Search results for AS 101

807 hits were found for AS 101

# Family MCID Name MIFTS Score
1
P LYM118 Lymphoma 68 0.200
2
P ADN016 Adenocarcinoma 64 0.189
3
P BRS047 Breast Cancer 97 0.180
4
P OVR042 Ovarian Cancer 88 0.180
5
P CLR023 Colorectal Cancer 99 0.173
6
DPR016 Depression 63 0.170
7
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.165
8
P MYL006 Myeloid Leukemia 60 0.165
9
ANR040 Aneurysm 59 0.162
10
P NTR004 Neutropenia 63 0.162
11
P HPT023 Hepatocellular Carcinoma 100 0.159
12
P KDN018 Kidney Disease 72 0.157
13
MYL069 Myeloma, Multiple 85 0.157
14
GLB015 Glioblastoma Multiforme 75 0.156
15
P LKM002 Leukemia 68 0.155
16
c LKM061 Leukemia, Acute Myeloid 84 0.153
17
P DRR001 Diarrhea 55 0.153
18
P VSC011 Vasculitis 62 0.151
19
P GST053 Gastric Cancer 83 0.151
20
P PRS040 Prostate Cancer 97 0.150
21
MNT002 Mental Depression 58 0.150
22
ATM095 Autoimmune Disease 62 0.149
23
P PNC035 Pancreatic Cancer 84 0.148
24
P LVR013 Liver Disease 68 0.147
25
48X005 48,xyyy 39 0.146
26
P NRP001 Neuropathy 56 0.145
27
ADN018 Adenoma 59 0.144
28
P BCL017 B-Cell Lymphoma 58 0.144
29
CNG034 Congestive Heart Failure 69 0.143
30
HMN044 Human Immunodeficiency Virus Type 1 71 0.143
31
ANX010 Anxiety 73 0.143
32
c SYS001 Systemic Lupus Erythematosus 86 0.142
33
THY029 Thyroid Carcinoma 59 0.141
34
P GLM045 Glioma 63 0.141
35
GLL048 Glial Tumor 45 0.140
36
P BLD134 Bladder Cancer 79 0.139
37
LNG099 Lung Disease 60 0.138
38
P HRT032 Heart Disease 75 0.137
39
P LKM062 Leukemia, Acute Lymphoblastic 69 0.136
40
CRH001 Crohn's Disease 74 0.136
41
SQM006 Squamous Cell Carcinoma 60 0.134
42
P MLN008 Melanoma 69 0.134
43
DYS073 Dysphagia 50 0.133
44
ISC004 Ischemia 58 0.133
45
P INF032 Infertility 57 0.133
46
P SZR006 Seizure Disorder 56 0.133
47
P NRB001 Neuroblastoma 72 0.131
48
LPP008 Lipoprotein Quantitative Trait Locus 62 0.129
49
LVR012 Liver Cirrhosis 62 0.128
50
PLM033 Pulmonary Embolism 59 0.128
51
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.128
52
DRM006 Dermatitis 61 0.128
53
VSL002 Visual Epilepsy 59 0.127
54
P END033 Endocarditis 57 0.127
55
P HDC001 Headache 57 0.126
56
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.126
57
P LPS004 Lupus Erythematosus 61 0.125
58
PNM008 Pneumothorax 56 0.125
59
SRC014 Sarcoma 65 0.124
60
SPN035 Spindle Cell Sarcoma 53 0.123
61
END086 End Stage Renal Disease 51 0.123
62
DWN001 Down Syndrome 70 0.122
63
P MNN013 Meningitis 66 0.122
64
P EXN002 Exanthem 57 0.122
65
LYM133 Lymphoma, Hodgkin, Classic 69 0.121
66
P THR014 Thrombocytopenia 67 0.121
67
P ENC018 Encephalopathy 61 0.121
68
BCK006 Back Pain 42 0.119
69
ALC007 Alcohol Dependence 66 0.119
70
OST159 Osteogenic Sarcoma 66 0.119
71
c CHR684 Chronic Kidney Disease 70 0.119
72
P LKM071 Leukemia, Chronic Lymphocytic 79 0.118
73
P HYP086 Hypothyroidism 69 0.118
74
P END044 Endometriosis 63 0.118
75
P BPL003 Bipolar Disorder 56 0.118
76
P MJR001 Major Depressive Disorder 68 0.118
77
CRV035 Cervical Cancer 76 0.117
78
ART140 Arteries, Anomalies of 52 0.117
79
P SRC025 Sarcoidosis 1 70 0.117
80
c MJR024 Major Affective Disorder 9 41 0.117
81
c MJR022 Major Affective Disorder 8 38 0.117
82
47X002 47,xyy 49 0.116
83
P CRN300 Coronary Heart Disease 1 63 0.116
84
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.115
85
P RCT021 Rectum Cancer 52 0.115
86
P ATS364 Autism 70 0.115
87
c HYP836 Hypercholesterolemia, Familial, 1 73 0.115
88
DFF005 Diffuse Large B-Cell Lymphoma 55 0.115
89
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.115
90
c THR092 Thrombophilia Due to Thrombin Defect 73 0.115
91
CYS001 Cystic Fibrosis 81 0.114
92
P INF037 Inflammatory Bowel Disease 54 0.114
93
PRT036 Peritonitis 64 0.114
94
P PRD008 Periodontitis 64 0.114
95
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.114
96
P OST002 Osteoporosis 74 0.113
97
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.112
98
c PRM038 Primary Agammaglobulinemia 44 0.112
99
IMM167 Immune Deficiency Disease 78 0.112
100
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.111
101
PNG002 Pain Agnosia 51 0.111
102
P ENC004 Encephalitis 61 0.111
103
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.110
104
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.110
105
P CRD119 Cardiac Arrest 67 0.110
106
DFC004 Deficiency Anemia 70 0.110
107
P INS002 in Situ Carcinoma 53 0.109
108
P RHM011 Rheumatoid Arthritis 80 0.109
109
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.109
110
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.108
111
CNS004 Constipation 58 0.108
112
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.108
113
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.108
114
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.108
115
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.108
116
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.108
117
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.108
118
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.108
119
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.108
120
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.108
121
CLT003 Colitis 62 0.108
122
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.108
123
PRP030 Purpura 54 0.108
124
ESP021 Esophageal Cancer 90 0.108
125
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.108
126
P RSP003 Respiratory Failure 74 0.108
127
TXC005 Toxic Shock Syndrome 62 0.107
128
c ATR087 Atrial Standstill 1 75 0.106
129
P PNC044 Pancreatitis 61 0.106
130
OST012 Osteoarthritis 78 0.106
131
THR024 Thrombosis 57 0.106
132
ART016 Aortic Aneurysm 69 0.105
133
c SVR001 Severe Acute Respiratory Syndrome 62 0.105
134
P ALC033 Alcohol Use Disorder 58 0.105
135
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.105
136
P PLM037 Pulmonary Hypertension 67 0.105
137
LYM019 Lymphosarcoma 46 0.104
138
P PNM007 Pneumonia 68 0.104
139
P MLT020 Multiple Sclerosis 72 0.104
140
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.104
141
APP008 Appendicitis 61 0.104
142
P LTR001 Lateral Sclerosis 54 0.104
143
SPN186 Spinal Cord Injury 60 0.104
144
P AMY004 Amyloidosis 70 0.104
145
MLR004 Malaria 81 0.104
146
ULC004 Ulcerative Colitis 73 0.104
147
P ART022 Arthritis 69 0.103
148
P EPL164 Epilepsy 71 0.103
149
PLM001 Pulmonary Tuberculosis 69 0.103
150
P ART005 Arteriovenous Malformation 65 0.103
151
BCT022 Bacterial Infectious Disease 56 0.103
152
P GST044 Gastritis 56 0.102
153
NRT001 Neurotic Disorder 53 0.102
154
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.102
155
P LNG064 Lung Cancer Susceptibility 3 78 0.102
156
OST017 Osteomyelitis 64 0.102
157
c ACT027 Acute Pancreatitis 60 0.102
158
P HYD006 Hydrocephalus 66 0.102
159
ACQ007 Acquired Immunodeficiency Syndrome 60 0.102
160
OCL069 Ocular Motor Apraxia 51 0.102
161
c ACT073 Acute Leukemia 58 0.101
162
TTN003 Tetanus 65 0.101
163
c HYP595 Hypertension, Essential 84 0.100
164
c HPT073 Hepatitis C Virus 72 0.100
165
P HYP069 Hyperparathyroidism 63 0.100
166
P KDN017 Kidney Cancer 60 0.099
167
END040 Endogenous Depression 55 0.099
168
P HRP006 Herpes Simplex 65 0.099
169
SKN016 Skin Disease 63 0.098
170
c ATS007 Autism Spectrum Disorder 67 0.098
171
P PSR002 Psoriasis 62 0.098
172
HLX001 Helix Syndrome 47 0.097
173
END057 Endometrial Cancer 74 0.097
174
SYN036 Syncope 45 0.097
175
CVD001 Covid-19 44 0.097
176
PST011 Pustulosis of Palm and Sole 52 0.097
177
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.096
178
AST005 Asthma 76 0.096
179
P PRS038 Personality Disorder 65 0.096
180
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.096
181
P MYP004 Myopathy 70 0.096
182
P CTR002 Cataract 60 0.096
183
MYL009 Myelodysplastic Syndrome 70 0.095
184
CHL067 Cholecystitis 57 0.095
185
P TRM003 Tremor 54 0.094
186
P AST007 Astrocytoma 51 0.094
187
IMP005 Impotence 52 0.094
188
ADL002 Adult Syndrome 70 0.094
189
P INF038 Influenza 68 0.094
190
P BNG032 Benign Mesothelioma 46 0.093
191
MNN042 Meningioma, Radiation-Induced 62 0.093
192
P THL005 Thalassemia 60 0.093
193
c MNN043 Meningioma, Familial 74 0.093
194
MSL001 Measles 62 0.093
195
PRP016 Paraplegia 52 0.093
196
c HPT001 Hepatitis C 62 0.093
197
P PRP019 Peripheral Nervous System Disease 58 0.093
198
c SCL052 Scleroderma, Familial Progressive 61 0.093
199
SPN021 Spinal Meningioma 50 0.093
200
SCR001 Secretory Meningioma 41 0.093
201
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.093
202
MDD011 Mood Disorder 62 0.093
203
DSS008 Disease of Mental Health 58 0.092
204
IRN002 Iron Metabolism Disease 57 0.092
205
CHR178 Chromosomal Triplication 35 0.092
206
AGN016 Aging 56 0.092
207
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.092
208
SPL018 Splenomegaly 48 0.092
209
P SNS001 Sensorineural Hearing Loss 60 0.091
210
P CND004 Candidiasis 58 0.091
211
P HMN010 Hemangioma 61 0.091
212
P HYP076 Hyperthyroidism 55 0.091
213
PRS045 Prostatic Hypertrophy 53 0.091
214
HDN002 Head Injury 46 0.091
215
c BRN108 Branchiootic Syndrome 1 62 0.090
216
VRC005 Varicose Veins 60 0.090
217
OTT002 Otitis Media 72 0.090
218
CLL003 Cellulitis 54 0.090
219
P FLL037 Follicular Lymphoma 67 0.090
220
HNS001 Hansen's Disease 34 0.090
221
P LPR021 Leprosy 3 69 0.089
222
CHL123 Chlamydia 59 0.089
223
CHG001 Chagas Disease 66 0.089
224
c LKM063 Leukemia, Chronic Myeloid 72 0.088
225
GTR002 Goiter 53 0.088
226
P UVT001 Uveitis 57 0.088
227
PRT013 Portal Hypertension 59 0.088
228
OVR094 Ovarian Epithelial Cancer 38 0.087
229
P SBS003 Substance Abuse 55 0.087
230
INF034 Infective Endocarditis 53 0.087
231
SBC016 Subacute Delirium 44 0.087
232
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.087
233
P MSC005 Muscular Dystrophy 66 0.086
234
c RHB024 Rhabdomyosarcoma 2 67 0.086
235
SKN019 Skin Melanoma 68 0.086
236
ATX019 Ataxia with Vitamin E Deficiency 42 0.086
237
ORL011 Oral Cancer 60 0.086
238
P OPN001 Open-Angle Glaucoma 49 0.086
239
PPT005 Peptic Ulcer Disease 59 0.086
240
PSY004 Psychotic Disorder 67 0.086
241
P HML002 Hemolytic Anemia 63 0.086
242
c VRL010 Viral Hepatitis 52 0.086
243
PRC013 Pericarditis 54 0.085
244
P RTN024 Retinoblastoma 73 0.085
245
P MCR115 Microvascular Complications of Diabetes 5 66 0.085
246
P SCL018 Scoliosis 60 0.084
247
c FML008 Familial Retinoblastoma 53 0.084
248
P OBS001 Obstructive Jaundice 50 0.084
249
P TRN020 Turner Syndrome 67 0.084
250
P OPT006 Optic Nerve Disease 60 0.084
251
SFT003 Soft Tissue Sarcoma 56 0.084
252
P ART023 Arthropathy 62 0.084
253
GST045 Gastroenteritis 59 0.084
254
CRD137 Cardiogenic Shock 47 0.084
255
CHL065 Cholangiocarcinoma 68 0.083
256
ETN001 Eating Disorder 60 0.083
257
P NSP012 Nasopharyngeal Carcinoma 66 0.083
258
INT075 Intracranial Hypertension 53 0.083
259
ECT026 Ectopic Pregnancy 50 0.083
260
INT079 Intrahepatic Cholangiocarcinoma 51 0.083
261
P FBR017 Fibrosarcoma 56 0.083
262
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.082
263
ING001 Inguinal Hernia 60 0.082
264
P HPT021 Hepatitis 67 0.082
265
P SCK005 Sickle Cell Disease 50 0.082
266
EXP004 Exophthalmos 52 0.082
267
P STR020 Strabismus 55 0.081
268
P SYS005 Systemic Scleroderma 68 0.081
269
MCH006 Mechanical Strabismus 42 0.081
270
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.081
271
ORL015 Oral Squamous Cell Carcinoma 43 0.080
272
RCK004 Rickets 68 0.080
273
PLM010 Pulmonary Edema 54 0.080
274
PRS021 Prostatic Adenoma 51 0.080
275
c BTT014 Beta-Thalassemia 74 0.080
276
DPH001 Diphtheria 60 0.079
277
PRS129 Prostatic Hyperplasia, Benign 49 0.079
278
MNT001 Mantle Cell Lymphoma 69 0.079
279
CNT047 Contact Dermatitis 58 0.078
280
CRD132 Cardiac Conduction Defect 58 0.078
281
OST003 Osteonecrosis 61 0.078
282
ENT004 Enthesopathy 49 0.078
283
PLC002 Plica Syndrome 36 0.078
284
THR016 Thrombophlebitis 51 0.078
285
P THY032 Thyroiditis 52 0.078
286
SYN007 Synovitis 54 0.077
287
P DYS154 Dystonia 65 0.077
288
ART074 Aortic Dissection 52 0.077
289
GST092 Gastroesophageal Reflux 67 0.077
290
PPL022 Papilloma 54 0.077
291
GT001 Gout 64 0.077
292
TRN018 Transitional Cell Carcinoma 56 0.076
293
HRP004 Herpes Zoster 60 0.076
294
P MSC003 Muscular Atrophy 52 0.076
295
P MYC084 Mycobacterium Tuberculosis 1 68 0.076
296
P OVR082 Overgrowth Syndrome 50 0.076
297
CHL068 Cholestasis 61 0.076
298
P PYL005 Pyelonephritis 56 0.075
299
c MLG068 Malignant Glioma 46 0.075
300
P BND020 Bone Disease 59 0.075
301
PLR007 Pleural Empyema 50 0.075
302
LMY002 Leiomyoma 52 0.075
303
HYD002 Hydronephrosis 60 0.074
304
HST010 Histiocytosis 48 0.074
305
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.074
306
c ACT134 Acute Liver Failure 56 0.074
307
P ESP024 Esophagitis 62 0.074
308
HYP005 Hypokalemia 55 0.074
309
c LKM005 Leukemia, T-Cell, Chronic 34 0.074
310
P GLM040 Glioma Susceptibility 1 81 0.074
311
ENT011 Enterocolitis 51 0.074
312
SQM002 Squamous Cell Papilloma 46 0.074
313
EYD002 Eye Disease 58 0.074
314
P MYS005 Myositis 56 0.073
315
CRV045 Cervical Intraepithelial Neoplasia 39 0.073
316
TRN015 Transient Cerebral Ischemia 63 0.073
317
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.073
318
DCT002 Ductal Carcinoma in Situ 59 0.073
319
P NRF002 Neurofibromatosis 56 0.073
320
AMN003 Amnestic Disorder 54 0.073
321
FSC004 Fasciitis 50 0.073
322
P CYS018 Cystitis 59 0.073
323
c GLC092 Glaucoma, Primary Open Angle 62 0.073
324
c GLL024 Gallbladder Disease 1 53 0.073
325
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.073
326
NRT004 Neuritis 52 0.073
327
INT007 Intermediate Coronary Syndrome 55 0.072
328
PTH003 Pathologic Nystagmus 52 0.072
329
P DRM010 Dermatomyositis 61 0.072
330
LYM021 Lymphadenitis 57 0.072
331
GST040 Gastric Adenocarcinoma 70 0.071
332
BRK010 Burkitt Lymphoma 67 0.071
333
CNN005 Connective Tissue Disease 68 0.071
334
ANR007 Anorexia Nervosa 63 0.071
335
AVD001 Avoidant Personality Disorder 51 0.071
336
CHL004 Cholelithiasis 49 0.070
337
P HYP061 Hypertrophic Cardiomyopathy 70 0.070
338
P MYS003 Myasthenia Gravis 68 0.070
339
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.070
340
P GRV001 Graves' Disease 55 0.070
341
MYL005 Myelofibrosis 70 0.070
342
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.070
343
P ART021 Arteriosclerosis 54 0.070
344
ACR007 Acromegaly 71 0.070
345
IRR002 Irritable Bowel Syndrome 65 0.069
346
c HPT003 Hepatitis a 62 0.069
347
MTB004 Metabolic Acidosis 50 0.069
348
P DNG005 Dengue Virus 59 0.069
349
P HYP750 Hypertriglyceridemia, Familial 62 0.069
350
P SLP005 Sleep Disorder 59 0.069
351
PLS011 Plasmacytoma 56 0.069
352
P DBT005 Diabetes Insipidus 55 0.068
353
INT066 Interstitial Lung Disease 60 0.068
354
ATR057 Atrioventricular Block 55 0.068
355
ART002 Arts Syndrome 64 0.068
356
DMY004 Demyelinating Disease 52 0.068
357
HRT011 Heart Septal Defect 50 0.068
358
P TMP003 Temporal Arteritis 68 0.067
359
RBS001 Rabies 58 0.067
360
BRN028 Brain Cancer 74 0.067
361
AMN001 Amenorrhea 54 0.067
362
VLV047 Volvulus of Midgut 49 0.067
363
CRP001 Carpal Tunnel Syndrome 67 0.067
364
CYT008 Cytomegalovirus Infection 57 0.066
365
P HMP007 Hemophilia 51 0.066
366
LKP003 Leukoplakia 39 0.066
367
BRN002 Bronchiolitis 59 0.066
368
SPS057 Spasticity 45 0.066
369
NRL016 Neural Tube Defects 82 0.065
370
P MJR007 Major Affective Disorder 1 43 0.065
371
HYP014 Hyperuricemia 52 0.065
372
LYM040 Lymphoblastic Lymphoma 54 0.065
373
CRN030 Coronary Stenosis 50 0.064
374
P BRS044 Breast Adenocarcinoma 59 0.064
375
LPT014 Leptin Deficiency or Dysfunction 74 0.064
376
c HPT007 Hepatitis E 53 0.064
377
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.064
378
FDL002 Food Allergy 51 0.064
379
WST005 West Nile Virus 54 0.064
380
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.064
381
P CHN012 Chondrosarcoma 56 0.063
382
NRN004 Neuroendocrine Tumor 55 0.063
383
SXL003 Sexual Disorder 47 0.063
384
LYM027 Lymphopenia 58 0.063
385
ATS010 Autosomal Recessive Disease 48 0.063
386
IGR001 Ige Responsiveness, Atopic 59 0.062
387
PST092 Posttransplant Acute Limbic Encephalitis 29 0.062
388
P NRV007 Nervous System Disease 66 0.062
389
ALL010 Allergic Contact Dermatitis 56 0.062
390
HPT004 Hepatic Coma 45 0.062
391
P OVR046 Ovarian Cyst 47 0.062
392
CYS005 Cysticercosis 53 0.062
393
CRT072 Creutzfeldt-Jakob Disease 70 0.062
394
SPT004 Septic Arthritis 58 0.061
395
P OPT009 Optic Neuritis 57 0.061
396
PRN019 Perinatal Necrotizing Enterocolitis 59 0.061
397
P PLY018 Polycythemia 56 0.061
398
CRT013 Carotid Stenosis 50 0.061
399
c PRS136 Prostate Cancer, Hereditary, 6 33 0.060
400
GRN037 Granulomatosis with Polyangiitis 65 0.060
401
c PRS130 Prostate Cancer, Hereditary, 8 32 0.060
402
HMP005 Hemiplegia 55 0.060
403
TLR001 Tularemia 51 0.060
404
WTH001 Withdrawal Disorder 48 0.060
405
MYC006 Mycosis Fungoides 66 0.060
406
MCR004 Macroglobulinemia 49 0.060
407
THR004 Thrombocytosis 51 0.059
408
P RBL001 Rubella 59 0.059
409
P PLY017 Polyarteritis Nodosa 58 0.059
410
ERY051 Erythroleukemia, Familial 56 0.059
411
HPT019 Hepatic Encephalopathy 60 0.059
412
PRS063 Paresthesia 41 0.059
413
P PLV020 Pelvic Organ Prolapse 57 0.059
414
c CHR064 Chronic Monocytic Leukemia 33 0.059
415
CLF001 Cleft Lip 53 0.059
416
CRH005 Crohn's Colitis 53 0.059
417
AZS001 Azoospermia 50 0.059
418
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.059
419
PNM010 Pneumothorax, Primary Spontaneous 60 0.058
420
URM002 Uremia 49 0.058
421
c MLG079 Malignant Pleural Mesothelioma 42 0.058
422
PPL002 Papillary Carcinoma 47 0.058
423
TND005 Tendinitis 54 0.058
424
c DWL002 Dowling-Degos Disease 1 58 0.058
425
c MJR003 Major Affective Disorder 6 33 0.058
426
c MJR006 Major Affective Disorder 5 33 0.058
427
c DNG003 Dengue Disease 59 0.058
428
PRP007 Priapism 47 0.058
429
OPT003 Opiate Dependence 50 0.058
430
MYL031 Myeloproliferative Neoplasm 66 0.057
431
P HYP265 Hypotonia 43 0.057
432
KRT006 Keratoconjunctivitis 53 0.057
433
c CNT035 Central Nervous System Disease 52 0.057
434
P BNG030 Benign Ependymoma 60 0.057
435
CLL010 Cellular Ependymoma 54 0.057
436
P VNT002 Ventricular Septal Defect 60 0.057
437
P ART018 Aortic Valve Insufficiency 49 0.057
438
P MLG074 Malignant Mesenchymoma 40 0.057
439
c MJR008 Major Affective Disorder 2 35 0.057
440
c MJR023 Major Affective Disorder 7 33 0.057
441
SMN007 Seminoma 43 0.057
442
P LYN001 Lynch Syndrome 77 0.057
443
P HYP083 Hypopituitarism 53 0.057
444
c MJR004 Major Affective Disorder 4 28 0.057
445
P SPN046 Spinal Muscular Atrophy 62 0.056
446
INT002 Intermittent Claudication 61 0.055
447
ACH005 Achalasia 51 0.055
448
c FLL041 Follicular Lymphoma 1 49 0.055
449
PNN001 Panniculitis 51 0.054
450
NRM004 Neuroma 51 0.054
451
MXD026 Mixed Glioma 45 0.054
452
c FNC043 Fanconi Anemia, Complementation Group E 62 0.054
453
P MTR003 Mitral Valve Stenosis 50 0.054
454
TBR011 Tuberculous Meningitis 48 0.054
455
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.054
456
PLY001 Polycythemia Vera 69 0.054
457
FCT007 Factor Vii Deficiency 67 0.054
458
OCL006 Ocular Hypertension 53 0.054
459
RFR003 Refractive Error 43 0.054
460
P CTN015 Cutaneous T Cell Lymphoma 49 0.054
461
MDD018 Middle East Respiratory Syndrome 43 0.054
462
c BCT013 Bacterial Pneumonia 48 0.054
463
MDS022 Mediastinitis 46 0.054
464
SPN019 Spondylolisthesis 51 0.053
465
CRB086 Cerebral Aneurysms 40 0.053
466
CRN036 Craniopharyngioma 65 0.053
467
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.053
468
c EXD008 Exudative Vitreoretinopathy 1 71 0.053
469
MMM001 Mammary Paget's Disease 53 0.053
470
MCR141 Mucormycosis 56 0.053
471
P MST009 Mastocytosis 64 0.053
472
GRD007 Grade Iii Astrocytoma 59 0.052
473
P MLN069 Melanoma, Uveal 59 0.052
474
PRT018 Portal Vein Thrombosis 50 0.052
475
P TTR001 Tetralogy of Fallot 70 0.052
476
P FBR003 Fibrous Histiocytoma 44 0.052
477
KRT001 Keratoconjunctivitis Sicca 49 0.052
478
P LNG028 Long Qt Syndrome 66 0.052
479
QDR001 Quadriplegia 48 0.052
480
c MLG084 Malignant Fibrous Histiocytoma 63 0.052
481
CHR001 Churg-Strauss Syndrome 61 0.052
482
P SJG008 Sjogren Syndrome 61 0.052
483
OST011 Osteomalacia 52 0.051
484
MRG003 Marginal Zone B-Cell Lymphoma 52 0.051
485
TNS005 Tonsillitis 57 0.051
486
SDD008 Sudden Sensorineural Hearing Loss 43 0.051
487
ADN011 Adenoid Cystic Carcinoma 70 0.051
488
P INT143 Interstitial Cystitis 61 0.051
489
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.051
490
P MCR010 Microcephaly 59 0.051
491
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.050
492
JPN002 Japanese Encephalitis 57 0.050
493
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.050
494
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.050
495
c FML021 Familial Hypercholesterolemia 66 0.050
496
BRN012 Bronchiolitis Obliterans 55 0.050
497
VRC001 Varicocele 49 0.050
498
P ESS003 Essential Thrombocythemia 68 0.049
499
ANK001 Ankylosis 51 0.049
500
ATN004 Autonomic Neuropathy 45 0.049
501
AMB002 Amblyopia 49 0.049
502
ASP007 Aspiration Pneumonia 48 0.049
503
MSC007 Muscle Hypertrophy 64 0.049
504
HYP020 Hyperprolactinemia 64 0.049
505
P EPD016 Epidermolysis Bullosa 53 0.049
506
PLL012 Pollen Allergy 46 0.049
507
DFF036 Differentiated Thyroid Carcinoma 52 0.049
508
SPP007 Suppression Amblyopia 39 0.049
509
DCB001 Decubitus Ulcer 61 0.049
510
P ANG001 Angelman Syndrome 69 0.048
511
FRZ001 Frozen Shoulder 53 0.048
512
CHR072 Chordoma 58 0.048
513
BLR001 Biliary Atresia 50 0.048
514
CHL147 Chlamydia Pneumonia 48 0.048
515
PHN003 Phenylketonuria 75 0.048
516
CMP010 Complex Regional Pain Syndrome 58 0.048
517
PSD007 Pseudomyxoma Peritonei 54 0.048
518
LPR001 Lepromatous Leprosy 50 0.048
519
ADN009 Adenosquamous Carcinoma 47 0.047
520
EXS001 Exostosis 46 0.047
521
c ACT042 Acute Pyelonephritis 46 0.047
522
TNS014 Tenosynovitis 44 0.047
523
ORB006 Orbital Cellulitis 37 0.047
524
HYP068 Hyperostosis 48 0.047
525
GRW007 Growth Hormone Deficiency 46 0.047
526
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.047
527
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.047
528
CHL039 Choledocholithiasis 38 0.047
529
ANG018 Angiomyolipoma 46 0.046
530
DNG002 Dengue Hemorrhagic Fever 60 0.046
531
INT071 Intestinal Perforation 51 0.046
532
CRY014 Cryptococcal Meningitis 48 0.046
533
CNN003 Conn's Syndrome 79 0.046
534
P TRT019 Torticollis 48 0.046
535
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.046
536
FLL027 Fallopian Tube Carcinoma 67 0.046
537
MYF001 Myofibroma 45 0.046
538
P MYM013 Moyamoya Disease 1 57 0.046
539
BRS064 Bursitis 48 0.046
540
MYM001 Myoma 54 0.046
541
CYS014 Cystadenocarcinoma 51 0.046
542
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.046
543
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.046
544
GST037 Gastroparesis 54 0.046
545
EPD005 Epidural Abscess 35 0.046
546
BRK012 Broken Heart Syndrome 35 0.046
547
c SYS004 Systemic Mastocytosis 63 0.045
548
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.045
549
MSN004 Mesenchymal Cell Neoplasm 41 0.045
550
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.045
551
P SCK002 Sick Sinus Syndrome 55 0.045
552
RHM028 Rheumatic Heart Disease 53 0.045
553
MST019 Mastoiditis 43 0.045
554
RGH001 Right Bundle Branch Block 48 0.045
555
END062 Endometrial Hyperplasia 48 0.045
556
RTC005 Reticulosarcoma 47 0.045
557
PTS001 Patau Syndrome 55 0.045
558
EST005 Esotropia 42 0.044
559
PNM001 Pneumocystosis 59 0.044
560
TND004 Tendinopathy 43 0.044
561
MNC001 Monocular Esotropia 30 0.044
562
PYR004 Pyuria 40 0.044
563
P PNL012 Penile Cancer 56 0.044
564
TRC005 Tracheal Stenosis 38 0.044
565
MCP006 Mucoepidermoid Carcinoma 50 0.044
566
MLG163 Malignant Tumor of Penis 29 0.044
567
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.043
568
CMM004 Common Variable Immunodeficiency 68 0.043
569
MGC001 Megacolon 46 0.043
570
INT003 Intracranial Hypotension 35 0.042
571
PPT001 Peptic Esophagitis 52 0.042
572
ESP020 Esophageal Atresia 62 0.042
573
CRN017 Coronary Thrombosis 47 0.042
574
GLM044 Glomerular Disease 37 0.042
575
P ECT006 Ectodermal Dysplasia 62 0.042
576
P PRD006 Prader-Willi Syndrome 59 0.041
577
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.041
578
PLS025 Plasmablastic Lymphoma 47 0.041
579
P LSS002 Lissencephaly 51 0.041
580
PRT038 Protein-Energy Malnutrition 54 0.041
581
LNT004 Lentigines 50 0.041
582
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.041
583
c ADN012 Adenocarcinoma in Situ 42 0.041
584
c HYD064 Hydrocephalus, Congenital, 1 48 0.041
585
HRN029 Hearing Loss, Noise-Induced 37 0.041
586
PGM001 Pigmented Villonodular Synovitis 56 0.040
587
P RNL015 Renal Hypertension 47 0.040
588
BNG077 Benign Idiopathic Neonatal Seizures 26 0.040
589
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.040
590
GLL008 Gilles De La Tourette Syndrome 66 0.040
591
OVR059 Ovary Adenocarcinoma 53 0.040
592
ORL012 Oral Leukoplakia 39 0.040
593
P HMF004 Hemifacial Spasm 38 0.040
594
c HMF011 Hemifacial Spasm, Familial 33 0.040
595
CLB002 Clubfoot 51 0.040
596
CRT015 Carotid Artery Occlusion 45 0.040
597
PLY024 Polymicrogyria 49 0.040
598
END011 Endometriosis of Ovary 39 0.040
599
P CRV031 Cervical Adenocarcinoma 49 0.040
600
LYM012 Lymphoplasmacytic Lymphoma 47 0.040
601
ART012 Aortitis 44 0.040
602
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.040
603
c ALP101 Alpha-Thalassemia 62 0.039
604
THR013 Thoracic Outlet Syndrome 54 0.039
605
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.039
606
PYL006 Pyloric Stenosis 48 0.039
607
INF058 Inflammatory Myofibroblastic Tumor 45 0.039
608
BLD063 Bile Duct Cysts 43 0.039
609
EXT022 Exotropia 41 0.039
610
ALT003 Alternating Exotropia 34 0.039
611
ACN002 Acanthosis Nigricans 60 0.039
612
P GLL020 Gallbladder Disease 57 0.039
613
JVN009 Juvenile Pilocytic Astrocytoma 55 0.039
614
CRC006 Carcinoid Syndrome 55 0.039
615
OST115 Osteonecrosis of the Jaw 40 0.039
616
BNN005 Bunion 33 0.039
617
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.039
618
P TRC086 Trichohepatoenteric Syndrome 1 62 0.039
619
CLL014 Cll/sll 45 0.039
620
VLL003 Villonodular Synovitis 42 0.039
621
P HYP055 Hypoplastic Left Heart Syndrome 63 0.038
622
CRT012 Cortical Blindness 37 0.038
623
UMB002 Umbilical Hernia 46 0.038
624
DRG024 Drug Allergy 42 0.038
625
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.038
626
SPN340 Spontaneous Intracranial Hypotension 29 0.038
627
HMN009 Hemangioblastoma 54 0.038
628
CLC001 Calciphylaxis 51 0.038
629
P NGH001 Night Blindness 48 0.038
630
CHL149 Childhood Acute Myeloid Leukemia 44 0.038
631
HYP457 Hypertrophic Scars 42 0.038
632
P HRD217 Hereditary Optic Neuropathy 36 0.038
633
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.038
634
CRT016 Carotid Artery Disease 52 0.038
635
MCR037 Macroglossia 45 0.038
636
P BNG095 Benign Giant Cell Tumor 44 0.038
637
P MXL015 Maxillary Sinusitis 36 0.038
638
FBR002 Fibrosarcoma of Bone 34 0.038
639
LSC001 Lesch-Nyhan Syndrome 62 0.037
640
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.037
641
DBL004 Double Discordia 23 0.037
642
PLS016 Plasma Cell Leukemia 53 0.037
643
CRD016 Cardiac Rupture 37 0.037
644
P CPL006 Capillary Hemangioma 51 0.037
645
LYM014 Lymphangitis 41 0.037
646
PPL018 Papillary Adenocarcinoma 45 0.037
647
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.037
648
DRY001 Dry Eye Syndrome 47 0.037
649
EPC002 Epicondylitis 41 0.037
650
CYT018 Cytochrome P450 2d6 Variant 27 0.037
651
P PGT001 Paget's Disease of Bone 58 0.036
652
BNG036 Bone Giant Cell Tumor 49 0.036
653
MYT011 Myotonia 34 0.036
654
WLD007 Waldenstroem's Macroglobulinemia 61 0.036
655
CYS010 Cystinosis 59 0.036
656
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.036
657
CNG134 Congenitally Corrected Transposition of the Great Arteries 41 0.036
658
c VRL012 Viral Meningitis 48 0.036
659
MST004 Mast Cell Neoplasm 42 0.036
660
MYS001 Myositis Ossificans 41 0.036
661
EXT007 Extracutaneous Mastocytoma 38 0.036
662
c ERY064 Erythrocytosis, Familial, 6 23 0.035
663
FCL022 Focal Dystonia 41 0.035
664
P DVL012 Developmental Dysplasia of the Hip 1 38 0.035
665
P LCT002 Lactose Intolerance 53 0.035
666
HYP082 Hypopharynx Cancer 47 0.035
667
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.035
668
GNG004 Ganglioglioma 54 0.035
669
RTR001 Retrograde Amnesia 44 0.035
670
GST020 Gastric Antral Vascular Ectasia 41 0.035
671
RCH001 Richter's Syndrome 45 0.034
672
EXC002 Exocrine Pancreatic Insufficiency 42 0.034
673
EMB007 Embryonal Sarcoma 41 0.034
674
PRP001 Propionic Acidemia 65 0.034
675
P ANR048 Aniridia 1 63 0.034
676
DSS010 Dissociative Disorder 39 0.034
677
INT146 Intervertebral Disc Disease 63 0.034
678
CNT033 Central Nervous System Cancer 47 0.034
679
c VRL005 Viral Pneumonia 52 0.034
680
PLN007 Plantar Fasciitis 32 0.034
681
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.034
682
PCK003 Pick Disease of Brain 68 0.033
683
DDN006 Duodenitis 49 0.033
684
DNG001 Dengue Shock Syndrome 43 0.033
685
GST007 Gastric Dilatation 31 0.033
686
CVR002 Cavernous Sinus Thrombosis 33 0.033
687
SCH018 Schizencephaly 52 0.033
688
c FML191 Familial Long Qt Syndrome 53 0.033
689
CRC014 Carcinoid Tumors, Intestinal 47 0.033
690
CNT046 Central Nervous System Vasculitis 44 0.033
691
P NNS072 Nonsyndromic Hearing Loss 41 0.033
692
ANS004 Anisometropia 35 0.033
693
VRR004 Verrucous Carcinoma 49 0.033
694
IMM003 Immunoglobulin Alpha Deficiency 45 0.033
695
PHH001 Phaeohyphomycosis 42 0.033
696
LYM005 Lymphocele 35 0.033
697
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 36 0.032
698
AND002 Androgen Insensitivity Syndrome 66 0.032
699
LBR030 Leber Optic Atrophy 60 0.032
700
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.032
701
P CNG010 Congenital Stationary Night Blindness 54 0.032
702
ESP018 Esophageal Candidiasis 44 0.032
703
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.032
704
EXF003 Exfoliative Dermatitis 27 0.032
705
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.031
706
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.031
707
P HYP035 Hypophosphatasia 61 0.031
708
P STR022 Stargardt Disease 58 0.031
709
SPN029 Spondylolysis 33 0.031
710
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.031
711
P HYP009 Hypertrophic Pyloric Stenosis 41 0.031
712
c MLT010 Multiple Personality Disorder 30 0.031
713
NDL001 Nodular Malignant Melanoma 44 0.030
714
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 0.030
715
DFF003 Diffuse Scleroderma 41 0.030
716
PPL058 Papilloma of Choroid Plexus 56 0.030
717
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.030
718
SYM002 Sympathetic Ophthalmia 47 0.030
719
P PTT014 Pitt-Hopkins Syndrome 63 0.030
720
ANL017 Anal Squamous Cell Carcinoma 44 0.030
721
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.029
722
GST014 Gastrointestinal Lymphoma 34 0.029
723
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.029
724
LNT002 Lentigo Maligna Melanoma 33 0.029
725
BNT001 Banti's Syndrome 21 0.029
726
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.029
727
CNT017 Central Nervous System Origin Vertigo 45 0.029
728
SRT003 Sertoli-Leydig Cell Tumor 38 0.029
729
MYP001 Myoepithelioma 38 0.029
730
P CNG048 Congenital Hepatic Fibrosis 38 0.029
731
END075 Endocervical Adenocarcinoma 37 0.029
732
c TRS012 Trisomy 22 25 0.029
733
PRL021 Perilymphatic Fistula 22 0.029
734
PND002 Pendred Syndrome 65 0.028
735
P AXN002 Axenfeld-Rieger Syndrome 59 0.028
736
TRC062 Tricuspid Atresia 54 0.028
737
FNG004 Fungal Meningitis 44 0.028
738
PLG004 Plagiocephaly 41 0.028
739
CRR002 Currarino Syndrome 48 0.028
740
ANP006 Anaplastic Ependymoma 46 0.028
741
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.028
742
ADP007 Adie Pupil 39 0.028
743
TNF001 Tinea Favosa 33 0.028
744
c SPN393 Spinal Muscular Atrophy, Type I 52 0.027
745
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.027
746
LMT001 Limited Scleroderma 47 0.027
747
MYP002 Myoepithelial Carcinoma 47 0.027
748
PRT049 Partial Deletion of Y 33 0.027
749
VST004 Vestibular Disease 41 0.027
750
c NNS007 Nonsyndromic Deafness 35 0.027
751
c CNG129 Congenital Torticollis 23 0.027
752
GRS011 Gerstmann-Straussler Disease 56 0.027
753
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 52 0.027
754
OVR047 Ovarian Cystadenocarcinoma 38 0.027
755
CHR463 Chronic Actinic Dermatitis 37 0.027
756
PTT001 Pituitary Hypoplasia 34 0.027
757
HMP030 Haemophilus Meningitis 24 0.027
758
MRZ001 Mirizzi Syndrome 20 0.027
759
CLL002 Collecting Duct Carcinoma 53 0.026
760
CRB151 Cerebral Creatine Deficiency Syndrome 1 52 0.026
761
PRS123 Persistent Generalized Lymphadenopathy 37 0.026
762
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.026
763
SHR107 Short Stature-Obesity Syndrome 26 0.026
764
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.026
765
SPL012 Splenic Disease 47 0.026
766
ANL011 Anal Canal Carcinoma 38 0.026
768
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 60 0.025
769
DBN001 Dubin-Johnson Syndrome 59 0.025
770
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.025
771
RSP023 Rasopathy 51 0.025
772
HYP835 Hypothalamic Obesity 38 0.025
773
ACT064 Acute Necrotizing Encephalitis 33 0.025
774
DSR074 Disorder of Purine Metabolism 29 0.025
775
NCR001 Necrotizing Ulcerative Gingivitis 28 0.025
776
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 66 0.024
777
CYS036 Cystinosis, Nephropathic 51 0.024
778
IMM154 Immunoglobulin a Deficiency 1 42 0.024
779
P ATS366 Autism X-Linked 2 42 0.024
780
SRC002 Sarcomatoid Renal Cell Carcinoma 38 0.024
781
ATX010 Ataxia Neuropathy Spectrum 34 0.024
782
BRN133 Bronchomalacia 33 0.024
783
c SPP012 Suppressor of Tumorigenicity 11 22 0.024
784
SPN092 Spinal Shock 19 0.024
785
c BRS110 Breast-Ovarian Cancer, Familial 1 56 0.024
786
P PRX014 Proximal Spinal Muscular Atrophy 45 0.024
787
c MSC171 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 40 0.024
788
END043 Endometrial Stromal Tumor 33 0.024
789
HLS001 Heel Spur 30 0.024
790
HNM002 Hinman Syndrome 27 0.024
791
ISL019 Isolated Duane Retraction Syndrome 22 0.024
792
SCP002 Scapuloperoneal Spinal Muscular Atrophy 56 0.023
793
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 51 0.023
794
CRT055 Creatine Deficiency Syndromes 38 0.023
795
c CLR081 Colorectal Cancer 6 24 0.023
796
P DNR001 Duane Retraction Syndrome 47 0.022
797
HPT082 Hepatic Adenomas, Familial 44 0.022
798
c NGH029 Night Blindness, Congenital Stationary, Type 1e 37 0.022
799
ALR002 Al-Raqad Syndrome 33 0.022
800
c DFN280 Deafness, Autosomal Recessive 27 0.022
801
XLN012 X-Linked Congenital Stationary Night Blindness 26 0.022
802
BLD137 Blood Group--Ahonen 16 0.022
803
CNR033 Cone-Rod Synaptic Disorder, Congenital Nonprogressive 35 0.021
804
CHR270 Chromosome 9p Duplication 29 0.021
805
c JVN001 Juvenile Astrocytoma 27 0.021
806
c ATS006 Autosomal Recessive Nonsyndromic Deafness 27 0.021
807
c SYS041 Systemic Lupus Erythematosus 9 19 0.021
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