Search results for pituitary tumor

990 hits were found for pituitary tumor

# Family MCID Name MIFTS Score
1
PTT037 Pituitary Tumors 49 3.859
2
PRL010 Prolactin Producing Pituitary Tumor 41 3.691
3
TSH001 Tsh Producing Pituitary Tumor 42 3.570
4
HRM003 Hormone Producing Pituitary Cancer 32 2.799
5
PST034 Posterior Pituitary Gland Neoplasm 7 2.053
6
ADN018 Adenoma 63 0.822
7
P PTT006 Pituitary Adenoma 57 0.715
8
P THY032 Thyroiditis 56 0.421
9
PTT004 Pituitary Apoplexy 47 0.402
10
P BRS047 Breast Cancer 100 0.388
11
PRS047 Prostatitis 59 0.351
12
NRN004 Neuroendocrine Tumor 58 0.347
13
P PNC044 Pancreatitis 64 0.342
14
P ADN016 Adenocarcinoma 71 0.341
15
END072 Endotheliitis 46 0.335
16
P LNG032 Lung Cancer 99 0.327
17
P GRM010 Germ Cells Tumors 37 0.327
18
P LYM118 Lymphoma 71 0.319
19
c BLD140 Blood Group, I System 37 0.296
20
GST019 Gastrointestinal Stromal Tumor 74 0.290
21
P LKM002 Leukemia 75 0.287
22
P PRS040 Prostate Cancer 88 0.284
23
ACR007 Acromegaly 70 0.282
24
MLN008 Melanoma 72 0.281
25
SRC014 Sarcoma 68 0.280
26
BRN028 Brain Cancer 72 0.273
27
NRV006 Nervous System Cancer 61 0.269
28
SQM006 Squamous Cell Carcinoma 74 0.267
29
P CLR023 Colorectal Cancer 98 0.263
30
P GLM045 Glioma 61 0.256
31
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.251
32
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.251
33
PTT009 Pituitary Gland Disease 56 0.248
34
P HPT023 Hepatocellular Carcinoma 94 0.240
35
P GRN010 Granular Cell Tumor 47 0.233
36
P HMN036 Hemangiopericytoma, Malignant 52 0.232
37
EWN002 Ewing's Family of Tumors 49 0.232
38
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.223
39
HYP266 Hypoxia 61 0.220
40
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 44 0.217
41
c SML038 Small Cell Cancer of the Lung 67 0.216
42
AGN016 Aging 65 0.212
43
NRN002 Neuronitis 43 0.211
44
P OVR042 Ovarian Cancer 82 0.211
45
CMB021 Combined Pituitary Hormone Deficiency 37 0.208
46
P HPT021 Hepatitis 75 0.207
47
P HYP083 Hypopituitarism 59 0.206
48
GST053 Gastric Cancer 84 0.205
49
GLB002 Glioblastoma 74 0.204
50
P NRB001 Neuroblastoma 73 0.203
51
P PNC035 Pancreatic Cancer 89 0.202
52
P CRV039 Cervicitis 49 0.201
53
NNF007 Non-Functioning Pituitary Adenoma 47 0.199
54
CRN036 Craniopharyngioma 63 0.199
55
FNC007 Functioning Pituitary Adenoma 37 0.197
56
c MNN043 Meningioma, Familial 69 0.197
57
P ART022 Arthritis 77 0.196
58
ISL001 Islet Cell Tumor 54 0.194
59
MLG077 Malignant Peripheral Nerve Sheath Tumor 59 0.193
60
P AST007 Astrocytoma 66 0.193
61
PTT008 Pituitary Carcinoma 51 0.191
62
P ESP024 Esophagitis 64 0.186
63
HYP085 Hypothalamic Disease 46 0.185
64
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.183
65
GGN002 Gigantism 36 0.182
66
P TST021 Testicular Germ Cell Tumor 70 0.180
67
P TRT010 Teratoma 53 0.178
68
P RHM011 Rheumatoid Arthritis 91 0.178
69
P HYP086 Hypothyroidism 62 0.177
70
P MLT074 Multiple Endocrine Neoplasia 55 0.176
71
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.176
72
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.175
73
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.175
74
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.175
75
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.175
76
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.175
77
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.175
78
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.175
79
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.175
80
P GRW001 Growth Hormone Secreting Pituitary Adenoma 43 0.174
81
CNN003 Conn's Syndrome 70 0.173
82
INS024 Insulin-Like Growth Factor I 83 0.171
83
P RTN024 Retinoblastoma 76 0.169
84
CRB009 Cerebritis 41 0.169
85
SFT003 Soft Tissue Sarcoma 58 0.166
86
P ACT010 Acth-Secreting Pituitary Adenoma 58 0.165
87
c PTT056 Pituitary Adenoma 1, Multiple Types 46 0.164
88
P DBT005 Diabetes Insipidus 54 0.163
89
HYP056 Hypoglycemia 62 0.162
90
P LYD001 Leydig Cell Tumor 47 0.161
91
c TST046 Testicular Germ Cell Tumor 1 26 0.161
92
ATY005 Atypical Teratoid Rhabdoid Tumor 57 0.161
93
P BCL006 B-Cell Lymphomas 70 0.160
94
HYP020 Hyperprolactinemia 64 0.160
95
P HRD009 Hereditary Wilms' Tumor 46 0.159
96
P MNN013 Meningitis 71 0.158
97
P MDL005 Medulloblastoma 76 0.157
98
ANR040 Aneurysm 61 0.157
99
PNC034 Pancreas Disease 59 0.156
100
P KDN018 Kidney Disease 69 0.156
101
SPR024 Supratentorial Cancer 26 0.155
102
P ENC018 Encephalopathy 58 0.154
103
P ANR048 Aniridia 1 68 0.152
104
PNC119 Pancreatic Neuroendocrine Tumor 49 0.151
105
GRW007 Growth Hormone Deficiency 52 0.148
106
DSM007 Desmoplastic Small Round Cell Tumor 53 0.148
107
MYL069 Myeloma, Multiple 86 0.147
108
P LVR013 Liver Disease 76 0.147
109
CHR034 Chromophobe Adenoma 43 0.145
110
GND003 Gonadal Disease 32 0.145
111
HYP002 Hypothalamic Neoplasm 23 0.143
112
GLB015 Glioblastoma Multiforme 68 0.142
113
P OVR049 Ovarian Disease 58 0.142
114
CRC006 Carcinoid Syndrome 59 0.142
115
P PHC003 Pheochromocytoma 72 0.141
116
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.141
117
NSP002 Nasopharyngitis 46 0.140
118
c CNT035 Central Nervous System Disease 65 0.140
119
P EPN002 Ependymoma 53 0.139
120
P RHB003 Rhabdomyosarcoma 61 0.139
121
BRS051 Breast Disease 67 0.138
122
THY028 Thyroid Cancer 72 0.138
123
HDC001 Headache 55 0.137
124
PTT041 Pituitary Stalk Interruption Syndrome 47 0.137
125
P NRV007 Nervous System Disease 75 0.137
126
URN009 Urinary System Disease 58 0.134
127
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.133
128
P INT068 Intestinal Disease 65 0.131
129
P PRG013 Paraganglioma 57 0.129
130
PNC053 Pancreatic Islet Cell Tumors 39 0.129
131
INS001 Insulinoma 66 0.129
132
EMP001 Empty Sella Syndrome 42 0.128
133
P BRN120 Bronchus Cancer 39 0.128
134
ANR038 Anorexia Nervosa 1 21 0.127
135
BLD137 Blood Group--Ahonen 17 0.127
136
AMN001 Amenorrhea 55 0.126
137
GNG005 Gangliocytoma 50 0.126
138
MXD032 Mixed Germ Cell Tumor 34 0.126
139
PTT003 Pituitary-Dependent Cushing's Disease 43 0.125
140
DFF005 Diffuse Large B-Cell Lymphoma 64 0.122
141
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.121
142
PTT001 Pituitary Hypoplasia 29 0.121
143
P RNG031 Ring Chromosome Y Syndrome 29 0.121
144
P MYL006 Myeloid Leukemia 69 0.121
145
P CRN038 Carney Complex Variant 59 0.119
146
CLN019 Colonic Disease 55 0.118
147
P HYP069 Hyperparathyroidism 58 0.118
148
P DBT009 Diabetes Mellitus 72 0.118
149
ORL015 Oral Squamous Cell Carcinoma 59 0.118
150
THY030 Thyroid Gland Disease 51 0.118
151
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.118
152
BNC003 Bone Cancer 59 0.117
153
GRN022 Granulosa Cell Tumor of the Ovary 41 0.117
154
P PRC019 Precocious Puberty 52 0.117
155
FML168 Familial Isolated Pituitary Adenoma 28 0.117
156
P SML001 Small Cell Carcinoma 58 0.116
157
ZLL002 Zollinger-Ellison Syndrome 57 0.115
158
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.115
159
BRR014 Barrett Esophagus 64 0.115
160
P OLG002 Oligodendroglioma 59 0.115
161
LYM043 Lymphocytic Hypophysitis 34 0.114
162
P INF032 Infertility 59 0.114
163
RCT017 Rectal Disease 38 0.113
164
MCC012 Mccune-Albright Syndrome 65 0.113
165
CHR072 Chordoma 61 0.113
166
TST014 Testicular Cancer 54 0.113
167
P FBR017 Fibrosarcoma 61 0.112
168
OST011 Osteomalacia 52 0.112
169
RTN023 Retinitis 52 0.112
170
P HMN010 Hemangioma 61 0.112
171
P HYP076 Hyperthyroidism 56 0.111
172
HYP070 Hyperpituitarism 43 0.110
173
c MLG068 Malignant Glioma 66 0.110
174
LMY002 Leiomyoma 58 0.110
175
ALR002 Al-Raqad Syndrome 30 0.110
176
P PSR002 Psoriasis 65 0.110
177
P NSP012 Nasopharyngeal Carcinoma 71 0.110
178
SLN005 Silent Pituitary Adenoma 23 0.109
179
LYM133 Lymphoma, Hodgkin, Classic 78 0.109
180
ESP021 Esophageal Cancer 79 0.109
181
ADR013 Adrenal Gland Hyperfunction 54 0.109
182
IMM136 Immune System Disease 57 0.109
183
END057 Endometrial Cancer 76 0.109
184
ADR012 Adrenal Gland Disease 51 0.109
185
ADN064 Adenohypophysitis 39 0.108
186
HMN009 Hemangioblastoma 56 0.108
187
MDS022 Mediastinitis 44 0.106
188
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.105
189
c LKM071 Leukemia, Chronic Lymphocytic 75 0.105
190
VNH007 Von Hippel-Lindau Syndrome 72 0.105
191
SPT006 Septooptic Dysplasia 54 0.105
192
P HYD006 Hydrocephalus 68 0.105
193
ISL003 Isolated Growth Hormone Deficiency 57 0.104
194
P MYC084 Mycobacterium Tuberculosis 1 69 0.103
195
CHR074 Choriocarcinoma 49 0.103
196
CHL065 Cholangiocarcinoma 70 0.103
197
P LRY019 Laryngitis 57 0.103
198
c LKM004 Leukemia, B-Cell, Chronic 37 0.102
199
THY111 Thyroid Carcinoma, Familial Medullary 63 0.102
200
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.101
201
CRC014 Carcinoid Tumors, Intestinal 46 0.100
202
LYM040 Lymphoblastic Lymphoma 58 0.100
203
P LYM026 Lymphoblastic Leukemia 66 0.100
204
OST159 Osteogenic Sarcoma 70 0.100
205
P HST010 Histiocytosis 60 0.100
206
P LPS004 Lupus Erythematosus 69 0.099
207
SPS003 Spastic Diplegia 55 0.099
208
PST011 Pustulosis of Palm and Sole 47 0.099
209
P HYP726 Hypercalcemia, Infantile, 1 57 0.099
210
ONC007 Oncocytoma 48 0.099
211
THR024 Thrombosis 61 0.098
212
HYP043 Hyperandrogenism 50 0.098
213
NRF007 Neurofibroma 65 0.098
214
c SYS001 Systemic Lupus Erythematosus 86 0.097
215
MCS002 Mucositis 61 0.097
216
P SNS014 Sinusitis 62 0.097
217
c PTT057 Pituitary Adenoma 4, Acth-Secreting 42 0.097
218
SKN016 Skin Disease 68 0.097
219
HYP080 Hypogonadism 54 0.096
220
P PLY011 Polycystic Ovary Syndrome 65 0.096
221
SKN027 Skin Conditions 48 0.096
222
AST005 Asthma 83 0.096
223
P MLT020 Multiple Sclerosis 85 0.096
224
P NRP001 Neuropathy 63 0.095
225
FBR019 Fibromatosis 47 0.095
226
P CYS017 Cystic Teratoma 40 0.095
227
P CNT036 Central Nervous System Germ Cell Tumor 39 0.095
228
AML029 Ameloblastoma 51 0.095
229
GST030 Gastrinoma 44 0.094
230
P END044 Endometriosis 71 0.094
231
c LKM061 Leukemia, Acute Myeloid 81 0.094
232
OSS002 Ossifying Fibromyxoid Tumor 29 0.094
233
LNG108 Langerhans Cell Histiocytosis 63 0.094
234
CLR030 Clear Cell Renal Cell Carcinoma 55 0.093
235
NRT004 Neuritis 55 0.093
236
PTC005 Pituicytoma 28 0.092
237
HYP730 Hypogonadotropic Hypogonadism 56 0.092
238
c BLM008 Bulimia Nervosa 2 53 0.092
239
PTT010 Pituitary Infarct 26 0.091
240
MRK001 Merkel Cell Carcinoma 59 0.091
241
FNC003 Functionless Pituitary Adenoma 15 0.091
242
P SCH015 Schizophrenia 71 0.091
243
FBR009 Fibrous Dysplasia 49 0.091
244
GLC036 Glucagonoma 52 0.090
245
c MLT086 Multiple Endocrine Neoplasia, Type Iv 52 0.090
246
P TCL004 T-Cell Leukemia 50 0.090
247
c PRM005 Primary Hyperparathyroidism 59 0.089
248
BRN071 Brain Injury 54 0.089
249
VRL011 Viral Infectious Disease 64 0.089
250
NLS001 Nelson Syndrome 49 0.088
251
ADR009 Adrenal Cortex Disease 40 0.088
252
PLM014 Pleomorphic Adenoma 55 0.088
253
CMB062 Combined Pituitary Hormone Deficiencies, Genetic Forms 36 0.088
254
ANX010 Anxiety 72 0.087
255
DND018 Dendritic Cell Tumor 41 0.087
256
PNL014 Pineal Gland Cancer 36 0.086
257
SHH001 Sheehan Syndrome 50 0.086
258
c HPT016 Hepatitis B 68 0.085
259
SMT003 Somatostatinoma 54 0.085
260
TRM010 Traumatic Brain Injury 54 0.085
261
ADR008 Adrenal Adenoma 51 0.085
262
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.085
263
GLC096 Galactorrhea 44 0.085
264
LNG099 Lung Disease 67 0.085
265
ADR001 Adrenal Rest Tumor 33 0.084
266
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 45 0.084
267
CHS002 Chiasmal Syndrome 35 0.084
268
PHC013 Phaeochromocytoma 44 0.084
269
CHR008 Choroiditis 47 0.084
270
HPT082 Hepatic Adenomas, Familial 52 0.084
271
GNG004 Ganglioglioma 51 0.083
272
NRM004 Neuroma 51 0.083
273
P THR014 Thrombocytopenia 65 0.083
274
GTR002 Goiter 53 0.083
275
HYP189 Hypoadrenalism 43 0.082
276
P BCK002 Beckwith-Wiedemann Syndrome 58 0.082
277
GNG002 Ganglioneuroma 50 0.082
278
ATM095 Autoimmune Disease 66 0.082
279
GYN001 Gynecomastia 47 0.082
280
CRB079 Cerebrospinal Fluid Leak 39 0.082
281
PNC006 Pancreatic Somatostatinoma 39 0.081
282
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.081
283
ECT093 Ectopic Cushing Syndrome 50 0.080
284
MLG041 Malignant Triton Tumor 36 0.080
285
PPL022 Papilloma 58 0.080
286
MYC006 Mycosis Fungoides 73 0.080
287
BRN053 Bronchial Adenomas/carcinoids Childhood 22 0.080
288
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.080
289
ALP046 Alport Syndrome, X-Linked 74 0.080
290
c HPT001 Hepatitis C 73 0.079
291
ORG010 Organ System Benign Neoplasm 28 0.079
292
END036 Endocrine Organ Benign Neoplasm 28 0.079
293
SPP011 Suppression of Tumorigenicity 12 41 0.078
294
c CNT075 Central Precocious Puberty 52 0.078
295
TBR007 Tuberculum Sellae Meningioma 28 0.078
296
P EPL164 Epilepsy 70 0.078
297
DDN006 Duodenitis 46 0.078
298
c CLL012 Cell Type Benign Neoplasm 32 0.078
299
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.078
300
P GLM040 Glioma Susceptibility 1 51 0.078
301
OLF005 Olfactory Neuroblastoma 48 0.078
302
BLS003 Blastoma 40 0.077
303
PNC008 Pancreatic Endocrine Carcinoma 40 0.077
304
PPL018 Papillary Adenocarcinoma 47 0.077
305
VSC008 Vascular Hemostatic Disease 36 0.077
306
CYS009 Cystadenoma 44 0.076
307
ACQ007 Acquired Immunodeficiency Syndrome 65 0.076
308
ANP006 Anaplastic Ependymoma 48 0.076
309
P LYN001 Lynch Syndrome 71 0.076
310
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.076
311
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.075
312
END041 Endometrial Adenocarcinoma 59 0.075
313
SPN051 Spondylitis 55 0.075
314
INF009 Inflammatory Spondylopathy 32 0.075
315
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.075
316
ANV001 Anovulation 48 0.074
317
c SPN225 Spondyloarthropathy 1 71 0.074
318
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.074
319
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.074
320
VPM001 Vipoma 52 0.074
321
c PTT060 Pituitary Adenoma 5, Multiple Types 14 0.074
322
P PLC011 Pilocytic Astrocytoma 63 0.073
323
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.073
324
ALV005 Alveolar Soft Part Sarcoma 56 0.073
325
P MYC007 Myocardial Infarction 81 0.073
326
SPN032 Spindle Cell Carcinoma 43 0.072
327
PLS011 Plasmacytoma 60 0.072
328
c SCN052 Secondary Adrenal Insufficiency 41 0.072
329
ACD001 Acidophil Adenoma 29 0.072
330
MNT002 Mental Depression 60 0.072
331
HDN002 Head Injury 48 0.072
332
ADN002 Adenoiditis 40 0.072
333
ARC002 Arachnoiditis 45 0.072
334
c PRG018 Paragangliomas 1 57 0.072
335
PRP021 Peripheral Nervous System Neoplasm 53 0.072
336
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.072
337
LVR012 Liver Cirrhosis 73 0.072
338
SRT004 Serotonin Syndrome 51 0.072
339
ISL114 Isolated Growth Hormone Deficiency, Type Ii 46 0.071
340
c LPM012 Lipomatosis, Multiple 64 0.071
341
ONC003 Oncogenic Osteomalacia 45 0.071
342
EXP004 Exophthalmos 50 0.071
343
P OST002 Osteoporosis 75 0.071
344
P HMR012 Hemorrhagic Fever 60 0.071
345
P HRP006 Herpes Simplex 70 0.070
346
PRN022 Perineurioma 38 0.070
347
MDD011 Mood Disorder 64 0.070
348
c PSD108 Pseudohypoparathyroidism, Type Ia 57 0.070
349
ISC004 Ischemia 66 0.070
350
MYX001 Myxopapillary Ependymoma 44 0.070
351
CNT043 Central Nervous System Organ Benign Neoplasm 23 0.070
352
HYP066 Hyperglycemia 64 0.070
353
LRN002 Laron Syndrome 63 0.069
354
P INF037 Inflammatory Bowel Disease 52 0.069
355
P OVR046 Ovarian Cyst 52 0.069
356
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.069
357
P CNT005 Central Nervous System Lymphoma 57 0.069
358
DRM013 Dermoid Cyst 43 0.069
359
DCT002 Ductal Carcinoma in Situ 56 0.068
360
ANX004 Anoxia 49 0.068
361
P EPN001 Ependymoblastoma 46 0.068
362
ACS001 Acoustic Neuroma 60 0.068
363
OVR029 Ovarian Hyperstimulation Syndrome 64 0.068
364
LMY014 Leiomyoma, Uterine 61 0.067
365
P ART023 Arthropathy 68 0.067
366
PPL058 Papilloma of Choroid Plexus 47 0.067
367
c PRM226 Primary Central Nervous System Lymphoma 51 0.067
368
INF021 Infant Gynecomastia 25 0.067
369
MNN001 Meningeal Melanocytoma 45 0.066
370
P SYR003 Syringoma 41 0.066
371
P ENC004 Encephalitis 66 0.066
372
c BCT007 Bacterial Meningitis 59 0.066
373
P PNM007 Pneumonia 70 0.066
374
ADR005 Adrenal Carcinoma 59 0.066
375
ISL015 Isolated Growth Hormone Deficiency, Type Ib 44 0.066
376
P LPM005 Lipomatosis 50 0.066
377
BRC012 Brucellosis 71 0.065
378
CHL068 Cholestasis 60 0.065
379
SLL002 Sella Turcica Neoplasm 23 0.065
380
P SPR013 Spiradenoma 39 0.065
381
CHR066 Chronic Fatigue Syndrome 67 0.065
382
SPR011 Suprasellar Meningioma 30 0.065
383
c PTT061 Pituitary Adenoma 3, Multiple Types 13 0.065
384
PTR001 Petrositis 25 0.065
385
c PTT058 Pituitary Adenoma 2, Growth Hormone-Secreting 14 0.065
386
PRT010 Parathyroid Carcinoma 64 0.064
387
SPN035 Spindle Cell Sarcoma 46 0.064
388
P GND004 Gonadal Dysgenesis 50 0.064
389
P HLP001 Holoprosencephaly 67 0.064
390
c GRV008 Graves Disease 1 52 0.064
391
P ENC008 Encephalocele 48 0.064
392
MYX004 Myxedema 44 0.064
393
CLN015 Colon Adenocarcinoma 53 0.064
394
MYB001 Myoblastoma 24 0.064
395
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.064
396
c ACT027 Acute Pancreatitis 61 0.064
397
GNG013 Gingivitis 64 0.064
398
OPT007 Optic Nerve Glioma 45 0.064
399
P HRT032 Heart Disease 80 0.064
400
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.064
401
P SDR002 Siderosis 48 0.064
402
PPL002 Papillary Carcinoma 51 0.063
403
c JVN009 Juvenile Pilocytic Astrocytoma 47 0.063
404
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 46 0.063
405
THY108 Thymic Neuroendocrine Tumor 37 0.063
406
CNG034 Congestive Heart Failure 74 0.063
407
MNN009 Meningoencephalitis 49 0.063
408
SCR024 Sacrococcygeal Teratoma 32 0.063
409
P CRN035 Cranial Nerve Palsy 42 0.063
410
ADN027 Adenomyosis 57 0.063
411
SYR002 Syringocystadenoma Papilliferum 45 0.062
412
NRS005 Neurosarcoidosis 26 0.062
413
P THY023 Thymoma 65 0.062
414
VGN023 Vaginitis 59 0.062
415
EPT008 Epithelioid Malignant Peripheral Nerve Sheath Tumor 29 0.062
416
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.062
417
STR067 Stroke, Ischemic 84 0.062
418
P INT030 Intracranial Aneurysm 58 0.062
419
OPT009 Optic Neuritis 53 0.062
420
EPD070 Epidermoid Cysts 46 0.062
421
PNC016 Pancreatic Cholera 41 0.062
422
ALL026 Allergic Hypersensitivity Disease 59 0.061
423
GLM004 Gliomatosis Cerebri 53 0.061
424
PNC027 Pancreatic Gastrinoma 37 0.061
425
CHN009 Chondroid Chordoma 31 0.061
426
LNT004 Lentigines 52 0.061
427
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.061
428
MCR013 Microphthalmia 61 0.061
429
P RNL003 Renal Clear Cell Carcinoma 58 0.060
430
OBS004 Obstructive Hydrocephalus 37 0.060
431
PRP083 Porphyria, Acute Intermittent 60 0.060
432
ACT029 Acute Interstitial Pneumonia 41 0.060
433
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 30 0.060
434
PRT029 Parathyroid Adenoma 50 0.060
435
PSD009 Pseudohermaphroditism 42 0.060
436
DNG002 Dengue Hemorrhagic Fever 66 0.059
437
P GRV001 Graves' Disease 62 0.059
438
P GST044 Gastritis 61 0.059
439
P TRN020 Turner Syndrome 69 0.059
440
HYP060 Hyperinsulinism 56 0.059
441
MLR004 Malaria 86 0.059
442
P LRY044 Larynx Cancer 57 0.059
443
CRB002 Cerebral Primitive Neuroectodermal Tumor 40 0.059
444
PLM019 Pleomorphic Liposarcoma 44 0.059
445
P ALP008 Alopecia 56 0.058
446
BLD163 Blood Group, Dombrock System 23 0.058
447
ADM013 Adamantinoma of Long Bones 55 0.058
448
P MJR001 Major Depressive Disorder 70 0.058
449
P AMY004 Amyloidosis 69 0.058
450
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.058
451
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.057
452
PLM026 Pilomatrixoma 53 0.057
453
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.057
454
CHR055 Chordoid Meningioma 32 0.057
455
P TRC086 Trichohepatoenteric Syndrome 1 54 0.057
456
ACN001 Acinar Cell Carcinoma 52 0.057
457
PLY040 Polymorphous Low-Grade Adenocarcinoma 42 0.057
458
MYX013 Myxofibrosarcoma 39 0.057
459
PLY150 Polykaryocytosis Inducer 20 0.057
460
NRM005 Neuromuscular Disease 60 0.057
461
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.057
462
c TYP010 Type C Thymoma 34 0.057
463
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.057
464
P MLT008 Multinodular Goiter 44 0.057
465
FST010 Fasting Hypoglycemia 36 0.056
466
DDN010 Duodenum Cancer 46 0.056
467
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.056
468
c CRN243 Carney Complex, Type 1 35 0.056
469
CHR033 Chordoid Glioma 33 0.056
470
MXD014 Mixed Ductal-Endocrine Carcinoma 29 0.056
471
PPM002 Ppoma 29 0.056
472
P MYP006 Myopia 56 0.056
473
KRT009 Keratosis 53 0.056
474
BRJ001 Borjeson-Forssman-Lehmann Syndrome 54 0.056
475
SXD001 Sex Differentiation Disease 37 0.056
476
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.056
477
PSY004 Psychotic Disorder 72 0.056
478
CVR006 Cavernous Hemangioma 48 0.056
479
THY043 Thymic Hyperplasia 38 0.056
480
CLR018 Clear Cell Meningioma 30 0.056
481
P FNC027 Fanconi Anemia, Complementation Group a 78 0.056
482
ALC007 Alcohol Dependence 65 0.056
483
MLN003 Melancholia 39 0.056
484
INT003 Intracranial Hypotension 36 0.056
485
NLL003 Null Pituitary Adenoma 11 0.056
486
P RHN004 Rhinitis 62 0.055
487
GST045 Gastroenteritis 65 0.055
488
CRB039 Cerebrovascular Disease 68 0.055
489
ARM001 Aromatase Deficiency 52 0.055
490
P ALZ034 Alzheimer Disease 95 0.055
491
DRM006 Dermatitis 67 0.055
492
P STR021 Struma Ovarii 40 0.055
493
CRB024 Cerebral Neuroblastoma 31 0.055
494
NSD001 Nose Disease 51 0.055
495
PHR003 Pharyngitis 59 0.055
496
ASK001 Askin's Tumor 33 0.055
497
P MYP004 Myopathy 69 0.054
498
IMM158 Immune Suppression 57 0.054
499
EXT039 Extrapontine Myelinolysis 18 0.054
500
NPH010 Nephrosclerosis 46 0.054
501
FBR083 Fibrous Dysplasia/mccune-Albright Syndrome 18 0.054
502
CHR177 Chromophobe Renal Cell Carcinoma 59 0.054
503
VLL006 Villous Adenoma 34 0.054
504
APR002 Aip-Related Familial Isolated Pituitary Adenomas 7 0.053
505
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.053
506
PRM020 Premenstrual Tension 49 0.053
507
MNN042 Meningioma, Radiation-Induced 38 0.053
508
END038 Endocrine Pancreas Disease 36 0.053
509
AND002 Androgen Insensitivity Syndrome 57 0.053
510
RTR011 Retroperitoneal Fibrosis 43 0.053
511
P OBS001 Obstructive Jaundice 53 0.052
512
GNG008 Ganglioneuroblastoma 44 0.052
513
PNC019 Pancreatoblastoma 33 0.052
514
ECC004 Eccrine Porocarcinoma 38 0.052
515
ADR041 Adrenal Cortical Adenoma 42 0.052
516
INV006 Inverted Papilloma 36 0.052
517
ATM052 Autoimmune Disease 1 30 0.051
518
HYP025 Hyperphosphatemia 48 0.051
519
CRT015 Carotid Artery Occlusion 42 0.051
520
AMN015 Amenorrhea-Galactorrhea Syndrome 20 0.051
521
P PLY041 Polymyositis 57 0.051
522
c PNS012 Paine Syndrome 52 0.051
523
DNC004 Diencephalic Syndrome 37 0.051
524
DDN005 Duodenal Somatostatinoma 30 0.051
525
P NPH012 Nephrotic Syndrome 60 0.051
526
P CNT037 Central Nervous System Germinoma 36 0.051
527
P TMP003 Temporal Arteritis 67 0.051
528
P THL005 Thalassemia 65 0.051
529
MST005 Mastitis 56 0.051
530
P KRT005 Keratoacanthoma 49 0.051
531
ADR010 Adrenal Cortical Hypofunction 41 0.050
532
P ANT006 Antiphospholipid Syndrome 59 0.050
533
SNS001 Sensorineural Hearing Loss 59 0.050
534
ERD001 Erdheim-Chester Disease 57 0.050
535
AML001 Amelanotic Melanoma 42 0.050
536
MNP001 Monophasic Synovial Sarcoma 26 0.050
537
ART140 Arteries, Anomalies of 51 0.050
538
MLG065 Malignant Fibroxanthoma 41 0.050
539
MNN006 Meninges Hemangiopericytoma 39 0.050
540
P CYS018 Cystitis 57 0.049
541
TRT001 Teratocarcinoma 41 0.049
542
OST012 Osteoarthritis 88 0.049
543
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.049
544
c THY107 Thymoma, Familial 34 0.049
545
ALL003 Allergic Rhinitis 68 0.049
546
HYP077 Hypertrichosis 49 0.049
547
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.049
548
PRP030 Purpura 61 0.049
549
ALL014 Allergic Encephalomyelitis 37 0.049
550
CHN010 Chondroma 44 0.049
551
c TRC078 Trichohepatoenteric Syndrome 2 34 0.049
552
P TST001 Testicular Leydig Cell Tumor 30 0.049
553
CRD119 Cardiac Arrest 63 0.049
554
SPN331 Spondyloocular Syndrome 34 0.049
555
MLT145 Multiple Enchondromatosis, Maffucci Type 51 0.048
556
P PTS002 Ptosis 50 0.048
557
SLP010 Slipped Capital Femoral Epiphysis 37 0.048
558
BRN040 Bronchus Adenoma 20 0.048
559
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.048
560
ASP003 Aseptic Meningitis 54 0.048
561
INT075 Intracranial Hypertension 53 0.048
562
FBR001 Fibrous Meningioma 25 0.048
563
MGR001 Migraine Without Aura 47 0.048
564
SCT002 Scotoma 42 0.048
565
BSP001 Basophil Adenoma 20 0.048
566
VSC011 Vasculitis 66 0.048
567
P STR035 Streptococcal Group a Invasive Disease 28 0.048
568
RNL078 Renal Dysplasia 49 0.047
569
c PSR018 Psoriasis 13 39 0.047
570
ECT026 Ectopic Pregnancy 52 0.047
571
c PRM196 Premature Ovarian Failure 1 68 0.047
572
OVR017 Ovarian Cystic Teratoma 30 0.047
573
LMY003 Leiomyomatosis 45 0.047
574
P LCT001 Lactic Acidosis 51 0.046
575
HRM002 Hermaphroditism 42 0.046
576
c PCH010 Pachyonychia Congenita 3 38 0.046
577
ILT001 Ileitis 52 0.046
578
AMP003 Ampulla of Vater Neoplasm 39 0.046
579
BRN106 Burns 57 0.046
580
SPN041 Spinal Cord Disease 54 0.046
581
MLN013 Melanoma Metastasis 37 0.046
582
P PNC025 Panic Disorder 57 0.046
583
P ACT150 Acute Adrenal Insufficiency 51 0.046
584
TRN007 Transsexualism 44 0.046
585
P CLS010 Cluster Headache 47 0.046
586
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 40 0.046
587
END045 Endometriosis of Uterus 38 0.046
588
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.046
589
HST016 Histiocytic Sarcoma 45 0.046
590
OVR063 Overnutrition 53 0.045
591
CCN002 Cocaine Abuse 50 0.045
592
STR002 Streptococcal Meningitis 40 0.045
593
ARC007 Arachnoid Cysts 39 0.045
594
ART005 Arteriovenous Malformation 64 0.045
595
PPL021 Papilledema 50 0.045
596
CHR178 Chromosomal Triplication 35 0.045
597
INT110 Intracranial Cysts 22 0.045
598
MGR028 Migraine with or Without Aura 1 55 0.045
599
P CHR342 Chiari Malformation 45 0.045
600
LMB002 Lambert-Eaton Myasthenic Syndrome 58 0.045
601
P CPL006 Capillary Hemangioma 56 0.045
602
HYP005 Hypokalemia 53 0.045
603
MSC033 Muscle Disorders 53 0.045
604
MSC004 Muscle Tissue Disease 39 0.045
605
HYP780 Hypoadrenocorticism, Familial 59 0.044
606
VRC001 Varicocele 52 0.044
607
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 34 0.044
608
EPG004 Epignathus 18 0.044
609
c MCR129 Microvascular Complications of Diabetes 1 62 0.044
610
P PLY006 Polydactyly 57 0.044
611
P MYM013 Moyamoya Disease 1 50 0.044
612
ANG004 Angioid Streaks 35 0.044
613
HSH003 Hashimoto Thyroiditis 67 0.044
614
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 60 0.044
615
P HYP040 Hypospadias 60 0.044
616
PNC001 Pancytopenia 50 0.044
617
c ATM024 Autoimmune Pancreatitis 49 0.044
618
c SCL052 Scleroderma, Familial Progressive 60 0.044
619
CRV022 Cervix Small Cell Carcinoma 38 0.044
620
ATY007 Atypical Follicular Adenoma 24 0.044
621
DMN002 Dementia 68 0.044
622
c DWL002 Dowling-Degos Disease 1 50 0.044
623
BLT006 Bilateral Breast Cancer 49 0.044
624
P MYS003 Myasthenia Gravis 73 0.043
625
P CNJ013 Conjunctivitis 67 0.043
626
P MNC007 Monocytic Leukemia 59 0.043
627
P SZR006 Seizure Disorder 55 0.043
628
MDD003 Middle Cerebral Artery Infarction 36 0.043
629
ENC014 Enchondroma 30 0.043
630
HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 51 0.043
631
SCL003 Social Phobia 50 0.043
632
SPN186 Spinal Cord Injury 67 0.043
633
c CNG006 Congenital Hypothyroidism 62 0.043
634
P LTR001 Lateral Sclerosis 58 0.043
635
P ACT105 Acute Mountain Sickness 58 0.043
636
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 54 0.043
637
INT303 Intracranial Hypertension, Idiopathic 49 0.043
638
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.043
639
TND004 Tendinopathy 45 0.043
640
RTC007 Reticular Perineurioma 21 0.043
641
BRS099 Breast Ductal Carcinoma 55 0.043
642
DFF036 Differentiated Thyroid Carcinoma 49 0.043
643
WDH001 Wdha Syndrome 31 0.043
644
P INT080 Intraocular Melanoma 28 0.043
645
c SBC007 Subacute Thyroiditis 43 0.042
646
PPL052 Papillomatosis, Confluent and Reticulated 26 0.042
647
IDP081 Idiopathic Hypertrophic Pachymeningitis 17 0.042
648
INT221 Intravascular Large B-Cell Lymphoma 42 0.042
649
ALD013 Aldosterone-Producing Adenoma 39 0.042
650
PRM290 Premature Centromere Division 19 0.042
651
P ECL001 Eclampsia 57 0.042
652
MYX007 Myxosarcoma 41 0.042
653
AGG003 Aggressive Digital Papillary Adenocarcinoma 33 0.042
654
FTT001 Fatty Liver Disease 62 0.041
655
CHL061 Childhood Leukemia 50 0.041
656
END035 Endocrine Gland Cancer 48 0.041
657
BNS003 Binswanger's Disease 43 0.041
658
P BPL003 Bipolar Disorder 61 0.041
659
c CHR089 Chronic Kidney Failure 72 0.041
660
P ALP009 Alopecia Areata 64 0.041
661
P PLY014 Polycystic Kidney Disease 60 0.041
662
TBR003 Tuberculous Epididymitis 27 0.041
663
CRB028 Cerebellar Medulloblastoma 23 0.040
664
P FRM004 Foramen Magnum Meningioma 23 0.040
665
TRG002 Trigeminal Neuralgia 60 0.040
666
c BTT014 Beta-Thalassemia 70 0.040
667
PLL001 Pallister-Hall Syndrome 59 0.040
668
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.040
669
ISL115 Isolated Growth Hormone Deficiency, Type Iii 42 0.040
670
c CNT101 Central Congenital Hypothyroidism 30 0.040
671
GRN033 Granulomatous Mastitis 27 0.040
672
LGR001 Laugier-Hunziker Syndrome 17 0.040
673
INF124 Infundibulo-Neurohypophysitis 13 0.040
674
P FNC043 Fanconi Anemia, Complementation Group E 52 0.039
675
P PRC012 Pericardial Effusion 52 0.039
676
CDQ001 Cauda Equina Syndrome 41 0.039
677
DWN001 Down Syndrome 70 0.039
678
P SLP006 Sleep Apnea 65 0.039
679
AZS001 Azoospermia 47 0.039
680
c MTR002 Mitral Valve Insufficiency 46 0.039
681
c MYS011 Myasthenia Gravis Congenital 28 0.039
682
P TXP001 Toxoplasmosis 65 0.039
683
OPT003 Opiate Dependence 54 0.039
684
P END047 Endophthalmitis 51 0.039
685
HYD001 Hydranencephaly 36 0.039
686
TLS001 Tolosa-Hunt Syndrome 35 0.039
687
ASP026 Asplenia, Isolated Congenital 29 0.039
688
P SLV001 Silver-Russell Syndrome 57 0.039
689
INP001 Inappropriate Adh Syndrome 39 0.039
690
c ACT075 Acute Myocardial Infarction 64 0.038
691
P SYR001 Syringomyelia 49 0.038
692
OVR109 Ovarian Germ Cell Teratoma 35 0.038
693
ADN088 Adenoma of the Pancreas 27 0.038
694
CHL014 Cholera 56 0.038
695
MMM006 Mammographic Density 43 0.038
696
EPT021 Epithelial Recurrent Erosion Dystrophy 35 0.038
697
LCL011 Localized Hypertrophic Neuropathy 16 0.038
698
SCL041 Sclerosing Perineurioma 14 0.038
699
VSC007 Vascular Disease 71 0.037
700
P MCR115 Microvascular Complications of Diabetes 5 66 0.037
701
P ASP006 Aspergillosis 65 0.037
702
INT004 Intraneural Perineurioma 36 0.037
703
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.037
704
STT001 Status Epilepticus 60 0.037
705
HYD002 Hydronephrosis 49 0.037
706
NRR001 Neuroretinitis 46 0.037
707
c PLY146 Polycystic Liver Disease 1 45 0.037
708
ILC002 Ileocolitis 43 0.037
709
WLL004 Wallerian Degeneration 40 0.037
710
SCR011 Scrapie 40 0.037
711
SKL005 Skull Base Meningioma 25 0.037
712
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 59 0.037
713
P RTN016 Retinal Degeneration 56 0.037
714
P SHR001 Short Bowel Syndrome 52 0.037
715
STS002 Situs Inversus 48 0.037
716
EVN001 Evans' Syndrome 45 0.037
717
PYR016 Pyridoxine Deficiency 37 0.037
718
OLF002 Olfactory Groove Meningioma 27 0.037
719
P CRN018 Coronary Artery Anomaly 69 0.037
720
CMP010 Complex Regional Pain Syndrome 58 0.037
721
P SBS003 Substance Abuse 57 0.036
722
TTR005 Tetrahydrobiopterin Deficiency 44 0.036
723
CRT008 Carotid Artery Dissection 42 0.036
724
LPT006 Leptin Receptor Deficiency 36 0.036
725
HYP029 Hyperthyroxinemia 27 0.036
726
CHR158 Charles Bonnet Syndrome 23 0.036
727
SNC001 Sunct Headache 19 0.036
728
P MSC005 Muscular Dystrophy 66 0.036
729
CRT072 Creutzfeldt-Jakob Disease 65 0.036
730
MLN007 Male Infertility 53 0.036
731
ANG054 Angina Pectoris 53 0.036
732
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.036
733
DFF012 Differentiating Neuroblastoma 34 0.036
734
P FCL005 Focal Segmental Glomerulosclerosis 60 0.036
735
END030 End Stage Renal Failure 59 0.036
736
RSD004 Rosai-Dorfman Disease 48 0.036
737
c PSR017 Psoriasis 2 40 0.036
738
MNN008 Meningeal Melanomatosis 38 0.036
739
c PSR028 Psoriasis 7 37 0.036
740
c PSR032 Psoriasis 11 35 0.036
741
BBS001 Babesiosis 51 0.035
742
HYD061 Hydrocephalus, Normal-Pressure 47 0.035
743
CNT025 Central Pontine Myelinolysis 45 0.035
744
EST005 Esotropia 43 0.035
745
CRB086 Cerebral Aneurysms 42 0.035
746
TRN012 Transient Global Amnesia 40 0.035
747
ETH004 Euthyroid Sick Syndrome 40 0.035
748
ALP097 Alopecia Universalis Congenita 40 0.035
749
ACR041 Acromelic Frontonasal Dysostosis 38 0.035
750
CSL001 Causalgia 38 0.035
751
AMR003 Amaurosis Fugax 37 0.035
752
FML063 Familial Glucocorticoid Deficiency 35 0.035
753
GST006 Gastric Leiomyoma 32 0.035
754
INT083 Intraventricular Meningioma 26 0.035
755
PRS024 Parasagittal Meningioma 25 0.035
756
FST001 Foster-Kennedy Syndrome 23 0.035
757
GRF006 Grfoma 19 0.035
758
TRN011 Transient Refractive Change 9 0.035
759
c PRC016 Pre-Eclampsia 65 0.034
760
PLS007 Plasmodium Falciparum Malaria 59 0.034
761
PRP016 Paraplegia 53 0.034
762
EXT010 Extramedullary Plasmacytoma 52 0.034
763
CST005 Castleman Disease 44 0.034
764
SPR066 Superficial Siderosis 40 0.034
765
c ACT053 Acute Thyroiditis 29 0.034
766
c GST091 Gastrointestinal Neuroendocrine Benign Tumor 21 0.034
767
IRR002 Irritable Bowel Syndrome 63 0.034
768
P GLY013 Glycogen Storage Disease 61 0.034
769
DBT010 Diabetic Neuropathy 60 0.034
770
GLC003 Glucose Intolerance 58 0.034
771
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.034
772
HYP231 Hypothalamic Hamartomas 49 0.034
773
P HYP263 Hypersomnia 45 0.034
774
P PRS062 Persistent Hyperplastic Primary Vitreous 41 0.034
775
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.034
776
FNT004 Fainting 36 0.034
777
PPL009 Papillary Craniopharyngioma 28 0.034
778
OTT002 Otitis Media 67 0.033
779
CHL123 Chlamydia 64 0.033
780
P HML002 Hemolytic Anemia 62 0.033
781
P LPR021 Leprosy 3 59 0.033
782
BCK006 Back Pain 46 0.033
783
c SRC023 Sarcoidosis 2 30 0.033
784
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.032
785
c HMC039 Hemochromatosis, Type 1 71 0.032
786
P ALC004 Alcohol Abuse 63 0.032
787
MRB003 Morbid Obesity 61 0.032
788
P DRM007 Dermatitis Herpetiformis 56 0.032
789
P TRM003 Tremor 54 0.032
790
SLP001 Sleeping Sickness 48 0.032
791
HDR003 Hidradenitis 47 0.032
792
MYC012 Mycetoma 46 0.032
793
DMP001 Dumping Syndrome 45 0.032
794
STT004 Steatorrhea 41 0.032
795
TNC002 Tinea Capitis 40 0.032
796
AYM001 Ayme-Gripp Syndrome 40 0.032
797
END028 Endemic Goiter 40 0.032
798
LPT014 Leptin Deficiency or Dysfunction 37 0.032
799
PST035 Postgastrectomy Syndrome 36 0.032
800
PHC004 Phace Syndrome 36 0.032
801
CLF027 Cleft Palate, Isolated 61 0.032
802
PST021 Postpartum Depression 54 0.032
803
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.032
804
CCH002 Coach Syndrome 51 0.032
805
PRN009 Paranoid Schizophrenia 49 0.032
806
SCH003 Schizophreniform Disorder 44 0.032
807
ART012 Aortitis 33 0.032
808
SCL002 Scleredema Adultorum 30 0.032
809
TST023 Testotoxicosis 27 0.032
810
GRN006 Granulomatous Angiitis 27 0.032
811
SPH007 Sphenoid Sinusitis 24 0.032
812
TNS005 Tonsillitis 61 0.032
813
TBR011 Tuberculous Meningitis 54 0.032
814
CRY005 Cryptococcosis 54 0.032
815
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 52 0.032
816
PRS045 Prostatic Hypertrophy 51 0.032
817
c BRN108 Branchiootic Syndrome 1 47 0.032
818
GST004 Gastric Neuroendocrine Neoplasm 25 0.032
819
CMM004 Common Variable Immunodeficiency 71 0.031
820
SMT004 Smith-Lemli-Opitz Syndrome 70 0.031
821
BRN038 Bronchial Disease 58 0.031
822
PRT038 Protein-Energy Malnutrition 52 0.031
823
NNL001 Non-Langerhans-Cell Histiocytosis 42 0.031
824
HMP001 Hemopericardium 34 0.031
825
BRN031 Brain Germinoma 28 0.031
826
FNC005 Functional Colonic Disease 24 0.031
827
PRT037 Pertussis 70 0.030
828
OBS002 Obsessive-Compulsive Disorder 68 0.030
829
P PLV020 Pelvic Organ Prolapse 63 0.030
830
GTL001 Gitelman Syndrome 62 0.030
831
P GRS003 Griscelli Syndrome 58 0.030
832
ECT006 Ectodermal Dysplasia 57 0.030
833
P HYP024 Hypoparathyroidism 55 0.030
834
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.030
835
PRP009 Peripartum Cardiomyopathy 53 0.030
836
BRL010 Buruli Ulcer 51 0.030
837
RPP001 Rapp-Hodgkin Syndrome 51 0.030
838
P HRP009 Herpes Simplex Encephalitis 50 0.030
839
RTN001 Retinal Vasculitis 47 0.030
840
CRD137 Cardiogenic Shock 45 0.030
841
P ANL018 Analbuminemia 45 0.030
842
ERY004 Erysipelas 43 0.030
843
c CNG208 Congenital Disorder of Glycosylation, Type Iic 42 0.030
844
TND005 Tendinitis 42 0.030
845
PST055 Postural Hypotension 40 0.030
846
c CHR087 Chronic Cystitis 26 0.030
847
P NRC002 Narcolepsy 64 0.029
848
P CND004 Candidiasis 61 0.029
849
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.029
850
RBR001 Roberts Syndrome 55 0.029
851
P SYP003 Syphilis 55 0.029
852
LST001 Listeriosis 55 0.029
853
INF039 Infratentorial Cancer 38 0.029
854
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.029
855
PFF001 Pfeiffer Syndrome 74 0.028
856
ATN002 Autonomic Nervous System Disease 51 0.028
857
ANG011 Angiodysplasia 48 0.028
858
BRN080 Brain Ischemia 45 0.028
859
TLR001 Tularemia 44 0.028
860
c CHR020 Chronic Interstitial Cystitis 44 0.028
861
SKN023 Skin Tag 41 0.028
862
GLC106 Glucocorticoid Resistance, Generalized 41 0.028
863
CLN006 Colonic Pseudo-Obstruction 36 0.028
864
P CMM008 Communicating Hydrocephalus 35 0.028
865
LRY007 Laryngeal Tuberculosis 33 0.028
866
ATN003 Autonomic Nervous System Neoplasm 32 0.028
867
PYL002 Pylorospasm 25 0.028
868
GRD004 Gardner-Diamond Syndrome 23 0.028
869
BLD138 Blood Group--Diego System 18 0.028
870
P RTN008 Retinitis Pigmentosa 81 0.027
871
P JBR020 Joubert Syndrome 1 68 0.027
872
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.027
873
c CNG021 Congenital Toxoplasmosis 57 0.027
874
P WRD001 Waardenburg's Syndrome 57 0.027
875
ESN005 Eosinophilic Gastroenteritis 56 0.027
876
HDR002 Hidradenitis Suppurativa 54 0.027
877
APP015 Apparent Mineralocorticoid Excess 54 0.027
878
P AXN002 Axenfeld-Rieger Syndrome 53 0.027
879
SCH012 Schizoaffective Disorder 51 0.027
880
HMS001 Hemosiderosis 50 0.027
881
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 46 0.027
882
STL001 St. Louis Encephalitis 43 0.027
883
DXR001 Doxorubicin Induced Cardiomyopathy 40 0.027
884
GLC042 Glucocorticoid Deficiency 1 39 0.027
885
GLC008 Glucose Metabolism Disease 38 0.027
886
CLC004 Calcific Tendinitis 38 0.027
887
NNT011 Neonatal Anemia 35 0.027
888
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.027
889
EXN003 Exencephaly 34 0.027
890
SBD001 Subdural Empyema 31 0.027
891
GRS001 Gerstmann Syndrome 30 0.027
892
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.027
893
SCL022 Scleredema 27 0.027
894
HRL002 Harlequin Syndrome 25 0.027
895
PNL021 Pineal Cyst 21 0.027
896
EPP010 Epiphysiolysis of the Hip 20 0.027
897
CNT047 Contact Dermatitis 64 0.026
898
P CFF008 Coffin-Siris Syndrome 1 59 0.026
899
P MGL013 Megalencephaly 54 0.026
900
DRG003 Drug Dependence 51 0.026
901
PNG002 Pain Agnosia 41 0.026
902
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.026
903
ALG001 Algoneurodystrophy 39 0.026
904
CLR014 Clear Cell Adenoma 39 0.026
905
c DRM040 Dermatitis Herpetiformis, Familial 32 0.026
906
CNJ017 Conjunctival Nevus 27 0.026
907
CRT005 Cortical Thymoma 27 0.026
908
STR018 Steroid Inherited Metabolic Disorder 27 0.026
909
CYT014 Cytochrome P450 Oxidoreductase Deficiency 25 0.026
910
HLX001 Helix Syndrome 25 0.026
911
SCK003 Sickle Cell Anemia 73 0.024
912
CHG001 Chagas Disease 72 0.024
913
DNH001 Donohue Syndrome 60 0.024
914
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.024
915
c HYP731 Hyperaldosteronism, Familial, Type I 56 0.024
916
IMP005 Impotence 54 0.024
917
P BLM007 Bulimia Nervosa 1 53 0.024
918
HYD012 Hydrops Fetalis 50 0.024
919
c CRB191 Cerebral Cavernous Malformations 2 49 0.024
920
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.024
921
P HRD021 Hereditary Sensory Neuropathy 47 0.024
922
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.024
923
ATN004 Autonomic Neuropathy 46 0.024
924
ANH002 Anhidrosis 45 0.024
925
LCH009 Lichen Sclerosus 45 0.024
926
STT007 Steatocystoma Multiplex 44 0.024
927
SWT003 Sweat Gland Disease 42 0.024
928
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 40 0.024
929
MRS001 Marasmus 39 0.024
930
CLS040 Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 37 0.024
931
LBR025 Lobar Holoprosencephaly 36 0.024
932
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 35 0.024
933
MCR173 Microform Holoprosencephaly 34 0.024
934
GNT019 Giant Cell Myocarditis 34 0.024
935
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.024
936
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 32 0.024
937
c PCH011 Pachyonychia Congenita 4 30 0.024
938
PNS014 Penis Agenesis 29 0.024
939
SPR032 Superficial Siderosis of the Central Nervous System 25 0.024
940
DRM046 Dermal Ridges-off-the-End 19 0.024
941
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.021
942
NRL016 Neural Tube Defects 79 0.021
943
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.021
944
ACH004 Achondroplasia 67 0.021
945
P LNG028 Long Qt Syndrome 63 0.021
946
P TRC072 Treacher Collins Syndrome 1 61 0.021
947
ALL010 Allergic Contact Dermatitis 60 0.021
948
SPN027 Spinal Stenosis 60 0.021
949
c PCH015 Pachyonychia Congenita 1 59 0.021
950
CHR103 Charge Syndrome 59 0.021
951
P BRC006 Brachydactyly 57 0.021
952
BLR001 Biliary Atresia 56 0.021
953
PNM001 Pneumocystosis 55 0.021
954
THR016 Thrombophlebitis 53 0.021
955
ACH005 Achalasia 52 0.021
956
CLB010 Coloboma of Macula 52 0.021
957
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 50 0.021
958
c BPL002 Bipolar I Disorder 50 0.021
959
ANS023 Anus, Imperforate 50 0.021
960
KLN009 Kleine-Levin Hibernation Syndrome 48 0.021
961
c LBR014 Leber Congenital Amaurosis 4 48 0.021
962
PLY020 Polyradiculoneuropathy 48 0.021
963
c PCH012 Pachyonychia Congenita 2 47 0.021
964
LYM004 Lymphoid Interstitial Pneumonia 47 0.021
965
FTL021 Fetal Macrosomia 46 0.021
966
CRB004 Cerebral Artery Occlusion 46 0.021
967
PRC038 Precocious Puberty, Male-Limited 46 0.021
968
NTR005 Nutritional Deficiency Disease 46 0.021
969
CHR492 Chromosome 13q14 Deletion Syndrome 43 0.021
970
GNT031 Genitopatellar Syndrome 43 0.021
971
KWS001 Kwashiorkor 43 0.021
972
CNV002 Conversion Disorder 42 0.021
973
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.021
974
FML039 Female Reproductive System Disease 40 0.021
975
c GLL024 Gallbladder Disease 1 39 0.021
976
P VSC018 Visceral Steatosis 38 0.021
977
c LKD009 Leukodystrophy, Hypomyelinating, 5 38 0.021
978
SML028 Semilobar Holoprosencephaly 38 0.021
979
ALB014 Alobar Holoprosencephaly 37 0.021
980
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 36 0.021
981
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.021
982
SCK001 Sick Building Syndrome 36 0.021
983
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 35 0.021
984
GRW036 Growth Control, Y-Chromosome Influenced 33 0.021
985
NNT019 Neonatal Hypothyroidism 33 0.021
986
SPT016 Septopreoptic Holoprosencephaly 31 0.021
987
ABD002 Abducens Nerve Disease 28 0.021
988
TTN001 Tetanus Neonatorum 28 0.021
989
FNC006 Functional Gastric Disease 26 0.021
990
CYT018 Cytochrome P450 2d6 Variant 13 0.021
Content
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