063
353
KRT002 Keratomalacia 54 0.063
354
P ALZ034 Alzheimer Disease 93 0.063
355
KLN001 Klinefelter's Syndrome 55 0.063
356
c ACT075 Acute Myocardial Infarction 60 0.063
357
ANV001 Anovulation 45 0.063
358
PSY004 Psychotic Disorder 67 0.062
359
RDN001 Reading Disorder 39 0.062
360
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.062
361
CVT001 Cavitary Optic Disc Anomalies 32 0.062
362
P HYP014 Hyperuricemia 50 0.062
363
NSY001 N Syndrome 39 0.061
364
GST078 Gastrointestinal Allergy 41 0.061
365
MDS022 Mediastinitis 41 0.061
366
VSC008 Vascular Hemostatic Disease 33 0.061
367
HDN002 Head Injury 45 0.060
368
CRV038 Cervical Squamous Cell Carcinoma 59 0.060
369
P GLY013 Glycogen Storage Disease 59 0.060
370
P INF038 Influenza 74 0.060
371
ADM013 Adamantinoma of Long Bones 59 0.060
372
ULC004 Ulcerative Colitis 75 0.060
373
HYP005 Hypokalemia 51 0.060
374
c CNT035 Central Nervous System Disease 59 0.060
375
EST007 Estrogen Resistance 45 0.060
376
P AST007 Astrocytoma 65 0.060
377
ATP002 Atopy 63 0.060
378
ALC007 Alcohol Dependence 65 0.060
379
CND002 Conduct Disorder 56 0.059
380
P ECL001 Eclampsia 54 0.059
381
P GST049 Gastrointestinal System Cancer 60 0.059
382
c MLG081 Malignant Teratoma 46 0.059
383
NWC001 Newcastle Disease 54 0.059
384
LRN004 Laron Dwarfism 59 0.059
385
P SHR001 Short Bowel Syndrome 48 0.059
386
c VRL010 Viral Hepatitis 61 0.059
387
c MTR002 Mitral Valve Insufficiency 44 0.059
388
P MYL006 Myeloid Leukemia 67 0.059
389
MVM001 Movement Disease 54 0.059
390
THY021 Thyroid Malformation 13 0.058
391
NSP002 Nasopharyngitis 41 0.058
392
c CLL013 Cell Type Cancer 48 0.058
393
P ALP009 Alopecia Areata 61 0.058
394
SVR004 Severe Combined Immunodeficiency 68 0.058
395
EXF001 Exfoliation Syndrome 57 0.058
396
P PLN008 Peeling Skin Syndrome 47 0.058
397
THY098 Thyroid Ectopia 27 0.058
398
P RNL015 Renal Hypertension 47 0.058
399
ACN011 Acne 63 0.058
400
c ACT073 Acute Leukemia 62 0.058
401
P PRM006 Primary Biliary Cirrhosis 52 0.058
402
CYS010 Cystinosis 51 0.058
403
HPT074 Hepatic Adenoma, Somatic 51 0.058
404
HMT018 Hematopoietic Stem Cell Transplantation 41 0.058
405
SNS023 Sensory System Cancer 46 0.058
406
EXT010 Extramedullary Plasmacytoma 49 0.058
407
P RTN024 Retinoblastoma 75 0.057
408
GNR004 Generalized Anxiety Disorder 51 0.057
409
DDN006 Duodenitis 44 0.057
410
ADR007 Adrenoleukodystrophy 71 0.057
411
P GLM007 Glomerulonephritis 56 0.057
412
INT253 Intestinal Benign Neoplasm 50 0.057
413
GLC006 Galactosemia 67 0.057
414
BLD053 Blood Platelet Disease 46 0.057
415
P INT068 Intestinal Disease 61 0.057
416
CRH001 Crohn's Disease 76 0.057
417
ETH004 Euthyroid Sick Syndrome 38 0.056
418
KWS001 Kwashiorkor 44 0.056
419
THY069 Thyroid Hormone Resistance, Selective Pituitary 21 0.056
420
SPC010 Speech and Communication Disorders 46 0.056
421
BNM008 Bone Mineral Density, Low 19 0.056
422
DFC004 Deficiency Anemia 65 0.056
423
NSD001 Nose Disease 52 0.056
424
c ADL017 Adult T-Cell Leukemia 58 0.056
425
ANR040 Aneurysm 57 0.056
426
P PNM007 Pneumonia 66 0.056
427
HYP189 Hypoadrenalism 40 0.056
428
P HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 36 0.056
429
P MYS003 Myasthenia Gravis 65 0.056
430
AYM001 Ayme-Gripp Syndrome 45 0.056
431
YNG002 Young Syndrome 26 0.056
432
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.055
433
ISL001 Islet Cell Tumor 50 0.055
434
IMM127 Immune System Cancer 42 0.055
435
P GLB002 Glioblastoma 66 0.055
436
DYS073 Dysphagia 49 0.055
437
c RNL003 Renal Clear Cell Carcinoma 52 0.055
438
IRN002 Iron Metabolism Disease 43 0.055
439
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.055
440
c INF067 Inflammatory Bowel Disease 10 51 0.055
441
OST011 Osteomalacia 48 0.055
442
MRG013 Mirage Syndrome 26 0.055
443
CHR008 Choroiditis 43 0.055
444
LKC003 Leukocyte Disease 47 0.055
445
P HYP192 Hypocalcemia, Autosomal Dominant 55 0.055
446
PLM011 Plummer's Disease 38 0.055
447
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.055
448
c MLG059 Malignant Struma Ovarii 35 0.055
449
P ACT074 Acute Lymphocytic Leukemia 55 0.055
450
P DRR001 Diarrhea 51 0.055
451
HDC001 Headache 54 0.055
452
NRL016 Neural Tube Defects 76 0.054
453
BRS099 Breast Ductal Carcinoma 52 0.054
454
P GST044 Gastritis 58 0.054
455
SWL001 Swallowing Disorders 34 0.054
456
P THY023 Thymoma 53 0.054
457
GST045 Gastroenteritis 60 0.054
458
c HPT003 Hepatitis a 59 0.054
459
ACT087 Acth Deficiency 43 0.054
460
PHS001 Phosphorus Metabolism Disease 42 0.054
461
PTT046 Pituitary Hormone Deficiency, Combined, 2 53 0.054
462
VSC011 Vasculitis 62 0.054
463
LYM024 Lymphatic System Disease 50 0.054
464
GLC077 Glucocorticoid Therapy, Response to 19 0.054
465
P DRM010 Dermatomyositis 58 0.053
466
P HMC003 Hemochromatosis 72 0.053
467
c ADL001 Adult Lymphoma 41 0.053
468
P GT001 Gout 58 0.053
469
LPM005 Lipomatosis 47 0.053
470
FNC006 Functional Gastric Disease 34 0.053
471
OPT006 Optic Nerve Disease 51 0.053
472
FST001 Foster-Kennedy Syndrome 34 0.053
473
c CRN176 Coronary Heart Disease 9 20 0.053
474
LYM023 Lymphatic System Cancer 35 0.053
475
VGN023 Vaginitis 42 0.053
476
NPH003 Nephrocalcinosis 46 0.053
477
c CHR090 Chronic Lymphocytic Leukemia 74 0.053
478
ACN002 Acanthosis Nigricans 57 0.053
479
DFF005 Diffuse Large B-Cell Lymphoma 56 0.053
480
PSR001 Psoriatic Arthritis 64 0.053
481
CRY002 Cryptorchidism 62 0.053
482
c ATM011 Autoimmune Hepatitis 58 0.052
483
RNL007 Renal Tubular Acidosis 50 0.052
484
GLC037 Glucocorticoid Resistance 62 0.052
485
P BLD051 Blood Coagulation Disease 45 0.052
486
AND015 Androgen Insensitivity 63 0.052
487
WRN001 Werner Syndrome 67 0.052
488
PST021 Postpartum Depression 49 0.052
489
P LMY004 Leiomyosarcoma 53 0.052
490
THL018 Thalassemia Major 42 0.052
491
BNM001 Bone Marrow Cancer 52 0.052
492
P ATR011 Atrial Fibrillation 64 0.052
493
P TRC086 Trichohepatoenteric Syndrome 1 46 0.052
494
PTT004 Pituitary Apoplexy 39 0.052
495
BRC012 Brucellosis 65 0.052
496
P MTR004 Maturity-Onset Diabetes of the Young 57 0.052
497
P MSC007 Muscle Hypertrophy 59 0.052
498
WLL001 Williams-Beuren Syndrome 61 0.052
499
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.052
500
c HMG004 Hemoglobin D Disease 33 0.051
501
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.051
502
PHC013 Phaeochromocytoma 41 0.051
503
CLN015 Colon Adenocarcinoma 49 0.051
504
THY041 Thyroxine-Binding Globulin Deficiency 25 0.051
505
c INF071 Inflammatory Bowel Disease 1 51 0.051
506
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.051
507
c HYP163 Hyperlipidemia Type 3 34 0.051
508
CNT098 Central Core Disease 66 0.051
509
P STR020 Strabismus 53 0.051
510
THY065 Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia 22 0.051
511
c MYC058 Myocardial Infarction 2 29 0.051
512
CHR074 Choriocarcinoma 46 0.051
513
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.051
514
c HYP615 Hyperparathyroidism, Familial Primary 55 0.051
515
P CTR002 Cataract 57 0.051
516
RTN018 Retinal Disease 56 0.051
517
ALL001 Allan-Herndon-Dudley Syndrome 47 0.051
518
P ENC004 Encephalitis 61 0.051
519
c CNG031 Congenital Nervous System Abnormality 39 0.051
520
CTS003 Coats Disease 57 0.051
521
P PNC025 Panic Disorder 60 0.051
522
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.051
523
FNC007 Functioning Pituitary Adenoma 41 0.050
524
RDT005 Radiation Induced Cancer 28 0.050
525
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.050
526
c SML034 Small Cell Neuroendocrine Carcinoma 40 0.050
527
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.050
528
P PRS038 Personality Disorder 61 0.050
529
NNT003 Neonatal Thyrotoxicosis 26 0.050
530
P MNN013 Meningitis 65 0.050
531
c DLT002 Dilated Cardiomyopathy 75 0.050
532
SPN186 Spinal Cord Injury 62 0.050
533
c SCH051 Schizophrenia 4 31 0.050
534
P GRN010 Granular Cell Tumor 47 0.050
535
P HML002 Hemolytic Anemia 60 0.050
536
VSC009 Vascular Skin Disease 22 0.050
537
CRB031 Cerebral Arterial Disease 31 0.050
538
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.050
539
P PLR004 Pleuropulmonary Blastoma 64 0.050
540
RNL101 Renal Cell Carcinoma, Papillary 67 0.050
541
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.049
542
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.049
543
P LCH002 Lichen Planus 53 0.049
544
IDN001 Iodine Hypothyroidism 14 0.049
545
P LCT001 Lactic Acidosis 52 0.049
546
c FML108 Familial Breast Cancer 57 0.049
547
SRT004 Serotonin Syndrome 49 0.049
548
c PLN017 Peeling Skin Syndrome 1 33 0.049
549
P HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 58 0.049
550
SFT003 Soft Tissue Sarcoma 56 0.049
551
HNM002 Hinman Syndrome 25 0.049
552
HRD059 Hereditary Peripheral Nervous Disorder 14 0.049
553
P CNN004 Connective Tissue Cancer 45 0.049
554
TST014 Testicular Cancer 52 0.049
555
c ACT020 Acute T Cell Leukemia 39 0.049
556
AND005 Androgen Insensitivity Syndrome, Mild 16 0.049
557
P DYS070 Dysalbuminemic Hyperthyroxinemia 20 0.049
558
RBR001 Roberts Syndrome 59 0.049
559
ADR010 Adrenal Cortical Hypofunction 38 0.049
560
FXF002 Fox-Fordyce Disease 39 0.049
561
P MTC003 Metachromatic Leukodystrophy 71 0.049
562
P ADL010 Adult Respiratory Distress Syndrome 60 0.049
563
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.048
564
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.048
565
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.048
566
P LYD001 Leydig Cell Tumor 44 0.048
567
P LKD001 Leukodystrophy 58 0.048
568
RFR004 Refractory Hematologic Cancer 29 0.048
569
BLT006 Bilateral Breast Cancer 52 0.048
570
ANG054 Angina Pectoris 51 0.048
571
CRV047 Cervical Cancer, Somatic 65 0.048
572
LYS002 Lysosomal Storage Disease 52 0.048
573
STT009 Sutton Disease 2 20 0.048
574
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.048
575
SPN369 Spinal Disease 41 0.048
576
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.048
577
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.048
578
HYP037 Hyperhomocysteinemia 50 0.047
579
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.047
580
ESP021 Esophageal Cancer 75 0.047
581
INT075 Intracranial Hypertension 53 0.047
582
P HRD018 Hair Disease 50 0.047
583
OCL006 Ocular Hypertension 48 0.047
584
c PSD067 Pseudohypoparathyroidism Ia 52 0.047
585
P PLM036 Pulmonary Fibrosis 68 0.047
586
CHL061 Childhood Leukemia 48 0.047
587
TRN007 Transsexualism 41 0.047
588
P TCL004 T-Cell Leukemia 46 0.047
589
c PLN021 Peeling Skin Syndrome 3 31 0.047
590
P CNJ013 Conjunctivitis 65 0.047
591
RHB003 Rhabdomyosarcoma 58 0.047
592
MLR004 Malaria 79 0.047
593
P OST005 Osteogenesis Imperfecta 67 0.047
594
P SZR006 Seizure Disorder 57 0.047
595
NNF007 Non-Functioning Pituitary Adenoma 40 0.047
596
c CNN010 Connective Tissue Benign Neoplasm 35 0.047
597
OST004 Osteitis Fibrosa 41 0.047
598
P ALX003 Alexander Disease 64 0.047
599
P OST001 Osteopetrosis 62 0.047
600
P SJG001 Sjogren's Syndrome 53 0.047
601
P FTT008 Fatty Liver Disease, Nonalcoholic 1 33 0.047
602
DRY001 Dry Eye Syndrome 51 0.046
603
P PRT013 Portal Hypertension 59 0.046
604
ATN005 Autonomic Dysfunction 45 0.046
605
JNT002 Joint Disorders 56 0.046
606
PRS045 Prostatic Hypertrophy 44 0.046
607
LYM067 Lymphoid Leukemia 43 0.046
608
MRG003 Marginal Zone B-Cell Lymphoma 50 0.046
609
c ACT027 Acute Pancreatitis 56 0.046
610
P ANG015 Angioedema 53 0.046
611
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.046
612
CRY004 Cryoglobulinemia 47 0.046
613
ADN021 Adenomatous Polyposis Coli 76 0.046
614
URC002 Urea Cycle Disorder 51 0.046
615
LBL001 Lobular Neoplasia 48 0.046
616
PRN039 Paraneoplastic Syndromes 33 0.046
617
P FLL037 Follicular Lymphoma 66 0.046
618
PRN011 Pernicious Anemia 46 0.046
619
c PLN018 Peeling Skin Syndrome 2 35 0.046
620
PRP074 Peripheral Resistance to Thyroid Hormones 17 0.046
621
LYM027 Lymphopenia 54 0.046
622
PHR003 Pharyngitis 58 0.046
623
P FBR017 Fibrosarcoma 56 0.045
624
DMY004 Demyelinating Disease 55 0.045
625
ORL015 Oral Squamous Cell Carcinoma 56 0.045
626
PLV005 Pelviureteric Junction Obstruction 45 0.045
627
PRT011 Protein C Deficiency 51 0.045
628
P ASP006 Aspergillosis 60 0.045
629
HYP344 Hyperthyroidism, Familial Gestational 27 0.045
630
BNN003 Bone Inflammation Disease 46 0.045
631
c FML297 Familial Thyroid Dyshormonogenesis 31 0.045
632
P PRC031 Preeclampsia/eclampsia 1 57 0.045
633
CRT015 Carotid Artery Occlusion 43 0.045
634
GST040 Gastric Adenocarcinoma 52 0.045
635
GST071 Gastrointestinal Carcinoma 41 0.045
636
FCT008 Factitious Disorder 43 0.045
637
NRF007 Neurofibroma 52 0.045
638
IRN001 Iron Deficiency Anemia 51 0.045
639
PRP016 Paraplegia 49 0.045
640
P MNN018 Mannosidosis 41 0.045
641
ANG049 Angioedema Induced by Ace Inhibitors 35 0.045
642
END080 Endometrial Disease 42 0.045
643
LYM021 Lymphadenitis 58 0.045
644
c BPL002 Bipolar I Disorder 47 0.045
645
PLM033 Pulmonary Embolism 59 0.045
646
CNV002 Conversion Disorder 42 0.045
647
P MYT002 Myotonic Dystrophy 47 0.045
648
PRM025 Primary Bacterial Infectious Disease 43 0.045
649
BRN080 Brain Ischemia 41 0.045
650
HYP249 Hyperthyroidism, Nonautoimmune 27 0.044
651
P PLY019 Polyneuropathy 54 0.044
652
EMP001 Empty Sella Syndrome 40 0.044
653
SYN036 Syncope 47 0.044
654
RCT017 Rectal Disease 39 0.044
655
PRT014 Protein S Deficiency 52 0.044
656
c THY071 Thyroid Dyshormonogenesis 1 23 0.044
657
APH001 Aphthous Stomatitis 62 0.044
658
GST023 Gastric Ulcer 55 0.044
659
P HYP237 Hypercalcemia, Infantile 51 0.044
660
FCT003 Factor X Deficiency 62 0.044
661
P UVT001 Uveitis 59 0.044
662
P THY061 Thyroid Dyshormonogenesis 2a 22 0.044
663
P CHL066 Cholangitis 49 0.044
664
INT066 Interstitial Lung Disease 58 0.044
665
P CYS017 Cystic Teratoma 41 0.044
666
P DYS154 Dystonia 64 0.044
667
BCL002 B Cell Deficiency 50 0.044
668
MRK001 Merkel Cell Carcinoma 51 0.044
669
VRL011 Viral Infectious Disease 59 0.043
670
ATN004 Autonomic Neuropathy 44 0.043
671
SPS057 Spasticity 42 0.043
672
GNG013 Gingivitis 60 0.043
673
ADN027 Adenomyosis 46 0.043
674
P TRM003 Tremor 54 0.043
675
CYT008 Cytomegalovirus Infection 51 0.043
676
PRM013 Premature Menopause 44 0.043
677
P RHN004 Rhinitis 61 0.043
678
MTR014 Motor Neuron Disease 59 0.043
679
LYM040 Lymphoblastic Lymphoma 54 0.043
680
P THY054 Thyrotoxic Periodic Paralysis 47 0.043
681
P HYP265 Hypotonia 39 0.043
682
c MCR115 Microvascular Complications of Diabetes 5 60 0.043
683
SPN051 Spondylitis 50 0.043
684
CRB150 Cerebral Creatine Deficiency Syndrome 2 48 0.043
685
P KLL001 Kallmann Syndrome 60 0.043
686
ORL013 Oral Lichen Planus 47 0.043
687
P HRP006 Herpes Simplex 65 0.043
688
SKL014 Skeletal Dysplasia 46 0.043
689
SKL017 Skeletal Dysplasias 45 0.043
690
GLB015 Glioblastoma Multiforme 62 0.043
691
P PLY041 Polymyositis 51 0.043
692
NCT008 Nicotine Dependence, Protection Against 52 0.043
693
P MYS005 Myositis 56 0.043
694
c MCR113 Microvascular Complications of Diabetes 3 49 0.043
695
P THR014 Thrombocytopenia 64 0.043
696
HYP002 Hypothalamic Neoplasm 23 0.042
697
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.042
698
NRL005 Neurilemmoma 51 0.042
699
c HMG003 Hemoglobin E Disease 44 0.042
700
c ACT210 Acute Respiratory Distress Syndrome 57 0.042
701
VTM002 Vitamin B12 Deficiency 44 0.042
702
GLB001 Gilbert Syndrome 61 0.042
703
P LYM033 Lymphoproliferative Syndrome 53 0.042
704
CHL123 Chlamydia 59 0.042
705
ALC009 Alcoholic Liver Cirrhosis 48 0.042
706
SPN041 Spinal Cord Disease 48 0.042
707
P EXN002 Exanthem 57 0.042
708
P NSP012 Nasopharyngeal Carcinoma 67 0.042
709
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.042
710
c DLT001 Delta Chain Disease 16 0.042
711
c RNL034 Renal Cell Carcinoma 4 21 0.042
712
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.042
713
GYN001 Gynecomastia 49 0.042
714
CRD001 Cardiac Tamponade 44 0.042
715
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.042
716
CLR030 Clear Cell Renal Cell Carcinoma 51 0.042
717
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.041
718
c HYP072 Hypersensitivity Reaction Type Iii Disease 41 0.041
719
P CHR345 Chronic Pain 49 0.041
720
SKN005 Skin Atrophy 43 0.041
721
c NRF018 Neurofibromatosis, Type 1 68 0.041
722
PRP030 Purpura 59 0.041
723
CHR066 Chronic Fatigue Syndrome 64 0.041
724
INS001 Insulinoma 59 0.041
725
ESP023 Esophageal Disease 53 0.041
726
AMN006 Aminoaciduria 42 0.041
727
BRS050 Breast Cyst 37 0.041
728
MDY004 Mody, Type Iii 37 0.041
729
ADN001 Adenosine Deaminase Deficiency 45 0.041
730
FCL014 Focal Epilepsy 56 0.041
731
BLM002 Bulimia Nervosa 54 0.041
732
P ATR005 Atrophic Gastritis 45 0.041
733
PRG014 Progesterone Resistance 41 0.041
734
P SCL009 Sclerosing Cholangitis 47 0.041
735
MNT001 Mantle Cell Lymphoma 70 0.041
736
CRD119 Cardiac Arrest 63 0.041
737
MYC033 Myoclonus 41 0.041
738
PTT043 Pituitary Hormone Deficiency, Combined, 6 19 0.041
739
RCT018 Rectal Neoplasm 55 0.041
740
PRX034 Peroxisome Disorders 40 0.041
741
MYM001 Myoma 51 0.040
742
c HYP058 Hypervitaminosis a 38 0.040
743
P DYS021 Dysautonomia 47 0.040
744
PRN021 Paranasal Sinus Disease 50 0.040
745
PRP036 Peripheral T-Cell Lymphoma 45 0.040
746
SCN001 Secondary Hyperparathyroidism of Renal Origin 41 0.040
747
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.040
748
MLT021 Multiple System Atrophy 71 0.040
749
c CSH004 Cushing Syndrome Due to Ectopic Acth Secretion 27 0.040
750
c CLL012 Cell Type Benign Neoplasm 41 0.040
751
HRT029 Heart Tumor of the Child 17 0.040
752
TXC005 Toxic Shock Syndrome 61 0.040
753
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.040
754
LYM115 Lymphoma, Non-Hodgkin 65 0.040
755
c MJR008 Major Affective Disorder 2 22 0.040
756
RTC005 Reticulosarcoma 48 0.040
757
ATH010 Athyreosis 30 0.040
758
P CHN012 Chondrosarcoma 57 0.040
759
ART016 Aortic Aneurysm 67 0.040
760
c CLR079 Colorectal Cancer 2 31 0.040
761
CLC006 Calcinosis 49 0.040
762
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 44 0.040
763
P SNS014 Sinusitis 60 0.040
764
P INT070 Intestinal Obstruction 56 0.040
765
MCN001 Mucinous Adenocarcinoma 50 0.040
766
c BSL007 Basal Cell Carcinoma 64 0.040
767
BCK006 Back Pain 42 0.040
768
P SLV002 Salivary Gland Cancer 61 0.040
769
TLL001 Tall Cell Variant Papillary Carcinoma 13 0.040
770
MYL009 Myelodysplastic Syndrome 74 0.040
771
SCK003 Sickle Cell Anemia 68 0.040
772
c CLR085 Colorectal Cancer 1 42 0.040
773
c THR092 Thrombophilia Due to Thrombin Defect 56 0.039
774
c LKM062 Leukemia, Acute Lymphoblastic 64 0.039
775
c MJR007 Major Affective Disorder 1 28 0.039
776
ARM001 Aromatase Deficiency 57 0.039
777
DBT008 Diabetic Angiopathy 45 0.039
778
c SCN052 Secondary Adrenal Insufficiency 36 0.039
779
c ANR038 Anorexia Nervosa 1 29 0.039
780
c HYP311 Hyperparathyroidism 3 34 0.039
781
ALL014 Allergic Encephalomyelitis 32 0.039
782
DST006 Diastolic Heart Failure 46 0.039
783
CLR109 Colorectal Adenocarcinoma 50 0.039
784
UTR033 Uterine Corpus Cancer 50 0.039
785
BSL008 Basal Ganglia Disease 43 0.039
786
VGN020 Vaginal Disease 45 0.039
787
P LRY044 Larynx Cancer 59 0.039
788
TTH006 Tooth Disease 52 0.039
789
P DRM007 Dermatitis Herpetiformis 46 0.039
790
GST088 Gastric Endocrine Tumor 17 0.039
791
MLG056 Malignant Hyperthermia 57 0.039
792
SMT003 Somatostatinoma 42 0.039
793
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
794
MND006 Mondor Disease 21 0.039
795
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.039
796
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.039
797
FNC005 Functional Colonic Disease 30 0.039
798
DBT002 Diabetic Autonomic Neuropathy 42 0.039
799
GRN016 Grant Syndrome 30 0.038
800
BRN002 Bronchiolitis 56 0.038
801
LYM104 Lymphoma, Malt, Somatic 54 0.038
802
P GLL020 Gallbladder Disease 59 0.038
803
MLK006 Milk Allergy 44 0.038
804
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.038
805
GLL018 Gallbladder Cancer 63 0.038
806
P SCL015 Scleritis 49 0.038
807
CRV069 Cervix Disease 34 0.038
808
c CHR418 Chronic Leukemia 48 0.038
809
P MYC008 Myocarditis 54 0.038
810
UPP004 Upper Respiratory Tract Disease 48 0.038
811
PLM001 Pulmonary Tuberculosis 68 0.038
812
ALC006 Alcoholic Hepatitis 59 0.038
813
CNT067 Central Cord Syndrome 24 0.038
814
P VNS003 Venous Insufficiency 53 0.038
815
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.038
816
CCN002 Cocaine Abuse 47 0.038
817
SNS001 Sensorineural Hearing Loss 57 0.038
818
P TMP003 Temporal Arteritis 60 0.038
819
PTZ001 Peutz-Jeghers Syndrome 70 0.038
820
OBS020 Obesity, Adrenal Insufficiency, and Red Hair Due to Pomc Deficiency 30 0.038
821
P THR015 Thrombophilia 59 0.038
822
P HVY001 Heavy Chain Disease 41 0.038
823
c CHR579 Chiari Malformation Type Ii 38 0.038
824
EYC003 Eye Accommodation Disease 26 0.038
825
P LNG064 Lung Cancer Susceptibility 3 62 0.038
826
MLG088 Malignant Germ Cell Tumor 36 0.038
827
HYP343 Hypothryoidism, Congenital, Nongoitrous 4 38 0.038
828
CRB037 Cerebral Palsy 54 0.038
829
TCL003 T Cell Deficiency 45 0.038
830
CWM001 Cow Milk Allergy 40 0.038
831
P PRK057 Parkinson Disease, Late-Onset 72 0.038
832
FBR019 Fibromatosis 42 0.038
833
ADT003 Auditory System Disease 51 0.038
834
P CRB088 Cerebral Atrophy 42 0.037
835
P RTN008 Retinitis Pigmentosa 79 0.037
836
c INV001 Invasive Aspergillosis 47 0.037
837
SLV003 Salivary Gland Disease 49 0.037
838
BRN038 Bronchial Disease 54 0.037
839
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.037
840
P ACT135 Acute Graft Versus Host Disease 53 0.037
841
DBT010 Diabetic Neuropathy 55 0.037
842
ADP007 Adie Pupil 34 0.037
843
MCP033 Mucopolysaccharidoses 39 0.037
844
P HMR012 Hemorrhagic Fever 55 0.037
845
THR004 Thrombocytosis 55 0.037
846
P DDN001 Duodenal Ulcer 51 0.037
847
THY039 Thyrotropin-Releasing Hormone Deficiency 28 0.037
848
IMM025 Immunoglobulin a Deficiency 2 27 0.037
849
P RTN014 Retinal Artery Occlusion 43 0.037
850
P OPN001 Open-Angle Glaucoma 48 0.037
851
ADL030 Adult-Onset Still's Disease 57 0.037
852
MYC002 Mycobacterium Avium Complex Disease 51 0.037
853
P RTT002 Rett Syndrome 78 0.037
854
P MMB011 Membranous Nephropathy 56 0.037
855
c ATM010 Autoimmune Hemolytic Anemia 60 0.037
856
NNT024 Neonatal Stroke 37 0.037
857
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.037
858
P PYL005 Pyelonephritis 52 0.037
859
LCT002 Lactose Intolerance 45 0.037
860
PRC013 Pericarditis 52 0.036
861
P ATP001 Atopic Dermatitis 62 0.036
862
HDR003 Hidradenitis 46 0.036
863
SMN007 Seminoma 42 0.036
864
P ACT150 Acute Adrenal Insufficiency 45 0.036
865
HPT020 Hepatic Vascular Disease 44 0.036
866
FSH003 Fish Allergy 30 0.036
867
TKY002 Takayasu Arteritis 60 0.036
868
ALP001 Alopecia Universalis 57 0.036
869
c GLY008 Glycogen Storage Disease Ii 61 0.036
870
ADN064 Adenohypophysitis 28 0.036
871
c HPT007 Hepatitis E 54 0.036
872
DSC009 Discoid Lupus Erythematosus 44 0.036
873
PST014 Postsurgical Hypothyroidism 23 0.036
874
BLD044 Bladder Disease 51 0.036
875
P CNT005 Central Nervous System Lymphoma 53 0.036
876
P CRB042 Cerebellar Ataxia 64 0.036
877
ADG002 Audiogenic Seizures 25 0.036
878
P MYL005 Myelofibrosis 67 0.036
879
GTL001 Gitelman Syndrome 60 0.036
880
SBP001 Subependymal Giant Cell Astrocytoma 47 0.036
881
IDP033 Idiopathic Edema 45 0.036
882
PLS016 Plasma Cell Leukemia 42 0.036
883
HYP030 Hypoactive Sexual Desire Disorder 48 0.036
884
VRC001 Varicocele 50 0.036
885
c HMP029 Hemophilia a 64 0.036
886
c SVR005 Severe Pre-Eclampsia 48 0.036
887
MLG097 Malignant Mesenchymal Tumor 37 0.036
888
PLY020 Polyradiculoneuropathy 44 0.036
889
CHR034 Chromophobe Adenoma 41 0.036
890
c BRS046 Breast Benign Neoplasm 34 0.036
891
P LYN001 Lynch Syndrome 69 0.036
892
P GNT008 Giant Cell Tumor 49 0.036
893
c CHR064 Chronic Monocytic Leukemia 43 0.036
894
MLG108 Malignant Melanoma, Somatic 67 0.035
895
RTN020 Retinal Vascular Disease 50 0.035
896
SDD007 Sudden Cardiac Death 46 0.035
897
EXC002 Exocrine Pancreatic Insufficiency 43 0.035
898
CHN016 Cohen Syndrome 55 0.035
899
c ATM007 Autoimmune Disease of Central Nervous System 28 0.035
900
MLL012 Miller Syndrome 49 0.035
901
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.035
902
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 24 0.035
903
BLS002 Blastomycosis 42 0.035
904
RNL013 Renal Adenoma 32 0.035
905
FNT004 Fainting 33 0.035
906
c MCP003 Mucopolysaccharidosis Vii 63 0.035
907
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.035
908
c XNT010 Xanthinuria, Type I 48 0.035
909
c PSD104 Pseudohypoparathyroidism, Type Ii 28 0.035
910
IMP005 Impotence 50 0.035
911
MXD023 Mixed Cell Type Cancer 47 0.035
912
c CLR075 Colorectal Cancer 3 30 0.035
913
ACT118 Acute Non Lymphoblastic Leukemia 29 0.035
914
CHL018 Childhood Medulloblastoma 48 0.035
915
DYS014 Dyspepsia 50 0.035
916
FBR012 Fabry Disease 69 0.035
917
PSD009 Pseudohermaphroditism 40 0.035
918
P HYD006 Hydrocephalus 67 0.035
919
BCT002 Bacterial Vaginosis 51 0.035
920
BHR001 Behr Syndrome 44 0.035
921
P FML012 Familial Partial Lipodystrophy 51 0.035
922
P HMR003 Hemorrhagic Disease 57 0.035
923
ABL002 Ablepharon-Macrostomia Syndrome 57 0.035
924
P PNC001 Pancytopenia 52 0.035
925
NWB001 Newborn Respiratory Distress Syndrome 47 0.035
926
CYS014 Cystadenocarcinoma 46 0.035
927
RSP007 Respiratory Distress Syndrome, Infant 26 0.035
928
ACT103 Acute Lymphoblastic Leukemia, Childhood 42 0.035
929
GLC036 Glucagonoma 40 0.035
930
CRC014 Carcinoid Tumors, Intestinal 40 0.035
931
UTR031 Uterine Benign Neoplasm 26 0.035
932
PMS001 Poems Syndrome 55 0.035
933
CNT047 Contact Dermatitis 62 0.035
934
ALL010 Allergic Contact Dermatitis 57 0.035
935
CRV040 Cervix Carcinoma 53 0.035
936
c HRD088 Hereditary Neuropathies 41 0.035
937
SCH003 Schizophreniform Disorder 41 0.035
938
VCC001 Vaccinia 46 0.035
939
P FML161 Familial Mediterranean Fever, Ar 63 0.035
940
TRN015 Transient Cerebral Ischemia 56 0.035
941
BLR001 Biliary Atresia 51 0.035
942
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 25 0.035
943
GST019 Gastrointestinal Stromal Tumor 72 0.035
944
KRT004 Keratitis 70 0.035
945
BRK010 Burkitt Lymphoma 66 0.035
946
PNN001 Panniculitis 50 0.035
947
HYP074 Hypersensitivity Vasculitis 47 0.035
948
IMM001 Immune-Complex Glomerulonephritis 42 0.035
949
AMY002 Amyloid Tumor 37 0.035
950
OBS002 Obsessive-Compulsive Disorder 66 0.034
951
TRN018 Transitional Cell Carcinoma 54 0.034
952
OST003 Osteonecrosis 45 0.034
953
c MJR004 Major Affective Disorder 4 18 0.034
954
c FML303 Familial/multiple Cancer 16 0.034
955
SMN008 Semantic Dementia 44 0.034
956
NRT004 Neuritis 52 0.034
957
KRN002 Kearns-Sayre Syndrome 59 0.034
958
c RTN162 Retinitis Pigmentosa 2 51 0.034
959
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.034
960
NSL022 Nasal Cavity Disease 42 0.034
961
CNN002 Cannabis Abuse 41 0.034
962
MNN009 Meningoencephalitis 45 0.034
963
P LFR001 Li-Fraumeni Syndrome 75 0.034
964
INC002 Inclusion Body Myositis 63 0.034
965
c SVR001 Severe Acute Respiratory Syndrome 57 0.034
966
CHP002 Chops Syndrome 36 0.034
967
MLN003 Melancholia 34 0.034
968
P ACT080 Acute Pulmonary Heart Disease 32 0.034
969
c LKM061 Leukemia, Acute Myeloid 71 0.034
970
NRC007 Neuroectodermal Endocrine Syndrome 22 0.034
971
EVN001 Evans' Syndrome 43 0.034
972
QDR001 Quadriplegia 52 0.034
973
CRH005 Crohn's Colitis 52 0.034
974
c CHR417 Chronic Graft Versus Host Disease 50 0.034
975
DDN009 Duodenal Obstruction 32 0.034
976
CLF001 Cleft Lip 49 0.033
977
BRD001 Brody Myopathy 49 0.033
978
PRM020 Premenstrual Tension 46 0.033
979
c GLL026 Gallbladder Disease 3 19 0.033
980
BRD004 Borderline Personality Disorder 46 0.033
981
ANG018 Angiomyolipoma 46 0.033
982
BNL002 Bone Lymphoma 33 0.033
983
PRM151 Primary Bone Lymphoma 27 0.033
984
P APL001 Aplastic Anemia 73 0.033
985
P SPN052 Spondyloarthropathy 60 0.033
986
P CTN015 Cutaneous T Cell Lymphoma 50 0.033
987
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.033
988
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 27 0.033
989
c PRK031 Parkinson Disease 1 55 0.033
990
P ALG002 Alagille Syndrome 72 0.033
991
STT004 Steatorrhea 40 0.033
992
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 32 0.033
993
P BRN120 Bronchus Cancer 46 0.033
994
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.033
995
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 38 0.033
996
c HYP354 Hypothyroidism, Congenital Nongoitrous, 5 20 0.033
997
GLC011 Galactose Epimerase Deficiency 40 0.033
998
CRB040 Cerebrum Cancer 36 0.033
999
c NPH055 Nephrotic Syndrome, Type 1 59 0.033
1000
P LYM007 Lymphangioleiomyomatosis 65 0.033
1001
FBR009 Fibrous Dysplasia 44 0.033
1002
c MLT094 Multiple Sclerosis 3 26 0.033
1003
P TXP001 Toxoplasmosis 60 0.033
1004
BLL006 Bullous Pemphigoid 58 0.033
1005
PLC007 Placental Abruption 47 0.033
1006
c ACT159 Acute Transverse Myelitis 42 0.033
1007
CRS001 Crescentic Glomerulonephritis 41 0.033
1008
PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.033
1009
EXT035 Extrinsic Cardiomyopathy 39 0.033
1010
CYT018 Cytochrome P450 2d6 Variant 20 0.033
1011
NVS004 Nova Syndrome 19 0.033
1012
MNT045 Montefiore Syndrome 13 0.033
1013
ART012 Aortitis 31 0.033
1014
MCK007 Muckle-Wells Syndrome 61 0.033
1015
P LPR003 Leprosy 68 0.032
1016
CNS004 Constipation 57 0.032
1017
INT079 Intrahepatic Cholangiocarcinoma 55 0.032
1018
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.032
1019
P CTS001 Cutis Laxa 59 0.032
1020
INT067 Interstitial Nephritis 47 0.032
1021
OCL011 Ocular Motility Disease 38 0.032
1022
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.032
1023
LSH001 Leishmaniasis 62 0.032
1024
PRL017 Prolymphocytic Leukemia 47 0.032
1025
APP015 Apparent Mineralocorticoid Excess 52 0.032
1026
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 0.032
1027
CHD001 Chediak-Higashi Syndrome 64 0.032
1028
ICH054 Ichthyosis, X-Linked 48 0.032
1029
P CHR562 Chronic Myelocytic Leukemia 41 0.032
1030
CPL005 Capillary Disease 40 0.032
1031
CNN001 Cannabis Dependence 37 0.032
1032
HYP077 Hypertrichosis 52 0.032
1033
c MLT095 Multiple Sclerosis 4 19 0.032
1034
ZLL002 Zollinger-Ellison Syndrome 47 0.032
1035
GND002 Gender Identity Disorder 44 0.032
1036