Search results for thyroid hormone metabolism

1076 hits were found for thyroid hormone metabolism

# Family MCID Name MIFTS Score
1
THY064 Thyroid Hormone Metabolism, Abnormal 19 5.777
2
P THY032 Thyroiditis 56 1.564
3
THY028 Thyroid Cancer 72 0.539
4
P HYP086 Hypothyroidism 62 0.535
5
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.427
6
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.407
7
HSH003 Hashimoto Thyroiditis 67 0.391
8
P BRS047 Breast Cancer 100 0.386
9
ADN018 Adenoma 63 0.371
10
GRW007 Growth Hormone Deficiency 52 0.353
11
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.351
12
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.351
13
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.351
14
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.351
15
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.351
16
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.351
17
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.351
18
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.351
19
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.351
20
AGN016 Aging 65 0.350
21
THY030 Thyroid Gland Disease 51 0.321
22
P DBT009 Diabetes Mellitus 72 0.318
23
P PRS040 Prostate Cancer 88 0.314
24
P HPT021 Hepatitis 75 0.312
25
c BLD140 Blood Group, I System 37 0.308
26
PRS047 Prostatitis 59 0.308
27
P ADN016 Adenocarcinoma 71 0.284
28
INS024 Insulin-Like Growth Factor I 83 0.283
29
GTR002 Goiter 53 0.283
30
P LYM118 Lymphoma 71 0.278
31
P GRV001 Graves' Disease 62 0.266
32
P HYP076 Hyperthyroidism 56 0.250
33
DFF036 Differentiated Thyroid Carcinoma 49 0.243
34
c SBC007 Subacute Thyroiditis 43 0.239
35
P PLY011 Polycystic Ovary Syndrome 65 0.230
36
GLC008 Glucose Metabolism Disease 38 0.229
37
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.226
38
HYP060 Hyperinsulinism 56 0.217
39
P KDN018 Kidney Disease 69 0.213
40
END072 Endotheliitis 46 0.213
41
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.202
42
P INF032 Infertility 59 0.199
43
ISL003 Isolated Growth Hormone Deficiency 57 0.199
44
NRN002 Neuronitis 43 0.199
45
ACR007 Acromegaly 70 0.198
46
P PNC044 Pancreatitis 64 0.196
47
P HYP083 Hypopituitarism 59 0.191
48
P PTT006 Pituitary Adenoma 57 0.190
49
P LKM002 Leukemia 75 0.189
50
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.187
51
c CNG006 Congenital Hypothyroidism 62 0.185
52
P HRT032 Heart Disease 80 0.184
53
PTT009 Pituitary Gland Disease 56 0.184
54
DWR001 Dwarfism 48 0.182
55
MTB004 Metabolic Acidosis 49 0.181
56
P OST002 Osteoporosis 75 0.181
57
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.180
58
P HYP069 Hyperparathyroidism 58 0.179
59
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.178
60
P ENC018 Encephalopathy 58 0.172
61
c GRV008 Graves Disease 1 52 0.171
62
P ART022 Arthritis 77 0.169
63
ATM095 Autoimmune Disease 66 0.169
64
CRB009 Cerebritis 41 0.167
65
SKN016 Skin Disease 68 0.164
66
P CRV039 Cervicitis 49 0.163
67
BRS051 Breast Disease 67 0.161
68
P TRN020 Turner Syndrome 69 0.157
69
P LNG032 Lung Cancer 99 0.157
70
SKN027 Skin Conditions 48 0.157
71
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.157
72
P LVR013 Liver Disease 76 0.153
73
P HYP726 Hypercalcemia, Infantile, 1 57 0.152
74
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 45 0.152
75
HYP056 Hypoglycemia 62 0.149
76
HYP085 Hypothalamic Disease 46 0.148
77
OVR063 Overnutrition 53 0.144
78
c CHR089 Chronic Kidney Failure 72 0.142
79
P RHM011 Rheumatoid Arthritis 91 0.141
80
HYP080 Hypogonadism 54 0.141
81
P OVR049 Ovarian Disease 58 0.141
82
P CRN018 Coronary Artery Anomaly 69 0.140
83
c HPT001 Hepatitis C 73 0.140
84
HYP266 Hypoxia 61 0.139
85
c PRM005 Primary Hyperparathyroidism 59 0.139
86
P PRC019 Precocious Puberty 52 0.139
87
CNN003 Conn's Syndrome 70 0.139
88
HYP066 Hyperglycemia 64 0.136
89
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.136
90
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.136
91
P HYP024 Hypoparathyroidism 55 0.136
92
P CRN300 Coronary Heart Disease 1 57 0.136
93
NRN004 Neuroendocrine Tumor 58 0.135
94
P MLT074 Multiple Endocrine Neoplasia 55 0.135
95
SQM006 Squamous Cell Carcinoma 74 0.134
96
PTT037 Pituitary Tumors 49 0.134
97
P GNR008 Generalized Resistance to Thyroid Hormone 36 0.134
98
IMM136 Immune System Disease 57 0.133
99
END028 Endemic Goiter 40 0.132
100
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.132
101
MYX004 Myxedema 44 0.131
102
MLN008 Melanoma 72 0.130
103
P ALZ034 Alzheimer Disease 95 0.130
104
NDL007 Nodular Goiter 50 0.130
105
P PRD006 Prader-Willi Syndrome 66 0.128
106
P SCH015 Schizophrenia 71 0.128
107
c HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 51 0.127
108
P OVR042 Ovarian Cancer 82 0.127
109
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.124
110
P CLR023 Colorectal Cancer 98 0.124
111
P PSD015 Pseudohypoparathyroidism 50 0.123
112
LPD008 Lipid Metabolism Disorder 59 0.122
113
ART140 Arteries, Anomalies of 51 0.122
114
FTT001 Fatty Liver Disease 62 0.121
115
P MYC007 Myocardial Infarction 81 0.121
116
CNG034 Congestive Heart Failure 74 0.121
117
SRC014 Sarcoma 68 0.121
118
ANX010 Anxiety 72 0.121
119
GLC003 Glucose Intolerance 58 0.121
120
P LPS004 Lupus Erythematosus 69 0.120
121
ACQ007 Acquired Immunodeficiency Syndrome 65 0.120
122
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.119
123
ISC004 Ischemia 66 0.118
124
ISC006 Ischemic Heart Disease 73 0.118
125
P HPT023 Hepatocellular Carcinoma 94 0.118
126
SPS003 Spastic Diplegia 55 0.118
127
MNT002 Mental Depression 60 0.117
128
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.117
129
P NRP001 Neuropathy 63 0.116
130
P PHC003 Pheochromocytoma 72 0.115
131
c SYS001 Systemic Lupus Erythematosus 86 0.114
132
HYP730 Hypogonadotropic Hypogonadism 56 0.114
133
PRT029 Parathyroid Adenoma 50 0.114
134
c BLM008 Bulimia Nervosa 2 53 0.113
135
THY001 Thyroid Crisis 30 0.113
136
P EPL164 Epilepsy 70 0.113
137
SPP011 Suppression of Tumorigenicity 12 41 0.113
138
AMN001 Amenorrhea 55 0.112
139
P NRB001 Neuroblastoma 73 0.112
140
P LPD010 Lipodystrophy 57 0.111
141
AST005 Asthma 83 0.110
142
c CNT075 Central Precocious Puberty 52 0.109
143
BRN106 Burns 57 0.109
144
URN009 Urinary System Disease 58 0.109
145
VSC007 Vascular Disease 71 0.107
146
GST033 Gestational Diabetes 62 0.107
147
MRB003 Morbid Obesity 61 0.107
148
P RNG031 Ring Chromosome Y Syndrome 29 0.106
149
END057 Endometrial Cancer 76 0.106
150
P END044 Endometriosis 71 0.106
151
P MYP004 Myopathy 69 0.105
152
MDD011 Mood Disorder 64 0.105
153
HYP043 Hyperandrogenism 50 0.103
154
P GLM045 Glioma 61 0.103
155
P ANR048 Aniridia 1 68 0.103
156
P PSR002 Psoriasis 65 0.102
157
DMN002 Dementia 68 0.101
158
PSY004 Psychotic Disorder 72 0.101
159
EXP004 Exophthalmos 50 0.101
160
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.101
161
P OVR046 Ovarian Cyst 52 0.100
162
P STR021 Struma Ovarii 40 0.100
163
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.100
164
GST053 Gastric Cancer 84 0.100
165
P ALP008 Alopecia 56 0.099
166
EWN002 Ewing's Family of Tumors 49 0.099
167
P CLC063 Celiac Disease 1 65 0.099
168
P NRV007 Nervous System Disease 75 0.098
169
LVR012 Liver Cirrhosis 73 0.098
170
P PRG013 Paraganglioma 57 0.098
171
PPL018 Papillary Adenocarcinoma 47 0.098
172
DWN001 Down Syndrome 70 0.098
173
P TRT010 Teratoma 53 0.097
174
c PRM196 Premature Ovarian Failure 1 68 0.097
175
BNF002 Bone Fracture 56 0.097
176
ANR038 Anorexia Nervosa 1 21 0.097
177
BLD137 Blood Group--Ahonen 17 0.097
178
c SML038 Small Cell Cancer of the Lung 67 0.096
179
HYP020 Hyperprolactinemia 64 0.096
180
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.096
181
c CNT035 Central Nervous System Disease 65 0.096
182
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.095
183
CNN005 Connective Tissue Disease 65 0.095
184
BRN071 Brain Injury 54 0.094
185
LNG099 Lung Disease 67 0.094
186
P LRY019 Laryngitis 57 0.094
187
P LYM026 Lymphoblastic Leukemia 66 0.094
188
c HYP595 Hypertension, Essential 78 0.094
189
P MLT020 Multiple Sclerosis 85 0.093
190
P DBT005 Diabetes Insipidus 54 0.093
191
c ACT053 Acute Thyroiditis 29 0.092
192
P BCL006 B-Cell Lymphomas 70 0.092
193
GST050 Gastrointestinal System Disease 66 0.091
194
THR024 Thrombosis 61 0.091
195
P PNC035 Pancreatic Cancer 89 0.091
196
RTN023 Retinitis 52 0.090
197
PLC008 Placenta Disease 48 0.090
198
RSP006 Respiratory System Disease 63 0.090
199
P AMY004 Amyloidosis 69 0.090
200
PRT030 Parathyroid Gland Disease 50 0.090
201
MYL069 Myeloma, Multiple 86 0.090
202
PND002 Pendred Syndrome 55 0.089
203
BRR014 Barrett Esophagus 64 0.089
204
NNT010 Nontoxic Goiter 37 0.089
205
P THL005 Thalassemia 65 0.088
206
ACT238 Acth Deficiency, Isolated 45 0.088
207
P MJR001 Major Depressive Disorder 70 0.088
208
NNL002 Nonalcoholic Steatohepatitis 56 0.087
209
c MNN043 Meningioma, Familial 69 0.087
210
P HST010 Histiocytosis 60 0.087
211
URT039 Urticaria 59 0.087
212
OVR029 Ovarian Hyperstimulation Syndrome 64 0.087
213
HYP029 Hyperthyroxinemia 27 0.087
214
P SLP006 Sleep Apnea 65 0.087
215
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.087
216
LMY002 Leiomyoma 58 0.086
217
PRT036 Peritonitis 67 0.086
218
c HPT073 Hepatitis C Virus 73 0.086
219
P MYP006 Myopia 56 0.086
220
ANV001 Anovulation 48 0.086
221
PRT010 Parathyroid Carcinoma 64 0.085
222
END030 End Stage Renal Failure 59 0.085
223
CYS001 Cystic Fibrosis 85 0.085
224
NNT019 Neonatal Hypothyroidism 33 0.085
225
P ESP024 Esophagitis 64 0.085
226
MCC012 Mccune-Albright Syndrome 65 0.084
227
TRM010 Traumatic Brain Injury 54 0.084
228
CLT003 Colitis 63 0.084
229
PRD004 Prediabetes Syndrome 46 0.084
230
PRT038 Protein-Energy Malnutrition 52 0.083
231
MDS022 Mediastinitis 44 0.083
232
P NPH012 Nephrotic Syndrome 60 0.083
233
ALR002 Al-Raqad Syndrome 30 0.083
234
GRW036 Growth Control, Y-Chromosome Influenced 33 0.083
235
PST011 Pustulosis of Palm and Sole 47 0.083
236
P INT068 Intestinal Disease 65 0.082
237
LYM019 Lymphosarcoma 58 0.082
238
c TRC078 Trichohepatoenteric Syndrome 2 34 0.082
239
P PRD008 Periodontitis 67 0.082
240
P PRP029 Porphyria 62 0.082
241
CHL068 Cholestasis 60 0.082
242
HYP189 Hypoadrenalism 43 0.082
243
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.082
244
PRM013 Premature Menopause 45 0.082
245
THY096 Thyroid Carcinoma, Hurthle Cell 27 0.081
246
c PRC016 Pre-Eclampsia 65 0.081
247
TTH032 Tooth Size 44 0.080
248
ANR040 Aneurysm 61 0.080
249
RHM027 Rheumatic Disease 62 0.080
250
THY069 Thyroid Hormone Resistance, Selective Pituitary 23 0.080
251
DRM006 Dermatitis 67 0.079
252
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.079
253
P GND004 Gonadal Dysgenesis 50 0.078
254
PLS011 Plasmacytoma 60 0.078
255
P SML001 Small Cell Carcinoma 58 0.078
256
PLM011 Plummer's Disease 38 0.078
257
P INF038 Influenza 77 0.078
258
P CHR084 Chromosomal Disease 40 0.077
259
P HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 39 0.077
260
P BPL003 Bipolar Disorder 61 0.077
261
APN008 Apnea, Obstructive Sleep 67 0.077
262
c ACT075 Acute Myocardial Infarction 64 0.076
263
P FML011 Familial Adenomatous Polyposis 71 0.076
264
CRN036 Craniopharyngioma 63 0.076
265
c HPT016 Hepatitis B 68 0.076
266
ISL001 Islet Cell Tumor 54 0.076
267
CRB039 Cerebrovascular Disease 68 0.076
268
P HMN010 Hemangioma 61 0.075
269
VRL011 Viral Infectious Disease 64 0.075
270
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.075
271
LYM133 Lymphoma, Hodgkin, Classic 78 0.075
272
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.075
273
HYP070 Hyperpituitarism 43 0.075
274
P ECL001 Eclampsia 57 0.075
275
ETN001 Eating Disorder 61 0.075
276
P MYL006 Myeloid Leukemia 69 0.074
277
END040 Endogenous Depression 53 0.074
278
MLN007 Male Infertility 53 0.074
279
LNG108 Langerhans Cell Histiocytosis 63 0.074
280
P HYP014 Hyperuricemia 54 0.074
281
GLB002 Glioblastoma 74 0.073
282
CHR008 Choroiditis 47 0.073
283
NSP002 Nasopharyngitis 46 0.073
284
KWS001 Kwashiorkor 43 0.073
285
HYP005 Hypokalemia 53 0.073
286
P INF037 Inflammatory Bowel Disease 52 0.073
287
ETH004 Euthyroid Sick Syndrome 40 0.072
288
ADR012 Adrenal Gland Disease 51 0.072
289
P GLM007 Glomerulonephritis 61 0.072
290
c MTR002 Mitral Valve Insufficiency 46 0.072
291
IRN002 Iron Metabolism Disease 45 0.072
292
c HPT003 Hepatitis a 63 0.072
293
SXD001 Sex Differentiation Disease 37 0.072
294
ULC004 Ulcerative Colitis 80 0.072
295
DDN006 Duodenitis 46 0.071
296
BRC012 Brucellosis 71 0.071
297
P AST007 Astrocytoma 66 0.071
298
P SHR001 Short Bowel Syndrome 52 0.071
299
P ACT074 Acute Lymphocytic Leukemia 61 0.071
300
P RTN024 Retinoblastoma 76 0.071
301
P DRR001 Diarrhea 60 0.071
302
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.071
303
c FML297 Familial Thyroid Dyshormonogenesis 38 0.071
304
c PSD108 Pseudohypoparathyroidism, Type Ia 57 0.071
305
CRB025 Carbohydrate Metabolic Disorder 38 0.070
306
c VRL010 Viral Hepatitis 59 0.070
307
VGN023 Vaginitis 59 0.070
308
HMN044 Human Immunodeficiency Virus Type 1 71 0.070
309
HDC001 Headache 55 0.070
310
P KDN017 Kidney Cancer 66 0.070
311
CRH001 Crohn's Disease 80 0.069
312
HPT082 Hepatic Adenomas, Familial 52 0.069
313
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.069
314
c ADL017 Adult T-Cell Leukemia 63 0.069
315
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 34 0.069
316
CHN070 Cohen-Gibson Syndrome 51 0.068
317
c OVR114 Ovarian Cancer 1 54 0.068
318
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.068
319
BRN028 Brain Cancer 72 0.068
320
P THY023 Thymoma 65 0.068
321
SVR004 Severe Combined Immunodeficiency 71 0.068
322
CYS010 Cystinosis 55 0.068
323
P DRM010 Dermatomyositis 65 0.068
324
P MYS003 Myasthenia Gravis 73 0.068
325
FXF002 Fox-Fordyce Disease 40 0.068
326
LYM024 Lymphatic System Disease 45 0.068
327
ATM052 Autoimmune Disease 1 30 0.068
328
P LPM005 Lipomatosis 50 0.068
329
P UTR058 Uterine Anomalies 55 0.068
330
DFF005 Diffuse Large B-Cell Lymphoma 64 0.067
331
P GST044 Gastritis 61 0.067
332
P ALP009 Alopecia Areata 64 0.067
333
P EST001 Estrogen-Receptor Positive Breast Cancer 52 0.067
334
NRL016 Neural Tube Defects 79 0.067
335
ACN002 Acanthosis Nigricans 60 0.067
336
P ENC004 Encephalitis 66 0.067
337
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.067
338
c BTT014 Beta-Thalassemia 70 0.067
339
OST011 Osteomalacia 52 0.067
340
P LMY004 Leiomyosarcoma 59 0.066
341
P NNN008 Noonan Syndrome 1 77 0.066
342
P MDL005 Medulloblastoma 76 0.066
343
P PRM006 Primary Biliary Cirrhosis 55 0.066
344
GLC006 Galactosemia 64 0.066
345
P PLM037 Pulmonary Hypertension 79 0.066
346
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.066
347
EXT010 Extramedullary Plasmacytoma 52 0.066
348
ADR013 Adrenal Gland Hyperfunction 54 0.066
349
c PTT056 Pituitary Adenoma 1, Multiple Types 46 0.066
350
P GLY013 Glycogen Storage Disease 61 0.066
351
c MLG059 Malignant Struma Ovarii 38 0.066
352
SPT006 Septooptic Dysplasia 54 0.065
353
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.065
354
PHC013 Phaeochromocytoma 44 0.065
355
SMT003 Somatostatinoma 54 0.065
356
ALL026 Allergic Hypersensitivity Disease 59 0.065
357
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.065
358
P RSP003 Respiratory Failure 71 0.065
359
GST045 Gastroenteritis 65 0.065
360
VSC011 Vasculitis 66 0.065
361
HMT018 Hematopoietic Stem Cell Transplantation 58 0.065
362
NNT003 Neonatal Thyrotoxicosis 28 0.065
363
PNC034 Pancreas Disease 59 0.065
364
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.065
365
CHR074 Choriocarcinoma 49 0.064
366
EMP001 Empty Sella Syndrome 42 0.064
367
RNL011 Renal Osteodystrophy 49 0.064
368
NPH003 Nephrocalcinosis 49 0.064
369
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.064
370
P PNM007 Pneumonia 70 0.064
371
P LCT001 Lactic Acidosis 51 0.064
372
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.064
373
P RNL003 Renal Clear Cell Carcinoma 58 0.064
374
PTT004 Pituitary Apoplexy 47 0.064
375
SPN186 Spinal Cord Injury 67 0.064
376
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.064
377
OST004 Osteitis Fibrosa 45 0.064
378
P ATS364 Autism 70 0.064
379
HLC007 Helicobacter Pylori Infection 64 0.064
380
DYS073 Dysphagia 47 0.063
381
P RNL007 Renal Tubular Acidosis 51 0.063
382
PSR001 Psoriatic Arthritis 66 0.063
383
HYP249 Hyperthyroidism, Nonautoimmune 27 0.063
384
MNG003 Mungan Syndrome 34 0.063
385
ADR007 Adrenoleukodystrophy 72 0.063
386
PST021 Postpartum Depression 54 0.063
387
ENT004 Enthesopathy 38 0.063
388
ALC007 Alcohol Dependence 65 0.063
389
WLL001 Williams-Beuren Syndrome 63 0.063
390
CMB081 Combined Immunodeficiency, X-Linked 64 0.062
391
c BRN108 Branchiootic Syndrome 1 47 0.062
392
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.062
393
P BLD134 Bladder Cancer 78 0.062
394
SFT003 Soft Tissue Sarcoma 58 0.062
395
P HYP265 Hypotonia 40 0.062
396
GT001 Gout 60 0.062
397
TST014 Testicular Cancer 54 0.062
398
CLN019 Colonic Disease 55 0.062
399
LMY014 Leiomyoma, Uterine 61 0.061
400
P CTR002 Cataract 60 0.061
401
P TRC086 Trichohepatoenteric Syndrome 1 54 0.061
402
CLN015 Colon Adenocarcinoma 53 0.061
403
P MYC084 Mycobacterium Tuberculosis 1 69 0.061
404
c LKM071 Leukemia, Chronic Lymphocytic 75 0.061
405
NNF007 Non-Functioning Pituitary Adenoma 47 0.061
406
FNC007 Functioning Pituitary Adenoma 37 0.061
407
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.060
408
ANG054 Angina Pectoris 53 0.060
409
CRC006 Carcinoid Syndrome 59 0.060
410
P CRV035 Cervical Cancer 72 0.060
411
PTT008 Pituitary Carcinoma 51 0.060
412
ACR006 Aceruloplasminemia 65 0.060
413
c ATM011 Autoimmune Hepatitis 63 0.060
414
P LCH002 Lichen Planus 58 0.060
415
HYP780 Hypoadrenocorticism, Familial 59 0.060
416
WRN001 Werner Syndrome 70 0.060
417
P HML002 Hemolytic Anemia 62 0.060
418
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.060
419
ALL001 Allan-Herndon-Dudley Syndrome 49 0.060
420
STR020 Strabismus 55 0.060
421
ADR010 Adrenal Cortical Hypofunction 41 0.060
422
PRN039 Paraneoplastic Syndromes 35 0.059
423
MLR004 Malaria 86 0.059
424
P ADL010 Adult Respiratory Distress Syndrome 67 0.059
425
P CHL066 Cholangitis 52 0.059
426
P PNC025 Panic Disorder 57 0.059
427
P ATR011 Atrial Fibrillation 68 0.059
428
P LYD001 Leydig Cell Tumor 47 0.059
429
P ICH004 Ichthyosis 54 0.059
430
PRN011 Pernicious Anemia 50 0.059
431
P FNC004 Fanconi Syndrome 54 0.059
432
CLC006 Calcinosis 51 0.059
433
PRP083 Porphyria, Acute Intermittent 60 0.059
434
P PRK057 Parkinson Disease, Late-Onset 78 0.059
435
SYN036 Syncope 46 0.059
436
P MCR115 Microvascular Complications of Diabetes 5 66 0.059
437
P RHB003 Rhabdomyosarcoma 61 0.058
438
ADN064 Adenohypophysitis 39 0.058
439
P MNN013 Meningitis 71 0.058
440
INS001 Insulinoma 66 0.058
441
ESP021 Esophageal Cancer 79 0.058
442
c LKM061 Leukemia, Acute Myeloid 81 0.058
443
LYM067 Lymphoid Leukemia 43 0.058
444
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.058
445
DMY004 Demyelinating Disease 58 0.058
446
P THY061 Thyroid Dyshormonogenesis 2a 24 0.058
447
ECT093 Ectopic Cushing Syndrome 50 0.057
448
ADR005 Adrenal Carcinoma 59 0.057
449
c LKM004 Leukemia, B-Cell, Chronic 37 0.057
450
ZLL002 Zollinger-Ellison Syndrome 57 0.057
451
P SZR006 Seizure Disorder 55 0.057
452
P KLL001 Kallmann Syndrome 63 0.057
453
P DLT002 Dilated Cardiomyopathy 76 0.057
454
DRY001 Dry Eye Syndrome 51 0.057
455
MYM001 Myoma 56 0.056
456
P CNJ013 Conjunctivitis 67 0.056
457
MYL009 Myelodysplastic Syndrome 75 0.056
458
SPN051 Spondylitis 55 0.056
459
TRN007 Transsexualism 44 0.056
460
PRP016 Paraplegia 53 0.056
461
c ACT027 Acute Pancreatitis 61 0.056
462
c THY071 Thyroid Dyshormonogenesis 1 23 0.056
463
IRN001 Iron Deficiency Anemia 55 0.056
464
AND014 Androgenic Alopecia 39 0.056
465
ALP046 Alport Syndrome, X-Linked 74 0.056
466
P ANG015 Angioedema 57 0.056
467
P EXN002 Exanthem 62 0.056
468
P TCL004 T-Cell Leukemia 50 0.056
469
P RHN004 Rhinitis 62 0.056
470
P PLY041 Polymyositis 57 0.055
471
c SCL052 Scleroderma, Familial Progressive 60 0.055
472
LYS002 Lysosomal Storage Disease 56 0.055
473
CRY004 Cryoglobulinemia 49 0.055
474
P PMP001 Pemphigus 55 0.055
475
c ACT020 Acute T Cell Leukemia 48 0.055
476
c SCN052 Secondary Adrenal Insufficiency 41 0.055
477
GLB015 Glioblastoma Multiforme 68 0.055
478
P ASP006 Aspergillosis 65 0.055
479
P ATR005 Atrophic Gastritis 51 0.055
480
HYP677 Hyperthyroxinemia, Familial Dysalbuminemic 25 0.055
481
P LPS002 Liposarcoma 61 0.055
482
P SJG008 Sjogren Syndrome 58 0.055
483
CHR034 Chromophobe Adenoma 43 0.055
484
P PLY019 Polyneuropathy 58 0.055
485
GNG013 Gingivitis 64 0.055
486
P MYS005 Myositis 63 0.055
487
GLC036 Glucagonoma 52 0.055
488
TSH001 Tsh Producing Pituitary Tumor 42 0.055
489
WLS001 Wilson Disease 72 0.055
490
CLR030 Clear Cell Renal Cell Carcinoma 55 0.054
491
P FML018 Familial Mediterranean Fever 73 0.054
492
P MYT002 Myotonic Dystrophy 50 0.054
493
BRT054 Brittle Bone Disorder 67 0.054
494
P THR014 Thrombocytopenia 65 0.054
495
c PSD047 Pseudo-Turner Syndrome 15 0.054
496
c ACT073 Acute Leukemia 61 0.054
497
P DYS154 Dystonia 61 0.054
498
BRS099 Breast Ductal Carcinoma 55 0.054
499
ALB001 Albright's Hereditary Osteodystrophy 55 0.054
500
P PRS038 Personality Disorder 65 0.054
501
PRP036 Peripheral T-Cell Lymphoma 48 0.053
502
INT075 Intracranial Hypertension 53 0.053
503
RTN018 Retinal Disease 56 0.053
504
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.053
505
c BSL007 Basal Cell Carcinoma 66 0.053
506
SKL017 Skeletal Dysplasias 48 0.053
507
CRD119 Cardiac Arrest 63 0.053
508
P STR035 Streptococcal Group a Invasive Disease 28 0.053
509
SPS057 Spasticity 41 0.053
510
P HRP006 Herpes Simplex 70 0.053
511
STR067 Stroke, Ischemic 84 0.053
512
P THY054 Thyrotoxic Periodic Paralysis 54 0.053
513
END041 Endometrial Adenocarcinoma 59 0.053
514
CHL061 Childhood Leukemia 50 0.053
515
ATH010 Athyreosis 37 0.053
516
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.053
517
PRD007 Periodontal Disease 64 0.053
518
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.053
519
FML037 Female Breast Cancer 52 0.052
520
PST014 Postsurgical Hypothyroidism 28 0.052
521
c ACT210 Acute Respiratory Distress Syndrome 63 0.052
522
P ATX030 Ataxia-Telangiectasia 80 0.052
523
c CRN243 Carney Complex, Type 1 35 0.052
524
NRT004 Neuritis 55 0.052
525
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.052
526
MRK001 Merkel Cell Carcinoma 59 0.052
527
MCS002 Mucositis 61 0.052
528
MYC033 Myoclonus 40 0.052
529
CHL065 Cholangiocarcinoma 70 0.052
530
HDR002 Hidradenitis Suppurativa 54 0.051
531
HDR003 Hidradenitis 47 0.051
532
P FBR017 Fibrosarcoma 61 0.051
533
NRF007 Neurofibroma 65 0.051
534
VPM001 Vipoma 52 0.051
535
P PMP005 Pemphigus Vulgaris 56 0.051
536
c THY107 Thymoma, Familial 34 0.051
537
GNR004 Generalized Anxiety Disorder 53 0.051
538
PNC001 Pancytopenia 50 0.051
539
P TRM003 Tremor 54 0.051
540
OST097 Osteoporotic Fracture 41 0.051
541
FBR009 Fibrous Dysplasia 49 0.051
542
CHL123 Chlamydia 64 0.051
543
c LKM062 Leukemia, Acute Lymphoblastic 64 0.051
544
NRV006 Nervous System Cancer 61 0.051
545
GST040 Gastric Adenocarcinoma 60 0.051
546
P CND004 Candidiasis 61 0.051
547
DFC004 Deficiency Anemia 62 0.050
548
CYT008 Cytomegalovirus Infection 57 0.050
549
c ALP061 Alopecia, Androgenetic, 1 44 0.050
550
P MYL005 Myelofibrosis 75 0.050
551
P SNS014 Sinusitis 62 0.050
552
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.050
553
P DYS021 Dysautonomia 47 0.050
554
LYM027 Lymphopenia 56 0.050
555
FBR019 Fibromatosis 47 0.050
556
PNC033 Pancreas Adenocarcinoma 63 0.050
557
MRG003 Marginal Zone B-Cell Lymphoma 56 0.050
558
P TMP003 Temporal Arteritis 67 0.050
559
P UVT001 Uveitis 61 0.050
560
P MYC008 Myocarditis 58 0.050
561
P GRF003 Graft-Versus-Host Disease 72 0.050
562
P PLY014 Polycystic Kidney Disease 60 0.050
563
c ALM001 Al Amyloidosis 56 0.050
564
CYS036 Cystinosis, Nephropathic 47 0.050
565
c JVN010 Juvenile Rheumatoid Arthritis 71 0.050
566
GYN001 Gynecomastia 47 0.050
567
c MCL042 Macular Degeneration, Age-Related, 1 79 0.050
568
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.050
569
PTZ001 Peutz-Jeghers Syndrome 70 0.050
570
TRN069 Transsexuality 23 0.050
571
P FLL037 Follicular Lymphoma 76 0.050
572
c SPN225 Spondyloarthropathy 1 71 0.050
573
MNT001 Mantle Cell Lymphoma 76 0.049
574
P PRT013 Portal Hypertension 59 0.049
575
P NSP012 Nasopharyngeal Carcinoma 71 0.049
576
MNN009 Meningoencephalitis 49 0.049
577
P END033 Endocarditis 58 0.049
578
P BRN120 Bronchus Cancer 39 0.049
579
INF009 Inflammatory Spondylopathy 32 0.049
580
CRB037 Cerebral Palsy 70 0.049
581
PLS009 Plasma Cell Neoplasm 51 0.049
582
INT067 Interstitial Nephritis 51 0.049
583
P MTR004 Maturity-Onset Diabetes of the Young 62 0.049
584
ADR008 Adrenal Adenoma 51 0.049
585
FNT004 Fainting 36 0.049
586
P LYN001 Lynch Syndrome 71 0.049
587
END035 Endocrine Gland Cancer 48 0.049
588
PRP030 Purpura 61 0.049
589
ADN001 Adenosine Deaminase Deficiency 52 0.049
590
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.049
591
PNC053 Pancreatic Islet Cell Tumors 39 0.049
592
P OST001 Osteopetrosis 70 0.048
593
CNS004 Constipation 57 0.048
594
ART016 Aortic Aneurysm 70 0.048
595
MTR014 Motor Neuron Disease 62 0.048
596
SNS001 Sensorineural Hearing Loss 59 0.048
597
GST023 Gastric Ulcer 57 0.048
598
ORL011 Oral Cancer 60 0.048
599
CLR109 Colorectal Adenocarcinoma 54 0.048
600
P PRC031 Preeclampsia/eclampsia 1 41 0.048
601
ALC006 Alcoholic Hepatitis 62 0.048
602
STM006 Stomach Disease 52 0.048
603
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 59 0.048
604
c MYS011 Myasthenia Gravis Congenital 28 0.048
605
SCK003 Sickle Cell Anemia 73 0.048
606
ORL013 Oral Lichen Planus 51 0.048
607
P PYL005 Pyelonephritis 56 0.048
608
P DRM007 Dermatitis Herpetiformis 56 0.048
609
P GRN010 Granular Cell Tumor 47 0.048
610
P SCL009 Sclerosing Cholangitis 53 0.048
611
c MLG074 Malignant Mesenchymoma 51 0.048
612
c THR092 Thrombophilia Due to Thrombin Defect 61 0.048
613
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.048
614
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 31 0.048
615
P FML012 Familial Partial Lipodystrophy 53 0.047
616
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.047
617
ALC009 Alcoholic Liver Cirrhosis 53 0.047
618
PRM020 Premenstrual Tension 49 0.047
619
GTL001 Gitelman Syndrome 62 0.047
620
SHH001 Sheehan Syndrome 50 0.047
621
SYS003 Systolic Heart Failure 44 0.047
622
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.047
623
MCN001 Mucinous Adenocarcinoma 54 0.047
624
AMN006 Aminoaciduria 41 0.047
625
LYM040 Lymphoblastic Lymphoma 58 0.047
626
SPP010 Suppressor of Tumorigenicity 3 55 0.047
627
BCK006 Back Pain 46 0.047
628
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.047
629
CRD001 Cardiac Tamponade 45 0.047
630
c PSD117 Pseudohypoparathyroidism, Type Ic 39 0.047
631
PRC013 Pericarditis 55 0.047
632
SMN007 Seminoma 49 0.047
633
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.047
634
MTH009 Mouth Disease 64 0.047
635
PLM033 Pulmonary Embolism 62 0.047
636
DYS014 Dyspepsia 54 0.047
637
CHR073 Choreatic Disease 40 0.047
638
ONC007 Oncocytoma 48 0.047
639
DBT008 Diabetic Angiopathy 48 0.047
640
PTT003 Pituitary-Dependent Cushing's Disease 43 0.047
641
KRT001 Keratoconjunctivitis Sicca 63 0.046
642
GLC011 Galactose Epimerase Deficiency 46 0.046
643
PNG002 Pain Agnosia 41 0.046
644
PHR003 Pharyngitis 59 0.046
645
APP015 Apparent Mineralocorticoid Excess 54 0.046
646
END036 Endocrine Organ Benign Neoplasm 28 0.046
647
c FML346 Familial Adenomatous Polyposis 1 63 0.046
648
c ACT042 Acute Pyelonephritis 48 0.046
649
NWB001 Newborn Respiratory Distress Syndrome 56 0.046
650
c BRS049 Breast Carcinoma in Situ 55 0.046
651
PRP037 Proopiomelanocortin Deficiency 34 0.046
652
RSP007 Respiratory Distress Syndrome, Infant 28 0.046
653
c CHL119 Cholangitis, Primary Sclerosing 60 0.046
654
ALL014 Allergic Encephalomyelitis 37 0.046
655
CRP001 Carpal Tunnel Syndrome 64 0.046
656
OST003 Osteonecrosis 63 0.046
657
c CHR579 Chiari Malformation Type Ii 42 0.046
658
INT066 Interstitial Lung Disease 63 0.046
659
BNN003 Bone Inflammation Disease 46 0.046
660
PPL022 Papilloma 58 0.046
661
c MLG068 Malignant Glioma 66 0.046
662
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.046
663
c LKM063 Leukemia, Chronic Myeloid 80 0.046
664
ESP023 Esophageal Disease 58 0.046
665
c INF071 Inflammatory Bowel Disease 1 54 0.046
666
ADR004 Adrenal Cortical Adenocarcinoma 47 0.045
667
BRS050 Breast Cyst 36 0.045
668
P CNT005 Central Nervous System Lymphoma 57 0.045
669
ALP072 Alpha-Fetoprotein Deficiency 32 0.045
670
KRT002 Keratomalacia 55 0.045
671
P RTN008 Retinitis Pigmentosa 81 0.045
672
PRM236 Primary Biliary Cholangitis 56 0.045
673
BRN002 Bronchiolitis 59 0.045
674
ORL015 Oral Squamous Cell Carcinoma 59 0.045
675
TKY002 Takayasu Arteritis 66 0.045
676
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.045
677
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.045
678
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 55 0.045
679
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.045
680
SWL001 Swallowing Disorders 36 0.044
681
PLL001 Pallister-Hall Syndrome 59 0.044
682
c WLM018 Wilms Tumor 5 49 0.044
683
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 21 0.044
684
SKN019 Skin Melanoma 63 0.044
685
P BLM007 Bulimia Nervosa 1 53 0.044
686
HYP077 Hypertrichosis 49 0.044
687
BLD163 Blood Group, Dombrock System 23 0.044
688
P HYP058 Hypervitaminosis a 48 0.044
689
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.044
690
c INF145 Infantile Liver Failure Syndrome 1 33 0.044
691
c SML034 Small Cell Neuroendocrine Carcinoma 39 0.044
692
GLL018 Gallbladder Cancer 67 0.044
693
P CTN015 Cutaneous T Cell Lymphoma 56 0.044
694
P OPN001 Open-Angle Glaucoma 51 0.044
695
PNN001 Panniculitis 48 0.044
696
CRD137 Cardiogenic Shock 45 0.044
697
c PSD104 Pseudohypoparathyroidism, Type Ii 34 0.044
698
VCC001 Vaccinia 50 0.044
699
ACT119 Acute Promyelocytic Leukemia 64 0.044
700
c INV001 Invasive Aspergillosis 51 0.044
701
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.044
702
P PRC012 Pericardial Effusion 52 0.044
703
CVR006 Cavernous Hemangioma 48 0.044
704
MLN003 Melancholia 39 0.043
705
RCT017 Rectal Disease 38 0.043
706
P ACT150 Acute Adrenal Insufficiency 51 0.043
707
CLF001 Cleft Lip 54 0.043
708
BRK010 Burkitt Lymphoma 71 0.043
709
FBR012 Fabry Disease 72 0.043
710
LYM007 Lymphangioleiomyomatosis 68 0.043
711
KRN002 Kearns-Sayre Syndrome 59 0.043
712
BLR001 Biliary Atresia 56 0.043
713
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.043
714
P ORT004 Orthostatic Intolerance 68 0.043
715
P LNG064 Lung Cancer Susceptibility 3 64 0.043
716
P THR117 Three M Syndrome 1 52 0.043
717
INF021 Infant Gynecomastia 25 0.043
718
c INS002 in Situ Carcinoma 56 0.043
719
CYS014 Cystadenocarcinoma 51 0.043
720
CRV040 Cervix Carcinoma 52 0.043
721
HYP081 Hypolipoproteinemia 49 0.043
722
BRN022 Bronchiectasis 55 0.043
723
HMT002 Hematologic Cancer 64 0.043
724
c MCR113 Microvascular Complications of Diabetes 3 55 0.043
725
APL001 Aplastic Anemia 74 0.043
726
P TBR001 Tuberous Sclerosis 69 0.043
727
ALL003 Allergic Rhinitis 68 0.043
728
ADL030 Adult-Onset Still's Disease 65 0.043
729
P CHN012 Chondrosarcoma 56 0.043
730
P RNL015 Renal Hypertension 46 0.043
731
LYM009 Lymphocytic Choriomeningitis 46 0.042
732
NLS001 Nelson Syndrome 49 0.042
733
CNT047 Contact Dermatitis 64 0.042
734
c ANM038 Anemia, Autoimmune Hemolytic 56 0.042
735
EXC002 Exocrine Pancreatic Insufficiency 45 0.042
736
P TRN034 Transverse Myelitis 53 0.042
737
SCH014 Schistosomiasis 62 0.042
738
GST030 Gastrinoma 44 0.042
739
INT303 Intracranial Hypertension, Idiopathic 49 0.042
740
THR004 Thrombocytosis 55 0.042
741
P THR015 Thrombophilia 58 0.042
742
P CRD132 Cardiac Conduction Defect 53 0.042
743
CHL018 Childhood Medulloblastoma 51 0.042
744
LCR008 Lacrimal Apparatus Disease 43 0.042
745
P FRD012 Friedreich Ataxia 1 58 0.042
746
BRN053 Bronchial Adenomas/carcinoids Childhood 22 0.042
747
NTR018 Neutrophilia, Hereditary 46 0.042
748
EPD070 Epidermoid Cysts 46 0.042
749
ADG002 Audiogenic Seizures 26 0.041
750
AGR002 Agoraphobia 47 0.041
751
c WLM011 Wilms Tumor 6 44 0.041
752
P DRM053 Dermatitis, Atopic 68 0.041
753
HYP741 Hyperparathyroidism 2 with Jaw Tumors 49 0.041
754
c DRM040 Dermatitis Herpetiformis, Familial 32 0.041
755
HYP344 Hyperthyroidism, Familial Gestational 22 0.041
756
DNT001 Dental Fluorosis 44 0.041
757
P DDN001 Duodenal Ulcer 53 0.041
758
c GLY005 Glycogen Storage Disease Vi 51 0.041
759
P TXP001 Toxoplasmosis 65 0.041
760
MCR011 Microinvasive Gastric Cancer 45 0.041
761
GST019 Gastrointestinal Stromal Tumor 74 0.041
762
OPT006 Optic Nerve Disease 53 0.041
763
c TYP010 Type C Thymoma 34 0.041
764
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 46 0.041
765
SBP001 Subependymal Giant Cell Astrocytoma 50 0.041
766
IDP033 Idiopathic Edema 42 0.041
767
c MYT021 Myotonic Dystrophy 1 68 0.041
768
SRT004 Serotonin Syndrome 51 0.041
769
c CHR417 Chronic Graft Versus Host Disease 65 0.041
770
P BRD002 Bardet-Biedl Syndrome 61 0.041
771
HRM003 Hormone Producing Pituitary Cancer 32 0.041
772
TRN015 Transient Cerebral Ischemia 58 0.041
773
CRC014 Carcinoid Tumors, Intestinal 46 0.041
774
PYC001 Pycnodysostosis 51 0.041
775
CLR014 Clear Cell Adenoma 39 0.041
776
c HYP762 Hypothyroidism, Congenital, Nongoitrous, 5 19 0.041
777
OST159 Osteogenic Sarcoma 70 0.041
778
ICH054 Ichthyosis, X-Linked 59 0.041
779
P CRB088 Cerebral Atrophy 38 0.040
780
STS003 Sitosterolemia 58 0.040
781
P GST049 Gastrointestinal System Cancer 60 0.040
782
MYL001 Myelitis 52 0.040
783
P INT070 Intestinal Obstruction 55 0.040
784
ANG018 Angiomyolipoma 50 0.040
785
INC002 Inclusion Body Myositis 64 0.040
786
PMS001 Poems Syndrome 64 0.040
787
INF034 Infective Endocarditis 56 0.040
788
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 50 0.040
789
VTM002 Vitamin B12 Deficiency 46 0.040
790
DSC009 Discoid Lupus Erythematosus 48 0.040
791
CYS005 Cysticercosis 57 0.040
792
c MCR130 Microvascular Complications of Diabetes 6 42 0.040
793
c MCR120 Microvascular Complications of Diabetes 7 34 0.040
794
c MCR133 Microvascular Complications of Diabetes 4 32 0.040
795
TNS005 Tonsillitis 61 0.040
796
P CYS018 Cystitis 57 0.040
797
MDD010 Middle Ear Disease 50 0.040
798
P PTS002 Ptosis 50 0.040
799
TRN018 Transitional Cell Carcinoma 58 0.040
800
c ACT135 Acute Graft Versus Host Disease 57 0.040
801
c PLM022 Pulmonary Valve Insufficiency 38 0.040
802
CRD223 Cardiac Arrhythmia 52 0.040
803
BRN038 Bronchial Disease 58 0.040
804
CRV045 Cervical Intraepithelial Neoplasia 43 0.040
805
OBS015 Obesity, Hyperphagia, and Developmental Delay 31 0.039
806
MTY001 Mutyh-Associated Polyposis 42 0.039
807
P MGL001 Megaloblastic Anemia 52 0.039
808
THY039 Thyrotropin-Releasing Hormone Deficiency 25 0.039
809
GNG011 Gingival Disease 50 0.039
810
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.039
811
P FNC027 Fanconi Anemia, Complementation Group a 78 0.039
812
CHP002 Chops Syndrome 40 0.039
813
APH002 Aphasia 58 0.039
814
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.039
815
LYM012 Lymphoplasmacytic Lymphoma 50 0.039
816
PPM002 Ppoma 29 0.039
817
BLL006 Bullous Pemphigoid 64 0.039
818
INT079 Intrahepatic Cholangiocarcinoma 60 0.039
819
HYP074 Hypersensitivity Vasculitis 52 0.039
820
CST005 Castleman Disease 44 0.039
821
c HYP562 Hypothyroidism, Congenital, Nongoitrous, 6 24 0.039
822
SPN369 Spinal Disease 42 0.039
823
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.039
824
P OVR106 Ovarian Clear Cell Carcinoma 45 0.039
825
c ADN012 Adenocarcinoma in Situ 45 0.039
826
P SYS005 Systemic Scleroderma 67 0.038
827
LMB024 Limbic Encephalitis 42 0.038
828
TCD001 Tic Disorder 54 0.038
829
SCH003 Schizophreniform Disorder 44 0.038
830
ADR040 Adrenal Gland Pheochromocytoma 41 0.038
831
STT003 Steatitis 22 0.038
832
c MLG079 Malignant Pleural Mesothelioma 54 0.038
833
ORG010 Organ System Benign Neoplasm 28 0.038
834
DYS011 Dyskinesia of Esophagus 39 0.038
835
c HRD002 Hereditary Angioedema 59 0.038
836
PPL052 Papillomatosis, Confluent and Reticulated 26 0.038
837
ADP007 Adie Pupil 41 0.038
838
P ALG028 Alagille Syndrome 1 68 0.038
839
P FTT008 Fatty Liver Disease, Nonalcoholic 1 25 0.038
840
THY025 Thymus Cancer 52 0.038
841
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.038
842
P ANT006 Antiphospholipid Syndrome 59 0.038
843
c CHR048 Chronic Rhinitis 41 0.037
844
HRY003 Hairy Cell Leukemia 60 0.037
845
c BRD014 Bardet-Biedl Syndrome 2 58 0.037
846
MSC007 Muscle Hypertrophy 57 0.037
847
c BRD011 Bardet-Biedl Syndrome 10 56 0.037
848
c BRD013 Bardet-Biedl Syndrome 12 55 0.037
849
c BRD012 Bardet-Biedl Syndrome 11 55 0.037
850
PGM003 Pigmentation Disease 36 0.037
851
CND002 Conduct Disorder 54 0.037
852
BRD004 Borderline Personality Disorder 50 0.037
853
BRN024 Bronchitis 67 0.037
854
MCK007 Muckle-Wells Syndrome 64 0.037
855
EXF003 Exfoliative Dermatitis 28 0.037
856
P SPN052 Spondyloarthropathy 61 0.037
857
c HNT011 Huntington Disease-Like 3 35 0.037
858
CRN019 Coronary Artery Vasospasm 42 0.037
859
IMM064 Immunodeficiency, Common Variable, 10 37 0.037
860
ZYG002 Zygomycosis 35 0.037
861
CNG376 Congenital Leptin Deficiency 21 0.037
862
PLY150 Polykaryocytosis Inducer 20 0.037
863
APH001 Aphthous Stomatitis 64 0.037
864
P INT030 Intracranial Aneurysm 58 0.037
865
PRL017 Prolymphocytic Leukemia 51 0.037
866
PNC016 Pancreatic Cholera 41 0.037
867
CRV002 Cervix Uteri Carcinoma in Situ 40 0.037
868
SKN006 Skin Sarcoidosis 39 0.037
869
c GLY003 Glycogen Storage Disease Iii 56 0.037
870
RNL024 Renal Glucosuria 50 0.037
871
STT004 Steatorrhea 41 0.037
872
LPT014 Leptin Deficiency or Dysfunction 37 0.037
873
BLD138 Blood Group--Diego System 18 0.037
874
STR039 Sturge-Weber Syndrome 59 0.037
875
WBR001 Weber Syndrome 40 0.037
876
HYP776 Hyperparathyroidism, Neonatal Severe 39 0.037
877
CHR072 Chordoma 61 0.036
878
DYS008 Dyshormonogenic Goiter 17 0.036
879
PLC007 Placental Abruption 50 0.036
880
WDH003 Woodhouse-Sakati Syndrome 47 0.036
881
SPL018 Splenomegaly 45 0.036
882
PLS016 Plasma Cell Leukemia 43 0.036
883
ALP097 Alopecia Universalis Congenita 40 0.036
884
TST043 Testicular Seminoma 36 0.036
885
c LPM012 Lipomatosis, Multiple 64 0.036
886
P OLG002 Oligodendroglioma 59 0.036
887
STM007 Stomatitis 52 0.036
888
PRR002 Pure Red-Cell Aplasia 52 0.036
889
BCL014 B-Cell Growth Factor 42 0.036
890
WDH001 Wdha Syndrome 31 0.036
891
FCT002 Factor Xi Deficiency 64 0.036
892
BLT006 Bilateral Breast Cancer 49 0.036
893
P BRN009 Burning Mouth Syndrome 56 0.036
894
c HMP029 Hemophilia a 69 0.036
895
P ACT008 Actinic Keratosis 56 0.036
896
c OST164 Osteoporosis, Juvenile 54 0.036
897
GNG002 Ganglioneuroma 50 0.036
898
c BSL024 Basal Cell Carcinoma 1 42 0.036
899
P GRS003 Griscelli Syndrome 58 0.036
900
HPT022 Hepatoblastoma 55 0.036
901
P NTR004 Neutropenia 60 0.036
902
P HMP007 Hemophilia 61 0.036
903
RSP002 Respiratory Syncytial Virus Infectious Disease 53 0.036
904
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.036
905
P SRC025 Sarcoidosis 1 63 0.036
906
QDR001 Quadriplegia 54 0.035
907
P MYM013 Moyamoya Disease 1 50 0.035
908
ATR003 Atrophic Rhinitis 34 0.035
909
ALL010 Allergic Contact Dermatitis 60 0.035
910
P SRT003 Sertoli-Leydig Cell Tumor 38 0.035
911
ERY017 Erythema Elevatum Diutinum 54 0.035
912
ANC002 Anca-Associated Vasculitis 42 0.035
913
END075 Endocervical Adenocarcinoma 36 0.035
914
c MST023 Mesothelioma, Malignant 61 0.035
915
VLV011 Vulvovaginal Candidiasis 53 0.035
916
c PRM126 Primary Peritoneal Carcinoma 59 0.035
917
P ORL007 Oral Cavity Cancer 59 0.035
918
PLR008 Pleurisy 52 0.035
919
GRN017 Granulocytopenia 49 0.035
920
P CTS001 Cutis Laxa 62 0.035
921
P LCT002 Lactose Intolerance 48 0.035
922
ATX010 Ataxia Neuropathy Spectrum 29 0.035
923
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.034
924
ACD001 Acidophil Adenoma 29 0.034
925
MYT011 Myotonia 41 0.034
926
PRT019 Protein-Losing Enteropathy 40 0.034
927
CLR108 Colorectal Adenoma 60 0.034
928
c HNT004 Huntington Disease-Like 2 37 0.034
929
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.034
930
CLF027 Cleft Palate, Isolated 61 0.034
931
c SRC023 Sarcoidosis 2 30 0.034
932
TST033 Testicular Regression Syndrome 32 0.034
933
MSL001 Measles 64 0.034
934
MTS001 Mutism 42 0.034
935
STT001 Status Epilepticus 60 0.034
936
P PLM036 Pulmonary Fibrosis 68 0.034
937
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.034
938
KRT008 Keratopathy 44 0.034
939
MNN006 Meninges Hemangiopericytoma 39 0.034
940
NRG003 Neurogenic Arthropathy 30 0.034
941
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.034
942
ACT017 Acute Chest Syndrome 50 0.034
943
CLN044 Colon Adenoma 45 0.034
944
TTN003 Tetanus 65 0.034
945
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.034
946
c ACT076 Acute Myocarditis 48 0.034
947
URM005 Uremic Pruritus 43 0.034
948
UTR024 Uterine Carcinosarcoma 57 0.033
949
PNH004 Panhypophysitis 21 0.033
950
c TBR025 Tuberous Sclerosis 1 63 0.033
951
CHL067 Cholecystitis 58 0.033
952
CCC002 Coccidiosis 52 0.033
953
c DPH024 Diaphragmatic Hernia, Congenital 63 0.033
954
c PLZ002 Pelizaeus-Merzbacher-Like Disease 30 0.033
955
DNG002 Dengue Hemorrhagic Fever 66 0.033
956
c SVR005 Severe Pre-Eclampsia 53 0.033
957
c CLL012 Cell Type Benign Neoplasm 32 0.032
958
END016 Endocervicitis 28 0.032
959
CTN007 Cutaneous Leishmaniasis 66 0.032
960
PLM012 Pulmonary Sarcoidosis 58 0.032
961
HDG004 Hodgkin's Granuloma 28 0.032
962
HDG006 Hodgkin's Paragranuloma 21 0.032
963
NDL013 Nodular Regenerative Hyperplasia 53 0.032
964
DBT062 Diabetic Foot Ulcers 59 0.032
965
c PRD040 Periodontitis, Chronic 49 0.032
966
FML063 Familial Glucocorticoid Deficiency 35 0.032
967
P PLC011 Pilocytic Astrocytoma 63 0.032
968
PNM001 Pneumocystosis 55 0.032
969
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 55 0.032
970
P PLY017 Polyarteritis Nodosa 51 0.032
971
CLD007 Cold Agglutinin Disease 50 0.032
972
P BRN035 Brain Stem Glioma 42 0.032
973
VSC009 Vascular Skin Disease 10 0.032
974
c ATR087 Atrial Standstill 1 59 0.032
975
P HRD009 Hereditary Wilms' Tumor 46 0.032
976
NRL004 Neuroleptic Malignant Syndrome 44 0.032
977
IMM003 Immunoglobulin Alpha Deficiency 37 0.032
978
HYP610 Hypothyroidism, Central, and Testicular Enlargement 21 0.032
979
GNT039 Genetic Transient Congenital Hypothyroidism 10 0.032
980
CRT046 Corticosteroid-Binding Globulin Deficiency 43 0.032
981
P MCR010 Microcephaly 57 0.032
982
PLC005 Placental Insufficiency 59 0.032
983
GRF006 Grfoma 19 0.032
984
ANN002 Anencephaly 57 0.032
985
EPD016 Epidermolysis Bullosa 57 0.032
986
RTR008 Root Resorption 44 0.032
987
LYM022 Lymphangioma 53 0.031
988
P PRT026 Parotitis 45 0.031
989
CRH005 Crohn's Colitis 53 0.031
990
PNC056 Pineocytoma 49 0.031
991
SLV003 Salivary Gland Disease 47 0.031
992
DFF003 Diffuse Scleroderma 44 0.031
993
GRN022 Granulosa Cell Tumor of the Ovary 41 0.031
994
PNL014 Pineal Gland Cancer 36 0.031
995
DDN004 Duodenogastric Reflux 33 0.031
996
TNG003 Tongue Cancer 63 0.031
997
STL001 St. Louis Encephalitis 43 0.031
998
ALX002 Alexithymia 40 0.031
999
17B003 17-Beta Hydroxysteroid Dehydrogenase Iii Deficiency 32 0.031
1000
DNH001 Donohue Syndrome 60 0.031
1001
SKN022 Skin Squamous Cell Carcinoma 46 0.031
1002
ESP025 Esophagus Adenocarcinoma 42 0.031
1003
c LBR014 Leber Congenital Amaurosis 4 48 0.030
1004
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.030
1005
GLS001 Gliosarcoma 61 0.030
1006
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.030
1007
RCT018 Rectal Neoplasm 53 0.030
1008
P PNB001 Pineoblastoma 51 0.030
1009
c SCN005 Secondary Hypertrophic Osteoarthropathy 44 0.030
1010
OVR105 Ovarian Serous Carcinoma 43 0.030
1011
SCR001 Secretory Meningioma 41 0.030
1012
CRB026 Cerebellar Astrocytoma 39 0.030
1013
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 30 0.030
1014
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 60 0.030
1015
IGR001 Ige Responsiveness, Atopic 56 0.030
1016
LTN011 Late-Onset Isolated Acth Deficiency 18 0.030
1017
OCC006 Occipital Horn Syndrome 49 0.029
1018
END038 Endocrine Pancreas Disease 36 0.029
1019
P GNT008 Giant Cell Tumor 49 0.029
1020
ART006 Arthus Reaction 39 0.029
1021
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.029
1022
SPR011 Suprasellar Meningioma 30 0.029
1023
ART005 Arteriovenous Malformation 64 0.029
1024
P RST002 Restrictive Cardiomyopathy 51 0.029
1025
ANT011 Antisocial Personality Disorder 51 0.029
1026
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.029
1027
P CRB059 Cerebellar Degeneration 40 0.029
1028
PST086 Posterior Cortical Atrophy 38 0.029
1029
SMT008 Smith-Magenis Syndrome 54 0.029
1030
DYS018 Dysostosis 48 0.029
1031
SHW001 Shwartzman Phenomenon 40 0.029
1032
SPN331 Spondyloocular Syndrome 34 0.029
1033
c HYP293 Hypophosphatasia, Adult 48 0.028
1034
PRD013 Periodic Fever, Familial, Autosomal Dominant 59 0.028
1035
c SPR009 Sporadic Breast Cancer 47 0.028
1036
PTT010 Pituitary Infarct 26 0.027
1037
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.027
1038
AND020 Androgen Insensitivity, Partial 49 0.027
1039
GLC096 Galactorrhea 44 0.027
1040
CHR063 Chronic Mucocutaneous Candidiasis 66 0.027
1041
CHR177 Chromophobe Renal Cell Carcinoma 59 0.027
1042
BBS001 Babesiosis 51 0.027
1043
OPH002 Ophthalmia Neonatorum 38 0.027
1044
ACT003 Acute Kidney Tubular Necrosis 34 0.027
1045
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 33 0.027
1046
TLG001 Telogen Effluvium 30 0.027
1047
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.027
1048
c ATM075 Autoimmune Encephalitis 40 0.027
1049
P BNG013 Benign Breast Phyllodes Tumor 33 0.027
1050
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 25 0.027
1051
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 37 0.027
1052
VNH007 Von Hippel-Lindau Syndrome 72 0.026
1053
P RNL017 Renal Oncocytoma 49 0.026
1054
GRD001 Giardiasis 45 0.026
1055
CNG002 Congenital Bile Acid Synthesis Defect 27 0.026
1056
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.025
1057
RSS007 Resistance to Thyrotropin-Releasing Hormone Syndrome 14 0.025
1058
CHS002 Chiasmal Syndrome 35 0.025
1059
c RHB024 Rhabdomyosarcoma 2 56 0.024
1060
P STS008 Sotos Syndrome 1 56 0.024
1061
MNN020 Meningococcal Infection 47 0.024
1062
P FNG006 Feingold Syndrome 1 44 0.024
1063
TBR007 Tuberculum Sellae Meningioma 28 0.024
1064
PRM206 Premature Aging Syndrome, Penttinen Type 25 0.024
1065
SLL002 Sella Turcica Neoplasm 23 0.024
1066
TXC005 Toxic Shock Syndrome 61 0.024
1067
ALB014 Alobar Holoprosencephaly 37 0.023
1068
CNT043 Central Nervous System Organ Benign Neoplasm 23 0.023
1069
IND012 Indifference to Pain, Congenital, Autosomal Recessive 42 0.022
1070
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 13 0.022
1071
P PTT014 Pitt-Hopkins Syndrome 52 0.020
1072
c VRL012 Viral Meningitis 49 0.020
1073
INT025 Intermittent Explosive Disorder 42 0.020
1074
TBR009 Tuberculous Empyema 35 0.020
1075
OVR093 Overhydrated Hereditary Stomatocytosis 35 0.020
1076
FBR010 Fibrogenesis Imperfecta Ossium 22 0.020
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