Search results for "thyroid hormone metabolism"

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

1369 hits were found for 'thyroid hormone metabolism'

# Family MCID Name MIFTS Score
1
THY064 Thyroid Hormone Metabolism, Abnormal 25 5.446
2
P THY032 Thyroiditis 54 1.356
3
THY028 Thyroid Cancer 69 0.481
4
P HYP086 Hypothyroidism 64 0.380
5
P OBS005 Obesity 92 0.330
6
ADN018 Adenoma 58 0.303
7
P BRS047 Breast Cancer 100 0.295
8
P HPT021 Hepatitis 69 0.268
9
GRW007 Growth Hormone Deficiency 50 0.268
10
THY030 Thyroid Gland Disease 48 0.266
11
GTR002 Goiter 52 0.244
12
PRS047 Prostatitis 56 0.236
13
P PRS040 Prostate Cancer 90 0.234
14
P LYM118 Lymphoma 69 0.234
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.230
16
P GRV001 Graves' Disease 59 0.229
17
P ADN016 Adenocarcinoma 69 0.218
18
PPL002 Papillary Carcinoma 51 0.216
19
GLC008 Glucose Metabolism Disease 42 0.212
20
c SBC007 Subacute Thyroiditis 40 0.212
21
INS024 Insulin-Like Growth Factor I 75 0.212
22
DFF036 Differentiated Thyroid Carcinoma 50 0.209
23
END035 Endocrine Gland Cancer 49 0.208
24
P HYP076 Hyperthyroidism 55 0.205
25
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.197
26
NTR005 Nutritional Deficiency Disease 36 0.194
27
LPD008 Lipid Metabolism Disorder 58 0.191
28
P PLY011 Polycystic Ovary Syndrome 65 0.182
29
P THY097 Thyroid Hormone Resistance 54 0.180
30
P HYP060 Hyperinsulinism 58 0.180
31
END072 Endotheliitis 42 0.178
32
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.172
33
ACD009 Acid-Labile Subunit, Deficiency of 45 0.169
34
ADL002 Adult Syndrome 52 0.163
35
P MLT074 Multiple Endocrine Neoplasia 56 0.162
36
P HRT032 Heart Disease 75 0.160
37
MTB004 Metabolic Acidosis 48 0.160
38
HSH003 Hashimoto Thyroiditis 62 0.159
39
NRN002 Neuronitis 41 0.159
40
P PNC044 Pancreatitis 61 0.159
41
P KDN018 Kidney Disease 66 0.157
42
c CNG006 Congenital Hypothyroidism 60 0.155
43
ACR007 Acromegaly 66 0.153
44
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.152
45
P LKM002 Leukemia 71 0.152
46
PTT006 Pituitary Adenoma 56 0.149
47
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.148
48
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.148
49
P INF032 Infertility 59 0.147
50
CRB025 Carbohydrate Metabolic Disorder 46 0.145
51
ISL003 Isolated Growth Hormone Deficiency 52 0.145
52
CRB009 Cerebritis 39 0.142
53
P HYP083 Hypopituitarism 54 0.142
54
P HYP069 Hyperparathyroidism 58 0.142
55
P OST002 Osteoporosis 64 0.141
56
ALL026 Allergic Hypersensitivity Disease 52 0.140
57
EYD002 Eye Disease 61 0.139
58
P ENC018 Encephalopathy 59 0.139
59
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.137
60
P ART022 Arthritis 75 0.137
61
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.137
62
MLR007 Male Reproductive System Disease 34 0.137
63
P CRV039 Cervicitis 45 0.136
64
BNS002 Bone Structure Disease 37 0.135
65
ORL011 Oral Cancer 56 0.133
66
DWR001 Dwarfism 47 0.132
67
P MYP004 Myopathy 67 0.132
68
BNC003 Bone Cancer 58 0.132
69
ATH003 Atherosclerosis 65 0.131
70
MSC004 Muscle Tissue Disease 34 0.131
71
PTT009 Pituitary Gland Disease 47 0.130
72
P ORL007 Oral Cavity Cancer 59 0.130
73
PRS042 Prostate Disease 52 0.130
74
P NRV006 Nervous System Cancer 60 0.129
75
P LVR013 Liver Disease 75 0.129
76
THY103 Thyroid Cancer, Monmedullary, 1 53 0.126
77
P LNG032 Lung Cancer 95 0.126
78
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.124
79
HYP085 Hypothalamic Disease 44 0.124
80
c HPT001 Hepatitis C 68 0.124
81
P OVR049 Ovarian Disease 56 0.122
82
PRM243 Primary Bone Cancer 29 0.122
83
CHL071 Child Syndrome 58 0.121
84
HYP056 Hypoglycemia 61 0.121
85
RPR002 Reproductive System Disease 41 0.120
86
P OVR042 Ovarian Cancer 76 0.120
87
SQM006 Squamous Cell Carcinoma 70 0.120
88
KDS001 Kid Syndrome 53 0.118
89
CSY001 C Syndrome 50 0.118
90
GLT021 Glutaricaciduria, Type I 46 0.118
91
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.117
92
ATM014 Autoimmune Disease of Endocrine System 36 0.117
93
OVR063 Overnutrition 50 0.117
94
P TRN020 Turner Syndrome 65 0.117
95
P RHM011 Rheumatoid Arthritis 89 0.116
96
BND014 Bone Development Disease 40 0.116
97
ACR002 Acrocapitofemoral Dysplasia 33 0.116
98
BRT030 Birth Defects 43 0.116
99
HYP266 Hypoxia 56 0.115
100
FML039 Female Reproductive System Disease 48 0.115
101
P CRN211 Coronary Artery Disease 74 0.115
102
MDY003 Mody, Type Ii 36 0.114
103
ACR041 Acromelic Frontonasal Dysostosis 45 0.114
104
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.113
105
NRN004 Neuroendocrine Tumor 56 0.113
106
P MSC033 Muscle Disorders 52 0.112
107
HYP066 Hyperglycemia 61 0.112
108
GNR008 Generalized Resistance to Thyroid Hormone 34 0.112
109
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.111
110
END028 Endemic Goiter 35 0.111
111
PTT037 Pituitary Tumors 45 0.111
112
P HPT023 Hepatocellular Carcinoma 92 0.110
113
P CSH001 Cushing's Syndrome 65 0.110
114
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.110
115
HYP080 Hypogonadism 53 0.110
116
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.110
117
BRS051 Breast Disease 61 0.109
118
P RNL014 Renal Cell Carcinoma 82 0.109
119
MYX004 Myxedema 35 0.108
120
SXL003 Sexual Disorder 42 0.108
121
P HYP024 Hypoparathyroidism 53 0.107
122
BLD054 Blood Protein Disease 37 0.107
123
NDL007 Nodular Goiter 46 0.106
124
P SCH015 Schizophrenia 77 0.106
125
P KDN017 Kidney Cancer 65 0.106
126
ETN001 Eating Disorder 58 0.105
127
MLN008 Melanoma 62 0.105
128
FTT001 Fatty Liver Disease 59 0.103
129
P CLR023 Colorectal Cancer 97 0.103
130
WTH001 Withdrawal Disorder 37 0.103
131
INC022 Inclusion-Cell Disease 46 0.102
132
FML037 Female Breast Cancer 50 0.102
133
P MDL005 Medulloblastoma 77 0.102
134
WLL006 Wells Syndrome 59 0.102
135
ALR002 Al-Raqad Syndrome 36 0.101
136
PCK002 Pick Disease 68 0.101
137
STM006 Stomach Disease 50 0.100
138
GLC003 Glucose Intolerance 55 0.100
139
P PRC019 Precocious Puberty 51 0.100
140
P MYC007 Myocardial Infarction 79 0.100
141
PPL018 Papillary Adenocarcinoma 46 0.100
142
MDD011 Mood Disorder 61 0.100
143
SKN016 Skin Disease 66 0.099
144
OCL009 Ocular Cancer 59 0.099
145
ART111 Artery Disease 55 0.098
146
GDS001 Good Syndrome 44 0.098
147
P PRD006 Prader-Willi Syndrome 62 0.098
148
P LPS004 Lupus Erythematosus 64 0.097
149
END040 Endogenous Depression 53 0.096
150
ATM052 Autoimmune Disease 1 25 0.096
151
P PSD015 Pseudohypoparathyroidism 46 0.096
152
ATM053 Autoimmune Disease 2 16 0.095
153
P SKN013 Skin Benign Neoplasm 43 0.095
154
c MLT136 Multiple Endocrine Neoplasia 1 69 0.095
155
SRC014 Sarcoma 66 0.095
156
PRT030 Parathyroid Gland Disease 47 0.094
157
P EPL164 Epilepsy 66 0.094
158
VTM003 Vitamin Metabolic Disorder 30 0.094
159
MSS002 Mass Syndrome 48 0.094
160
TST021 Testicular Germ Cell Tumor 69 0.094
161
CNG034 Congestive Heart Failure 72 0.094
162
P NRP001 Neuropathy 59 0.094
163
c SYS001 Systemic Lupus Erythematosus 86 0.093
164
c INH020 Inherited Metabolic Disorder 49 0.093
165
SKN023 Skin Tag 44 0.092
166
P ANR007 Anorexia Nervosa 61 0.092
167
c CRN214 Coronary Heart Disease 5 22 0.092
168
P SPS003 Spastic Diplegia 52 0.092
169
P PHC003 Pheochromocytoma 71 0.092
170
PRT029 Parathyroid Adenoma 48 0.091
171
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.091
172
CRC006 Carcinoid Syndrome 52 0.091
173
EWN003 Ewing Sarcoma 66 0.091
174
c CRN172 Coronary Heart Disease 3 19 0.091
175
ACQ007 Acquired Immunodeficiency Syndrome 60 0.091
176
IMM136 Immune System Disease 51 0.091
177
GST033 Gestational Diabetes 57 0.090
178
ALN001 Aland Island Eye Disease 45 0.090
179
GRM001 Germ Cell and Embryonal Cancer 36 0.090
180
P NRB001 Neuroblastoma 70 0.089
181
P LPD010 Lipodystrophy 55 0.089
182
DWN001 Down Syndrome 66 0.089
183
ATM054 Autoimmune Disease 3 15 0.088
184
MNR003 Mineral Metabolism Disease 38 0.088
185
MRB003 Morbid Obesity 59 0.088
186
ISC004 Ischemia 61 0.088
187
C3D001 C3 Deficiency 53 0.088
188
P CRV031 Cervical Adenocarcinoma 53 0.088
189
P GLM045 Glioma 60 0.088
190
c CRN174 Coronary Heart Disease 2 20 0.087
191
SXD001 Sex Differentiation Disease 38 0.087
192
BRN106 Burns 52 0.087
193
ADR014 Adrenal Medulla Cancer 36 0.087
194
HMT002 Hematologic Cancer 64 0.087
195
MLN007 Male Infertility 55 0.087
196
ATM055 Autoimmune Disease 4 15 0.086
197
c CRN175 Coronary Heart Disease 4 19 0.086
198
P PSR002 Psoriasis 61 0.086
199
AMN001 Amenorrhea 50 0.085
200
GST053 Gastric Cancer 78 0.085
201
PRP027 Peripheral Vascular Disease 69 0.085
202
P STR021 Struma Ovarii 39 0.085
203
ISC006 Ischemic Heart Disease 68 0.085
204
P CLC005 Celiac Disease 68 0.085
205
LPD004 Lipoid Nephrosis 48 0.084
206
P CRN178 Coronary Heart Disease 6 21 0.084
207
ALP008 Alopecia 57 0.084
208
DMN002 Dementia 65 0.083
209
CRD118 Cardiovascular Cancer 44 0.083
210
DSS008 Disease of Mental Health 52 0.083
211
NNL002 Nonalcoholic Steatohepatitis 50 0.083
212
PHY002 Physical Disorder 43 0.083
213
PLC008 Placenta Disease 33 0.082
214
END057 Endometrial Cancer 75 0.082
215
P MCR129 Microvascular Complications of Diabetes 1 54 0.082
216
P PRM019 Premature Ovarian Failure 64 0.082
217
c GRV008 Graves Disease 1 44 0.081
218
VND001 Vein Disease 47 0.081
219
HRT007 Heart Cancer 46 0.081
220
P HRT017 Heart Tumor 32 0.081
221
EMB004 Embryonal Carcinoma 57 0.081
222
ATN002 Autonomic Nervous System Disease 48 0.081
223
ATM012 Autoimmune Disease of Blood 35 0.081
224
P END044 Endometriosis 66 0.081
225
SKN027 Skin Conditions 43 0.081
226
LYM116 Lymph Node Disease 47 0.080
227
MTH009 Mouth Disease 61 0.080
228
c ADL079 Adult Heart Tumor 16 0.080
229
P TRT010 Teratoma 52 0.080
230
ADJ001 Adjustment Disorder 38 0.080
231
LVR012 Liver Cirrhosis 67 0.080
232
P PRG013 Paraganglioma 54 0.080
233
HYP043 Hyperandrogenism 47 0.079
234
P PRT010 Parathyroid Carcinoma 63 0.079
235
BRN028 Brain Cancer 70 0.079
236
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.079
237
SLP005 Sleep Disorder 53 0.079
238
GLB003 Globe Disease 32 0.079
239
c ACT053 Acute Thyroiditis 30 0.079
240
P CRD011 Cardiomyopathy 68 0.078
241
P LRY019 Laryngitis 54 0.078
242
VSC006 Vascular Cancer 51 0.078
243
PRD004 Prediabetes Syndrome 43 0.078
244
VSC007 Vascular Disease 67 0.078
245
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.077
246
SPC003 Specific Developmental Disorder 38 0.077
247
P LYM026 Lymphoblastic Leukemia 62 0.077
248
P OCY001 Oocyte Maturation Defect 38 0.077
249
CNN005 Connective Tissue Disease 62 0.077
250
P BCL006 B-Cell Lymphomas 65 0.077
251
LYM020 Lymph Node Cancer 39 0.077
252
ADR012 Adrenal Gland Disease 48 0.077
253
RSP006 Respiratory System Disease 58 0.077
254
P OVR046 Ovarian Cyst 51 0.077
255
P ADD001 Addison's Disease 62 0.076
256
BRN071 Brain Injury 52 0.076
257
P AST005 Asthma 82 0.076
258
c CNT075 Central Precocious Puberty 49 0.076
259
MSC072 Muscle Cancer 49 0.076
260
RTN023 Retinitis 50 0.076
261
MNT002 Mental Depression 53 0.075
262
PPL010 Papillary Follicular Thyroid Adenocarcinoma 14 0.075
263
BNF002 Bone Fracture 50 0.075
264
END036 Endocrine Organ Benign Neoplasm 33 0.075
265
P SLP006 Sleep Apnea 61 0.075
266
PRP021 Peripheral Nervous System Neoplasm 46 0.074
267
HYP020 Hyperprolactinemia 60 0.074
268
c HPT073 Hepatitis C Virus 73 0.074
269
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.074
270
c TRC078 Trichohepatoenteric Syndrome 2 29 0.074
271
ETH011 Ethylmalonic Encephalopathy 56 0.073
272
P HST010 Histiocytosis 58 0.073
273
BNR001 Bone Remodeling Disease 37 0.073
274
FRB001 Farber Lipogranulomatosis 53 0.073
275
PLS009 Plasma Cell Neoplasm 48 0.073
276
FDL002 Food Allergy 53 0.073
277
LNG099 Lung Disease 64 0.073
278
LRN003 Learning Disability 49 0.073
279
c HYP595 Hypertension, Essential 69 0.073
280
P ESP024 Esophagitis 61 0.072
281
P PND002 Pendred Syndrome 55 0.072
282
THY096 Thyroid Carcinoma, Hurthle Cell 28 0.072
283
P EST001 Estrogen-Receptor Positive Breast Cancer 48 0.072
284
THR024 Thrombosis 57 0.072
285
P THL005 Thalassemia 64 0.072
286
URT039 Urticaria 57 0.072
287
P AMY004 Amyloidosis 65 0.072
288
P MTC069 Mitochondrial Disorders 53 0.072
289
P UTR038 Uterine Disease 37 0.071
290
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.071
291
CYS001 Cystic Fibrosis 83 0.071
292
CRV034 Cervical Benign Neoplasm 9 0.071
293
OBS061 Obstructive Sleep Apnea 66 0.071
294
P BPL003 Bipolar Disorder 62 0.071
295
ADR005 Adrenal Carcinoma 57 0.070
296
PRT036 Peritonitis 63 0.070
297
P RCK004 Rickets 61 0.070
298
P PNC035 Pancreatic Cancer 87 0.070
299
c HMG001 Hemoglobin C Disease 47 0.070
300
PRT038 Protein-Energy Malnutrition 49 0.070
301
HYP029 Hyperthyroxinemia 26 0.070
302
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.070
303
P INT063 Intellectual Disability 49 0.070
304
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.070
305
P DBT005 Diabetes Insipidus 53 0.070
306
CLT003 Colitis 60 0.070
307
P NPH012 Nephrotic Syndrome 59 0.069
308
P ATX004 Ataxia 53 0.069
309
P FML011 Familial Adenomatous Polyposis 68 0.069
310
P MLT019 Multiple Myeloma 83 0.069
311
ADR021 Adrenocorticotropic Hormone Deficiency 45 0.069
312
P RSP003 Respiratory Failure 71 0.069
313
P NRV007 Nervous System Disease 71 0.068
314
SML033 Small Cell Cancer of the Lung, Somatic 54 0.068
315
ATR060 Atrial Standstill, Digenic 51 0.068
316
PRD011 Proud Syndrome 42 0.068
317
P PLM037 Pulmonary Hypertension 79 0.068
318
ATM059 Autoimmune Disease 6 22 0.068
319
LPM004 Lipoma 60 0.068
320
PRM097 Primary Immunodeficiency Disease 60 0.067
321
LMY002 Leiomyoma 54 0.067
322
CCN007 Cocoon Syndrome 45 0.067
323
PRP019 Peripheral Nervous System Disease 55 0.067
324
NNT019 Neonatal Hypothyroidism 34 0.067
325
c CRN173 Coronary Heart Disease 8 18 0.067
326
OVR029 Ovarian Hyperstimulation Syndrome 61 0.067
327
ANX002 Anxiety Disorder 67 0.067
328
IMP003 Impaired Renal Function Disease 34 0.067
329
TRM010 Traumatic Brain Injury 52 0.067
330
STR067 Stroke, Ischemic 75 0.067
331
PNC034 Pancreas Disease 58 0.067
332
PLS011 Plasmacytoma 56 0.067
333
NNT010 Nontoxic Goiter 35 0.066
334
P PRD008 Periodontitis 63 0.066
335
P PRP029 Porphyria 59 0.066
336
PTT008 Pituitary Carcinoma 45 0.066
337
c CRN177 Coronary Heart Disease 7 20 0.066
338
MTC005 Mitochondrial Metabolism Disease 36 0.066
339
CRB039 Cerebrovascular Disease 63 0.066
340
c HPT016 Hepatitis B 65 0.066
341
DRG001 Drug Psychosis 38 0.066
342
END030 End Stage Renal Failure 55 0.066
343
P GND004 Gonadal Dysgenesis 51 0.066
344
WLS001 Wilson Disease 72 0.066
345
c PNC106 Pancreatic Agenesis 1 37 0.066
346
KRT002 Keratomalacia 52 0.066
347
GST050 Gastrointestinal System Disease 56 0.065
348
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.065
349
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.065
350
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.065
351
DRM006 Dermatitis 66 0.065
352
URN009 Urinary System Disease 50 0.064
353
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.064
354
P CHR084 Chromosomal Disease 32 0.064
355
P INF037 Inflammatory Bowel Disease 63 0.064
356
c ACT075 Acute Myocardial Infarction 60 0.064
357
KLN001 Klinefelter's Syndrome 50 0.064
358
RDN001 Reading Disorder 34 0.064
359
CHL068 Cholestasis 59 0.064
360
GST078 Gastrointestinal Allergy 40 0.064
361
LYM019 Lymphosarcoma 53 0.063
362
TBR010 Tuberculosis 70 0.063
363
P URF003 Urofacial Syndrome 1 50 0.063
364
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.063
365
WST001 West Syndrome 57 0.063
366
NRM005 Neuromuscular Disease 56 0.063
367
MVM001 Movement Disease 49 0.063
368
CNG368 Congenital Adrenal Hyperplasia 62 0.063
369
HDN002 Head Injury 45 0.063
370
HDG012 Hodgkin Lymphoma 77 0.062
371
P GST049 Gastrointestinal System Cancer 60 0.062
372
ADM013 Adamantinoma of Long Bones 57 0.062
373
P HYP014 Hyperuricemia 50 0.062
374
ANV001 Anovulation 44 0.062
375
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.062
376
c PRC016 Pre-Eclampsia 56 0.062
377
NSY001 N Syndrome 36 0.061
378
c PND001 Pain Disorder 54 0.061
379
c VRL010 Viral Hepatitis 60 0.061
380
HPT074 Hepatic Adenoma, Somatic 50 0.061
381
P INF038 Influenza 72 0.061
382
ULC004 Ulcerative Colitis 76 0.061
383
CVT001 Cavitary Optic Disc Anomalies 31 0.061
384
MDS022 Mediastinitis 41 0.060
385
P GLY013 Glycogen Storage Disease 60 0.060
386
P ALZ034 Alzheimer Disease 92 0.060
387
ADR007 Adrenoleukodystrophy 72 0.060
388
c CLL013 Cell Type Cancer 46 0.060
389
THY021 Thyroid Malformation 11 0.060
390
c EST002 Estrogen-Receptor Negative Breast Cancer 42 0.060
391
HV1006 Hiv-1 80 0.060
392
CLN019 Colonic Disease 51 0.060
393
c CNT035 Central Nervous System Disease 60 0.060
394
ETH004 Euthyroid Sick Syndrome 36 0.060
395
ATP002 Atopy 66 0.059
396
BLD053 Blood Platelet Disease 46 0.059
397
EST007 Estrogen Resistance 46 0.059
398
P PRM006 Primary Biliary Cirrhosis 51 0.059
399
ALC007 Alcohol Dependence 63 0.059
400
SVR004 Severe Combined Immunodeficiency 69 0.059
401
HYP005 Hypokalemia 51 0.059
402
VSC008 Vascular Hemostatic Disease 30 0.059
403
P MYL006 Myeloid Leukemia 66 0.059
404
c MTR002 Mitral Valve Insufficiency 44 0.059
405
THY098 Thyroid Ectopia 25 0.059
406
DFC004 Deficiency Anemia 64 0.059
407
P RNL015 Renal Hypertension 48 0.059
408
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.059
409
ACN011 Acne 62 0.059
410
P AST007 Astrocytoma 65 0.058
411
c ACT073 Acute Leukemia 60 0.058
412
NWC001 Newcastle Disease 54 0.058
413
P SHR001 Short Bowel Syndrome 49 0.058
414
GNR004 Generalized Anxiety Disorder 51 0.058
415
P ECL001 Eclampsia 54 0.058
416
c MLG081 Malignant Teratoma 46 0.058
417
NSP002 Nasopharyngitis 40 0.058
418
EXF001 Exfoliation Syndrome 57 0.058
419
P PLN008 Peeling Skin Syndrome 45 0.058
420
CRV038 Cervical Squamous Cell Carcinoma 60 0.058
421
INT253 Intestinal Benign Neoplasm 47 0.058
422
RHM027 Rheumatic Disease 58 0.058
423
CND002 Conduct Disorder 54 0.058
424
CYS010 Cystinosis 53 0.057
425
EXT010 Extramedullary Plasmacytoma 49 0.057
426
SPC010 Speech and Communication Disorders 41 0.057
427
DYS073 Dysphagia 48 0.057
428
c HPT003 Hepatitis a 59 0.057
429
BNM008 Bone Mineral Density, Low 16 0.057
430
HMT018 Hematopoietic Stem Cell Transplantation 41 0.057
431
P RTN024 Retinoblastoma 74 0.057
432
MRG013 Mirage Syndrome 29 0.057
433
GLC006 Galactosemia 64 0.057
434
DDN006 Duodenitis 42 0.057
435
P DRR001 Diarrhea 60 0.057
436
LYM024 Lymphatic System Disease 52 0.057
437
P MYS003 Myasthenia Gravis 67 0.057
438
P THY023 Thymoma 57 0.057
439
P ALP009 Alopecia Areata 62 0.057
440
LYM023 Lymphatic System Cancer 33 0.057
441
P GLM007 Glomerulonephritis 59 0.057
442
KWS001 Kwashiorkor 40 0.057
443
P GLB002 Glioblastoma 68 0.056
444
LKC003 Leukocyte Disease 43 0.056
445
BNM001 Bone Marrow Cancer 51 0.056
446
P PNM007 Pneumonia 68 0.056
447
P INT068 Intestinal Disease 60 0.056
448
YNG002 Young Syndrome 26 0.056
449
THY069 Thyroid Hormone Resistance, Selective Pituitary 21 0.056
450
NSD001 Nose Disease 48 0.056
451
SNS023 Sensory System Cancer 43 0.056
452
LRN004 Laron Dwarfism 58 0.056
453
c ADL017 Adult T-Cell Leukemia 60 0.055
454
P HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 36 0.055
455
BLT006 Bilateral Breast Cancer 53 0.055
456
ANR040 Aneurysm 57 0.055
457
P ACT074 Acute Lymphocytic Leukemia 56 0.055
458
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.055
459
P HMC003 Hemochromatosis 72 0.055
460
ISL001 Islet Cell Tumor 50 0.055
461
OST011 Osteomalacia 49 0.055
462
AYM001 Ayme-Gripp Syndrome 41 0.055
463
HNM002 Hinman Syndrome 25 0.055
464
CHR008 Choroiditis 44 0.055
465
P GST044 Gastritis 56 0.055
466
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.055
467
NRL016 Neural Tube Defects 76 0.054
468
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.054
469
c HMG004 Hemoglobin D Disease 31 0.054
470
CNT098 Central Core Disease 65 0.054
471
INT007 Intermediate Coronary Syndrome 50 0.054
472
CRH001 Crohn's Disease 75 0.054
473
c RNL003 Renal Clear Cell Carcinoma 54 0.054
474
P BLD051 Blood Coagulation Disease 42 0.054
475
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.054
476
DFF005 Diffuse Large B-Cell Lymphoma 59 0.054
477
ACT087 Acth Deficiency 43 0.054
478
HDC001 Headache 54 0.054
479
SWL001 Swallowing Disorders 33 0.054
480
P PLR004 Pleuropulmonary Blastoma 65 0.054
481
c CRN176 Coronary Heart Disease 9 18 0.054
482
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.054
483
PTT004 Pituitary Apoplexy 46 0.054
484
CLN015 Colon Adenocarcinoma 50 0.053
485
P TRC086 Trichohepatoenteric Syndrome 1 48 0.053
486
P LMY004 Leiomyosarcoma 55 0.053
487
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.053
488
c ATM011 Autoimmune Hepatitis 60 0.053
489
LPM005 Lipomatosis 47 0.053
490
AND005 Androgen Insensitivity Syndrome, Mild 16 0.053
491
RTN018 Retinal Disease 53 0.053
492
P DRM010 Dermatomyositis 62 0.053
493
GLC077 Glucocorticoid Therapy, Response to 16 0.053
494
VSC011 Vasculitis 62 0.053
495
P MTR004 Maturity-Onset Diabetes of the Young 58 0.053
496
FNC006 Functional Gastric Disease 32 0.053
497
ACN002 Acanthosis Nigricans 57 0.053
498
GST045 Gastroenteritis 59 0.053
499
NPH003 Nephrocalcinosis 48 0.053
500
P MSC007 Muscle Hypertrophy 58 0.053
501
THL018 Thalassemia Major 48 0.052
502
AND015 Androgen Insensitivity 64 0.052
503
PSR001 Psoriatic Arthritis 64 0.052
504
VGN023 Vaginitis 42 0.052
505
RNL007 Renal Tubular Acidosis 50 0.052
506
CRY002 Cryptorchidism 60 0.052
507
VSC009 Vascular Skin Disease 19 0.052
508
c CHR090 Chronic Lymphocytic Leukemia 76 0.052
509
OPT006 Optic Nerve Disease 52 0.052
510
c ADL001 Adult Lymphoma 39 0.052
511
WRN001 Werner Syndrome 67 0.052
512
c CNG031 Congenital Nervous System Abnormality 37 0.052
513
THY065 Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia 23 0.052
514
P ATR011 Atrial Fibrillation 66 0.052
515
CTS003 Coats Disease 57 0.052
516
P GRN010 Granular Cell Tumor 47 0.052
517
c MYC058 Myocardial Infarction 2 28 0.052
518
PHS001 Phosphorus Metabolism Disease 38 0.052
519
BRS099 Breast Ductal Carcinoma 50 0.051
520
RDT005 Radiation Induced Cancer 28 0.051
521
P GT001 Gout 58 0.051
522
FST001 Foster-Kennedy Syndrome 31 0.051
523
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.051
524
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.051
525
WLL001 Williams-Beuren Syndrome 60 0.051
526
P ENC004 Encephalitis 63 0.051
527
THY041 Thyroxine-Binding Globulin Deficiency 20 0.051
528
ANG054 Angina Pectoris 50 0.051
529
P STR020 Strabismus 51 0.051
530
PLM011 Plummer's Disease 35 0.051
531
c MLG059 Malignant Struma Ovarii 36 0.051
532
ART002 Arts Syndrome 51 0.050
533
P CTR002 Cataract 58 0.050
534
CHR074 Choriocarcinoma 46 0.050
535
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.050
536
c FML108 Familial Breast Cancer 57 0.050
537
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.050
538
SPN186 Spinal Cord Injury 63 0.050
539
P HML002 Hemolytic Anemia 62 0.050
540
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.050
541
CRB031 Cerebral Arterial Disease 27 0.050
542
P LCT001 Lactic Acidosis 51 0.050
543
PST021 Postpartum Depression 49 0.050
544
PHC013 Phaeochromocytoma 41 0.050
545
P FNC004 Fanconi Syndrome 49 0.050
546
c SCH051 Schizophrenia 4 28 0.050
547
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.050
548
P ADL010 Adult Respiratory Distress Syndrome 61 0.050
549
FNC007 Functioning Pituitary Adenoma 41 0.049
550
P NRF002 Neurofibromatosis 71 0.049
551
ESP021 Esophageal Cancer 76 0.049
552
c HYP615 Hyperparathyroidism, Familial Primary 56 0.049
553
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.049
554
RNL101 Renal Cell Carcinoma, Papillary 63 0.049
555
P LCH002 Lichen Planus 53 0.049
556
RBR001 Roberts Syndrome 60 0.049
557
SPN369 Spinal Disease 39 0.049
558
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.049
559
NNT003 Neonatal Thyrotoxicosis 27 0.049
560
BRC012 Brucellosis 66 0.049
561
P ICH004 Ichthyosis 52 0.049
562
OCL006 Ocular Hypertension 48 0.049
563
VRL011 Viral Infectious Disease 55 0.049
564
c SML034 Small Cell Neuroendocrine Carcinoma 42 0.048
565
P DYS070 Dysalbuminemic Hyperthyroxinemia 16 0.048
566
TST014 Testicular Cancer 53 0.048
567
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.048
568
P HRD018 Hair Disease 51 0.048
569
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.048
570
c PLN017 Peeling Skin Syndrome 1 34 0.048
571
P PNC025 Panic Disorder 60 0.048
572
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.048
573
c ACT020 Acute T Cell Leukemia 35 0.048
574
HYP189 Hypoadrenalism 37 0.048
575
P MNN013 Meningitis 67 0.048
576
MXD005 Mixed Connective Tissue Disease 62 0.048
577
SFT003 Soft Tissue Sarcoma 57 0.048
578
HYP540 Hypertension, Diastolic 39 0.048
579
P LYD001 Leydig Cell Tumor 44 0.048
580
P SZR006 Seizure Disorder 56 0.048
581
P PRS038 Personality Disorder 62 0.048
582
PRP016 Paraplegia 49 0.047
583
CHL061 Childhood Leukemia 49 0.047
584
HRD059 Hereditary Peripheral Nervous Disorder 11 0.047
585
DCT002 Ductal Carcinoma in Situ 51 0.047
586
SYN036 Syncope 47 0.047
587
ALL001 Allan-Herndon-Dudley Syndrome 46 0.047
588
c PSD066 Pseudohypoparathyroidism, Type Ib 51 0.047
589
RHB003 Rhabdomyosarcoma 57 0.047
590
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.047
591
P PRT013 Portal Hypertension 60 0.047
592
RFR004 Refractory Hematologic Cancer 28 0.047
593
ATN005 Autonomic Dysfunction 49 0.047
594
CRT015 Carotid Artery Occlusion 43 0.047
595
P CNN004 Connective Tissue Cancer 40 0.047
596
c DLT002 Dilated Cardiomyopathy 76 0.047
597
ADN021 Adenomatous Polyposis Coli 70 0.047
598
PRN039 Paraneoplastic Syndromes 32 0.047
599
P PLM036 Pulmonary Fibrosis 71 0.047
600
GST071 Gastrointestinal Carcinoma 42 0.047
601
c ACT027 Acute Pancreatitis 57 0.047
602
LYM067 Lymphoid Leukemia 44 0.047
603
DRY001 Dry Eye Syndrome 50 0.047
604
c PLN018 Peeling Skin Syndrome 2 40 0.047
605
c PLN021 Peeling Skin Syndrome 3 29 0.047
606
IDN001 Iodine Hypothyroidism 12 0.046
607
TRN007 Transsexualism 41 0.046
608
NNF007 Non-Functioning Pituitary Adenoma 41 0.046
609
P FBR017 Fibrosarcoma 56 0.046
610
P CLL015 Collagen Disease 50 0.046
611
P TCL004 T-Cell Leukemia 47 0.046
612
P ALX003 Alexander Disease 63 0.046
613
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.046
614
LYS002 Lysosomal Storage Disease 52 0.046
615
OST004 Osteitis Fibrosa 41 0.046
616
P PLY019 Polyneuropathy 56 0.046
617
URC002 Urea Cycle Disorder 51 0.046
618
ATN003 Autonomic Nervous System Neoplasm 40 0.046
619
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.046
620
DDN007 Duodenal Disease 33 0.046
621
BCL002 B Cell Deficiency 49 0.046
622
P SJG001 Sjogren's Syndrome 50 0.046
623
MDY004 Mody, Type Iii 34 0.046
624
PRS045 Prostatic Hypertrophy 45 0.046
625
c MCR113 Microvascular Complications of Diabetes 3 45 0.046
626
P OST005 Osteogenesis Imperfecta 69 0.046
627
P ANG015 Angioedema 52 0.046
628
ADR010 Adrenal Cortical Hypofunction 36 0.046
629
INT075 Intracranial Hypertension 50 0.046
630
SMT003 Somatostatinoma 48 0.046
631
EMP001 Empty Sella Syndrome 40 0.046
632
ORL015 Oral Squamous Cell Carcinoma 57 0.045
633
FXF002 Fox-Fordyce Disease 36 0.045
634
PRP074 Peripheral Resistance to Thyroid Hormones 16 0.045
635
STT009 Sutton Disease 2 18 0.045
636
P ASP006 Aspergillosis 61 0.045
637
SKL014 Skeletal Dysplasia 46 0.045
638
SKL017 Skeletal Dysplasias 45 0.045
639
IRN001 Iron Deficiency Anemia 52 0.045
640
c PSD067 Pseudohypoparathyroidism Ia 52 0.045
641
HRF001 Hair Follicle Neoplasm 32 0.045
642
APH001 Aphthous Stomatitis 62 0.045
643
UTR033 Uterine Corpus Cancer 49 0.045
644
P KLL001 Kallmann Syndrome 61 0.045
645
FCT008 Factitious Disorder 41 0.044
646
ANG049 Angioedema Induced by Ace Inhibitors 34 0.044
647
PRM025 Primary Bacterial Infectious Disease 41 0.044
648
CNV002 Conversion Disorder 41 0.044
649
ESP023 Esophageal Disease 54 0.044
650
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.044
651
P MYT002 Myotonic Dystrophy 48 0.044
652
ECT093 Ectopic Cushing Syndrome 43 0.044
653
BRN080 Brain Ischemia 41 0.044
654
HYP249 Hyperthyroidism, Nonautoimmune 26 0.044
655
c CNN010 Connective Tissue Benign Neoplasm 32 0.044
656
P RHN004 Rhinitis 60 0.044
657
P THY054 Thyrotoxic Periodic Paralysis 48 0.044
658
LYM021 Lymphadenitis 58 0.044
659
c FML297 Familial Thyroid Dyshormonogenesis 31 0.044
660
c THY071 Thyroid Dyshormonogenesis 1 22 0.044
661
GLC036 Glucagonoma 46 0.044
662
LBL001 Lobular Neoplasia 46 0.044
663
RCT017 Rectal Disease 40 0.044
664
END041 Endometrial Adenocarcinoma 56 0.044
665
CYT008 Cytomegalovirus Infection 52 0.044
666
P THY061 Thyroid Dyshormonogenesis 2a 21 0.044
667
DBT008 Diabetic Angiopathy 44 0.044
668
P TRM003 Tremor 54 0.044
669
PHR003 Pharyngitis 56 0.044
670
P CNJ013 Conjunctivitis 64 0.044
671
PLM033 Pulmonary Embolism 60 0.044
672
ATN004 Autonomic Neuropathy 45 0.044
673
BRN038 Bronchial Disease 51 0.044
674
SPS057 Spasticity 42 0.044
675
P FLL037 Follicular Lymphoma 70 0.043
676
CRV047 Cervical Cancer, Somatic 65 0.043
677
P DYS154 Dystonia 65 0.043
678
NRL005 Neurilemmoma 51 0.043
679
PMP001 Pemphigus 50 0.043
680
c AST039 Asthma 2 28 0.043
681
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.043
682
SPN041 Spinal Cord Disease 51 0.043
683
MXD023 Mixed Cell Type Cancer 45 0.043
684
CRD001 Cardiac Tamponade 44 0.043
685
INT066 Interstitial Lung Disease 59 0.043
686
LYM040 Lymphoblastic Lymphoma 53 0.043
687
P PRC031 Preeclampsia/eclampsia 1 51 0.043
688
c MCR115 Microvascular Complications of Diabetes 5 57 0.043
689
P OST001 Osteopetrosis 63 0.043
690
c CLR085 Colorectal Cancer 1 45 0.043
691
PRT014 Protein S Deficiency 53 0.043
692
PRM013 Premature Menopause 41 0.043
693
VTM002 Vitamin B12 Deficiency 45 0.043
694
P HRP006 Herpes Simplex 65 0.043
695
CLR109 Colorectal Adenocarcinoma 51 0.043
696
CHL123 Chlamydia 60 0.043
697
NRF007 Neurofibroma 53 0.043
698
c ACT210 Acute Respiratory Distress Syndrome 57 0.042
699
GLB001 Gilbert Syndrome 60 0.042
700
c RNL016 Renal Infectious Disease 20 0.042
701
P PLY041 Polymyositis 52 0.042
702
GNG013 Gingivitis 61 0.042
703
P MYS005 Myositis 57 0.042
704
TCL003 T Cell Deficiency 45 0.042
705
c DLT001 Delta Chain Disease 13 0.042
706
FCL014 Focal Epilepsy 55 0.042
707
c CLR079 Colorectal Cancer 2 29 0.042
708
PRN011 Pernicious Anemia 44 0.042
709
MRK001 Merkel Cell Carcinoma 52 0.042
710
FNT004 Fainting 33 0.042
711
HYP002 Hypothalamic Neoplasm 20 0.042
712
GST023 Gastric Ulcer 56 0.042
713
P CHR345 Chronic Pain 50 0.042
714
LYM027 Lymphopenia 56 0.042
715
GLB015 Glioblastoma Multiforme 63 0.042
716
P THR014 Thrombocytopenia 64 0.042
717
SPN051 Spondylitis 51 0.042
718
ALC009 Alcoholic Liver Cirrhosis 49 0.042
719
CHR066 Chronic Fatigue Syndrome 64 0.042
720
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.042
721
ZLL002 Zollinger-Ellison Syndrome 53 0.042
722
TTH006 Tooth Disease 52 0.041
723
GST040 Gastric Adenocarcinoma 52 0.041
724
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.041
725
CLR030 Clear Cell Renal Cell Carcinoma 53 0.041
726
c PRM196 Premature Ovarian Failure 1 42 0.041
727
ALC006 Alcoholic Hepatitis 59 0.041
728
GYN001 Gynecomastia 48 0.041
729
c NRF018 Neurofibromatosis, Type 1 67 0.041
730
TKY002 Takayasu Arteritis 61 0.041
731
ORL013 Oral Lichen Planus 47 0.041
732
P DYS021 Dysautonomia 44 0.041
733
DBT010 Diabetic Neuropathy 55 0.041
734
AMN006 Aminoaciduria 41 0.041
735
PRP030 Purpura 58 0.041
736
P SNS014 Sinusitis 60 0.041
737
SCK003 Sickle Cell Anemia 71 0.041
738
MND006 Mondor Disease 21 0.041
739
PTT043 Pituitary Hormone Deficiency, Combined, 6 19 0.041
740
DST006 Diastolic Heart Failure 46 0.041
741
P ATR005 Atrophic Gastritis 45 0.041
742
BRS050 Breast Cyst 36 0.041
743
P HYP265 Hypotonia 38 0.041
744
P EXN002 Exanthem 57 0.041
745
BLM002 Bulimia Nervosa 52 0.041
746
P NSP012 Nasopharyngeal Carcinoma 66 0.041
747
P UVT001 Uveitis 58 0.041
748
P SCL009 Sclerosing Cholangitis 48 0.041
749
FBR019 Fibromatosis 43 0.041
750
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 0.040
751
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.040
752
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.040
753
P BRS044 Breast Adenocarcinoma 58 0.040
754
PRG014 Progesterone Resistance 40 0.040
755
P FNC043 Fanconi Anemia, Complementation Group E 55 0.040
756
c HYP058 Hypervitaminosis a 39 0.040
757
c BPL002 Bipolar I Disorder 47 0.040
758
MYC033 Myoclonus 42 0.040
759
PRN021 Paranasal Sinus Disease 49 0.040
760
SNS001 Sensorineural Hearing Loss 57 0.040
761
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.040
762
P VNS003 Venous Insufficiency 54 0.040
763
P HMR003 Hemorrhagic Disease 57 0.040
764
CLC006 Calcinosis 50 0.040
765
MLT021 Multiple System Atrophy 70 0.040
766
P BRN120 Bronchus Cancer 44 0.040
767
c RNL034 Renal Cell Carcinoma 4 18 0.040
768
PRP036 Peripheral T-Cell Lymphoma 45 0.040
769
MYM001 Myoma 52 0.040
770
c LKM062 Leukemia, Acute Lymphoblastic 64 0.040
771
CRD119 Cardiac Arrest 61 0.040
772
P OPN001 Open-Angle Glaucoma 49 0.040
773
MLG088 Malignant Germ Cell Tumor 38 0.040
774
c RTN162 Retinitis Pigmentosa 2 48 0.040
775
PTZ001 Peutz-Jeghers Syndrome 71 0.040
776
P CRB088 Cerebral Atrophy 43 0.040
777
P CHN012 Chondrosarcoma 56 0.040
778
c BSL007 Basal Cell Carcinoma 65 0.040
779
SKN005 Skin Atrophy 40 0.040
780
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.040
781
ATH010 Athyreosis 31 0.040
782
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.040
783
P LYN001 Lynch Syndrome 69 0.040
784
RCT018 Rectal Neoplasm 54 0.040
785
ADT003 Auditory System Disease 40 0.039
786
c MJR008 Major Affective Disorder 2 19 0.039
787
MYL009 Myelodysplastic Syndrome 73 0.039
788
MTR014 Motor Neuron Disease 58 0.039
789
HRT029 Heart Tumor of the Child 15 0.039
790
TLL001 Tall Cell Variant Papillary Carcinoma 13 0.039
791
BCK006 Back Pain 43 0.039
792
BLD044 Bladder Disease 51 0.039
793
DMY004 Demyelinating Disease 53 0.039
794
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.039
795
P MMB011 Membranous Nephropathy 54 0.039
796
c THR092 Thrombophilia Due to Thrombin Defect 54 0.039
797
CRB037 Cerebral Palsy 66 0.039
798
ALL014 Allergic Encephalomyelitis 32 0.039
799
P MYL005 Myelofibrosis 67 0.039
800
ARM001 Aromatase Deficiency 58 0.039
801
PRX034 Peroxisome Disorders 39 0.039
802
CYS036 Cystinosis, Nephropathic 41 0.039
803
P MYC008 Myocarditis 54 0.039
804
P PRK057 Parkinson Disease, Late-Onset 70 0.039
805
MLK006 Milk Allergy 47 0.039
806
P GLL020 Gallbladder Disease 59 0.039
807
GLL018 Gallbladder Cancer 63 0.039
808
P ATP001 Atopic Dermatitis 62 0.039
809
c CHR418 Chronic Leukemia 47 0.039
810
c HPT007 Hepatitis E 54 0.039
811
P GNT008 Giant Cell Tumor 49 0.039
812
RTN020 Retinal Vascular Disease 48 0.039
813
ADN001 Adenosine Deaminase Deficiency 45 0.039
814
MLG056 Malignant Hyperthermia 58 0.039
815
P DRM007 Dermatitis Herpetiformis 51 0.039
816
OLG001 Oligospermia 36 0.039
817
ART016 Aortic Aneurysm 69 0.038
818
VGN020 Vaginal Disease 41 0.038
819
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.038
820
c MJR007 Major Affective Disorder 1 24 0.038
821
c ANR038 Anorexia Nervosa 1 26 0.038
822
P INT070 Intestinal Obstruction 57 0.038
823
c CLR075 Colorectal Cancer 3 28 0.038
824
BRN002 Bronchiolitis 56 0.038
825
P HVY001 Heavy Chain Disease 41 0.038
826
P RTN014 Retinal Artery Occlusion 44 0.038
827
BLL006 Bullous Pemphigoid 59 0.038
828
UPP004 Upper Respiratory Tract Disease 46 0.038
829
c PSR017 Psoriasis 2 37 0.038
830
CNT067 Central Cord Syndrome 23 0.038
831
P SCL015 Scleritis 49 0.038
832
c SCN052 Secondary Adrenal Insufficiency 37 0.038
833
MNT001 Mantle Cell Lymphoma 72 0.038
834
EXC002 Exocrine Pancreatic Insufficiency 43 0.038
835
c CLL012 Cell Type Benign Neoplasm 39 0.038
836
BHR001 Behr Syndrome 42 0.038
837
MCN001 Mucinous Adenocarcinoma 50 0.038
838
PLS016 Plasma Cell Leukemia 42 0.038
839
BNL002 Bone Lymphoma 32 0.038
840
PRM151 Primary Bone Lymphoma 26 0.038
841
CCN002 Cocaine Abuse 48 0.038
842
P THR015 Thrombophilia 59 0.038
843
INT067 Interstitial Nephritis 46 0.038
844
c CHR579 Chiari Malformation Type Ii 37 0.038
845
c PSD058 Pseudohypoparathyroidism Ic 28 0.038
846
GRN016 Grant Syndrome 29 0.038
847
ALB001 Albright's Hereditary Osteodystrophy 41 0.037
848
HYP344 Hyperthyroidism, Familial Gestational 22 0.037
849
KRN002 Kearns-Sayre Syndrome 61 0.037
850
c INV001 Invasive Aspergillosis 47 0.037
851
P RTN008 Retinitis Pigmentosa 80 0.037
852
HDR002 Hidradenitis Suppurativa 51 0.037
853
HDR003 Hidradenitis 45 0.037
854
P CRB042 Cerebellar Ataxia 63 0.037
855
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 45 0.037
856
SCN001 Secondary Hyperparathyroidism of Renal Origin 38 0.037
857
LYM115 Lymphoma, Non-Hodgkin 63 0.037
858
IDP033 Idiopathic Edema 42 0.037
859
EYC003 Eye Accommodation Disease 24 0.037
860
CHL018 Childhood Medulloblastoma 47 0.037
861
ANG018 Angiomyolipoma 46 0.037
862
RNL013 Renal Adenoma 32 0.037
863
MLL012 Miller Syndrome 49 0.037
864
OBS020 Obesity, Adrenal Insufficiency, and Red Hair Due to Pomc Deficiency 32 0.037
865
MCS002 Mucositis 55 0.037
866
SDD007 Sudden Cardiac Death 47 0.037
867
PTT048 Pituitary Adenoma, Prolactin-Secreting 53 0.037
868
THY039 Thyrotropin-Releasing Hormone Deficiency 28 0.037
869
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.036
870
LCT002 Lactose Intolerance 46 0.036
871
CHN016 Cohen Syndrome 54 0.036
872
P LFR001 Li-Fraumeni Syndrome 75 0.036
873
c ATM010 Autoimmune Hemolytic Anemia 61 0.036
874
CRV040 Cervix Carcinoma 53 0.036
875
CNN002 Cannabis Abuse 40 0.036
876
MNN009 Meningoencephalitis 47 0.036
877
BRD001 Brody Myopathy 47 0.036
878
KRT004 Keratitis 71 0.036
879
P LNG064 Lung Cancer Susceptibility 3 62 0.036
880
PRC013 Pericarditis 51 0.036
881
SMN007 Seminoma 45 0.036
882
P ACT150 Acute Adrenal Insufficiency 45 0.036
883
c CHR064 Chronic Monocytic Leukemia 42 0.036
884
GST019 Gastrointestinal Stromal Tumor 73 0.036
885
CRV069 Cervix Disease 32 0.036
886
ALP001 Alopecia Universalis 58 0.036
887
UTR031 Uterine Benign Neoplasm 23 0.036
888
c GLY008 Glycogen Storage Disease Ii 59 0.036
889
c HYP311 Hyperparathyroidism 3 33 0.036
890
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.036
891
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.036
892
P CHL066 Cholangitis 42 0.036
893
c SVR001 Severe Acute Respiratory Syndrome 57 0.036
894
CRC014 Carcinoid Tumors, Intestinal 40 0.036
895
ADG002 Audiogenic Seizures 24 0.036
896
DDN009 Duodenal Obstruction 32 0.036
897
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.036
898
c PSD104 Pseudohypoparathyroidism, Type Ii 32 0.036
899
THY026 Thymus Gland Disease 27 0.036
900
ACT118 Acute Non Lymphoblastic Leukemia 30 0.036
901
ADN064 Adenohypophysitis 28 0.036
902
P TMP003 Temporal Arteritis 60 0.036
903
SBP001 Subependymal Giant Cell Astrocytoma 47 0.036
904
STT004 Steatorrhea 40 0.036
905
P PYL005 Pyelonephritis 52 0.036
906
c PRM023 Pre-Malignant Neoplasm 41 0.036
907
c INF023 Inflammatory Breast Carcinoma 52 0.036
908
P CNT005 Central Nervous System Lymphoma 53 0.035
909
P CTN015 Cutaneous T Cell Lymphoma 50 0.035
910
CRN017 Coronary Thrombosis 48 0.035
911
HYP030 Hypoactive Sexual Desire Disorder 39 0.035
912
PLM001 Pulmonary Tuberculosis 67 0.035
913
PLY020 Polyradiculoneuropathy 45 0.035
914
CHR034 Chromophobe Adenoma 40 0.035
915
ADL030 Adult-Onset Still's Disease 59 0.035
916
EVN001 Evans' Syndrome 43 0.035
917
c ATM007 Autoimmune Disease of Central Nervous System 25 0.035
918
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.035
919
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.035
920
P LYM007 Lymphangioleiomyomatosis 66 0.035
921
BRS015 Breast Medullary Carcinoma 37 0.035
922
c HRD088 Hereditary Neuropathies 40 0.035
923
c INS002 in Situ Carcinoma 53 0.035
924
CLF001 Cleft Lip 50 0.035
925
CWM001 Cow Milk Allergy 40 0.035
926
MYC002 Mycobacterium Avium Complex Disease 52 0.035
927
DBT002 Diabetic Autonomic Neuropathy 42 0.035
928
CD4004 Cd4 Deficiency 14 0.035
929
HYP343 Hypothryoidism, Congenital, Nongoitrous 4 37 0.035
930
P DDN001 Duodenal Ulcer 50 0.035
931
CRN019 Coronary Artery Vasospasm 40 0.035
932
DYS014 Dyspepsia 50 0.035
933
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.035
934
GLM004 Gliomatosis Cerebri 49 0.035
935
PSD009 Pseudohermaphroditism 40 0.035
936
P ACT080 Acute Pulmonary Heart Disease 31 0.035
937
GTL001 Gitelman Syndrome 61 0.034
938
HPT020 Hepatic Vascular Disease 42 0.034
939
MLT016 Multicentric Reticulohistiocytosis 46 0.034
940
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.034
941
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 25 0.034
942
IMM071 Immunodeficiency 12 26 0.034
943
TRN015 Transient Cerebral Ischemia 56 0.034
944
BLR001 Biliary Atresia 52 0.034
945
VCC001 Vaccinia 46 0.034
946
FBR012 Fabry Disease 69 0.034
947
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 30 0.034
948
ABL002 Ablepharon-Macrostomia Syndrome 57 0.034
949
c MLT094 Multiple Sclerosis 3 24 0.034
950
P PNC001 Pancytopenia 52 0.034
951
NWB001 Newborn Respiratory Distress Syndrome 45 0.034
952
RSP007 Respiratory Distress Syndrome, Infant 22 0.034
953
BRK010 Burkitt Lymphoma 69 0.034
954
KRT001 Keratoconjunctivitis Sicca 59 0.034
955
IMM001 Immune-Complex Glomerulonephritis 42 0.034
956
P FML012 Familial Partial Lipodystrophy 52 0.034
957
SMN008 Semantic Dementia 44 0.034
958
c HMP029 Hemophilia a 63 0.034
959
OST003 Osteonecrosis 45 0.034
960
c ADL096 Adult Hepatocellular Carcinoma 24 0.034
961
c MJR004 Major Affective Disorder 4 16 0.034
962
c FML303 Familial/multiple Cancer 14 0.034
963
PRM236 Primary Biliary Cholangitis 47 0.034
964
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.034
965
IMM025 Immunoglobulin a Deficiency 2 24 0.034
966
CNT047 Contact Dermatitis 61 0.034
967
P HMP007 Hemophilia 57 0.034
968
PMS001 Poems Syndrome 52 0.034
969
ACT017 Acute Chest Syndrome 48 0.034
970
NNT024 Neonatal Stroke 36 0.034
971
CHP002 Chops Syndrome 35 0.034
972
MLN003 Melancholia 34 0.034
973
PST014 Postsurgical Hypothyroidism 23 0.034
974
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.034
975
NSL022 Nasal Cavity Disease 38 0.034
976
GLC011 Galactose Epimerase Deficiency 41 0.034
977
TXC005 Toxic Shock Syndrome 60 0.034
978
MTY001 Mutyh-Associated Polyposis 49 0.033
979
c LKM061 Leukemia, Acute Myeloid 73 0.033
980
c BRS046 Breast Benign Neoplasm 32 0.033
981
CRH005 Crohn's Colitis 52 0.033
982
P TBR001 Tuberous Sclerosis 67 0.033
983
MSL001 Measles 61 0.033
984
WBR001 Weber Syndrome 41 0.033
985
THR004 Thrombocytosis 55 0.033
986
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 43 0.033
987
MGL001 Megaloblastic Anemia 50 0.033
988
P IDP010 Idiopathic Generalized Epilepsy 61 0.033
989
CYT002 Cytokine Deficiency 30 0.033
990
P ALG002 Alagille Syndrome 72 0.033
991
c HYP354 Hypothyroidism, Congenital Nongoitrous, 5 20 0.033
992
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 39 0.033
993
c PRK031 Parkinson Disease 1 51 0.033
994
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.033
995
TRN018 Transitional Cell Carcinoma 53 0.033
996
NRT004 Neuritis 52 0.033
997
c SVR005 Severe Pre-Eclampsia 49 0.033
998
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.033
999
c PLM022 Pulmonary Valve Insufficiency 34 0.033
1000
PRM020 Premenstrual Tension 44 0.033
1001
FSH003 Fish Allergy 29 0.033
1002
MDD010 Middle Ear Disease 48 0.033
1003
P CHR562 Chronic Myelocytic Leukemia 41 0.033
1004
ADP007 Adie Pupil 34 0.033
1005
HTS001 Hiatus Hernia 40 0.033
1006
CHR073 Choreatic Disease 37 0.033
1007
SNS003 Sensory Peripheral Neuropathy 45 0.033
1008
CYT018 Cytochrome P450 2d6 Variant 19 0.032
1009
c ACT159 Acute Transverse Myelitis 42 0.032
1010
CRS001 Crescentic Glomerulonephritis 42 0.032
1011
TMP012 Temple Syndrome 38 0.032
1012
FLL027 Fallopian Tube Carcinoma 60 0.032
1013
SPN040 Spinal Cancer 39 0.032
1014
NVS004 Nova Syndrome 13 0.032
1015
MNT045 Montefiore Syndrome 10 0.032
1016
BRN024 Bronchitis 64 0.032
1017
TCD001 Tic Disorder 48 0.032
1018
DSC009 Discoid Lupus Erythematosus 45 0.032
1019
SCH003 Schizophreniform Disorder 40 0.032
1020
CNS004 Constipation 57 0.032
1021
PNN001 Panniculitis 51 0.032
1022
c SCN036 Secondary Progressive Multiple Sclerosis 49 0.032
1023
PPM002 Ppoma 23 0.032
1024
NRC007 Neuroectodermal Endocrine Syndrome 19 0.032
1025
MCK007 Muckle-Wells Syndrome 61 0.032
1026
c CHR417 Chronic Graft Versus Host Disease 51 0.032
1027
CHD001 Chediak-Higashi Syndrome 64 0.032
1028
SNL007 Senile Cataract 37 0.032
1029
GNR003 Generalized Atherosclerosis 37 0.032
1030
APP015 Apparent Mineralocorticoid Excess 51 0.032
1031
ICH054 Ichthyosis, X-Linked 46 0.032
1032
P CTS001 Cutis Laxa 58 0.032
1033
FBR009 Fibrous Dysplasia 45 0.032
1034
HYP077 Hypertrichosis 44 0.032
1035
c MLT095 Multiple Sclerosis 4 16 0.032
1036
GND002