Search results for Human calcitonin

725 hits were found for Human calcitonin

# Family MCID Name MIFTS Score
1
THY029 Thyroid Carcinoma 59 0.615
2
BNR002 Bone Resorption Disease 48 0.503
3
THY111 Thyroid Carcinoma, Familial Medullary 67 0.499
4
THY125 Thyroid Gland Medullary Carcinoma 51 0.491
5
P OST002 Osteoporosis 73 0.474
6
HMN044 Human Immunodeficiency Virus Type 1 71 0.456
7
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.436
8
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.434
9
P BRS047 Breast Cancer 96 0.403
10
c MGR028 Migraine with or Without Aura 1 69 0.384
11
MMM001 Mammary Paget's Disease 53 0.361
12
P ADN016 Adenocarcinoma 64 0.318
13
P NRB001 Neuroblastoma 71 0.314
14
P CLR023 Colorectal Cancer 98 0.311
15
ADN018 Adenoma 58 0.309
16
P LKM002 Leukemia 66 0.301
17
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.300
18
P PRS040 Prostate Cancer 97 0.298
19
OST159 Osteogenic Sarcoma 66 0.296
20
GLB015 Glioblastoma Multiforme 75 0.292
21
PRT037 Pertussis 65 0.286
22
P GLM045 Glioma 63 0.279
23
P OVR042 Ovarian Cancer 89 0.277
24
CRV035 Cervical Cancer 76 0.269
25
P LNG032 Lung Cancer 97 0.269
26
P BND020 Bone Disease 59 0.268
27
GLL048 Glial Tumor 45 0.266
28
P HPT023 Hepatocellular Carcinoma 100 0.266
29
CYT002 Cytokine Deficiency 44 0.264
30
OST012 Osteoarthritis 78 0.261
31
P HYP069 Hyperparathyroidism 62 0.255
32
HLX001 Helix Syndrome 47 0.254
33
P DRR001 Diarrhea 57 0.248
34
ATM095 Autoimmune Disease 61 0.246
35
P PNC035 Pancreatic Cancer 84 0.243
36
PPL022 Papilloma 54 0.234
37
P LYM031 Lymphocytic Leukemia 55 0.234
38
48X005 48,xyyy 39 0.233
39
P HYP086 Hypothyroidism 68 0.232
40
P PGT001 Paget's Disease of Bone 60 0.232
41
P TCL004 T-Cell Leukemia 47 0.232
42
P KDN018 Kidney Disease 70 0.229
43
SQM002 Squamous Cell Papilloma 42 0.226
44
CHL014 Cholera 55 0.226
45
SQM006 Squamous Cell Carcinoma 60 0.225
46
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.222
47
ALL026 Allergic Hypersensitivity Disease 64 0.222
48
P PRD008 Periodontitis 62 0.221
49
GTR002 Goiter 52 0.217
50
c PCH010 Pachyonychia Congenita 3 43 0.210
51
LVR012 Liver Cirrhosis 63 0.207
52
INS024 Insulin-Like Growth Factor I 79 0.206
53
c PRC016 Pre-Eclampsia 63 0.205
54
P HDC001 Headache 57 0.199
55
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.198
56
LNG099 Lung Disease 61 0.198
57
P INF032 Infertility 57 0.197
58
P MYL006 Myeloid Leukemia 60 0.196
59
HYP266 Hypoxia 56 0.196
60
HYP056 Hypoglycemia 66 0.193
61
HYP066 Hyperglycemia 61 0.193
62
P HRP006 Herpes Simplex 65 0.192
63
c SML038 Small Cell Cancer of the Lung 65 0.190
64
c HYP595 Hypertension, Essential 84 0.190
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.189
66
P THY032 Thyroiditis 53 0.189
67
MYL069 Myeloma, Multiple 85 0.189
68
P PHC003 Pheochromocytoma 71 0.188
69
SPP010 Suppressor of Tumorigenicity 3 51 0.186
70
47X002 47,xyy 49 0.184
71
P LYM118 Lymphoma 68 0.184
72
P MLT074 Multiple Endocrine Neoplasia 55 0.183
73
ADR040 Adrenal Gland Pheochromocytoma 46 0.182
74
c LKM061 Leukemia, Acute Myeloid 83 0.179
75
P VSC007 Vascular Disease 63 0.178
76
P LVR013 Liver Disease 68 0.176
77
TXC005 Toxic Shock Syndrome 61 0.176
78
KPS004 Kaposi Sarcoma 75 0.175
79
SPN186 Spinal Cord Injury 60 0.174
80
CNG034 Congestive Heart Failure 70 0.174
81
P INF037 Inflammatory Bowel Disease 56 0.173
82
P LKM062 Leukemia, Acute Lymphoblastic 68 0.173
83
P CHR345 Chronic Pain 50 0.169
84
P AST007 Astrocytoma 50 0.169
85
BCT022 Bacterial Infectious Disease 56 0.169
86
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.169
87
P ENC004 Encephalitis 61 0.168
88
CHR074 Choriocarcinoma 46 0.167
89
RCK004 Rickets 69 0.167
90
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.167
91
AGN016 Aging 56 0.167
92
P NRP001 Neuropathy 56 0.167
93
P SML001 Small Cell Carcinoma 52 0.165
94
c PRM005 Primary Hyperparathyroidism 58 0.165
95
c ACT027 Acute Pancreatitis 59 0.163
96
PNG002 Pain Agnosia 51 0.162
97
GST045 Gastroenteritis 59 0.162
98
c PRM038 Primary Agammaglobulinemia 43 0.158
99
SRC014 Sarcoma 65 0.158
100
P SKN015 Skin Carcinoma 67 0.157
101
TTN003 Tetanus 64 0.156
102
P HYP076 Hyperthyroidism 55 0.156
103
SKN016 Skin Disease 63 0.155
104
P CTR002 Cataract 60 0.155
105
P DBT009 Diabetes Mellitus 64 0.155
106
P HYP726 Hypercalcemia, Infantile, 1 57 0.153
107
P LTR001 Lateral Sclerosis 53 0.153
108
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.152
109
c ACT073 Acute Leukemia 58 0.152
110
ISC004 Ischemia 60 0.151
111
c CHR684 Chronic Kidney Disease 66 0.151
112
END057 Endometrial Cancer 74 0.151
113
P GRV001 Graves' Disease 55 0.150
114
P EXN002 Exanthem 57 0.150
115
P HRT032 Heart Disease 75 0.150
116
SPN035 Spindle Cell Sarcoma 51 0.150
117
PRS045 Prostatic Hypertrophy 52 0.150
118
EMB004 Embryonal Carcinoma 57 0.150
119
BRN071 Brain Injury 49 0.149
120
P PSR002 Psoriasis 62 0.147
121
CLN015 Colon Adenocarcinoma 63 0.147
122
DWN001 Down Syndrome 70 0.146
123
NRN004 Neuroendocrine Tumor 55 0.146
124
P ART022 Arthritis 70 0.146
125
INS001 Insulinoma 60 0.144
126
PST011 Pustulosis of Palm and Sole 52 0.143
127
TRM010 Traumatic Brain Injury 53 0.142
128
P ALZ034 Alzheimer Disease 88 0.142
129
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.141
130
c LKM071 Leukemia, Chronic Lymphocytic 79 0.141
131
CYS001 Cystic Fibrosis 80 0.141
132
PRS021 Prostatic Adenoma 51 0.140
133
P RHM011 Rheumatoid Arthritis 80 0.140
134
P PLM037 Pulmonary Hypertension 68 0.139
135
PRS129 Prostatic Hyperplasia, Benign 49 0.138
136
P PNC044 Pancreatitis 61 0.138
137
P END044 Endometriosis 62 0.138
138
THY030 Thyroid Gland Disease 51 0.138
139
CLT003 Colitis 62 0.137
140
HYP060 Hyperinsulinism 54 0.136
141
TRT001 Teratocarcinoma 46 0.136
142
c SYS001 Systemic Lupus Erythematosus 86 0.135
143
BRT054 Brittle Bone Disorder 70 0.135
144
ULC004 Ulcerative Colitis 73 0.133
145
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.132
146
P TRT010 Teratoma 51 0.132
147
c SCN007 Secondary Hyperparathyroidism 50 0.132
148
c MLG068 Malignant Glioma 45 0.130
149
ERY051 Erythroleukemia, Familial 56 0.130
150
P TRN020 Turner Syndrome 65 0.130
151
ARG004 Argyria 28 0.129
152
P KDN017 Kidney Cancer 61 0.129
153
P CRN300 Coronary Heart Disease 1 63 0.129
154
c LKM063 Leukemia, Chronic Myeloid 71 0.129
155
GST023 Gastric Ulcer 53 0.128
157
P FBR017 Fibrosarcoma 56 0.128
158
MYL009 Myelodysplastic Syndrome 70 0.127
159
P GST044 Gastritis 55 0.126
160
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.126
161
HYP017 Hypophosphatemia 49 0.126
162
DRM006 Dermatitis 61 0.125
163
BCK006 Back Pain 42 0.125
164
c DLT002 Dilated Cardiomyopathy 79 0.125
165
P ENC018 Encephalopathy 61 0.125
166
P ART023 Arthropathy 62 0.125
167
PTT037 Pituitary Tumors 44 0.125
168
P DRM053 Dermatitis, Atopic 66 0.125
169
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.124
170
P MYP004 Myopathy 64 0.124
171
END030 End Stage Renal Failure 58 0.123
172
HSH003 Hashimoto Thyroiditis 62 0.123
173
P INS002 in Situ Carcinoma 52 0.123
174
RTR008 Root Resorption 45 0.122
175
P AMY004 Amyloidosis 70 0.122
176
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.122
177
CRH001 Crohn's Disease 74 0.121
178
P PTT006 Pituitary Adenoma 54 0.121
179
P PLM036 Pulmonary Fibrosis 61 0.121
180
IDP011 Idiopathic Interstitial Pneumonia 63 0.120
181
P HYP098 Hypereosinophilic Syndrome 66 0.120
182
URM002 Uremia 49 0.120
183
P CRD246 Cardiovascular System Disease 56 0.119
184
AST005 Asthma 77 0.119
185
c BRN108 Branchiootic Syndrome 1 61 0.119
186
CHC001 Chickenpox 60 0.118
187
NRN001 Neuroendocrine Carcinoma 47 0.118
188
c PRD040 Periodontitis, Chronic 54 0.118
189
SPS019 Spastic Paraparesis 40 0.118
190
P HYP024 Hypoparathyroidism 55 0.117
191
P PRP019 Peripheral Nervous System Disease 57 0.117
192
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.117
193
HYP064 Hypogonadotropism 40 0.117
194
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.117
195
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.117
196
PPT005 Peptic Ulcer Disease 58 0.117
197
HYP080 Hypogonadism 50 0.117
198
P RHN004 Rhinitis 57 0.117
199
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.117
200
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.116
201
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.116
202
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.116
203
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.116
204
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.116
205
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.116
206
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.116
207
P PNM007 Pneumonia 68 0.116
208
P RSP003 Respiratory Failure 74 0.115
209
P CRN018 Coronary Artery Anomaly 63 0.115
210
P SZR006 Seizure Disorder 58 0.114
211
P ECL001 Eclampsia 51 0.114
212
ADL002 Adult Syndrome 69 0.113
213
P DDN001 Duodenal Ulcer 50 0.113
214
CRB004 Cerebral Artery Occlusion 44 0.113
215
FTT001 Fatty Liver Disease 61 0.113
216
P CLS010 Cluster Headache 43 0.112
217
P MYC007 Myocardial Infarction 70 0.112
218
ALL014 Allergic Encephalomyelitis 39 0.112
219
ACR007 Acromegaly 71 0.111
220
VSL002 Visual Epilepsy 58 0.111
221
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.110
222
PRT036 Peritonitis 65 0.110
223
IMP005 Impotence 52 0.110
224
MNN042 Meningioma, Radiation-Induced 62 0.110
225
PLY150 Polykaryocytosis Inducer 31 0.107
226
P ALC033 Alcohol Use Disorder 58 0.107
227
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.107
228
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.106
229
DPH001 Diphtheria 60 0.106
230
P THL005 Thalassemia 60 0.106
231
ALC007 Alcohol Dependence 66 0.106
232
c MNN043 Meningioma, Familial 74 0.106
233
c ACT071 Acute Kidney Failure 59 0.105
234
SPN021 Spinal Meningioma 47 0.105
235
P MLT020 Multiple Sclerosis 72 0.105
236
SCR001 Secretory Meningioma 37 0.105
237
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.105
238
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.105
239
LPD008 Lipid Metabolism Disorder 62 0.104
240
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.104
241
THY122 Thyroid Gland Cancer 58 0.104
242
RFL001 Reflex Sympathetic Dystrophy 53 0.104
243
ART140 Arteries, Anomalies of 53 0.103
244
P ALP008 Alopecia 56 0.103
245
P LPS004 Lupus Erythematosus 61 0.102
246
PRP030 Purpura 55 0.102
247
c SCL052 Scleroderma, Familial Progressive 62 0.102
248
DPR016 Depression 63 0.101
249
GNT001 Giant Cell Reparative Granuloma 40 0.101
250
OST011 Osteomalacia 52 0.101
251
P PLY011 Polycystic Ovary Syndrome 56 0.101
252
P OVR082 Overgrowth Syndrome 50 0.100
253
ANG054 Angina Pectoris 66 0.100
254
c RHB024 Rhabdomyosarcoma 2 65 0.100
255
P HPT021 Hepatitis 67 0.100
256
LYM133 Lymphoma, Hodgkin, Classic 69 0.100
257
c ATR087 Atrial Standstill 1 74 0.099
258
BRN028 Brain Cancer 73 0.099
259
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.099
260
CRB039 Cerebrovascular Disease 69 0.099
261
RYN005 Raynaud Phenomenon 46 0.099
262
PRT029 Parathyroid Adenoma 50 0.099
263
CNN005 Connective Tissue Disease 66 0.098
264
THR024 Thrombosis 56 0.098
265
P PRM006 Primary Biliary Cirrhosis 61 0.098
266
P MYS003 Myasthenia Gravis 68 0.098
267
P SRC025 Sarcoidosis 1 70 0.098
268
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.097
269
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.097
270
NDL007 Nodular Goiter 47 0.097
271
PLG002 Plague 57 0.096
272
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.096
273
ANX010 Anxiety 72 0.096
274
PPL002 Papillary Carcinoma 47 0.095
275
CHL068 Cholestasis 60 0.095
276
BRN024 Bronchitis 68 0.095
277
OCL069 Ocular Motor Apraxia 51 0.094
278
DBT010 Diabetic Neuropathy 55 0.094
279
BRN056 Bronchopulmonary Dysplasia 57 0.094
280
THY124 Thyroid Gland Papillary Carcinoma 52 0.094
281
P PRK057 Parkinson Disease, Late-Onset 76 0.094
282
c GRV008 Graves Disease 1 55 0.094
283
OST017 Osteomyelitis 64 0.094
284
ACT119 Acute Promyelocytic Leukemia 63 0.093
285
LMY002 Leiomyoma 50 0.093
286
RNL011 Renal Osteodystrophy 49 0.093
287
P GNT008 Giant Cell Tumor 44 0.092
288
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.092
289
DGN001 Degenerative Disc Disease 48 0.092
290
MNT002 Mental Depression 57 0.092
291
c ACT075 Acute Myocardial Infarction 56 0.092
292
SPN051 Spondylitis 52 0.092
293
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.091
294
INF009 Inflammatory Spondylopathy 32 0.091
295
c SPN225 Spondyloarthropathy 1 73 0.091
296
KRT019 Keratitis, Hereditary 67 0.091
297
GLC003 Glucose Intolerance 54 0.091
298
EWN003 Ewing Sarcoma 68 0.091
299
P ART021 Arteriosclerosis 54 0.091
300
PLP001 Pulpitis 48 0.091
301
HYP025 Hyperphosphatemia 47 0.090
302
CNT047 Contact Dermatitis 57 0.090
303
P LRY044 Larynx Cancer 54 0.090
304
c THR092 Thrombophilia Due to Thrombin Defect 73 0.090
305
STR067 Stroke, Ischemic 80 0.090
306
END041 Endometrial Adenocarcinoma 63 0.090
307
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.089
308
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.089
309
P NPH012 Nephrotic Syndrome 63 0.089
310
P TRM003 Tremor 53 0.089
311
PRP016 Paraplegia 53 0.089
312
ALL003 Allergic Rhinitis 67 0.089
313
P CHN012 Chondrosarcoma 56 0.088
314
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.088
315
P URT039 Urticaria 58 0.088
316
P CRD119 Cardiac Arrest 67 0.088
317
DMY004 Demyelinating Disease 52 0.088
318
OTT002 Otitis Media 71 0.088
319
P MGR001 Migraine Without Aura 48 0.088
320
P DMN002 Dementia 67 0.088
321
P SYS005 Systemic Scleroderma 70 0.087
322
P PLY019 Polyneuropathy 56 0.087
323
DNT012 Dental Caries 51 0.087
324
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.087
325
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.087
326
IRR002 Irritable Bowel Syndrome 63 0.087
327
P CYS018 Cystitis 59 0.087
328
ATX019 Ataxia with Vitamin E Deficiency 48 0.087
329
OST003 Osteonecrosis 61 0.086
330
MTB004 Metabolic Acidosis 50 0.086
331
P MYC008 Myocarditis 59 0.086
332
HYP020 Hyperprolactinemia 64 0.085
333
c GLL024 Gallbladder Disease 1 52 0.085
334
c ACT068 Acute Cystitis 63 0.085
335
ZLL002 Zollinger-Ellison Syndrome 55 0.085
336
P RRT020 Rare Tumor 41 0.084
337
P BPL003 Bipolar Disorder 56 0.084
338
GNG013 Gingivitis 59 0.084
339
P MTR014 Motor Neuron Disease 64 0.084
340
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.084
341
P RTN016 Retinal Degeneration 53 0.084
342
DFF036 Differentiated Thyroid Carcinoma 51 0.083
343
BNN003 Bone Inflammation Disease 48 0.083
344
c MJR024 Major Affective Disorder 9 41 0.083
345
c MJR022 Major Affective Disorder 8 38 0.083
346
c PNS012 Paine Syndrome 61 0.083
347
P MJR001 Major Depressive Disorder 68 0.083
348
SMN007 Seminoma 44 0.083
349
P DBT005 Diabetes Insipidus 55 0.083
350
P THY023 Thymoma 65 0.083
351
c THY107 Thymoma, Familial 54 0.082
352
BRS051 Breast Disease 58 0.082
353
PPL052 Papillomatosis, Confluent and Reticulated 34 0.082
354
SPN027 Spinal Stenosis 59 0.082
355
P MLT008 Multinodular Goiter 42 0.082
356
P CNJ013 Conjunctivitis 65 0.081
357
CRH005 Crohn's Colitis 52 0.081
358
ISL001 Islet Cell Tumor 56 0.081
359
P MGR003 Migraine with Aura 50 0.081
360
HLC007 Helicobacter Pylori Infection 59 0.081
361
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.081
362
HYP005 Hypokalemia 55 0.081
363
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.081
364
PRP027 Peripheral Vascular Disease 71 0.081
365
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.081
366
VRC005 Varicose Veins 60 0.080
367
P HYP730 Hypogonadotropic Hypogonadism 53 0.080
368
SYN007 Synovitis 55 0.080
369
ANX004 Anoxia 42 0.080
370
c LRG001 Large Cell Carcinoma 49 0.080
371
P SCL018 Scoliosis 60 0.080
372
BLL006 Bullous Pemphigoid 62 0.080
373
P HMP006 Hemiplegic Migraine 44 0.079
374
NTR005 Nutritional Deficiency Disease 61 0.078
375
YLL002 Yellow Fever 60 0.078
376
P OST001 Osteopetrosis 71 0.078
377
CNS004 Constipation 57 0.078
378
P MYS005 Myositis 56 0.078
379
P PSD015 Pseudohypoparathyroidism 56 0.078
380
DSS008 Disease of Mental Health 57 0.078
381
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.077
382
CHR066 Chronic Fatigue Syndrome 61 0.077
383
ALG001 Algoneurodystrophy 39 0.077
384
PLC008 Placenta Disease 49 0.077
385
ENT004 Enthesopathy 48 0.077
386
AMN001 Amenorrhea 54 0.077
387
RHM027 Rheumatic Disease 56 0.077
388
c FML023 Familial Hemiplegic Migraine 54 0.077
389
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.076
390
NRM004 Neuroma 51 0.076
391
c CNG006 Congenital Hypothyroidism 65 0.076
392
IGG001 Iga Glomerulonephritis 48 0.075
393
P NRV007 Nervous System Disease 66 0.075
394
P HYD006 Hydrocephalus 65 0.075
395
PLS011 Plasmacytoma 56 0.075
396
P GLL022 Guillain-Barre Syndrome 59 0.074
397
P GND004 Gonadal Dysgenesis 49 0.074
398
THY128 Thyroid Tumor 47 0.074
399
P PMP001 Pemphigus 55 0.074
400
MDD011 Mood Disorder 62 0.074
401
ALL010 Allergic Contact Dermatitis 55 0.073
402
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.073
403
c INF071 Inflammatory Bowel Disease 1 68 0.073
404
BNG036 Bone Giant Cell Tumor 48 0.073
405
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.073
406
WLL001 Williams-Beuren Syndrome 62 0.073
407
P INT143 Interstitial Cystitis 61 0.073
408
CLC006 Calcinosis 48 0.073
409
RTN017 Retinal Detachment 60 0.072
410
LNG031 Lung Benign Neoplasm 50 0.072
411
CMP010 Complex Regional Pain Syndrome 58 0.072
412
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.072
413
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.072
414
SCT005 Scott Syndrome 48 0.072
415
P GCH001 Gaucher's Disease 64 0.072
416
DYS073 Dysphagia 50 0.071
417
MSC007 Muscle Hypertrophy 63 0.071
418
SPT004 Septic Arthritis 57 0.071
419
P DYS154 Dystonia 65 0.071
420
LMY014 Leiomyoma, Uterine 56 0.071
421
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.071
422
P SLP006 Sleep Apnea 69 0.070
423
ADR016 Adrenal Cortical Carcinoma 48 0.070
424
FLL031 Follicular Adenoma 39 0.070
425
PRT013 Portal Hypertension 60 0.070
426
P FLL037 Follicular Lymphoma 66 0.070
427
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.070
428
FBR009 Fibrous Dysplasia 48 0.069
429
CHL079 Children's Interstitial Lung Disease 27 0.069
430
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.069
431
DCT002 Ductal Carcinoma in Situ 59 0.069
432
WTH001 Withdrawal Disorder 48 0.069
433
PLM010 Pulmonary Edema 55 0.069
434
LNG039 Lung Squamous Cell Carcinoma 65 0.069
435
ADR004 Adrenal Cortical Adenocarcinoma 38 0.069
436
P PRC019 Precocious Puberty 47 0.068
437
c JVN010 Juvenile Rheumatoid Arthritis 67 0.068
438
BRS050 Breast Cyst 38 0.068
439
MLT157 Multiple System Atrophy 1 70 0.068
440
TRG002 Trigeminal Neuralgia 60 0.068
441
GT001 Gout 63 0.068
442
P INT068 Intestinal Disease 52 0.068
443
THY123 Thyroid Gland Follicular Carcinoma 48 0.068
444
CRC014 Carcinoid Tumors, Intestinal 48 0.068
445
P MYP006 Myopia 55 0.068
446
PSR001 Psoriatic Arthritis 62 0.068
447
ANR009 Aneurysmal Bone Cysts 43 0.068
448
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.067
449
P VTR007 Vitreoretinopathy 46 0.067
450
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.066
451
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.066
452
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.066
453
SDD001 Sudden Infant Death Syndrome 61 0.066
454
P CHL066 Cholangitis 50 0.066
455
c GCH015 Gaucher Disease, Type I 70 0.066
456
P LCH002 Lichen Planus 54 0.065
457
HYD038 Hydrops Fetalis, Nonimmune 61 0.065
458
CRN030 Coronary Stenosis 50 0.065
459
HRD005 Hard Palate Cancer 46 0.065
460
CHR005 Chorioamnionitis 51 0.065
461
GST050 Gastrointestinal System Disease 56 0.065
462
CLF027 Cleft Palate, Isolated 64 0.064
463
P OTS001 Otosclerosis 50 0.064
464
ILS001 Ileus 51 0.064
465
HML018 Homologous Wasting Disease 22 0.064
466
RTN020 Retinal Vascular Disease 48 0.064
468
PRS063 Paresthesia 43 0.063
469
P RNV001 Renovascular Hypertension 49 0.063
470
PRT010 Parathyroid Carcinoma 66 0.063
471
P PYL005 Pyelonephritis 56 0.063
472
P PLY018 Polycythemia 55 0.063
473
NRT004 Neuritis 53 0.063
474
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.063
475
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
476
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
477
FBR047 Fibromyalgia 59 0.062
478
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.062
479
LPT014 Leptin Deficiency or Dysfunction 73 0.062
480
HYP457 Hypertrophic Scars 43 0.062
481
LNG020 Lung Oat Cell Carcinoma 43 0.062
482
SCR003 Secretory Diarrhea 36 0.062
483
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.062
484
BRN004 Brain Edema 55 0.061
485
P ALP009 Alopecia Areata 60 0.061
486
HRT011 Heart Septal Defect 50 0.061
487
P ESP024 Esophagitis 62 0.061
488
TND005 Tendinitis 52 0.061
489
P FCL005 Focal Segmental Glomerulosclerosis 58 0.060
490
CRC006 Carcinoid Syndrome 55 0.060
491
c SVR005 Severe Pre-Eclampsia 49 0.060
492
INT030 Intracranial Aneurysm 56 0.059
493
c SBC007 Subacute Thyroiditis 46 0.059
494
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.059
495
P BRN022 Bronchiectasis 59 0.059
496
P ATR005 Atrophic Gastritis 50 0.059
497
SNS003 Sensory Peripheral Neuropathy 53 0.059
498
P HST010 Histiocytosis 53 0.058
499
MYL005 Myelofibrosis 67 0.058
500
ATM052 Autoimmune Disease 1 37 0.058
501
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.058
502
HMP005 Hemiplegia 54 0.058
503
PRN011 Pernicious Anemia 52 0.058
504
CHL004 Cholelithiasis 49 0.057
505
INT066 Interstitial Lung Disease 59 0.057
506
CRC021 Carcinosarcoma 61 0.057
507
MST020 Mast Cell Activation Syndrome 27 0.057
508
NWB001 Newborn Respiratory Distress Syndrome 58 0.057
509
MNN017 Mononeuropathy 39 0.057
510
P RNL015 Renal Hypertension 48 0.056
511
ATR057 Atrioventricular Block 55 0.056
512
STT001 Status Epilepticus 59 0.056
513
INT002 Intermittent Claudication 61 0.056
514
PPL018 Papillary Adenocarcinoma 46 0.056
515
MLD001 Melioidosis 67 0.056
516
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.056
517
VPM001 Vipoma 50 0.056
518
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.056
519
P LYM025 Lymphedema 53 0.055
520
INT007 Intermediate Coronary Syndrome 55 0.055
521
LYM040 Lymphoblastic Lymphoma 54 0.055
522
VTM027 Vitamin D-Dependent Rickets, Type 2a 55 0.055
523
PPL001 Papillary Adenoma 45 0.055
524
CRP001 Carpal Tunnel Syndrome 67 0.054
525
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.054
526
P BNC003 Bone Cancer 57 0.054
527
P SCL009 Sclerosing Cholangitis 47 0.054
528
EXS001 Exostosis 46 0.054
529
QDR001 Quadriplegia 48 0.054
530
c DPH024 Diaphragmatic Hernia, Congenital 64 0.053
531
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.053
532
FDB001 Foodborne Botulism 56 0.053
533
RRD056 Rare Disease in Surgical Orthopedic 28 0.053
534
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.053
535
WLL004 Wallerian Degeneration 39 0.053
536
IDP070 Idiopathic Scoliosis 37 0.053
537
PLY001 Polycythemia Vera 69 0.052
538
RFR010 Refractory Anemia 48 0.052
539
KHL003 Kohlschutter-Tonz Syndrome 64 0.052
540
MTN003 Motion Sickness 52 0.052
541
CNN003 Conn's Syndrome 79 0.052
542
c PNC106 Pancreatic Agenesis 1 50 0.052
543
MRK001 Merkel Cell Carcinoma 66 0.052
544
MYL001 Myelitis 51 0.051
545
PNC034 Pancreas Disease 46 0.051
546
c MGR032 Migraine, Familial Hemiplegic, 1 40 0.051
547
NPH003 Nephrocalcinosis 51 0.051
548
NSP002 Nasopharyngitis 41 0.051
549
c CHL119 Cholangitis, Primary Sclerosing 57 0.051
550
CRT013 Carotid Stenosis 50 0.051
551
P HYP733 Hypercalciuria, Absorptive, 2 46 0.051
552
P PRG013 Paraganglioma 52 0.050
553
TQP001 Taqi Polymorphism 32 0.050
554
P OBS001 Obstructive Jaundice 48 0.050
555
P ATR010 Atrial Heart Septal Defect 60 0.050
556
FCT007 Factor Vii Deficiency 66 0.049
557
IDP073 Idiopathic Hypercalciuria 43 0.049
558
P OPT009 Optic Neuritis 56 0.049
559
P SBR004 Seborrheic Dermatitis 45 0.049
560
PRM020 Premenstrual Tension 39 0.049
561
HYP043 Hyperandrogenism 48 0.047
562
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.047
563
OPT003 Opiate Dependence 50 0.047
564
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.047
565
PSY004 Psychotic Disorder 67 0.047
566
CRN017 Coronary Thrombosis 47 0.047
567
OST004 Osteitis Fibrosa 40 0.046
568
VSC002 Vascular Dementia 57 0.046
569
P SCL048 Sclerosteosis 53 0.046
570
P MTR003 Mitral Valve Stenosis 50 0.046
571
GNG008 Ganglioneuroblastoma 47 0.046
572
LCK001 Locked-in Syndrome 46 0.046
573
P CRN026 Corneal Edema 40 0.046
574
END035 Endocrine Gland Cancer 44 0.046
575
P ACT105 Acute Mountain Sickness 52 0.045
576
FLL008 Folliculitis 46 0.045
577
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.045
578
SMT003 Somatostatinoma 51 0.045
579
RSC001 Rosacea 55 0.045
580
ADR041 Adrenal Cortical Adenoma 43 0.045
581
BRN053 Bronchial Adenomas/carcinoids Childhood 25 0.044
582
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.044
583
NRG002 Neurogenic Bladder 54 0.044
584
BCT021 Bacterial Sepsis 44 0.044
585
END028 Endemic Goiter 37 0.044
586
HYP068 Hyperostosis 48 0.044
587
P DYS021 Dysautonomia 39 0.044
588
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.043
589
FRZ001 Frozen Shoulder 53 0.043
590
P SCL057 Scoliosis, Isolated 1 41 0.043
591
c CHR418 Chronic Leukemia 50 0.043
592
P TMP003 Temporal Arteritis 67 0.043
593
CRT015 Carotid Artery Occlusion 44 0.043
594
CHR003 Cherubism 57 0.043
595
c OST164 Osteoporosis, Juvenile 53 0.043
596
PLC007 Placental Abruption 48 0.042
597
ACT088 Acute Insulin Response 41 0.042
598
GST030 Gastrinoma 45 0.042
599
SPR004 Supravalvular Aortic Stenosis 58 0.042
600
PLM011 Plummer's Disease 34 0.042
601
P SPN052 Spondyloarthropathy 54 0.042
602
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.041
603
GNG002 Ganglioneuroma 53 0.041
604
MCC012 Mccune-Albright Syndrome 70 0.041
605
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.041
606
P ESS003 Essential Thrombocythemia 67 0.041
607
P CRB059 Cerebellar Degeneration 37 0.041
608
LNG108 Langerhans Cell Histiocytosis 58 0.041
609
MYF002 Myofascial Pain Syndrome 42 0.041
610
c OVR058 Ovarian Small Cell Carcinoma 38 0.041
611
NNT010 Nontoxic Goiter 32 0.040
612
HRP009 Herpes Simplex Encephalitis 50 0.040
613
SCT002 Scotoma 43 0.040
614
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.040
615
c HYP243 Hyperparathyroidism 1 49 0.040
616
P GLL020 Gallbladder Disease 58 0.039
617
ADR008 Adrenal Adenoma 56 0.039
618
GNG005 Gangliocytoma 55 0.039
619
c MLG054 Malignant Histiocytosis 50 0.039
620
NPH010 Nephrosclerosis 49 0.039
621
URT010 Ureteral Obstruction 46 0.039
622
PRT019 Protein-Losing Enteropathy 46 0.039
623
P MCH002 Machado-Joseph Disease 63 0.039
624
P INT070 Intestinal Obstruction 58 0.039
625
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.039
626
PNC016 Pancreatic Cholera 38 0.039
627
ULN001 Ulnar Neuropathy 30 0.039
628
c EXS019 Exostoses, Multiple, Type I 52 0.039
629
DNT006 Dental Pulp Necrosis 40 0.039
630
PSD014 Pseudopseudohypoparathyroidism 56 0.039
631
RYN001 Raynaud Disease 49 0.039
632
HPT014 Hepatorenal Syndrome 50 0.038
633
LYM035 Lymphangiectasis 30 0.038
634
FBR019 Fibromatosis 44 0.038
635
c CHR098 Chronic Pyelonephritis 35 0.038
636
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.038
637
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 42 0.038
638
SCR037 Sucrase-Isomaltase Deficiency, Congenital 41 0.038
639
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 38 0.038
640
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.037
641
ILT001 Ileitis 50 0.037
642
PNN001 Panniculitis 49 0.037
643
ALC009 Alcoholic Liver Cirrhosis 53 0.037
644
LCH001 Leech Infestation 36 0.037
645
DBT004 Diabetic Polyneuropathy 50 0.037
646
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.036
647
END081 Endosteal Hyperostosis, Autosomal Dominant 59 0.036
648
c PGT008 Paget Disease of Bone 5, Juvenile-Onset 47 0.036
649
NRV004 Nerve Compression Syndrome 38 0.036
650
PNC006 Pancreatic Somatostatinoma 29 0.036
651
DYS018 Dysostosis 43 0.036
652
ESP002 Esophageal Varix 51 0.036
653
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.036
654
c EXS020 Exostoses, Multiple, Type Ii 39 0.036
655
PRN039 Paraneoplastic Syndromes 38 0.036
656
BRN009 Burning Mouth Syndrome 49 0.035
657
CYN002 Cyanosis, Transient Neonatal 45 0.035
658
SPN369 Spinal Disease 41 0.035
659
c MLG157 Malignant Pheochromocytoma 39 0.035
660
GRN007 Granuloma Annulare 45 0.035
661
PST053 Postherpetic Neuralgia 42 0.035
662
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.035
663
P HRD021 Hereditary Sensory Neuropathy 47 0.034
664
ACT162 Acute Sensory Ataxic Neuropathy 26 0.034
665
c MLT159 Multiple Endocrine Neoplasia, Type Iib 59 0.034
666
HLL004 Hellp Syndrome 53 0.034
667
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.034
668
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.034
669
ASP004 Asphyxia Neonatorum 45 0.034
670
EXC002 Exocrine Pancreatic Insufficiency 41 0.034
671
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 55 0.033
672
P BLP003 Blepharospasm 44 0.033
673
ART006 Arthus Reaction 42 0.033
674
CNT105 Central Core Disease of Muscle 61 0.033
675
P SYR001 Syringomyelia 46 0.033
676
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.033
677
PNC008 Pancreatic Endocrine Carcinoma 39 0.033
678
SPN032 Spindle Cell Carcinoma 45 0.032
679
P CMM008 Communicating Hydrocephalus 43 0.032
680
P CLD001 Cleidocranial Dysplasia 65 0.032
681
ANH002 Anhidrosis 46 0.032
682
SPN119 Spondylarthropathy 44 0.032
683
P CYS017 Cystic Teratoma 42 0.032
684
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 56 0.032
685
SRT004 Serotonin Syndrome 46 0.031
686
BNM001 Bone Marrow Cancer 43 0.031
687
GTL001 Gitelman Syndrome 66 0.030
688
PYC001 Pycnodysostosis 55 0.030
689
EPC002 Epicondylitis 41 0.030
690
PYR004 Pyuria 39 0.030
691
c PGT007 Paget Disease of Bone 3 36 0.030
692
PRL008 Paralytic Ileus 44 0.028
693
MYS001 Myositis Ossificans 40 0.028
694
PRR013 Prurigo Nodularis 36 0.028
695
c OST135 Osteogenesis Imperfecta, Type I 55 0.028
696
P HMF004 Hemifacial Spasm 38 0.028
697
P MXL015 Maxillary Sinusitis 37 0.028
698
CLD011 Cold Urticaria 34 0.028
699
CRB036 Cerebral Meningioma 34 0.028
700
c HMF011 Hemifacial Spasm, Familial 33 0.028
701
PHY008 Physical Urticaria 36 0.027
702
SPN011 Spongiotic Dermatitis 32 0.027
703
NRD001 Neurodermatitis 32 0.027
704
P EPL003 Epulis 29 0.027
705
P VNB005 Van Buchem Disease 55 0.026
706
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 62 0.025
707
P CMR001 Camurati-Engelmann Disease 58 0.024
708
CSL001 Causalgia 45 0.024
709
c MGR030 Migraine, Familial Hemiplegic, 2 36 0.024
710
c SPR094 Sporadic Pheochromocytoma 32 0.024
711
VLK001 Volkmann Contracture 32 0.024
712
PRS120 Persistent Idiopathic Facial Pain 28 0.024
713
c EXS021 Exostoses, Multiple, Type Iii 20 0.024
714
CCC003 Coccygodynia 17 0.024
715
PRT030 Parathyroid Gland Disease 45 0.022
716
THY009 Thyroid Lymphoma 45 0.022
717
URM005 Uremic Pruritus 39 0.022
718
PRC054 Perching Syndrome 33 0.022
719
PRX009 Paroxysmal Hemicrania 33 0.022
720
OST008 Osteosclerotic Myeloma 32 0.022
721
PLM039 Pulmonary Neuroendocrine Tumor 31 0.022
722
EXT001 Extragonadal Seminoma 27 0.022
723
c RTN032 Retinal Cone Dystrophy 1 24 0.022
724
c SBC039 Subacute Cerebellar Degeneration 21 0.022
725
CTN020 Cutaneous Sclerosis 17 0.022
Content
Loading form....