Search results for Cobalt

666 hits were found for Cobalt

# Family MCID Name MIFTS Score
1
CBL009 Cobalt Allergic Contact Dermatitis 7 2.782
2
CBL010 Cobalt Allergic Asthma 4 2.770
3
DRM006 Dermatitis 61 0.260
4
CNT047 Contact Dermatitis 58 0.243
5
DFC004 Deficiency Anemia 70 0.240
6
HYP266 Hypoxia 57 0.233
7
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.229
8
P PLY018 Polycythemia 56 0.194
9
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.192
10
HRW001 Hair Whorl 36 0.192
11
ALL010 Allergic Contact Dermatitis 56 0.180
12
LPP008 Lipoprotein Quantitative Trait Locus 62 0.172
13
c ATR087 Atrial Standstill 1 75 0.160
14
ALL026 Allergic Hypersensitivity Disease 62 0.160
15
ISC004 Ischemia 58 0.160
16
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.158
17
ART140 Arteries, Anomalies of 52 0.156
18
LNG099 Lung Disease 60 0.146
19
P CRN300 Coronary Heart Disease 1 63 0.141
20
P EPL164 Epilepsy 71 0.136
21
VTM002 Vitamin B12 Deficiency 48 0.136
22
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.136
23
IRN002 Iron Metabolism Disease 57 0.133
24
c VRL010 Viral Hepatitis 52 0.124
25
GTR002 Goiter 53 0.115
26
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.115
27
INT066 Interstitial Lung Disease 60 0.112
28
BNR002 Bone Resorption Disease 48 0.112
29
P HYP086 Hypothyroidism 69 0.108
30
47X002 47,xyy 49 0.108
31
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.108
32
P PLM036 Pulmonary Fibrosis 65 0.105
33
48X005 48,xyyy 39 0.101
34
OST159 Osteogenic Sarcoma 66 0.098
35
MTL005 Metal Allergy 41 0.098
36
P MYC007 Myocardial Infarction 70 0.094
37
P LVR013 Liver Disease 68 0.094
38
P NRP001 Neuropathy 56 0.094
39
ATH013 Atherosclerosis Susceptibility 65 0.090
40
P PRP019 Peripheral Nervous System Disease 58 0.090
41
INT007 Intermediate Coronary Syndrome 55 0.090
42
P SPP010 Suppressor of Tumorigenicity 3 51 0.090
43
ESP021 Esophageal Cancer 90 0.086
44
P BLD134 Bladder Cancer 79 0.086
45
P RTN024 Retinoblastoma 73 0.086
46
P NRB001 Neuroblastoma 72 0.086
47
ANG054 Angina Pectoris 66 0.086
48
IRN001 Iron Deficiency Anemia 59 0.086
49
THR024 Thrombosis 57 0.086
50
P PNM006 Pneumoconiosis 56 0.086
51
c FML008 Familial Retinoblastoma 53 0.086
52
ANT018 Anthracosis 48 0.086
53
c PCH010 Pachyonychia Congenita 3 44 0.086
54
P BRS047 Breast Cancer 97 0.081
55
AST005 Asthma 76 0.081
56
P SCL018 Scoliosis 60 0.081
57
c ACT075 Acute Myocardial Infarction 57 0.081
58
P SZR006 Seizure Disorder 56 0.081
59
HLX001 Helix Syndrome 47 0.081
60
CYN003 Cyanide Poisoning 24 0.081
61
OST012 Osteoarthritis 78 0.077
62
P HRT032 Heart Disease 75 0.077
63
P KDN018 Kidney Disease 72 0.077
64
P VSC007 Vascular Disease 63 0.077
65
HYP066 Hyperglycemia 61 0.077
66
P OPT006 Optic Nerve Disease 60 0.077
67
VSL002 Visual Epilepsy 59 0.077
68
FCL014 Focal Epilepsy 54 0.077
69
RFR010 Refractory Anemia 48 0.077
70
IDP070 Idiopathic Scoliosis 42 0.077
71
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.077
72
PST092 Posttransplant Acute Limbic Encephalitis 29 0.077
73
MTH071 Methane Production 26 0.077
74
P CLR023 Colorectal Cancer 99 0.072
75
P PHC003 Pheochromocytoma 71 0.072
76
PRP027 Peripheral Vascular Disease 71 0.072
77
PLM001 Pulmonary Tuberculosis 69 0.072
78
P MYC084 Mycobacterium Tuberculosis 1 68 0.072
79
SKN016 Skin Disease 63 0.072
80
P VSC011 Vasculitis 62 0.072
81
P MLN069 Melanoma, Uveal 59 0.072
82
ANR040 Aneurysm 59 0.072
83
PRP080 Peripheral Artery Disease 53 0.072
84
CRV040 Cervix Carcinoma 51 0.072
85
ADR040 Adrenal Gland Pheochromocytoma 46 0.072
86
OCC001 Occupational Dermatitis 29 0.072
87
c VSC053 Visceral Steatosis, Congenital 25 0.072
88
P HPT023 Hepatocellular Carcinoma 100 0.066
89
P LNG064 Lung Cancer Susceptibility 3 78 0.066
90
P MLN008 Melanoma 69 0.066
91
P LYM118 Lymphoma 68 0.066
92
P RHB003 Rhabdomyosarcoma 63 0.066
93
c BRN108 Branchiootic Syndrome 1 62 0.066
94
P RHN004 Rhinitis 57 0.066
95
P TRM003 Tremor 54 0.066
96
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.066
97
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.066
98
P SCL057 Scoliosis, Isolated 1 41 0.066
99
PPL052 Papillomatosis, Confluent and Reticulated 33 0.066
100
P LNG032 Lung Cancer 98 0.061
101
P MDL005 Medulloblastoma 77 0.061
102
P LKM002 Leukemia 68 0.061
103
RCK004 Rickets 68 0.061
104
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.061
105
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.061
106
SRC014 Sarcoma 65 0.061
107
P GLM045 Glioma 63 0.061
108
P BCL017 B-Cell Lymphoma 58 0.061
109
EXT034 Extrinsic Allergic Alveolitis 58 0.061
110
SPN035 Spindle Cell Sarcoma 53 0.061
111
CRN030 Coronary Stenosis 50 0.061
112
LYM019 Lymphosarcoma 46 0.061
113
GLL048 Glial Tumor 45 0.061
114
CRB086 Cerebral Aneurysms 40 0.061
115
CRV035 Cervical Cancer 76 0.054
116
GLB015 Glioblastoma Multiforme 75 0.054
117
SCK003 Sickle Cell Anemia 74 0.054
118
SVR004 Severe Combined Immunodeficiency 73 0.054
119
CNG034 Congestive Heart Failure 69 0.054
120
P NSP012 Nasopharyngeal Carcinoma 66 0.054
121
KRT019 Keratitis, Hereditary 65 0.054
122
P HRP006 Herpes Simplex 65 0.054
123
CLF027 Cleft Palate, Isolated 64 0.054
124
LVR012 Liver Cirrhosis 62 0.054
125
NTR005 Nutritional Deficiency Disease 62 0.054
126
P HMN010 Hemangioma 61 0.054
127
P MYL006 Myeloid Leukemia 60 0.054
128
P BRS044 Breast Adenocarcinoma 59 0.054
129
P SYP003 Syphilis 58 0.054
130
P URT039 Urticaria 58 0.054
131
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.054
132
EYD002 Eye Disease 58 0.054
133
P LRY044 Larynx Cancer 55 0.054
134
SYN007 Synovitis 54 0.054
135
PLM010 Pulmonary Edema 54 0.054
136
HMS001 Hemosiderosis 54 0.054
137
PRN011 Pernicious Anemia 53 0.054
138
EXP004 Exophthalmos 52 0.054
139
CLR109 Colorectal Adenocarcinoma 51 0.054
140
P AST007 Astrocytoma 51 0.054
141
RTN003 Retinal Ischemia 50 0.054
142
CHL061 Childhood Leukemia 48 0.054
143
CYT002 Cytokine Deficiency 42 0.054
144
P AVS003 Avascular Necrosis 42 0.054
145
ATX019 Ataxia with Vitamin E Deficiency 42 0.054
146
c PST022 Posterior Uveal Melanoma 42 0.054
147
P RRH023 Rare Hereditary Hemochromatosis 41 0.054
148
ANX004 Anoxia 40 0.054
149
END028 Endemic Goiter 37 0.054
150
PLC002 Plica Syndrome 36 0.054
151
MLG061 Malignant Choroid Melanoma 34 0.054
152
ANM001 Anemia of Prematurity 31 0.054
153
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.054
154
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.054
155
ARG006 Aregenerative Anemia 27 0.054
156
P PRS040 Prostate Cancer 97 0.047
157
P OVR042 Ovarian Cancer 88 0.047
159
c HYP595 Hypertension, Essential 84 0.047
160
P GST053 Gastric Cancer 83 0.047
161
c NRF023 Neurofibromatosis, Type Ii 80 0.047
162
c DLT002 Dilated Cardiomyopathy 79 0.047
163
c HMC039 Hemochromatosis, Type 1 74 0.047
164
c HYP836 Hypercholesterolemia, Familial, 1 73 0.047
165
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.047
166
P GRF003 Graft-Versus-Host Disease 72 0.047
167
P SRC025 Sarcoidosis 1 70 0.047
168
c CHR684 Chronic Kidney Disease 70 0.047
169
ADL002 Adult Syndrome 70 0.047
170
P SLP006 Sleep Apnea 69 0.047
171
BRN024 Bronchitis 68 0.047
172
ALC007 Alcohol Dependence 66 0.047
173
P DRM053 Dermatitis, Atopic 66 0.047
174
c SML038 Small Cell Cancer of the Lung 65 0.047
175
TTN003 Tetanus 65 0.047
176
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.047
177
P PRD008 Periodontitis 64 0.047
178
P HML002 Hemolytic Anemia 63 0.047
179
P NTR004 Neutropenia 63 0.047
180
TYP007 Typhoid Fever 63 0.047
181
ATM095 Autoimmune Disease 62 0.047
182
RTN017 Retinal Detachment 61 0.047
183
DPH001 Diphtheria 60 0.047
184
P CTR002 Cataract 60 0.047
185
IGR001 Ige Responsiveness, Atopic 59 0.047
186
P ANP001 Anaplastic Large Cell Lymphoma 58 0.047
187
P EXN002 Exanthem 57 0.047
188
P FBR017 Fibrosarcoma 56 0.047
189
TRN018 Transitional Cell Carcinoma 56 0.047
190
ERY051 Erythroleukemia, Familial 56 0.047
191
BCT022 Bacterial Infectious Disease 56 0.047
192
P PLY019 Polyneuropathy 56 0.047
193
P MNC007 Monocytic Leukemia 53 0.047
194
P RTN016 Retinal Degeneration 53 0.047
195
c PRD040 Periodontitis, Chronic 53 0.047
196
P RTN018 Retinal Disease 53 0.047
197
P PRR016 Pierre Robin Syndrome 52 0.047
198
P PRC012 Pericardial Effusion 51 0.047
199
STM007 Stomatitis 50 0.047
200
HMP001 Hemopericardium 48 0.047
201
RNL077 Renal Fibrosis 47 0.047
202
CRD137 Cardiogenic Shock 47 0.047
203
ISL075 Isolated Pierre Robin Sequence 29 0.047
204
CHL079 Children's Interstitial Lung Disease 26 0.047
205
HVY002 Heavy Metal Poisoning 22 0.047
206
CRN311 Coronary Ostial Stenosis or Atresia 20 0.047
207
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.038
208
MYL069 Myeloma, Multiple 85 0.038
209
c LKM061 Leukemia, Acute Myeloid 84 0.038
210
MLR004 Malaria 81 0.038
211
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.038
212
STR067 Stroke, Ischemic 81 0.038
213
P RSP003 Respiratory Failure 74 0.038
214
c MNN043 Meningioma, Familial 74 0.038
215
c THR092 Thrombophilia Due to Thrombin Defect 73 0.038
216
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.038
217
c LKM063 Leukemia, Chronic Myeloid 72 0.038
218
GST040 Gastric Adenocarcinoma 70 0.038
219
P MYP004 Myopathy 70 0.038
220
LYM133 Lymphoma, Hodgkin, Classic 69 0.038
221
EWN003 Ewing Sarcoma 69 0.038
222
P LKM062 Leukemia, Acute Lymphoblastic 69 0.038
223
P PNM007 Pneumonia 68 0.038
224
P INF038 Influenza 68 0.038
225
CRB039 Cerebrovascular Disease 67 0.038
226
P TRN020 Turner Syndrome 67 0.038
227
c RHB024 Rhabdomyosarcoma 2 67 0.038
228
P MCR115 Microvascular Complications of Diabetes 5 66 0.038
229
PRT037 Pertussis 65 0.038
230
P THY023 Thymoma 65 0.038
231
P DBT009 Diabetes Mellitus 64 0.038
232
P ADN016 Adenocarcinoma 64 0.038
233
LSH001 Leishmaniasis 63 0.038
234
c PRC016 Pre-Eclampsia 63 0.038
235
P ANR048 Aniridia 1 63 0.038
236
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.038
237
ANR007 Anorexia Nervosa 63 0.038
238
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.038
239
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
240
P PSR002 Psoriasis 62 0.038
241
MNN042 Meningioma, Radiation-Induced 62 0.038
242
MDD011 Mood Disorder 62 0.038
243
P ENC018 Encephalopathy 61 0.038
244
ACN002 Acanthosis Nigricans 60 0.038
245
SQM006 Squamous Cell Carcinoma 60 0.038
246
c ACT071 Acute Kidney Failure 60 0.038
247
P THL005 Thalassemia 60 0.038
248
CHL014 Cholera 59 0.038
249
P CYS018 Cystitis 59 0.038
250
P DNG005 Dengue Virus 59 0.038
251
c ACT073 Acute Leukemia 58 0.038
252
LYM027 Lymphopenia 58 0.038
253
P END033 Endocarditis 57 0.038
254
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.038
255
P BPL003 Bipolar Disorder 56 0.038
256
ALL006 Allergic Asthma 56 0.038
257
SFT003 Soft Tissue Sarcoma 56 0.038
258
P GST044 Gastritis 56 0.038
259
ORP003 Oropharynx Cancer 55 0.038
260
DFF005 Diffuse Large B-Cell Lymphoma 55 0.038
261
P SBS003 Substance Abuse 55 0.038
262
BRN014 Bronchopneumonia 54 0.038
263
P ART021 Arteriosclerosis 54 0.038
264
PPL022 Papilloma 54 0.038
265
MYM001 Myoma 54 0.038
266
INT075 Intracranial Hypertension 53 0.038
267
GST023 Gastric Ulcer 53 0.038
268
DNT012 Dental Caries 53 0.038
269
ALC009 Alcoholic Liver Cirrhosis 53 0.038
270
c MCR113 Microvascular Complications of Diabetes 3 52 0.038
271
PST011 Pustulosis of Palm and Sole 52 0.038
272
P RCT021 Rectum Cancer 52 0.038
273
c THY107 Thymoma, Familial 52 0.038
274
P ACT105 Acute Mountain Sickness 52 0.038
275
P OTS014 Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant 52 0.038
276
c ACT135 Acute Graft Versus Host Disease 52 0.038
277
ANK001 Ankylosis 51 0.038
278
CCC002 Coccidiosis 51 0.038
279
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.038
280
SPN021 Spinal Meningioma 50 0.038
281
MTB004 Metabolic Acidosis 50 0.038
282
IRR003 Irritant Dermatitis 49 0.038
283
CHL056 Cheilitis 48 0.038
284
CRN017 Coronary Thrombosis 47 0.038
285
c MCR120 Microvascular Complications of Diabetes 7 47 0.038
286
KRT002 Keratomalacia 47 0.038
287
RTC005 Reticulosarcoma 47 0.038
288
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.038
289
ALB002 Albinism 46 0.038
290
CYN002 Cyanosis, Transient Neonatal 45 0.038
291
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.038
292
P SDR002 Siderosis 44 0.038
293
c PRM038 Primary Agammaglobulinemia 44 0.038
294
HPT082 Hepatic Adenomas, Familial 44 0.038
295
SMN007 Seminoma 43 0.038
296
MYX004 Myxedema 43 0.038
297
c CHR546 Chronic Mountain Sickness 43 0.038
298
DRG024 Drug Allergy 42 0.038
299
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.038
300
BCK006 Back Pain 42 0.038
301
P KLZ004 Kala-Azar 1 41 0.038
302
c MCR130 Microvascular Complications of Diabetes 6 41 0.038
303
c MCR133 Microvascular Complications of Diabetes 4 41 0.038
304
c MJR024 Major Affective Disorder 9 41 0.038
305
SCR001 Secretory Meningioma 41 0.038
306
KLD004 Keloid Disorder 40 0.038
307
CRN020 Coronary Restenosis 39 0.038
308
ADP007 Adie Pupil 39 0.038
309
c MJR022 Major Affective Disorder 8 38 0.038
310
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.038
311
ATX010 Ataxia Neuropathy Spectrum 34 0.038
312
MTH047 Methanol Poisoning 34 0.038
313
SLN001 Silent Myocardial Infarction 34 0.038
314
GNT167 Genetic Obesity 33 0.038
315
ACT064 Acute Necrotizing Encephalitis 33 0.038
316
CND006 Candida Glabrata 32 0.038
317
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.038
319
GRN004 Granulomatous Amebic Encephalitis 30 0.038
320
ARG004 Argyria 27 0.038
321
HNM002 Hinman Syndrome 27 0.038
322
TXC008 Toxic Optic Neuropathy 23 0.038
323
BLD165 Blood Group, Colton System 20 0.038
324
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.038
325
BLD137 Blood Group--Ahonen 16 0.038
326
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.027
327
P ALZ034 Alzheimer Disease 88 0.027
328
P PNC035 Pancreatic Cancer 84 0.027
329
P GLM040 Glioma Susceptibility 1 81 0.027
330
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.027
331
P LKM071 Leukemia, Chronic Lymphocytic 79 0.027
332
PFF001 Pfeiffer Syndrome 79 0.027
333
INS024 Insulin-Like Growth Factor I 79 0.027
334
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.027
335
KPS004 Kaposi Sarcoma 75 0.027
336
PHN003 Phenylketonuria 75 0.027
337
CRH001 Crohn's Disease 74 0.027
338
BSL036 Basal Cell Nevus Syndrome 73 0.027
339
P CNR004 Cone-Rod Dystrophy 2 73 0.027
340
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.027
341
ACR007 Acromegaly 71 0.027
342
HMN044 Human Immunodeficiency Virus Type 1 71 0.027
343
WLS001 Wilson Disease 71 0.027
344
MYL009 Myelodysplastic Syndrome 70 0.027
345
DWN001 Down Syndrome 70 0.027
346
P HYP061 Hypertrophic Cardiomyopathy 70 0.027
347
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.027
348
PLY001 Polycythemia Vera 69 0.027
349
P ART022 Arthritis 69 0.027
350
CRB037 Cerebral Palsy 69 0.027
351
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.027
352
ART016 Aortic Aneurysm 69 0.027
353
MNT001 Mantle Cell Lymphoma 69 0.027
354
c BSL007 Basal Cell Carcinoma 68 0.027
355
SKN019 Skin Melanoma 68 0.027
356
PNC129 Pancreatic Adenocarcinoma 68 0.027
357
P THR014 Thrombocytopenia 67 0.027
358
P CRD119 Cardiac Arrest 67 0.027
359
P HPT021 Hepatitis 67 0.027
360
FCT007 Factor Vii Deficiency 67 0.027
361
BRK010 Burkitt Lymphoma 67 0.027
362
P FLL037 Follicular Lymphoma 67 0.027
363
P PLM037 Pulmonary Hypertension 67 0.027
364
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.027
365
c FML021 Familial Hypercholesterolemia 66 0.027
366
P MSC005 Muscular Dystrophy 66 0.027
367
P SKN015 Skin Carcinoma 66 0.027
368
HYP056 Hypoglycemia 66 0.027
369
LNG039 Lung Squamous Cell Carcinoma 66 0.027
370
P CNJ013 Conjunctivitis 65 0.027
371
c ART101 Aortic Valve Disease 2 65 0.027
372
MRK001 Merkel Cell Carcinoma 65 0.027
373
PRT036 Peritonitis 64 0.027
374
ANG020 Angiosarcoma 64 0.027
375
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.027
376
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.027
377
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.027
378
ALS001 Alstrom Syndrome 64 0.027
379
DGR001 Digeorge Syndrome 64 0.027
380
LYM017 Lyme Disease 64 0.027
381
OST017 Osteomyelitis 64 0.027
382
KRN002 Kearns-Sayre Syndrome 63 0.027
383
PLG002 Plague 63 0.027
384
CHN016 Cohen Syndrome 63 0.027
385
P MVM001 Movement Disease 63 0.027
386
c ACT068 Acute Cystitis 63 0.027
387
c OPT053 Optic Atrophy 1 63 0.027
388
HMT002 Hematologic Cancer 62 0.027
389
LPD008 Lipid Metabolism Disorder 62 0.027
390
c HPT003 Hepatitis a 62 0.027
391
P HYP750 Hypertriglyceridemia, Familial 62 0.027
392
P ART023 Arthropathy 62 0.027
393
HSH003 Hashimoto Thyroiditis 62 0.027
394
CRC021 Carcinosarcoma 62 0.027
395
CHL068 Cholestasis 61 0.027
396
OST003 Osteonecrosis 61 0.027
397
FTT001 Fatty Liver Disease 61 0.027
398
YLL002 Yellow Fever 61 0.027
399
WLD007 Waldenstroem's Macroglobulinemia 61 0.027
400
WHM001 Whim Syndrome 61 0.027
401
NTH001 Netherton Syndrome 60 0.027
402
SPN186 Spinal Cord Injury 60 0.027
403
SHG001 Shigellosis 60 0.027
404
TTH002 Tooth Agenesis 60 0.027
405
TRG002 Trigeminal Neuralgia 60 0.027
406
HPT019 Hepatic Encephalopathy 60 0.027
407
ACQ007 Acquired Immunodeficiency Syndrome 60 0.027
408
VRC005 Varicose Veins 60 0.027
409
CHC001 Chickenpox 60 0.027
410
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.027
411
SPP011 Suppression of Tumorigenicity 12 59 0.027
412
P MYC008 Myocarditis 59 0.027
413
P MCR010 Microcephaly 59 0.027
414
SPN027 Spinal Stenosis 59 0.027
415
PLM033 Pulmonary Embolism 59 0.027
416
GRD007 Grade Iii Astrocytoma 59 0.027
417
GNG013 Gingivitis 59 0.027
418
GST045 Gastroenteritis 59 0.027
419
PPT005 Peptic Ulcer Disease 59 0.027
420
CRY005 Cryptococcosis 58 0.027
421
ANT024 Anthrax Disease 58 0.027
422
CHR072 Chordoma 58 0.027
423
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.027
424
ERY003 Erythema Multiforme 58 0.027
425
CRV038 Cervical Squamous Cell Carcinoma 58 0.027
426
P CND004 Candidiasis 58 0.027
427
PMP006 Pemphigus Vulgaris, Familial 57 0.027
428
CHL067 Cholecystitis 57 0.027
429
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.027
430
c MST023 Mesothelioma, Malignant 57 0.027
431
BLR008 Bilirubin Metabolic Disorder 57 0.027
432
c LKM070 Leukemia, Acute Monocytic 57 0.027
433
PHR003 Pharyngitis 57 0.027
434
PGM001 Pigmented Villonodular Synovitis 56 0.027
435
P PYL005 Pyelonephritis 56 0.027
436
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.027
437
HPT046 Hepatic Veno-Occlusive Disease 56 0.027
438
PLS011 Plasmacytoma 56 0.027
439
LMY014 Leiomyoma, Uterine 56 0.027
440
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.027
441
SPN041 Spinal Cord Disease 56 0.027
442
ISL001 Islet Cell Tumor 56 0.027
443
MTH009 Mouth Disease 56 0.027
444
EMB004 Embryonal Carcinoma 56 0.027
445
GST050 Gastrointestinal System Disease 56 0.027
446
ORL005 Oral Candidiasis 56 0.027
447
INT030 Intracranial Aneurysm 56 0.027
448
MCS002 Mucositis 56 0.027
449
SLC006 Silicosis 56 0.027
450
BRN004 Brain Edema 56 0.027
451
AGN016 Aging 56 0.027
452
MCL006 Macular Retinal Edema 55 0.027
453
c PRG126 Progressive Familial Heart Block 55 0.027
454
P MLN007 Male Infertility 55 0.027
455
P GRV001 Graves' Disease 55 0.027
456
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.027
457
GNG005 Gangliocytoma 55 0.027
458
P HYP076 Hyperthyroidism 55 0.027
459
P AML002 Amelogenesis Imperfecta 55 0.027
460
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.027
461
CLF004 Cleft Lip/palate 54 0.027
462
HYP060 Hyperinsulinism 54 0.027
463
P PMP001 Pemphigus 54 0.027
464
CRT017 Cartilage Disease 54 0.027
465
P ALP008 Alopecia 54 0.027
466
THR013 Thoracic Outlet Syndrome 54 0.027
467
PRC013 Pericarditis 54 0.027
468
DBT010 Diabetic Neuropathy 54 0.027
469
P LTR001 Lateral Sclerosis 54 0.027
470
LYM040 Lymphoblastic Lymphoma 54 0.027
471
P LNG035 Lung Large Cell Carcinoma 54 0.027
472
WST005 West Nile Virus 54 0.027
473
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.027
474
PNC001 Pancytopenia 54 0.027
475
PRS045 Prostatic Hypertrophy 53 0.027
476
CLR030 Clear Cell Renal Cell Carcinoma 53 0.027
477
P LCH002 Lichen Planus 53 0.027
478
P END047 Endophthalmitis 53 0.027
479
FRZ001 Frozen Shoulder 53 0.027
480
P INS002 in Situ Carcinoma 53 0.027
481
KRT006 Keratoconjunctivitis 53 0.027
482
NVS001 Neovascular Glaucoma 53 0.027
483
CLF001 Cleft Lip 53 0.027
484
HMC014 Homocysteinemia 53 0.027
485
NNT012 Neonatal Jaundice 53 0.027
486
GSG001 Gas Gangrene 53 0.027
487
P RTN022 Retinal Vein Occlusion 53 0.027
488
GNG002 Ganglioneuroma 52 0.027
489
P LRY019 Laryngitis 52 0.027
490
ACR041 Acromelic Frontonasal Dysostosis 52 0.027
491
P DDN001 Duodenal Ulcer 52 0.027
492
MRG003 Marginal Zone B-Cell Lymphoma 52 0.027
493
DYS015 Dysentery 52 0.027
494
THY030 Thyroid Gland Disease 52 0.027
495
P MSC003 Muscular Atrophy 52 0.027
496
P THY032 Thyroiditis 52 0.027
497
BWN001 Bowen-Conradi Syndrome 52 0.027
498
ACT200 Acute Monoblastic Leukemia 52 0.027
499
TLN003 Telangiectasis 52 0.027
500
LMY002 Leiomyoma 52 0.027
501
PRS021 Prostatic Adenoma 51 0.027
502
MYL001 Myelitis 51 0.027
503
PLS009 Plasma Cell Neoplasm 51 0.027
504
MGL001 Megaloblastic Anemia 51 0.027
505
P LCT001 Lactic Acidosis 51 0.027
506
THR016 Thrombophlebitis 51 0.027
507
LNG031 Lung Benign Neoplasm 51 0.027
508
SPN019 Spondylolisthesis 51 0.027
509
SPL004 Splenic Marginal Zone Lymphoma 51 0.027
510
TNG007 Tongue Carcinoma 51 0.027
511
P HYP040 Hypospadias 51 0.027
512
END086 End Stage Renal Disease 51 0.027
513
PNM005 Pneumonic Plague 51 0.027
514
BRX001 Bruxism 50 0.027
515
P SCK005 Sickle Cell Disease 50 0.027
516
PYD002 Pyoderma 50 0.027
517
NTR046 Neutrophil Migration 50 0.027
518
P PNB001 Pineoblastoma 50 0.027
519
OCL022 Ocular Melanoma 50 0.027
520
VRR004 Verrucous Carcinoma 49 0.027
521
ENT004 Enthesopathy 49 0.027
522
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.027
523
MCN001 Mucinous Adenocarcinoma 49 0.027
524
LFT001 Left Bundle Branch Hemiblock 49 0.027
525
PCT003 Pectus Excavatum 49 0.027
526
PRS129 Prostatic Hyperplasia, Benign 49 0.027
527
MCR004 Macroglobulinemia 49 0.027
528
c FLL041 Follicular Lymphoma 1 49 0.027
529
P CMP008 Compartment Syndrome 49 0.027
530
P SDR003 Sideroblastic Anemia 49 0.027
531
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.027
532
P CTN015 Cutaneous T Cell Lymphoma 49 0.027
533
VCC001 Vaccinia 49 0.027
534
HST010 Histiocytosis 48 0.027
535
BRS064 Bursitis 48 0.027
536
P SCL015 Scleritis 48 0.027
537
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.027
538
FBR009 Fibrous Dysplasia 48 0.027
539
c PRM226 Primary Central Nervous System Lymphoma 48 0.027
540
PYL006 Pyloric Stenosis 48 0.027
541
P PRR002 Pure Red-Cell Aplasia 47 0.027
542
PRC003 Proctitis 47 0.027
543
NDL007 Nodular Goiter 47 0.027
544
KHN001 Kuhnt-Junius Degeneration 47 0.027
545
LYM012 Lymphoplasmacytic Lymphoma 47 0.027
546
PLS025 Plasmablastic Lymphoma 47 0.027
547
CNT033 Central Nervous System Cancer 47 0.027
548
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.027
549
HYP034 Hypertensive Encephalopathy 46 0.027
550
LPD004 Lipoid Nephrosis 46 0.027
551
CMP034 Complete Androgen Insensitivity Syndrome 46 0.027
552
P BRB001 Beriberi 46 0.027
553
P LPC002 Lip Cancer 46 0.027
554
FLL008 Folliculitis 46 0.027
555
P BNG032 Benign Mesothelioma 46 0.027
556
P MTH007 Methemoglobinemia 46 0.027
557
c MLG068 Malignant Glioma 46 0.027
558
URT010 Ureteral Obstruction 45 0.027
559
TRT001 Teratocarcinoma 45 0.027
560
ORL013 Oral Lichen Planus 45 0.027
561
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.027
562
HPT004 Hepatic Coma 45 0.027
563
CRB004 Cerebral Artery Occlusion 45 0.027
564
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.027
565
ESP027 Esophagus Squamous Cell Carcinoma 45 0.027
566
MLK003 Melkersson-Rosenthal Syndrome 45 0.027
567
SYN005 Synostosis 45 0.027
568
NNS002 Nonspecific Interstitial Pneumonia 45 0.027
569
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 45 0.027
570
MSC072 Muscle Cancer 45 0.027
572
APP009 Appendix Adenocarcinoma 44 0.027
573
CHL149 Childhood Acute Myeloid Leukemia 44 0.027
574
PTT037 Pituitary Tumors 44 0.027
575
IRT001 Iritis 44 0.027
576
GNG003 Gingival Recession 44 0.027
577
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.027
578
SCT002 Scotoma 44 0.027
579
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
580
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.027
581
P EPN001 Ependymoblastoma 44 0.027
582
CRB090 Cerebral Hypoxia 44 0.027
583
AND001 Anodontia 43 0.027
584
SKN005 Skin Atrophy 43 0.027
585
ANR009 Aneurysmal Bone Cysts 43 0.027
586
RDC006 Red Cell Aplasia 43 0.027
587
LWC001 Low Compliance Bladder 43 0.027
588
ORL015 Oral Squamous Cell Carcinoma 43 0.027
589
TRP009 Triple X Syndrome 42 0.027
590
PRS115 Prosthetic Joint Infection 42 0.027
591
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.027
592
OBS082 Obstructive Nephropathy 42 0.027
593
GST020 Gastric Antral Vascular Ectasia 41 0.027
594
LTX001 Latex Allergy 41 0.027
595
49X006 49, Xxxxy Syndrome 41 0.027
596
KLB003 Klebsiella Pneumonia 41 0.027
597
HMN035 Hemangioma-Thrombocytopenia Syndrome 40 0.027
598
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.027
599
BLT001 Bilateral Retinoblastoma 39 0.027
600
CRN006 Coronary Aneurysm 39 0.027
601
P FML340 Familial Episodic Pain Syndrome 39 0.027
602
THR017 Thoracoabdominal Syndrome 39 0.027
603
ORF044 Orofacial Granulomatosis 38 0.027
604
c MLG157 Malignant Pheochromocytoma 38 0.027
605
c ACT067 Acute Conjunctivitis 38 0.027
606
KLD003 Keloid Formation 38 0.027
607
PMP010 Pompholyx 37 0.027
608
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 37 0.027
609
HRN029 Hearing Loss, Noise-Induced 37 0.027
610
CHR463 Chronic Actinic Dermatitis 37 0.027
611
PST035 Postgastrectomy Syndrome 37 0.027
612
TTH032 Tooth Size 36 0.027
613
P ADT009 Auditory Neuropathy Spectrum Disorder 36 0.027
614
PSD088 Pseudobulbar Affect 36 0.027
615
ENP001 Enophthalmos 35 0.027
616
ACT149 Acetaminophen Metabolism 35 0.027
617
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.027
618
RTR010 Retroperitoneal Sarcoma 34 0.027
619
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.027
621
c LVR030 Liver Failure, Infantile, Transient 34 0.027
622
BNS001 Bone Osteosarcoma 33 0.027
623
c CHR064 Chronic Monocytic Leukemia 33 0.027
624
RTC003 Root Caries 33 0.027
625
BRN034 Brain Meningioma 33 0.027
626
c PRS136 Prostate Cancer, Hereditary, 6 33 0.027
627
c EPL115 Epilepsy, Familial Temporal Lobe, 2 33 0.027
628
HND015 Hand Skill, Relative 33 0.027
629
NSL006 Nasal Cavity Squamous Cell Carcinoma 33 0.027
630
c PRS130 Prostate Cancer, Hereditary, 8 32 0.027
631
MXL008 Maxillary Sinus Cancer 32 0.027
632
PRT112 Portal Hypertension, Noncirrhotic 31 0.027
633
SPN011 Spongiotic Dermatitis 31 0.027
634
PNT003 Pinta Disease 31 0.027
635
ACN019 Acanthamoeba Keratitis 31 0.027
636
c RNG008 Ring Chromosome 13 31 0.027
637
PLY150 Polykaryocytosis Inducer 31 0.027
638
c PRG019 Paragangliomas 2 31 0.027
639
c THY056 Thyroid Dyshormonogenesis 3 30 0.027
640
PYR016 Pyridoxine Deficiency 30 0.027
641
ACT228 Acute Radiation Syndrome 29 0.027
642
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.027
643
ORB011 Orbit Rhabdomyosarcoma 29 0.027
644
LRY011 Larynx Verrucous Carcinoma 28 0.027
645
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.027
646
PHS025 Phosphatase, Acid, of Tissues 28 0.027
647
MST020 Mast Cell Activation Syndrome 26 0.027
648
AST054 Australia Antigen 26 0.027
649
PRL018 Purulent Endophthalmitis 25 0.027
650
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.027
651
VSC052 Vasculitis, Lymphocytic, Nodular 25 0.027
652
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.027
653
DFF002 Diffuse Pulmonary Fibrosis 25 0.027
654
RDT005 Radiation Induced Cancer 25 0.027
655
TXC004 Toxic Diffuse Goiter 24 0.027
656
AND017 Anodontia of Permanent Dentition 23 0.027
657
HDG004 Hodgkin's Granuloma 23 0.027
658
HMG009 Hemoglobin Zurich 22 0.027
659
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 22 0.027
660
HDG006 Hodgkin's Paragranuloma 22 0.027
661
HML018 Homologous Wasting Disease 22 0.027
662
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.027
663
TMP006 Temporomandibular Ankylosis 20 0.027
664
MGB001 Megabladder, Congenital 18 0.027
665
RCT006 Rectum Mucinous Adenocarcinoma 13 0.027
666
P VTM031 Vitamin B12 Plasma Level Quantitative Trait Locus 1 13 0.027
Content
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