Search results for ADP

927 hits were found for ADP

# Family MCID Name MIFTS Score
1
c BLD120 Bleeding Disorder, Platelet-Type, 8 35 6.115
2
GLT038 Glutamyl Ribose-5-Phosphate Storage Disease 8 2.715
3
CHL014 Cholera 59 0.439
4
PRT037 Pertussis 65 0.392
5
DPH001 Diphtheria 60 0.265
6
ISC004 Ischemia 58 0.195
7
P OVR042 Ovarian Cancer 88 0.176
8
ART002 Arts Syndrome 64 0.172
9
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.154
10
P GLM045 Glioma 63 0.141
11
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.140
12
GLL048 Glial Tumor 45 0.136
13
P NRB001 Neuroblastoma 72 0.134
14
P BRS047 Breast Cancer 97 0.130
15
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.130
16
P ATX030 Ataxia-Telangiectasia 82 0.127
17
TLN003 Telangiectasis 52 0.127
18
CRB004 Cerebral Artery Occlusion 45 0.127
19
GLB015 Glioblastoma Multiforme 75 0.123
20
P CLR023 Colorectal Cancer 99 0.114
21
P NRP001 Neuropathy 56 0.114
22
c SYS001 Systemic Lupus Erythematosus 86 0.109
23
OST159 Osteogenic Sarcoma 66 0.109
24
TRM010 Traumatic Brain Injury 51 0.109
25
HLX001 Helix Syndrome 47 0.109
26
P LKM002 Leukemia 68 0.107
27
DBT010 Diabetic Neuropathy 54 0.101
28
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.101
29
c SVR001 Severe Acute Respiratory Syndrome 62 0.099
30
ATM095 Autoimmune Disease 62 0.099
31
HYP066 Hyperglycemia 61 0.099
32
P VSC007 Vascular Disease 63 0.096
33
TXC005 Toxic Shock Syndrome 62 0.096
34
P PRS040 Prostate Cancer 97 0.093
35
P PNC035 Pancreatic Cancer 84 0.093
36
P THR014 Thrombocytopenia 67 0.093
37
LPP008 Lipoprotein Quantitative Trait Locus 62 0.093
38
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.093
39
BRN071 Brain Injury 49 0.093
40
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.090
41
c DLT002 Dilated Cardiomyopathy 79 0.087
42
c LKM061 Leukemia, Acute Myeloid 84 0.084
43
P LPS004 Lupus Erythematosus 61 0.084
44
c ACT075 Acute Myocardial Infarction 57 0.084
45
P HPT023 Hepatocellular Carcinoma 100 0.081
46
P HRT032 Heart Disease 75 0.081
47
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.081
48
WRN001 Werner Syndrome 69 0.081
49
P LYM118 Lymphoma 68 0.081
50
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.081
51
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.081
52
ALL026 Allergic Hypersensitivity Disease 62 0.081
53
P MYL006 Myeloid Leukemia 60 0.081
54
INS001 Insulinoma 60 0.081
55
HYP266 Hypoxia 57 0.081
56
THR035 Thrombasthenia 40 0.081
57
OVR094 Ovarian Epithelial Cancer 38 0.081
58
P GLM040 Glioma Susceptibility 1 81 0.077
59
P MYP004 Myopathy 70 0.077
60
CRB039 Cerebrovascular Disease 67 0.077
61
P MCR115 Microvascular Complications of Diabetes 5 66 0.077
62
P NTR004 Neutropenia 63 0.077
63
48X005 48,xyyy 39 0.077
64
ALL014 Allergic Encephalomyelitis 38 0.077
65
CRV035 Cervical Cancer 76 0.074
66
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.074
67
P BCL017 B-Cell Lymphoma 58 0.074
68
P LTR001 Lateral Sclerosis 54 0.074
69
ART140 Arteries, Anomalies of 52 0.074
70
P AST007 Astrocytoma 51 0.074
71
c MLG068 Malignant Glioma 46 0.074
72
PRM329 Premature Aging 35 0.074
73
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.070
74
P LNG064 Lung Cancer Susceptibility 3 78 0.070
75
P KDN018 Kidney Disease 72 0.070
76
HMN044 Human Immunodeficiency Virus Type 1 71 0.070
77
P PLM036 Pulmonary Fibrosis 65 0.070
78
P HRP006 Herpes Simplex 65 0.070
79
SPN186 Spinal Cord Injury 60 0.070
80
ANX004 Anoxia 40 0.070
81
P LKM071 Leukemia, Chronic Lymphocytic 79 0.066
82
P MDL005 Medulloblastoma 77 0.066
83
c ATR087 Atrial Standstill 1 75 0.066
84
P PHC003 Pheochromocytoma 71 0.066
85
MYL009 Myelodysplastic Syndrome 70 0.066
86
P MLN008 Melanoma 69 0.066
87
EWN003 Ewing Sarcoma 69 0.066
88
P CRD119 Cardiac Arrest 67 0.066
89
P DBT009 Diabetes Mellitus 64 0.066
90
P ADN016 Adenocarcinoma 64 0.066
91
P PRP019 Peripheral Nervous System Disease 58 0.066
92
THR024 Thrombosis 57 0.066
93
c MCR113 Microvascular Complications of Diabetes 3 52 0.066
94
STM007 Stomatitis 50 0.066
95
47X002 47,xyy 49 0.066
96
c MCR120 Microvascular Complications of Diabetes 7 47 0.066
97
MDD018 Middle East Respiratory Syndrome 43 0.066
98
c MCR130 Microvascular Complications of Diabetes 6 41 0.066
99
c MCR133 Microvascular Complications of Diabetes 4 41 0.066
100
P ALZ034 Alzheimer Disease 88 0.062
101
MYL069 Myeloma, Multiple 85 0.062
102
P PRK057 Parkinson Disease, Late-Onset 78 0.062
103
P FML011 Familial Adenomatous Polyposis 72 0.062
104
P MYC007 Myocardial Infarction 70 0.062
105
P CRN300 Coronary Heart Disease 1 63 0.062
106
c ACT027 Acute Pancreatitis 60 0.062
107
P BRS044 Breast Adenocarcinoma 59 0.062
108
ERY051 Erythroleukemia, Familial 56 0.062
109
P SPP010 Suppressor of Tumorigenicity 3 51 0.062
110
BNR002 Bone Resorption Disease 48 0.062
111
ADR040 Adrenal Gland Pheochromocytoma 46 0.062
112
TRT001 Teratocarcinoma 45 0.062
113
CYT002 Cytokine Deficiency 42 0.062
114
CLP006 Clopidogrel Resistance 40 0.062
115
P LNG032 Lung Cancer 98 0.057
116
c FNC027 Fanconi Anemia, Complementation Group a 81 0.057
117
CYS001 Cystic Fibrosis 81 0.057
118
STR067 Stroke, Ischemic 81 0.057
119
P BLD134 Bladder Cancer 79 0.057
120
IMM167 Immune Deficiency Disease 78 0.057
121
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.057
122
P HNT016 Huntington Disease 72 0.057
123
P LVR013 Liver Disease 68 0.057
124
P CCK001 Cockayne Syndrome 66 0.057
125
c SML038 Small Cell Cancer of the Lung 65 0.057
126
TTN003 Tetanus 65 0.057
127
SRC014 Sarcoma 65 0.057
128
SQM006 Squamous Cell Carcinoma 60 0.057
129
ANT024 Anthrax Disease 58 0.057
130
CHK001 Chikungunya 57 0.057
131
P CRD246 Cardiovascular System Disease 57 0.057
132
P MTC069 Mitochondrial Disorders 56 0.057
133
P DRR001 Diarrhea 55 0.057
134
INT007 Intermediate Coronary Syndrome 55 0.057
135
P RTN016 Retinal Degeneration 53 0.057
136
SPN035 Spindle Cell Sarcoma 53 0.057
137
MTC005 Mitochondrial Metabolism Disease 49 0.057
138
ACT003 Acute Kidney Tubular Necrosis 45 0.057
139
c OVR114 Ovarian Cancer 1 38 0.057
140
END057 Endometrial Cancer 74 0.052
141
SVR004 Severe Combined Immunodeficiency 73 0.052
142
P RTN024 Retinoblastoma 73 0.052
143
c HPT073 Hepatitis C Virus 72 0.052
144
PRP027 Peripheral Vascular Disease 71 0.052
145
P HYP086 Hypothyroidism 69 0.052
146
BRK010 Burkitt Lymphoma 67 0.052
147
P PLM037 Pulmonary Hypertension 67 0.052
148
ANG054 Angina Pectoris 66 0.052
149
HYP056 Hypoglycemia 66 0.052
150
ATH013 Atherosclerosis Susceptibility 65 0.052
151
PRT036 Peritonitis 64 0.052
152
P PRD008 Periodontitis 64 0.052
153
TRN015 Transient Cerebral Ischemia 63 0.052
154
c SCL052 Scleroderma, Familial Progressive 61 0.052
155
c ACT071 Acute Kidney Failure 60 0.052
156
P MYC008 Myocarditis 59 0.052
157
ADN018 Adenoma 59 0.052
158
GST045 Gastroenteritis 59 0.052
159
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.052
160
BRN004 Brain Edema 56 0.052
161
AGN016 Aging 56 0.052
162
P MLN007 Male Infertility 55 0.052
163
c HPT007 Hepatitis E 53 0.052
164
c FML008 Familial Retinoblastoma 53 0.052
165
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.052
166
PLR008 Pleurisy 50 0.052
167
VTM033 Vitamin K Deficiency Bleeding 48 0.052
168
VNZ002 Venezuelan Equine Encephalitis 47 0.052
169
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.052
170
P BNG032 Benign Mesothelioma 46 0.052
171
MXD026 Mixed Glioma 45 0.052
172
c SPR009 Sporadic Breast Cancer 45 0.052
173
c LKM005 Leukemia, T-Cell, Chronic 34 0.052
174
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 34 0.052
175
PPL052 Papillomatosis, Confluent and Reticulated 33 0.052
176
P RTN008 Retinitis Pigmentosa 79 0.047
177
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.047
178
c HYP836 Hypercholesterolemia, Familial, 1 73 0.047
179
P PNM007 Pneumonia 68 0.047
180
SKN019 Skin Melanoma 68 0.047
181
c RHB024 Rhabdomyosarcoma 2 67 0.047
182
P SKN015 Skin Carcinoma 66 0.047
183
P VNW001 Von Willebrand's Disease 65 0.047
184
P PRS038 Personality Disorder 65 0.047
185
CLN015 Colon Adenocarcinoma 65 0.047
186
P THY023 Thymoma 65 0.047
187
P HRM001 Hermansky-Pudlak Syndrome 64 0.047
188
SKN016 Skin Disease 63 0.047
189
CLT003 Colitis 62 0.047
190
c HPT001 Hepatitis C 62 0.047
191
P PRP029 Porphyria 62 0.047
192
FTT001 Fatty Liver Disease 61 0.047
193
ORL011 Oral Cancer 60 0.047
194
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.047
195
P BPL003 Bipolar Disorder 56 0.047
196
BCT022 Bacterial Infectious Disease 56 0.047
197
P HYP076 Hyperthyroidism 55 0.047
198
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.047
199
P INF037 Inflammatory Bowel Disease 54 0.047
200
P RTN018 Retinal Disease 53 0.047
201
IMP005 Impotence 52 0.047
202
c THY107 Thymoma, Familial 52 0.047
203
AVD001 Avoidant Personality Disorder 51 0.047
204
AZS001 Azoospermia 50 0.047
205
P MTC133 Mitochondrial Myopathy 49 0.047
206
VCC001 Vaccinia 49 0.047
207
RTN023 Retinitis 46 0.047
208
NRR001 Neuroretinitis 42 0.047
209
c MJR024 Major Affective Disorder 9 41 0.047
210
c MJR022 Major Affective Disorder 8 38 0.047
211
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.047
212
HYP114 Hypertensive Nephropathy 36 0.047
213
c PRS136 Prostate Cancer, Hereditary, 6 33 0.047
214
c PRS130 Prostate Cancer, Hereditary, 8 32 0.047
215
PLY150 Polykaryocytosis Inducer 31 0.047
216
ARG004 Argyria 27 0.047
217
ESP021 Esophageal Cancer 90 0.040
218
c HYP595 Hypertension, Essential 84 0.040
219
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.040
220
AST005 Asthma 76 0.040
221
KPS004 Kaposi Sarcoma 75 0.040
222
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.040
223
c LKM063 Leukemia, Chronic Myeloid 72 0.040
224
DFC004 Deficiency Anemia 70 0.040
225
DWN001 Down Syndrome 70 0.040
226
ADL002 Adult Syndrome 70 0.040
227
PLY001 Polycythemia Vera 69 0.040
228
P LKM062 Leukemia, Acute Lymphoblastic 69 0.040
229
P ESS003 Essential Thrombocythemia 68 0.040
230
BRN024 Bronchitis 68 0.040
231
PNC129 Pancreatic Adenocarcinoma 68 0.040
232
ALL003 Allergic Rhinitis 67 0.040
233
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.040
234
P BRD002 Bardet-Biedl Syndrome 66 0.040
235
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.040
236
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.040
237
P RHB003 Rhabdomyosarcoma 63 0.040
238
ACT119 Acute Promyelocytic Leukemia 63 0.040
239
HMT002 Hematologic Cancer 62 0.040
240
c BRN108 Branchiootic Syndrome 1 62 0.040
241
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.040
242
P ENC018 Encephalopathy 61 0.040
243
P ENC004 Encephalitis 61 0.040
244
P PNC044 Pancreatitis 61 0.040
245
VRL011 Viral Infectious Disease 61 0.040
246
P BNG030 Benign Ependymoma 60 0.040
247
LNG099 Lung Disease 60 0.040
248
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.040
249
THY029 Thyroid Carcinoma 59 0.040
250
CHL123 Chlamydia 59 0.040
251
P MLN069 Melanoma, Uveal 59 0.040
252
P EXN002 Exanthem 57 0.040
253
P RHN004 Rhinitis 57 0.040
254
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.040
255
P PLY018 Polycythemia 56 0.040
256
P FBR017 Fibrosarcoma 56 0.040
257
ALL006 Allergic Asthma 56 0.040
258
PLS011 Plasmacytoma 56 0.040
259
SFT003 Soft Tissue Sarcoma 56 0.040
260
P GST044 Gastritis 56 0.040
261
LMB062 Limb Ischemia 55 0.040
262
P ANT006 Antiphospholipid Syndrome 55 0.040
263
HYP060 Hyperinsulinism 54 0.040
264
GLS001 Gliosarcoma 54 0.040
265
CLL010 Cellular Ependymoma 54 0.040
266
PPL022 Papilloma 54 0.040
267
HMC014 Homocysteinemia 53 0.040
268
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.040
269
THR004 Thrombocytosis 51 0.040
270
ENT011 Enterocolitis 51 0.040
271
RTN003 Retinal Ischemia 50 0.040
272
c LRG001 Large Cell Carcinoma 50 0.040
273
BLD053 Blood Platelet Disease 49 0.040
274
HPR003 Heparin-Induced Thrombocytopenia 48 0.040
275
SQM002 Squamous Cell Papilloma 46 0.040
276
c PCH010 Pachyonychia Congenita 3 44 0.040
277
P EPN001 Ependymoblastoma 44 0.040
278
CVD001 Covid-19 44 0.040
280
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.033
281
P GST053 Gastric Cancer 83 0.033
282
P RHM011 Rheumatoid Arthritis 80 0.033
283
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.033
284
c NRF023 Neurofibromatosis, Type Ii 80 0.033
285
INS024 Insulin-Like Growth Factor I 79 0.033
286
OST012 Osteoarthritis 78 0.033
287
c TBR025 Tuberous Sclerosis 1 77 0.033
288
BRN028 Brain Cancer 74 0.033
289
c MNN043 Meningioma, Familial 74 0.033
290
P CNR004 Cone-Rod Dystrophy 2 73 0.033
291
P JBR020 Joubert Syndrome 1 72 0.033
292
P SRC025 Sarcoidosis 1 70 0.033
293
GST040 Gastric Adenocarcinoma 70 0.033
294
P FRG001 Fragile X Syndrome 70 0.033
295
c CHR684 Chronic Kidney Disease 70 0.033
296
P ART022 Arthritis 69 0.033
297
LYM133 Lymphoma, Hodgkin, Classic 69 0.033
298
P LPR021 Leprosy 3 69 0.033
299
LYM007 Lymphangioleiomyomatosis 69 0.033
300
MNT001 Mantle Cell Lymphoma 69 0.033
301
CNN005 Connective Tissue Disease 68 0.033
302
FCT007 Factor Vii Deficiency 67 0.033
303
P OLG002 Oligodendroglioma 67 0.033
304
P FLL037 Follicular Lymphoma 67 0.033
305
P TRN020 Turner Syndrome 67 0.033
306
FLL027 Fallopian Tube Carcinoma 67 0.033
307
P HYP098 Hypereosinophilic Syndrome 67 0.033
308
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.033
309
P MSC005 Muscular Dystrophy 66 0.033
310
GLN010 Glanzmann Thrombasthenia 66 0.033
311
P NSP012 Nasopharyngeal Carcinoma 66 0.033
312
P ATR011 Atrial Fibrillation 66 0.033
313
P MNN013 Meningitis 66 0.033
314
P DRM053 Dermatitis, Atopic 66 0.033
315
CRN036 Craniopharyngioma 65 0.033
316
c FML001 Familial Atrial Fibrillation 65 0.033
317
P LPS002 Liposarcoma 65 0.033
318
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.033
319
P ADL010 Adult Respiratory Distress Syndrome 65 0.033
320
ANG020 Angiosarcoma 64 0.033
321
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.033
322
KRN002 Kearns-Sayre Syndrome 63 0.033
323
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.033
324
TYP007 Typhoid Fever 63 0.033
325
P LMY004 Leiomyosarcoma 63 0.033
326
RHB001 Rhabdoid Cancer 63 0.033
327
PRM126 Primary Peritoneal Carcinoma 62 0.033
328
MNN042 Meningioma, Radiation-Induced 62 0.033
329
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.033
330
CHL068 Cholestasis 61 0.033
331
P SJG008 Sjogren Syndrome 61 0.033
332
P CTR002 Cataract 60 0.033
333
P CHR285 Chronic Myelomonocytic Leukemia 60 0.033
334
GRD007 Grade Iii Astrocytoma 59 0.033
335
CNT047 Contact Dermatitis 58 0.033
336
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.033
337
CHL028 Childhood Type Dermatomyositis 58 0.033
338
CNS004 Constipation 58 0.033
339
LYM027 Lymphopenia 58 0.033
340
P FNC044 Fanconi Anemia, Complementation Group C 57 0.033
341
P UVT001 Uveitis 57 0.033
342
P PRN023 Prion Disease 57 0.033
343
c MST023 Mesothelioma, Malignant 57 0.033
344
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.033
345
c LKM070 Leukemia, Acute Monocytic 57 0.033
346
P ADL017 Adult T-Cell Leukemia 56 0.033
347
SPN041 Spinal Cord Disease 56 0.033
348
EMB004 Embryonal Carcinoma 56 0.033
349
c BCT007 Bacterial Meningitis 55 0.033
350
DFF005 Diffuse Large B-Cell Lymphoma 55 0.033
351
P DBT005 Diabetes Insipidus 55 0.033
352
P SLM003 Salmonellosis 55 0.033
353
PLM010 Pulmonary Edema 54 0.033
354
P ART021 Arteriosclerosis 54 0.033
355
LYM040 Lymphoblastic Lymphoma 54 0.033
356
SNS003 Sensory Peripheral Neuropathy 54 0.033
357
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.033
358
P PTS002 Ptosis 53 0.033
359
c VRL010 Viral Hepatitis 52 0.033
360
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.033
361
P RCT021 Rectum Cancer 52 0.033
362
THY030 Thyroid Gland Disease 52 0.033
363
P LCT001 Lactic Acidosis 51 0.033
364
P THR015 Thrombophilia 51 0.033
365
CRV040 Cervix Carcinoma 51 0.033
366
SCB001 Scabies 50 0.033
367
SPN021 Spinal Meningioma 50 0.033
368
P SCK005 Sickle Cell Disease 50 0.033
369
MTB004 Metabolic Acidosis 50 0.033
370
P PNB001 Pineoblastoma 50 0.033
371
VRC001 Varicocele 49 0.033
372
c FLL041 Follicular Lymphoma 1 49 0.033
373
URM002 Uremia 49 0.033
374
P CTN015 Cutaneous T Cell Lymphoma 49 0.033
375
ATS010 Autosomal Recessive Disease 48 0.033
376
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.033
377
CRN017 Coronary Thrombosis 47 0.033
378
RNL077 Renal Fibrosis 47 0.033
379
TTR011 Tetraploidy 47 0.033
380
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.033
381
CNT033 Central Nervous System Cancer 47 0.033
382
CRD137 Cardiogenic Shock 47 0.033
383
LYM019 Lymphosarcoma 46 0.033
384
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.033
385
RTN020 Retinal Vascular Disease 46 0.033
386
P CHR573 Choroid Plexus Cancer 46 0.033
387
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.033
388
CWP001 Cowpox 46 0.033
389
LKS001 Leukostasis 46 0.033
390
PNC056 Pineocytoma 45 0.033
391
CRT015 Carotid Artery Occlusion 45 0.033
392
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 45 0.033
393
CYS009 Cystadenoma 44 0.033
394
SPN040 Spinal Cancer 44 0.033
395
c PRM038 Primary Agammaglobulinemia 44 0.033
396
P OVR106 Ovarian Clear Cell Carcinoma 44 0.033
397
CRB090 Cerebral Hypoxia 44 0.033
398
MRG013 Mirage Syndrome 43 0.033
399
ORL015 Oral Squamous Cell Carcinoma 43 0.033
400
HMP009 Haemophilus Influenzae 43 0.033
401
PNL014 Pineal Gland Cancer 41 0.033
402
SCR001 Secretory Meningioma 41 0.033
403
P MLG074 Malignant Mesenchymoma 40 0.033
404
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.033
405
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 40 0.033
406
ASP030 Aspirin Resistance 39 0.033
407
P PRP021 Peripheral Nervous System Neoplasm 39 0.033
408
DBT007 Diabetic Cataract 38 0.033
409
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.033
410
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.033
411
HNS001 Hansen's Disease 34 0.033
412
GRM010 Germ Cells Tumors 34 0.033
413
KDN013 Kidney Hypertrophy 32 0.033
414
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.033
415
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.033
416
INT358 Intestinal Polyposis Syndrome 25 0.033
417
PLT033 Platelet Signal Processing Defect 9 0.033
419
MLR004 Malaria 81 0.023
420
P RTT002 Rett Syndrome 80 0.023
421
PHN003 Phenylketonuria 75 0.023
422
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.023
423
P RSP003 Respiratory Failure 74 0.023
424
SCK003 Sickle Cell Anemia 74 0.023
425
c HMC039 Hemochromatosis, Type 1 74 0.023
426
CRH001 Crohn's Disease 74 0.023
427
P NJM001 Nijmegen Breakage Syndrome 74 0.023
428
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.023
429
ANX010 Anxiety 73 0.023
430
MSC157 Muscular Dystrophy, Duchenne Type 72 0.023
431
SCH036 Scheie Syndrome 72 0.023
432
c TBR026 Tuberous Sclerosis 2 72 0.023
433
P MLT020 Multiple Sclerosis 72 0.023
434
P LFR001 Li-Fraumeni Syndrome 72 0.023
435
P GRF003 Graft-Versus-Host Disease 72 0.023
436
c EXD008 Exudative Vitreoretinopathy 1 71 0.023
437
MYL005 Myelofibrosis 70 0.023
438
LGH007 Leigh Syndrome 70 0.023
439
P OST001 Osteopetrosis 70 0.023
440
P HYP061 Hypertrophic Cardiomyopathy 70 0.023
441
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.023
442
CRT072 Creutzfeldt-Jakob Disease 70 0.023
443
P TBR001 Tuberous Sclerosis 70 0.023
444
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.023
445
P PRM011 Primary Ciliary Dyskinesia 69 0.023
446
P SLP006 Sleep Apnea 69 0.023
447
ART016 Aortic Aneurysm 69 0.023
448
P MYC084 Mycobacterium Tuberculosis 1 68 0.023
449
CHL065 Cholangiocarcinoma 68 0.023
450
P MYS003 Myasthenia Gravis 68 0.023
451
P INF038 Influenza 68 0.023
452
P MJR001 Major Depressive Disorder 68 0.023
453
MLD001 Melioidosis 68 0.023
454
P FRN006 Frontotemporal Dementia 68 0.023
455
P KBK002 Kabuki Syndrome 1 67 0.023
456
P HPT021 Hepatitis 67 0.023
457
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.023
458
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.023
459
P HLP001 Holoprosencephaly 67 0.023
460
BLM001 Bloom Syndrome 67 0.023
461
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.023
462
THY111 Thyroid Carcinoma, Familial Medullary 67 0.023
463
P BLD062 Bile Duct Cancer 67 0.023
464
P MLG056 Malignant Hyperthermia 67 0.023
465
MYC006 Mycosis Fungoides 66 0.023
466
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 66 0.023
467
GLL008 Gilles De La Tourette Syndrome 66 0.023
468
CHD001 Chediak-Higashi Syndrome 66 0.023
469
P DMN002 Dementia 66 0.023
470
c FML021 Familial Hypercholesterolemia 66 0.023
471
c MCR129 Microvascular Complications of Diabetes 1 66 0.023
472
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.023
473
CHG001 Chagas Disease 66 0.023
474
LNG039 Lung Squamous Cell Carcinoma 66 0.023
475
MYL031 Myeloproliferative Neoplasm 66 0.023
476
P NRV007 Nervous System Disease 66 0.023
477
P CNJ013 Conjunctivitis 65 0.023
478
KRT019 Keratitis, Hereditary 65 0.023
479
AFB002 Afibrinogenemia, Congenital 65 0.023
480
P MTR014 Motor Neuron Disease 65 0.023
481
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.023
482
MSM014 Mismatch Repair Cancer Syndrome 65 0.023
483
BRR014 Barrett Esophagus 65 0.023
484
c ART101 Aortic Valve Disease 2 65 0.023
485
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.023
486
MRK001 Merkel Cell Carcinoma 65 0.023
487
c WLM013 Wilms Tumor 1 65 0.023
488
c DBT099 Diabetes Mellitus, Type I 65 0.023
489
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.023
490
NRM005 Neuromuscular Disease 64 0.023
491
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.023
492
c JVN010 Juvenile Rheumatoid Arthritis 64 0.023
493
MSC007 Muscle Hypertrophy 64 0.023
494
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.023
495
MGK001 Megakaryocytic Leukemia 64 0.023
496
HYP020 Hyperprolactinemia 64 0.023
497
LSH001 Leishmaniasis 63 0.023
498
c PRC016 Pre-Eclampsia 63 0.023
499
P ANR048 Aniridia 1 63 0.023
500
PLG002 Plague 63 0.023
501
END041 Endometrial Adenocarcinoma 63 0.023
502
DPR016 Depression 63 0.023
503
P END044 Endometriosis 63 0.023
504
c OPT053 Optic Atrophy 1 63 0.023
505
c FNC043 Fanconi Anemia, Complementation Group E 62 0.023
506
P PLY014 Polycystic Kidney Disease 62 0.023
507
P PSR002 Psoriasis 62 0.023
508
LSC001 Lesch-Nyhan Syndrome 62 0.023
509
BRS099 Breast Ductal Carcinoma 62 0.023
510
CRC021 Carcinosarcoma 62 0.023
511
BLD131 Bladder Urothelial Carcinoma 62 0.023
512
P DRM010 Dermatomyositis 61 0.023
513
MCK005 Mckusick-Kaufman Syndrome 61 0.023
514
DRM006 Dermatitis 61 0.023
515
YLL002 Yellow Fever 61 0.023
516
WLD007 Waldenstroem's Macroglobulinemia 61 0.023
517
c WLM018 Wilms Tumor 5 61 0.023
518
GST033 Gestational Diabetes 61 0.023
519
P HMN010 Hemangioma 61 0.023
520
P KDN017 Kidney Cancer 60 0.023
521
SZR001 Sezary's Disease 60 0.023
522
P TST021 Testicular Germ Cell Tumor 60 0.023
523
c JVN061 Juvenile Arthritis 60 0.023
524
P TXP001 Toxoplasmosis 60 0.023
525
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 0.023
526
P SNS001 Sensorineural Hearing Loss 60 0.023
527
STT001 Status Epilepticus 60 0.023
528
VGN017 Vaginal Cancer 60 0.023
529
P BRN019 Bernard-Soulier Syndrome 60 0.023
530
P OPT006 Optic Nerve Disease 60 0.023
531
SPP011 Suppression of Tumorigenicity 12 59 0.023
532
P RBL001 Rubella 59 0.023
533
P MCR010 Microcephaly 59 0.023
534
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.023
535
c HPT016 Hepatitis B 59 0.023
536
UTR024 Uterine Carcinosarcoma 59 0.023
537
PRN019 Perinatal Necrotizing Enterocolitis 59 0.023
538
VSL002 Visual Epilepsy 59 0.023
539
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.023
540
P CYS018 Cystitis 59 0.023
541
AVN001 Avian Influenza 59 0.023
542
GRY002 Gray Platelet Syndrome 59 0.023
543
BRN002 Bronchiolitis 59 0.023
544
P GLL022 Guillain-Barre Syndrome 59 0.023
545
P DNG005 Dengue Virus 59 0.023
546
P PLY006 Polydactyly 59 0.023
547
PPT005 Peptic Ulcer Disease 59 0.023
548
c ACT073 Acute Leukemia 58 0.023
549
GLB001 Gilbert Syndrome 58 0.023
550
P TYR004 Tyrosinemia 58 0.023
551
CRD132 Cardiac Conduction Defect 58 0.023
552
CHR072 Chordoma 58 0.023
553
c PRG018 Paragangliomas 1 58 0.023
554
BRS051 Breast Disease 58 0.023
555
ADR005 Adrenal Carcinoma 58 0.023
556
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.023
557
EYD002 Eye Disease 58 0.023
558
MNT002 Mental Depression 58 0.023
559
P BNC003 Bone Cancer 58 0.023
560
LNG108 Langerhans Cell Histiocytosis 58 0.023
561
MXD005 Mixed Connective Tissue Disease 58 0.023
562
P GLL018 Gallbladder Cancer 57 0.023
563
P INF032 Infertility 57 0.023
564
P GLM007 Glomerulonephritis 57 0.023
565
GLS018 Glass Syndrome 57 0.023
566
P PLV020 Pelvic Organ Prolapse 57 0.023
567
c CHR417 Chronic Graft Versus Host Disease 57 0.023
568
MCR013 Microphthalmia 57 0.023
569
IRN002 Iron Metabolism Disease 57 0.023
570
MNR012 Meniere Disease 57 0.023
571
P PLY041 Polymyositis 57 0.023
572
P HDC001 Headache 57 0.023
573
DSS009 Disseminated Intravascular Coagulation 57 0.023
574
THY122 Thyroid Gland Cancer 57 0.023
575
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.023
576
APH001 Aphthous Stomatitis 57 0.023
577
BLR008 Bilirubin Metabolic Disorder 57 0.023
578
PGM001 Pigmented Villonodular Synovitis 56 0.023
579
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.023
580
P CHN012 Chondrosarcoma 56 0.023
581
CMR002 Coumarin Resistance 56 0.023
582
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.023
583
P PLY011 Polycystic Ovary Syndrome 56 0.023
584
TRN018 Transitional Cell Carcinoma 56 0.023
585
c ACT134 Acute Liver Failure 56 0.023
586
c ESS001 Essential Tremor 56 0.023
587
P SZR006 Seizure Disorder 56 0.023
588
ALL010 Allergic Contact Dermatitis 56 0.023
589
c BRS110 Breast-Ovarian Cancer, Familial 1 56 0.023
590
ISL001 Islet Cell Tumor 56 0.023
591
P PSD015 Pseudohypoparathyroidism 56 0.023
592
MTH009 Mouth Disease 56 0.023
593
c MCR256 Microphthalmia, Syndromic 9 56 0.023
594
MCR141 Mucormycosis 56 0.023
595
SLC006 Silicosis 56 0.023
596
P PLY019 Polyneuropathy 56 0.023
597
HPT022 Hepatoblastoma 56 0.023
598
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.023
599
BRN012 Bronchiolitis Obliterans 55 0.023
600
HYP005 Hypokalemia 55 0.023
601
NRN004 Neuroendocrine Tumor 55 0.023
602
ADR008 Adrenal Adenoma 55 0.023
603
AMB001 Amebiasis 55 0.023
604
P GRV001 Graves' Disease 55 0.023
605
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.023
606
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.023
607
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.023
608
P LRY044 Larynx Cancer 55 0.023
609
HRY003 Hairy Cell Leukemia 55 0.023
610
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.023
611
SYN007 Synovitis 54 0.023
612
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.023
613
GLC003 Glucose Intolerance 54 0.023
614
c CCK007 Cockayne Syndrome B 54 0.023
615
BRN014 Bronchopneumonia 54 0.023
616
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.023
617
HMS001 Hemosiderosis 54 0.023
618
WST005 West Nile Virus 54 0.023
619
SLP001 Sleeping Sickness 54 0.023
620
P TRM003 Tremor 54 0.023
621
PRS045 Prostatic Hypertrophy 53 0.023
622
CLR030 Clear Cell Renal Cell Carcinoma 53 0.023
623
MMM001 Mammary Paget's Disease 53 0.023
624
RHM028 Rheumatic Heart Disease 53 0.023
625
HRT012 Heart Valve Disease 53 0.023
626
P MNC007 Monocytic Leukemia 53 0.023
627
PRP036 Peripheral T-Cell Lymphoma 53 0.023
628
MST005 Mastitis 53 0.023
629
P HML001 Hemolytic-Uremic Syndrome 53 0.023
630
P HMR003 Hemorrhagic Disease 53 0.023
631
FNG017 Fungal Infectious Disease 53 0.023
632
GSG001 Gas Gangrene 53 0.023
633
GST023 Gastric Ulcer 53 0.023
634
TXC002 Toxic Encephalopathy 53 0.023
635
DNT012 Dental Caries 53 0.023
636
P RTN022 Retinal Vein Occlusion 53 0.023
637
P INT068 Intestinal Disease 53 0.023
638
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.023
639
c CNT035 Central Nervous System Disease 52 0.023
640
CHR073 Choreatic Disease 52 0.023
641
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.023
642
DMY004 Demyelinating Disease 52 0.023
643
P PRG013 Paraganglioma 52 0.023
644
LYS002 Lysosomal Storage Disease 52 0.023
645
ACR041 Acromelic Frontonasal Dysostosis 52 0.023
646
P SML001 Small Cell Carcinoma 52 0.023
647
PST011 Pustulosis of Palm and Sole 52 0.023
648
MRG003 Marginal Zone B-Cell Lymphoma 52 0.023
649
P MSC003 Muscular Atrophy 52 0.023
650
P PRV002 Periventricular Nodular Heterotopia 52 0.023
651
APR001 Apraxia 52 0.023
652
ACT200 Acute Monoblastic Leukemia 52 0.023
653
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 0.023
654
P OVR049 Ovarian Disease 52 0.023
655
P BRN035 Brain Stem Glioma 52 0.023
656
SRS001 Serous Cystadenocarcinoma 52 0.023
657
P TRT010 Teratoma 52 0.023
658
PNG002 Pain Agnosia 51 0.023
659
OCL069 Ocular Motor Apraxia 51 0.023
660
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.023
661
PRS021 Prostatic Adenoma 51 0.023
662
PLS009 Plasma Cell Neoplasm 51 0.023
663
LNG095 Lung Abscess 51 0.023
664
c PNC106 Pancreatic Agenesis 1 51 0.023
665
CYS014 Cystadenocarcinoma 51 0.023
666
INT079 Intrahepatic Cholangiocarcinoma 51 0.023
667
LNG031 Lung Benign Neoplasm 51 0.023
668
HND002 Hand, Foot and Mouth Disease 51 0.023
669
P PST095 Post-Thrombotic Syndrome 51 0.023
670
ASP003 Aseptic Meningitis 51 0.023
671
SKN013 Skin Benign Neoplasm 51 0.023
672
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.023
673
GNT002 Giant Cell Glioblastoma 50 0.023
674
c PRM012 Primary Polycythemia 50 0.023
675
P FNC004 Fanconi Syndrome 50 0.023
676
P OVR082 Overgrowth Syndrome 50 0.023
677
P ECL001 Eclampsia 50 0.023
678
HPT014 Hepatorenal Syndrome 50 0.023
679
CRN030 Coronary Stenosis 50 0.023
680
c MTC059 Mitochondrial Dna Depletion Syndrome 5 50 0.023
681
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.023
682
FSC004 Fasciitis 50 0.023
683
c INF145 Infantile Liver Failure Syndrome 1 50 0.023
684
TRY001 Trypanosomiasis 50 0.023
685
TRP002 Tropical Spastic Paraparesis 50 0.023
686
CLR003 Clear Cell Adenocarcinoma 50 0.023
687
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.023
688
OCL022 Ocular Melanoma 50 0.023
689
c INF023 Inflammatory Breast Carcinoma 50 0.023
690
P ATR005 Atrophic Gastritis 50 0.023
691
c FML347 Familial Adenomatous Polyposis 2 50 0.023
692
DBT004 Diabetic Polyneuropathy 49 0.023
693
ATY042 Atypical Chronic Myeloid Leukemia 49 0.023
694
c CHR418 Chronic Leukemia 49 0.023
695
INP001 Inappropriate Adh Syndrome 49 0.023
696
c THR090 Thrombocythemia 1 49 0.023
697
ENT004 Enthesopathy 49 0.023
698
CHL018 Childhood Medulloblastoma 49 0.023
699
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.023
700
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.023
701
MCN001 Mucinous Adenocarcinoma 49 0.023
702
P ART018 Aortic Valve Insufficiency 49 0.023
703
PRS129 Prostatic Hyperplasia, Benign 49 0.023
704
MCR004 Macroglobulinemia 49 0.023
705
c OST126 Osteopetrosis, Autosomal Recessive 1 49 0.023
706
GST049 Gastrointestinal System Cancer 49 0.023
707
c TCL005 T-Cell Prolymphocytic Leukemia 49 0.023
708
P CRV031 Cervical Adenocarcinoma 49 0.023
709
c FNC028 Fanconi Anemia, Complementation Group L 49 0.023
710
LRN003 Learning Disability 49 0.023
711
HST010 Histiocytosis 48 0.023
712
HYP043 Hyperandrogenism 48 0.023
713
INT054 Intraocular Lymphoma 48 0.023
714
NCR007 Necrotizing Fasciitis 48 0.023
715
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.023
716
CLS016 Clostridium Difficile Colitis 48 0.023
717
PNC034 Pancreas Disease 48 0.023
718
END062 Endometrial Hyperplasia 48 0.023
719
c BRD015 Bardet-Biedl Syndrome 3 48 0.023
720
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.023
721
RCT020 Rectum Adenocarcinoma 48 0.023
722
ADN009 Adenosquamous Carcinoma 47 0.023
723
GRM005 Germ Cell Cancer 47 0.023
724
PRL017 Prolymphocytic Leukemia 47 0.023
725
ASB001 Asbestosis 47 0.023
726
c PRK085 Parkinson Disease 1, Autosomal Dominant 47 0.023
727
PPL002 Papillary Carcinoma 47 0.023
728
THY128 Thyroid Tumor 47 0.023
729
CRN027 Corneal Neovascularization 47 0.023
730
NRN001 Neuroendocrine Carcinoma 47 0.023
731
STR089 Storage Pool Platelet Disease 47 0.023
732
RTC005 Reticulosarcoma 47 0.023
733
LYM012 Lymphoplasmacytic Lymphoma 47 0.023
734
LNG020 Lung Oat Cell Carcinoma 47 0.023
735
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.023
736
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 47 0.023
737
GST071 Gastrointestinal Carcinoma 47 0.023
738
PLS025 Plasmablastic Lymphoma 47 0.023
739
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.023
740
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.023
741
TST044 Testicular Torsion 47 0.023
742
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.023
743
TST014 Testicular Cancer 46 0.023
744
CLN045 Colonic Benign Neoplasm 46 0.023
745
ANP006 Anaplastic Ependymoma 46 0.023
746
CHN056 Chondrosarcoma, Extraskeletal Myxoid 46 0.023
747
GST012 Gastroesophageal Junction Adenocarcinoma 46 0.023
748
c DRR009 Diarrhea 6 46 0.023
749
c FNC045 Fanconi Anemia, Complementation Group F 46 0.023
750
PHS014 Phosphoglycerate Kinase 1 Deficiency 46 0.023
751
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.023
752
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.023
753
c LFR007 Li-Fraumeni Syndrome 2 45 0.023
754
PPL018 Papillary Adenocarcinoma 45 0.023
755
URT010 Ureteral Obstruction 45 0.023
756
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.023
757
STS002 Situs Inversus 45 0.023
758
LYM051 Lymphomatoid Granulomatosis 45 0.023
759
URT051 Ureter, Cancer of 45 0.023
760
P END084 Endocrine System Disease 45 0.023
761
ATN004 Autonomic Neuropathy 45 0.023
762
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.023
763
FML005 Female Reproductive Endometrioid Cancer 45 0.023
764
OVR112 Ovarian Germ Cell Cancer 45 0.023
765
P DFF019 Diffuse Gastric Cancer 45 0.023
766
MXD023 Mixed Cell Type Cancer 44 0.023
767
c JVN003 Juvenile Xanthogranuloma 44 0.023
768
APP009 Appendix Adenocarcinoma 44 0.023
769
IMM064 Immunodeficiency, Common Variable, 10 44 0.023
770
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.023
771
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.023
772
HPT067 Hepatocellular Adenoma 44 0.023
773
NTM002 Nut Midline Carcinoma 44 0.023
774
c DFN196 Deafness, Autosomal Dominant 22 44 0.023
775
P FBR003 Fibrous Histiocytoma 44 0.023
776
PRT035 Peritoneum Cancer 44 0.023
777
ART006 Arthus Reaction 44 0.023
778
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.023
779
P CRN024 Corneal Disease 44 0.023
780
END085 Endometrial Serous Adenocarcinoma 44 0.023
781
ANP009 Anaplastic Oligodendroglioma 43 0.023
782
FLL013 Follicular Dendritic Cell Sarcoma 43 0.023
783
CLP005 Ciliopathy 43 0.023
784
MND023 Mend Syndrome 43 0.023
785
SMN007 Seminoma 43 0.023
786
P TST026 Testicular Germ Cell Cancer 43 0.023
787
QBC001 Quebec Platelet Disorder 43 0.023
788
TST015 Testicular Disease 43 0.023
789
BNM001 Bone Marrow Cancer 43 0.023
790
LWC001 Low Compliance Bladder 43 0.023
791
MYC013 Mycobacterium Abscessus 43 0.023
792
PRS042 Prostate Disease 43 0.023
793
P HYP265 Hypotonia 43 0.023
794
P MJR007 Major Affective Disorder 1 43 0.023
795
BLR013 Biliary Tract Cancer 42 0.023
796
MST004 Mast Cell Neoplasm 42 0.023
797
TRP009 Triple X Syndrome 42 0.023
798
PNM013 Pneumococcal Meningitis 42 0.023
799
c RTN047 Retinitis Pigmentosa 18 42 0.023
800
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.023
801
OVR044 Ovarian Carcinosarcoma 42 0.023
802
GST105 Gastroesophageal Adenocarcinoma 42 0.023
803
BCK006 Back Pain 42 0.023
804
ATX019 Ataxia with Vitamin E Deficiency 42 0.023
805
c MLG079 Malignant Pleural Mesothelioma 42 0.023
806
OBS082 Obstructive Nephropathy 42 0.023
807
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.023
808
VLL003 Villonodular Synovitis 42 0.023
809
c WLF009 Wolfram Syndrome 2 42 0.023
810
EHR002 Ehrlichiosis 42 0.023
811
c MLG064 Malignant Ependymoma 41 0.023
812
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 41 0.023
813
P KLZ004 Kala-Azar 1 41 0.023
814
49X006 49, Xxxxy Syndrome 41 0.023
815
DBT002 Diabetic Autonomic Neuropathy 41 0.023
816
P RRH023 Rare Hereditary Hemochromatosis 41 0.023
817
PCD001 Pica Disease 41 0.023
818
c FNC030 Fanconi Anemia, Complementation Group G 41 0.023
819
P RRT020 Rare Tumor 41 0.023
820
c MCR112 Microvascular Complications of Diabetes 2 41 0.023
821
GRM004 Germinoma 40 0.023
822
MCN008 Mucinous Cystadenocarcinoma 40 0.023
823
PPL007 Papillary Serous Adenocarcinoma 40 0.023
824
MLR006 Male Reproductive Organ Cancer 40 0.023
825
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.023
826
PLY100 Polyploidy 40 0.023
827
CHL045 Choline Deficiency Disease 39 0.023
828
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.023
829
HST016 Histiocytic Sarcoma 39 0.023
830
SKN020 Skin Papilloma 39 0.023
831
FLL031 Follicular Adenoma 39 0.023
832
CRV045 Cervical Intraepithelial Neoplasia 39 0.023
833
PCH007 Pouchitis 39 0.023
834
MYL057 Myelopathy, Htlv-1-Associated 39 0.023
835
TNP004 Tn Polyagglutination Syndrome 39 0.023
836
FML039 Female Reproductive System Disease 39 0.023
837
DSS010 Dissociative Disorder 39 0.023
838
AMP013 Ampulla of Vater Cancer 39 0.023
839
c CHR682 Chronic Bilirubin Encephalopathy 39 0.023
840
SCR011 Scrapie 39 0.023
841
EXT007 Extracutaneous Mastocytoma 38 0.023
842
SPS019 Spastic Paraparesis 38 0.023
843
P OVR010 Ovarian Brenner Tumor 38 0.023
844
NST002 Nestor-Guillermo Progeria Syndrome 38 0.023
845
SHW001 Shwartzman Phenomenon 37 0.023
846
STR077 Streptococcal Toxic-Shock Syndrome 37 0.023
847
GLM044 Glomerular Disease 37 0.023
848
OCL015 Oculomotor Apraxia 37 0.023
849
c CHR020 Chronic Interstitial Cystitis 37 0.023
850
HRN029 Hearing Loss, Noise-Induced 37 0.023
851
c WLM011 Wilms Tumor 6 37 0.023
852
c ATS282 Autosomal Recessive Malignant Osteopetrosis 37 0.023
853
SYS071 Systemic Autoimmune Disease 37 0.023
854
P PHC019 Pheochromocytoma-Paraganglioma 36 0.023
855
BRN018 Borna Disease 36 0.023
856
PLC002 Plica Syndrome 36 0.023
857
ASC009 Ascites, Chylous 35 0.023
858
MTG002 Mutagen Sensitivity 35 0.023
859
c WLL036 Weill-Marchesani Syndrome 1 35 0.023
860
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.023
861
P EXT030 Extraosseous Chondrosarcoma 35 0.023
862
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 35 0.023
863
c RTN152 Retinitis Pigmentosa 66 34 0.023
864
MLR007 Male Reproductive System Disease 34 0.023
865
NNT024 Neonatal Stroke 34 0.023
866
c ADL008 Adult Oligodendroglioma 34 0.023
867
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.023
868
c CHR064 Chronic Monocytic Leukemia 33 0.023
869
LTT002 Letterer-Siwe Disease 33 0.023
870
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.023
871
P MYX008 Myxoid Chondrosarcoma 32 0.023
872
HMN002 Human Granulocytic Anaplasmosis 32 0.023
873
FLL003 Fallopian Tube Endometrioid Adenocarcinoma 32 0.023
874
HGH041 High-Grade Astrocytoma 32 0.023
875
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.023
876
FLL015 Fallopian Tube Serous Adenocarcinoma 31 0.023
877
c HYP708 Hyperaldosteronism, Familial, Type Iv 30 0.023
878
c ADL054 Adult Brain Stem Glioma 30 0.023
879
ACT228 Acute Radiation Syndrome 29 0.023
880
UND007 Undifferentiated Connective Tissue Disease 29 0.023
881
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.023
882
ISL099 Isolated Methylmalonic Acidemia 29 0.023
883
c FML339 Familial Adenomatous Polyposis 4 29 0.023
884
OCC001 Occupational Dermatitis 29 0.023
885
PLT031 Platelet Membrane Fluidity 29 0.023
886
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.023
888
FLL022 Fallopian Tube Clear Cell Adenocarcinoma 28 0.023
889
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.023
890
c FML299 Familial Adenomatous Polyposis 3 28 0.023
891
CYT018 Cytochrome P450 2d6 Variant 27 0.023
892
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 27 0.023
893
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.023
894
CHL079 Children's Interstitial Lung Disease 26 0.023
895
MST020 Mast Cell Activation Syndrome 26 0.023
896
STR033 Storm Syndrome 26 0.023
897
SPN026 Spinal Cord Lymphoma 26 0.023
898
MLG164 Malignant Epithelial Tumor of Ovary 26 0.023
899
ASB003 Asbestos Intoxication 26 0.023
900
SHR097 Short Tarsus with Absence of Lower Eyelashes 26 0.023
901
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.023
902
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.023
903
c CLR068 Ciliary Dyskinesia, Primary, 5 25 0.023
904
c BLD133 Bleeding Disorder, Platelet-Type, 20 24 0.023
905
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.023
906
c RTN032 Retinal Cone Dystrophy 1 24 0.023
907
PRD041 Periodic Fever, Menstrual Cycle-Dependent 24 0.023
908
c JBR047 Joubert Syndrome 35 24 0.023
909
BLD163 Blood Group, Dombrock System 24 0.023
910
NRD058 Neurodegeneration, Childhood-Onset, Stress-Induced, with Variable Ataxia and Seizures 24 0.023
911
RTN216 Retinitis Pigmentosa 82 with or Without Situs Inversus 23 0.023
912
c BRN132 Bernard-Soulier Syndrome, Type A2, Autosomal Dominant 23 0.023
913
HDG004 Hodgkin's Granuloma 23 0.023
914
P ZNC008 Zinc Finger Protein 1 22 0.023
915
c PRS080 Prostate Cancer, Hereditary, 7 22 0.023
916
CHL131 Chlorpropamide-Alcohol Flushing 22 0.023
917
HDG006 Hodgkin's Paragranuloma 22 0.023
918
NCL007 Nuclear Gene-Encoded Leigh Syndrome 22 0.023
919
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.023
920
IQS001 Iqsec2 19 0.023
921
NRN046 Neuronal Tumor 18 0.023
922
c MLG023 Malignant Adult Ependymoma 15 0.023
923
PNL001 Pineal Gland Astrocytoma 14 0.023
924
OVR040 Ovarian Clear Cell Cystadenocarcinoma 13 0.023
925
UND002 Undifferentiated Carcinoma of the Corpus Uteri 12 0.023
926
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.023
927
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 7 0.023
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