Search results for was

2796 hits were found for was

# Family MCID Name MIFTS Score
1
P WSK001 Wiskott-Aldrich Syndrome 72 20.575
3
c THR071 Thrombocytopenia 1 50 5.734
4
NTR036 Neutropenia, Severe Congenital, X-Linked 30 5.421
5
P THR014 Thrombocytopenia 67 4.933
6
P NTR004 Neutropenia 63 4.144
7
c SVR003 Severe Congenital Neutropenia 59 3.166
8
P DRR001 Diarrhea 55 2.712
9
IMM167 Immune Deficiency Disease 78 2.628
10
P DRM053 Dermatitis, Atopic 66 2.608
11
AGM019 Agammaglobulinemia, X-Linked 71 2.580
12
XLN228 X-Linked Recessive Disease 26 2.580
13
c JVN004 Juvenile Myelomonocytic Leukemia 67 2.573
14
LKC009 Leukocyte Adhesion Deficiency, Type I 69 2.564
15
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 1.825
16
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 55 1.825
17
BLD053 Blood Platelet Disease 49 1.825
18
OMN001 Omenn Syndrome 67 1.813
19
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 1.813
20
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 51 1.813
21
CMB003 Combined T Cell and B Cell Immunodeficiency 49 1.813
22
P BLD051 Blood Coagulation Disease 46 1.813
23
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 42 1.813
24
OPH003 Ophthalmia Nodosa 22 1.813
25
c XLN230 X-Linked Monogenic Disease 18 1.813
26
P CLR023 Colorectal Cancer 99 0.111
27
P MYC007 Myocardial Infarction 70 0.108
28
P GST053 Gastric Cancer 83 0.101
29
OST012 Osteoarthritis 78 0.095
30
ESP021 Esophageal Cancer 90 0.087
31
CNG034 Congestive Heart Failure 69 0.084
32
BCK006 Back Pain 42 0.084
33
P PNC035 Pancreatic Cancer 84 0.078
34
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.078
35
P HPT023 Hepatocellular Carcinoma 100 0.077
36
ADN018 Adenoma 59 0.077
37
P RSP003 Respiratory Failure 74 0.076
38
P KDN018 Kidney Disease 72 0.076
39
P CRD119 Cardiac Arrest 67 0.076
40
DRM006 Dermatitis 61 0.076
41
PLM033 Pulmonary Embolism 59 0.076
42
ISC004 Ischemia 58 0.076
43
c SYS001 Systemic Lupus Erythematosus 86 0.074
44
P OST002 Osteoporosis 74 0.074
45
PRT036 Peritonitis 64 0.074
46
P ADN016 Adenocarcinoma 64 0.074
47
48X005 48,xyyy 39 0.074
48
LVR012 Liver Cirrhosis 62 0.073
49
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.073
50
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.073
51
P VSC011 Vasculitis 62 0.072
52
P HDC001 Headache 57 0.072
53
P RCT021 Rectum Cancer 52 0.072
54
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.070
55
P ATR011 Atrial Fibrillation 66 0.070
56
LPP008 Lipoprotein Quantitative Trait Locus 62 0.070
57
P HRT032 Heart Disease 75 0.069
58
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.069
59
P CRN300 Coronary Heart Disease 1 63 0.069
60
ATM095 Autoimmune Disease 62 0.069
61
HMN044 Human Immunodeficiency Virus Type 1 71 0.068
62
c SVR001 Severe Acute Respiratory Syndrome 62 0.068
63
c ACT075 Acute Myocardial Infarction 57 0.068
64
P LNG032 Lung Cancer 98 0.066
65
CRV035 Cervical Cancer 76 0.066
66
P SYP003 Syphilis 58 0.066
67
P BCL017 B-Cell Lymphoma 58 0.066
68
PRP030 Purpura 54 0.066
69
P ATS364 Autism 70 0.065
70
P EXN002 Exanthem 57 0.065
71
47X002 47,xyy 49 0.065
72
c HPT073 Hepatitis C Virus 72 0.063
73
TXC005 Toxic Shock Syndrome 62 0.063
74
P NRP001 Neuropathy 56 0.063
75
PNG002 Pain Agnosia 51 0.063
76
DYS073 Dysphagia 50 0.063
77
P LNG064 Lung Cancer Susceptibility 3 78 0.062
78
P SLP006 Sleep Apnea 69 0.062
79
TTN003 Tetanus 65 0.062
80
GT001 Gout 64 0.062
81
c PRC016 Pre-Eclampsia 63 0.062
82
DPR016 Depression 63 0.062
83
P LPS004 Lupus Erythematosus 61 0.062
84
SQM006 Squamous Cell Carcinoma 60 0.062
85
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.062
86
MLR004 Malaria 81 0.060
87
c ATR087 Atrial Standstill 1 75 0.060
88
c THR092 Thrombophilia Due to Thrombin Defect 73 0.060
89
PLM001 Pulmonary Tuberculosis 69 0.060
90
P LVR013 Liver Disease 68 0.060
91
P INF038 Influenza 68 0.060
92
HYP056 Hypoglycemia 66 0.060
93
P MNN013 Meningitis 66 0.060
94
PRT037 Pertussis 65 0.060
95
P ENC018 Encephalopathy 61 0.060
96
THY029 Thyroid Carcinoma 59 0.060
97
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.059
98
ULC004 Ulcerative Colitis 73 0.059
99
P PHC003 Pheochromocytoma 71 0.059
100
PLG002 Plague 63 0.059
101
CLT003 Colitis 62 0.059
102
LNG099 Lung Disease 60 0.059
103
GST045 Gastroenteritis 59 0.059
104
ART140 Arteries, Anomalies of 52 0.059
105
OCL069 Ocular Motor Apraxia 51 0.059
106
ADR040 Adrenal Gland Pheochromocytoma 46 0.059
107
CVD001 Covid-19 44 0.059
108
P OVR042 Ovarian Cancer 88 0.057
109
CRH001 Crohn's Disease 74 0.057
110
P MLT020 Multiple Sclerosis 72 0.057
111
P PNM007 Pneumonia 68 0.057
112
SRC014 Sarcoma 65 0.057
113
P GLM045 Glioma 63 0.057
114
MSL001 Measles 62 0.057
115
FTT001 Fatty Liver Disease 61 0.057
116
P MYL006 Myeloid Leukemia 60 0.057
117
c ACT027 Acute Pancreatitis 60 0.057
118
SPN035 Spindle Cell Sarcoma 53 0.057
119
GLL048 Glial Tumor 45 0.057
120
P BRS047 Breast Cancer 97 0.055
121
GST019 Gastrointestinal Stromal Tumor 78 0.055
122
END057 Endometrial Cancer 74 0.055
123
P HYP086 Hypothyroidism 69 0.055
124
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.055
125
P HYD006 Hydrocephalus 66 0.055
126
HYP066 Hyperglycemia 61 0.055
127
P GLM007 Glomerulonephritis 57 0.055
128
PNM008 Pneumothorax 56 0.055
129
P ALZ034 Alzheimer Disease 88 0.053
130
c LKM061 Leukemia, Acute Myeloid 84 0.053
131
P BLD134 Bladder Cancer 79 0.053
132
MYL009 Myelodysplastic Syndrome 70 0.053
133
RCK004 Rickets 68 0.053
134
c MGR028 Migraine with or Without Aura 1 67 0.053
135
PLM031 Poliomyelitis 64 0.053
136
P HYP069 Hyperparathyroidism 63 0.053
137
P PSR002 Psoriasis 62 0.053
138
P ENC004 Encephalitis 61 0.053
139
P CTR002 Cataract 60 0.053
140
ANR040 Aneurysm 59 0.053
141
MNT002 Mental Depression 58 0.053
142
SML019 Smallpox 56 0.053
143
PST011 Pustulosis of Palm and Sole 52 0.053
144
P OBS001 Obstructive Jaundice 50 0.053
145
c HYP836 Hypercholesterolemia, Familial, 1 73 0.052
146
P DMN002 Dementia 66 0.052
147
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.052
148
P NPH012 Nephrotic Syndrome 60 0.052
149
P INF032 Infertility 57 0.052
150
P HYP076 Hyperthyroidism 55 0.052
151
P INF037 Inflammatory Bowel Disease 54 0.052
152
MYL069 Myeloma, Multiple 85 0.050
153
STR067 Stroke, Ischemic 81 0.050
154
ANX010 Anxiety 73 0.050
155
P GRF003 Graft-Versus-Host Disease 72 0.050
156
DFC004 Deficiency Anemia 70 0.050
157
P MLN008 Melanoma 69 0.050
158
ANG054 Angina Pectoris 66 0.050
159
P VSC007 Vascular Disease 63 0.050
160
c HPT001 Hepatitis C 62 0.050
161
c SCL052 Scleroderma, Familial Progressive 61 0.050
162
DPH001 Diphtheria 60 0.050
163
CHL014 Cholera 59 0.050
164
P END033 Endocarditis 57 0.050
165
DFF005 Diffuse Large B-Cell Lymphoma 55 0.050
166
PRC013 Pericarditis 54 0.050
167
P CHL066 Cholangitis 51 0.050
168
P RHM011 Rheumatoid Arthritis 80 0.048
169
c DLT002 Dilated Cardiomyopathy 79 0.048
170
c CHR684 Chronic Kidney Disease 70 0.048
171
P LYM118 Lymphoma 68 0.048
172
P MJR001 Major Depressive Disorder 68 0.048
173
c ATS007 Autism Spectrum Disorder 67 0.048
174
TYP007 Typhoid Fever 63 0.048
175
ALL026 Allergic Hypersensitivity Disease 62 0.048
176
P HMN010 Hemangioma 61 0.048
177
CNS004 Constipation 58 0.048
178
THR024 Thrombosis 57 0.048
179
BLR008 Bilirubin Metabolic Disorder 57 0.048
180
P SZR006 Seizure Disorder 56 0.048
181
P GRV001 Graves' Disease 55 0.048
182
c MCR113 Microvascular Complications of Diabetes 3 52 0.048
183
HRT011 Heart Septal Defect 50 0.048
184
c MCR120 Microvascular Complications of Diabetes 7 47 0.048
185
c MCR130 Microvascular Complications of Diabetes 6 41 0.048
186
c MCR133 Microvascular Complications of Diabetes 4 41 0.048
187
HNS001 Hansen's Disease 34 0.048
188
P PRS040 Prostate Cancer 97 0.046
189
c NRF023 Neurofibromatosis, Type Ii 80 0.046
190
GLB015 Glioblastoma Multiforme 75 0.046
191
P SRC025 Sarcoidosis 1 70 0.046
192
P MYP004 Myopathy 70 0.046
193
P LPR021 Leprosy 3 69 0.046
194
P LKM062 Leukemia, Acute Lymphoblastic 69 0.046
195
P HYP098 Hypereosinophilic Syndrome 67 0.046
196
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.046
197
P SKN015 Skin Carcinoma 66 0.046
198
OST017 Osteomyelitis 64 0.046
199
c BRN108 Branchiootic Syndrome 1 62 0.046
200
c HPT016 Hepatitis B 59 0.046
201
APH002 Aphasia 57 0.046
202
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.046
203
P SBS003 Substance Abuse 55 0.046
204
P TRM003 Tremor 54 0.046
205
P INS002 in Situ Carcinoma 53 0.046
206
IMP005 Impotence 52 0.046
207
END086 End Stage Renal Disease 51 0.046
208
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.046
209
HRW001 Hair Whorl 36 0.046
210
c MNN043 Meningioma, Familial 74 0.044
211
P NRB001 Neuroblastoma 72 0.044
212
ACR007 Acromegaly 71 0.044
213
LYM133 Lymphoma, Hodgkin, Classic 69 0.044
214
BRN024 Bronchitis 68 0.044
215
P PLM037 Pulmonary Hypertension 67 0.044
216
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.044
217
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.044
218
ART002 Arts Syndrome 64 0.044
219
LYM017 Lyme Disease 64 0.044
220
SKN016 Skin Disease 63 0.044
221
P END044 Endometriosis 63 0.044
222
P DRM010 Dermatomyositis 61 0.044
223
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.044
224
ACQ007 Acquired Immunodeficiency Syndrome 60 0.044
225
VRC005 Varicose Veins 60 0.044
226
c ACT071 Acute Kidney Failure 60 0.044
227
VSL002 Visual Epilepsy 59 0.044
228
BRN002 Bronchiolitis 59 0.044
229
P INT070 Intestinal Obstruction 58 0.044
230
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.044
231
P PRP019 Peripheral Nervous System Disease 58 0.044
232
CHL067 Cholecystitis 57 0.044
233
BRN056 Bronchopulmonary Dysplasia 57 0.044
234
DSS009 Disseminated Intravascular Coagulation 57 0.044
235
P MYS005 Myositis 56 0.044
236
ATR057 Atrioventricular Block 55 0.044
237
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.044
238
SYN007 Synovitis 54 0.044
239
AMN003 Amnestic Disorder 54 0.044
240
HYP014 Hyperuricemia 52 0.044
241
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.044
242
PLR007 Pleural Empyema 50 0.044
243
MTB004 Metabolic Acidosis 50 0.044
244
P BNG032 Benign Mesothelioma 46 0.044
245
P CHR345 Chronic Pain 44 0.044
246
VRL003 Variola Major 42 0.044
247
PLC002 Plica Syndrome 36 0.044
248
NRL016 Neural Tube Defects 82 0.041
249
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.041
250
P EPL164 Epilepsy 71 0.041
251
P ASP006 Aspergillosis 69 0.041
252
CRB037 Cerebral Palsy 69 0.041
253
OBS002 Obsessive-Compulsive Disorder 68 0.041
254
P MYS003 Myasthenia Gravis 68 0.041
255
OST159 Osteogenic Sarcoma 66 0.041
256
LPD008 Lipid Metabolism Disorder 62 0.041
257
c HPT003 Hepatitis a 62 0.041
258
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.041
259
P PNC044 Pancreatitis 61 0.041
260
SDD001 Sudden Infant Death Syndrome 61 0.041
261
APP008 Appendicitis 61 0.041
262
CHL123 Chlamydia 59 0.041
263
P CYS018 Cystitis 59 0.041
264
AVN001 Avian Influenza 59 0.041
265
DSS008 Disease of Mental Health 58 0.041
266
IRN002 Iron Metabolism Disease 57 0.041
267
SCH014 Schistosomiasis 57 0.041
268
P PLY011 Polycystic Ovary Syndrome 56 0.041
269
ART074 Aortic Dissection 52 0.041
270
c ACT135 Acute Graft Versus Host Disease 52 0.041
271
SPN051 Spondylitis 51 0.041
272
CHL004 Cholelithiasis 49 0.041
273
SPL018 Splenomegaly 48 0.041
274
HLX001 Helix Syndrome 47 0.041
275
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 47 0.041
276
MCR011 Microinvasive Gastric Cancer 43 0.041
277
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.041
278
INF009 Inflammatory Spondylopathy 31 0.041
279
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.039
280
AST005 Asthma 76 0.039
281
P SCH015 Schizophrenia 74 0.039
282
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.039
283
MSC157 Muscular Dystrophy, Duchenne Type 72 0.039
284
OTT002 Otitis Media 72 0.039
285
P HYP061 Hypertrophic Cardiomyopathy 70 0.039
286
CRT072 Creutzfeldt-Jakob Disease 70 0.039
287
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.039
288
ART016 Aortic Aneurysm 69 0.039
289
P MSC005 Muscular Dystrophy 66 0.039
290
P CNJ013 Conjunctivitis 65 0.039
291
P LPS002 Liposarcoma 65 0.039
292
P THY023 Thymoma 65 0.039
293
P DBT009 Diabetes Mellitus 64 0.039
294
CLF027 Cleft Palate, Isolated 64 0.039
295
c JVN010 Juvenile Rheumatoid Arthritis 64 0.039
296
P HML002 Hemolytic Anemia 63 0.039
297
c ACT068 Acute Cystitis 63 0.039
298
ANR007 Anorexia Nervosa 63 0.039
299
MNN042 Meningioma, Radiation-Induced 62 0.039
300
RTN017 Retinal Detachment 61 0.039
301
SPN186 Spinal Cord Injury 60 0.039
302
P ATR010 Atrial Heart Septal Defect 60 0.039
303
HYD002 Hydronephrosis 60 0.039
304
ETN001 Eating Disorder 60 0.039
305
P BPL003 Bipolar Disorder 56 0.039
306
AMN001 Amenorrhea 54 0.039
307
PNC001 Pancytopenia 54 0.039
308
CLF001 Cleft Lip 53 0.039
309
c GLL024 Gallbladder Disease 1 53 0.039
310
c THY107 Thymoma, Familial 52 0.039
311
LMY002 Leiomyoma 52 0.039
312
SPN021 Spinal Meningioma 50 0.039
313
P ECL001 Eclampsia 50 0.039
314
AZS001 Azoospermia 50 0.039
315
FCL012 Facial Paralysis 46 0.039
316
HDN002 Head Injury 46 0.039
317
SYN036 Syncope 45 0.039
318
ASC004 Ascending Colon Cancer 42 0.039
319
c MJR024 Major Affective Disorder 9 41 0.039
320
SCR001 Secretory Meningioma 41 0.039
321
P RRT020 Rare Tumor 41 0.039
322
c MJR022 Major Affective Disorder 8 38 0.039
323
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.039
325
CYS001 Cystic Fibrosis 81 0.037
326
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.037
327
PRP027 Peripheral Vascular Disease 71 0.037
328
P AMY004 Amyloidosis 70 0.037
329
GST040 Gastric Adenocarcinoma 70 0.037
330
ADL002 Adult Syndrome 70 0.037
331
PNC129 Pancreatic Adenocarcinoma 68 0.037
332
CRB039 Cerebrovascular Disease 67 0.037
333
LNG039 Lung Squamous Cell Carcinoma 66 0.037
334
ATH013 Atherosclerosis Susceptibility 65 0.037
335
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.037
336
CHL068 Cholestasis 61 0.037
337
c PNS012 Paine Syndrome 61 0.037
338
CHR066 Chronic Fatigue Syndrome 61 0.037
339
GST033 Gestational Diabetes 61 0.037
340
IGR001 Ige Responsiveness, Atopic 59 0.037
341
HLC007 Helicobacter Pylori Infection 59 0.037
342
PPT005 Peptic Ulcer Disease 59 0.037
343
FBR047 Fibromyalgia 58 0.037
344
P ALC033 Alcohol Use Disorder 58 0.037
345
P GLL018 Gallbladder Cancer 57 0.037
346
PHR003 Pharyngitis 57 0.037
347
P PTT006 Pituitary Adenoma 55 0.037
348
c ATM024 Autoimmune Pancreatitis 55 0.037
349
PLM010 Pulmonary Edema 54 0.037
350
P LTR001 Lateral Sclerosis 54 0.037
351
MMM001 Mammary Paget's Disease 53 0.037
352
GST023 Gastric Ulcer 53 0.037
353
INT051 Intussusception 53 0.037
354
P TRT010 Teratoma 52 0.037
355
ILS001 Ileus 51 0.037
356
ENT011 Enterocolitis 51 0.037
357
STM007 Stomatitis 50 0.037
358
ECT026 Ectopic Pregnancy 50 0.037
359
LRN003 Learning Disability 49 0.037
360
P SCL009 Sclerosing Cholangitis 48 0.037
361
c MTR002 Mitral Valve Insufficiency 48 0.037
362
SXL003 Sexual Disorder 47 0.037
363
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.037
364
CYS009 Cystadenoma 44 0.037
365
EPC002 Epicondylitis 41 0.037
366
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.037
367
c LKM005 Leukemia, T-Cell, Chronic 34 0.037
368
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.037
369
c SPN225 Spondyloarthropathy 1 73 0.034
370
P RTN024 Retinoblastoma 73 0.034
371
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.034
372
P SYS005 Systemic Scleroderma 68 0.034
373
SKN019 Skin Melanoma 68 0.034
374
P HPT021 Hepatitis 67 0.034
375
c SML038 Small Cell Cancer of the Lung 65 0.034
376
P PRS038 Personality Disorder 65 0.034
377
P CHR071 Charcot-Marie-Tooth Disease 65 0.034
378
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.034
379
BRC012 Brucellosis 64 0.034
380
P HYP750 Hypertriglyceridemia, Familial 62 0.034
381
P PRM006 Primary Biliary Cirrhosis 62 0.034
382
P PRP029 Porphyria 62 0.034
383
OST003 Osteonecrosis 61 0.034
384
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.034
385
NRL005 Neurilemmoma 60 0.034
386
P KDN017 Kidney Cancer 60 0.034
387
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.034
388
P SCL018 Scoliosis 60 0.034
389
INT066 Interstitial Lung Disease 60 0.034
390
RHM001 Rheumatic Fever 60 0.034
391
CHC001 Chickenpox 60 0.034
392
ING001 Inguinal Hernia 60 0.034
393
P THL005 Thalassemia 60 0.034
394
P RBL001 Rubella 59 0.034
395
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.034
396
P BRN022 Bronchiectasis 59 0.034
397
P GLL022 Guillain-Barre Syndrome 59 0.034
398
P CND004 Candidiasis 58 0.034
399
LNG108 Langerhans Cell Histiocytosis 58 0.034
400
P UVT001 Uveitis 57 0.034
401
P RHN004 Rhinitis 57 0.034
402
c ACT134 Acute Liver Failure 56 0.034
403
HYP005 Hypokalemia 55 0.034
404
P MYP006 Myopia 55 0.034
405
FLR002 Filariasis 55 0.034
406
P DBT005 Diabetes Insipidus 55 0.034
407
WST005 West Nile Virus 54 0.034
408
CLL003 Cellulitis 54 0.034
409
CRH005 Crohn's Colitis 53 0.034
410
INF034 Infective Endocarditis 53 0.034
411
c HPT007 Hepatitis E 53 0.034
412
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.034
413
NRT004 Neuritis 52 0.034
414
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.034
415
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.034
416
TLN003 Telangiectasis 52 0.034
417
P HMP007 Hemophilia 51 0.034
418
CRT013 Carotid Stenosis 50 0.034
419
MCN001 Mucinous Adenocarcinoma 49 0.034
420
HST010 Histiocytosis 48 0.034
421
ATS010 Autosomal Recessive Disease 48 0.034
422
PYL006 Pyloric Stenosis 48 0.034
423
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.034
424
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.034
425
RYN005 Raynaud Phenomenon 47 0.034
426
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.034
427
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.034
428
SGN002 Signet Ring Cell Adenocarcinoma 45 0.034
429
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.034
430
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.034
431
APP009 Appendix Adenocarcinoma 44 0.034
432
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.034
433
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.034
434
DVR002 Diverticulitis 43 0.034
435
CYT002 Cytokine Deficiency 42 0.034
436
TBL003 Tubular Adenocarcinoma 40 0.034
437
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
438
P APL001 Aplastic Anemia 74 0.031
439
c HMC039 Hemochromatosis, Type 1 74 0.031
440
P FML011 Familial Adenomatous Polyposis 72 0.031
441
c LKM063 Leukemia, Chronic Myeloid 72 0.031
442
c EXD008 Exudative Vitreoretinopathy 1 71 0.031
443
MYL005 Myelofibrosis 70 0.031
444
P ART022 Arthritis 69 0.031
445
CHL065 Cholangiocarcinoma 68 0.031
446
P BLD062 Bile Duct Cancer 67 0.031
447
CRP001 Carpal Tunnel Syndrome 67 0.031
448
P MLG056 Malignant Hyperthermia 67 0.031
449
P CLC063 Celiac Disease 1 66 0.031
450
P PLM036 Pulmonary Fibrosis 65 0.031
451
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.031
452
P DYS154 Dystonia 65 0.031
453
KRT019 Keratitis, Hereditary 65 0.031
454
P HRP006 Herpes Simplex 65 0.031
455
ANG020 Angiosarcoma 64 0.031
456
ACT119 Acute Promyelocytic Leukemia 63 0.031
457
P LMY004 Leiomyosarcoma 63 0.031
458
c ATM011 Autoimmune Hepatitis 63 0.031
459
P ESP024 Esophagitis 62 0.031
460
BLL006 Bullous Pemphigoid 62 0.031
461
c ANM038 Anemia, Autoimmune Hemolytic 62 0.031
462
CHR001 Churg-Strauss Syndrome 61 0.031
463
YLL002 Yellow Fever 61 0.031
464
c JVN061 Juvenile Arthritis 60 0.031
465
QFV001 Q Fever 60 0.031
466
STT001 Status Epilepticus 60 0.031
467
P MCR010 Microcephaly 59 0.031
468
P BND020 Bone Disease 59 0.031
469
PST028 Post-Traumatic Stress Disorder 58 0.031
470
c PRM005 Primary Hyperparathyroidism 58 0.031
471
c GLC112 Galactosemia Iii 56 0.031
472
P ADL017 Adult T-Cell Leukemia 56 0.031
473
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.031
474
MTH009 Mouth Disease 56 0.031
475
P GST044 Gastritis 56 0.031
476
FLR001 Filarial Elephantiasis 55 0.031
477
P SCK002 Sick Sinus Syndrome 55 0.031
478
c BCT007 Bacterial Meningitis 55 0.031
479
INT007 Intermediate Coronary Syndrome 55 0.031
480
PRS045 Prostatic Hypertrophy 53 0.031
481
GTR002 Goiter 53 0.031
482
P PTS002 Ptosis 53 0.031
483
c FML008 Familial Retinoblastoma 53 0.031
484
P INT068 Intestinal Disease 53 0.031
485
P LRY019 Laryngitis 52 0.031
486
c VRL010 Viral Hepatitis 52 0.031
487
P SML001 Small Cell Carcinoma 52 0.031
489
PRS021 Prostatic Adenoma 51 0.031
490
INT079 Intrahepatic Cholangiocarcinoma 51 0.031
491
P PRC012 Pericardial Effusion 51 0.031
492
c SCN007 Secondary Hyperparathyroidism 51 0.031
493
PRT029 Parathyroid Adenoma 50 0.031
494
P MTR003 Mitral Valve Stenosis 50 0.031
495
FSC004 Fasciitis 50 0.031
496
PRS129 Prostatic Hyperplasia, Benign 49 0.031
497
BNR002 Bone Resorption Disease 48 0.031
498
ASP007 Aspiration Pneumonia 48 0.031
499
IGG001 Iga Glomerulonephritis 48 0.031
500
CHL147 Chlamydia Pneumonia 48 0.031
501
HMP001 Hemopericardium 48 0.031
502
NRN001 Neuroendocrine Carcinoma 47 0.031
503
ACT055 Actinomycosis 47 0.031
504
ACT084 Acute Stress Disorder 47 0.031
505
P KRN004 Kernicterus 47 0.031
506
CRD137 Cardiogenic Shock 47 0.031
507
CHR074 Choriocarcinoma 47 0.031
508
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.031
509
KR002 Kuru 45 0.031
510
PTT037 Pituitary Tumors 44 0.031
511
HMP009 Haemophilus Influenzae 43 0.031
512
PRS063 Paresthesia 41 0.031
513
OCH001 Ochronosis 38 0.031
514
MLN003 Melancholia 38 0.031
515
TRN003 Transverse Colon Cancer 38 0.031
516
DTH005 Diethylstilbestrol Syndrome 25 0.031
517
ELC001 Elective Mutism 23 0.031
518
c HYP595 Hypertension, Essential 84 0.028
519
P LKM071 Leukemia, Chronic Lymphocytic 79 0.028
520
CNN003 Conn's Syndrome 79 0.028
521
P HNT016 Huntington Disease 72 0.028
522
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.028
523
EWN003 Ewing Sarcoma 69 0.028
524
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.028
525
P TMP003 Temporal Arteritis 68 0.028
526
MLD001 Melioidosis 68 0.028
527
P LNG028 Long Qt Syndrome 66 0.028
528
ALC007 Alcohol Dependence 66 0.028
529
c FML021 Familial Hypercholesterolemia 66 0.028
530
P NSP012 Nasopharyngeal Carcinoma 66 0.028
531
IRR002 Irritable Bowel Syndrome 65 0.028
532
LYS012 Lysosomal Acid Lipase Deficiency 65 0.028
533
APN008 Apnea, Obstructive Sleep 64 0.028
534
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.028
535
PRP083 Porphyria, Acute Intermittent 64 0.028
536
P RHB003 Rhabdomyosarcoma 63 0.028
537
c DPH024 Diaphragmatic Hernia, Congenital 63 0.028
538
LSH001 Leishmaniasis 63 0.028
539
CHN016 Cohen Syndrome 63 0.028
540
TRN015 Transient Cerebral Ischemia 63 0.028
541
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.028
542
P PLY014 Polycystic Kidney Disease 62 0.028
543
PSR001 Psoriatic Arthritis 61 0.028
544
HRP004 Herpes Zoster 60 0.028
545
PTN001 Patent Foramen Ovale 60 0.028
546
PNM010 Pneumothorax, Primary Spontaneous 60 0.028
547
P VNT002 Ventricular Septal Defect 60 0.028
548
ORL011 Oral Cancer 60 0.028
549
INS001 Insulinoma 60 0.028
550
P MYC008 Myocarditis 59 0.028
551
PRT013 Portal Hypertension 59 0.028
552
c DNG003 Dengue Disease 59 0.028
553
P SLP005 Sleep Disorder 59 0.028
554
P LYM033 Lymphoproliferative Syndrome 59 0.028
555
c LTN004 Late-Onset Retinal Degeneration 59 0.028
556
DCT002 Ductal Carcinoma in Situ 59 0.028
557
P PLY017 Polyarteritis Nodosa 58 0.028
558
c ACT073 Acute Leukemia 58 0.028
559
ALK013 Alkaptonuria 58 0.028
560
ANT024 Anthrax Disease 58 0.028
561
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.028
562
SPT004 Septic Arthritis 58 0.028
563
P URT039 Urticaria 58 0.028
564
P MMP001 Mumps 58 0.028
565
MXD005 Mixed Connective Tissue Disease 58 0.028
566
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.028
567
LYM021 Lymphadenitis 57 0.028
568
P PRN023 Prion Disease 57 0.028
569
c MST023 Mesothelioma, Malignant 57 0.028
570
TRN018 Transitional Cell Carcinoma 56 0.028
571
c ESS001 Essential Tremor 56 0.028
572
BCT022 Bacterial Infectious Disease 56 0.028
573
SBC001 Subacute Sclerosing Panencephalitis 56 0.028
574
P NRF002 Neurofibromatosis 56 0.028
575
ORL005 Oral Candidiasis 56 0.028
576
c GRV008 Graves Disease 1 56 0.028
577
MCS002 Mucositis 56 0.028
578
BRN004 Brain Edema 56 0.028
579
AGN016 Aging 56 0.028
580
NRN004 Neuroendocrine Tumor 55 0.028
581
P PLM034 Pulmonary Emphysema 55 0.028
582
P SLM003 Salmonellosis 55 0.028
583
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.028
584
GLC003 Glucose Intolerance 54 0.028
585
P ART021 Arteriosclerosis 54 0.028
586
DBT010 Diabetic Neuropathy 54 0.028
587
PPL022 Papilloma 54 0.028
588
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.028
589
P EPD016 Epidermolysis Bullosa 53 0.028
590
ECH003 Echinococcosis 53 0.028
591
DNT012 Dental Caries 53 0.028
592
OST011 Osteomalacia 52 0.028
593
SRS001 Serous Cystadenocarcinoma 52 0.028
594
P SPP010 Suppressor of Tumorigenicity 3 51 0.028
595
FDL002 Food Allergy 51 0.028
596
P LCT001 Lactic Acidosis 51 0.028
597
ACT049 Acute Disseminated Encephalomyelitis 51 0.028
598
TRM010 Traumatic Brain Injury 51 0.028
599
HYP781 Hypoascorbemia 51 0.028
600
c SVR005 Severe Pre-Eclampsia 50 0.028
601
STT002 Status Asthmaticus 50 0.028
602
PRT018 Portal Vein Thrombosis 50 0.028
603
BLR001 Biliary Atresia 50 0.028
604
HYP080 Hypogonadism 50 0.028
605
URT001 Urethritis 49 0.028
606
CVR006 Cavernous Hemangioma 49 0.028
607
P ART018 Aortic Valve Insufficiency 49 0.028
608
LFT001 Left Bundle Branch Hemiblock 49 0.028
609
DYS009 Dysthymic Disorder 49 0.028
610
BCT004 Bacteriuria 49 0.028
611
c BCT013 Bacterial Pneumonia 48 0.028
612
CRY004 Cryoglobulinemia 48 0.028
613
RGH001 Right Bundle Branch Block 48 0.028
614
PPL002 Papillary Carcinoma 47 0.028
615
CLF056 Cleft Lip with or Without Cleft Palate 47 0.028
617
P CLL015 Collagen Disease 47 0.028
618
RFT001 Rift Valley Fever 47 0.028
619
TTH006 Tooth Disease 46 0.028
620
P HMR005 Hemorrhoid 46 0.028
621
SQM002 Squamous Cell Papilloma 46 0.028
622
EPD015 Epidemic Typhus 45 0.028
623
PPL018 Papillary Adenocarcinoma 45 0.028
624
CYN002 Cyanosis, Transient Neonatal 45 0.028
625
SPS057 Spasticity 45 0.028
626
SBC016 Subacute Delirium 44 0.028
627
DWR001 Dwarfism 44 0.028
628
CRP002 Croup 44 0.028
629
MTR010 Mature Teratoma 44 0.028
630
SMN007 Seminoma 43 0.028
631
MRG013 Mirage Syndrome 43 0.028
632
ANG011 Angiodysplasia 43 0.028
633
ORL015 Oral Squamous Cell Carcinoma 43 0.028
634
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.028
635
ANC002 Anca-Associated Vasculitis 41 0.028
636
P CYS017 Cystic Teratoma 41 0.028
637
P KLZ004 Kala-Azar 1 41 0.028
638
MSN004 Mesenchymal Cell Neoplasm 41 0.028
639
NNT008 Neonatal Abstinence Syndrome 41 0.028
640
ART008 Arteriosclerosis Obliterans 40 0.028
641
SCR011 Scrapie 39 0.028
642
CHL039 Choledocholithiasis 38 0.028
643
c XLN227 X-Linked Chondrodysplasia Punctata 1 36 0.028
644
c CNG223 Congenital Methemoglobinemia 36 0.028
645
WHP002 Whiplash 36 0.028
646
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.028
647
CHR178 Chromosomal Triplication 35 0.028
648
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 32 0.028
649
BRR001 Barre-Lieou Syndrome 28 0.028
650
MTH071 Methane Production 26 0.028
651
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.028
652
ALL012 Allergic Angiitis 24 0.028
653
LRR002 Lrrk2 Parkinson Disease 19 0.028
654
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 13 0.028
655
YSH001 Yusho Disease 11 0.028
656
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.024
657
INS024 Insulin-Like Growth Factor I 79 0.024
658
LPT014 Leptin Deficiency or Dysfunction 74 0.024
659
SCH036 Scheie Syndrome 72 0.024
660
DWN001 Down Syndrome 70 0.024
661
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.024
662
P TTR001 Tetralogy of Fallot 70 0.024
663
SMT004 Smith-Lemli-Opitz Syndrome 70 0.024
664
P TBR001 Tuberous Sclerosis 70 0.024
665
LYM007 Lymphangioleiomyomatosis 69 0.024
666
MNT001 Mantle Cell Lymphoma 69 0.024
667
P MYC084 Mycobacterium Tuberculosis 1 68 0.024
668
P LKM002 Leukemia 68 0.024
669
c HMP004 Hemophilia B 68 0.024
670
CNN005 Connective Tissue Disease 68 0.024
671
STH001 Saethre-Chotzen Syndrome 67 0.024
672
THY111 Thyroid Carcinoma, Familial Medullary 67 0.024
673
LPT001 Leptospirosis 66 0.024
674
P MCR115 Microvascular Complications of Diabetes 5 66 0.024
675
MYL031 Myeloproliferative Neoplasm 66 0.024
676
BRR014 Barrett Esophagus 65 0.024
677
DRM014 Dermatofibrosarcoma Protuberans 65 0.024
678
KWS002 Kawasaki Disease 65 0.024
679
c DBT099 Diabetes Mellitus, Type I 65 0.024
680
P ADL010 Adult Respiratory Distress Syndrome 65 0.024
681
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.024
682
NRF007 Neurofibroma 64 0.024
683
CLR108 Colorectal Adenoma 64 0.024
684
P PRD008 Periodontitis 64 0.024
685
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.024
686
DSM004 Desmoid Tumor 64 0.024
687
P ANR048 Aniridia 1 63 0.024
688
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.024
689
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.024
690
c GLC092 Glaucoma, Primary Open Angle 62 0.024
691
P ART023 Arthropathy 62 0.024
692
CRC021 Carcinosarcoma 62 0.024
693
MDD011 Mood Disorder 62 0.024
694
NTR005 Nutritional Deficiency Disease 62 0.024
695
NRM001 Neuromyelitis Optica 61 0.024
696
INT002 Intermittent Claudication 61 0.024
697
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.024
698
VGN017 Vaginal Cancer 60 0.024
699
P OPT006 Optic Nerve Disease 60 0.024
700
CRT002 Cartilage-Hair Hypoplasia 59 0.024
701
SPN027 Spinal Stenosis 59 0.024
702
IRN001 Iron Deficiency Anemia 59 0.024
703
SRC027 Sarcoma, Synovial 58 0.024
704
CRY005 Cryptococcosis 58 0.024
705
RBS001 Rabies 58 0.024
706
CRD132 Cardiac Conduction Defect 58 0.024
707
c BNG091 Benign Chronic Pemphigus 58 0.024
708
CCC001 Coccidioidomycosis 58 0.024
709
ADL030 Adult-Onset Still's Disease 58 0.024
710
P EHL001 Ehlers-Danlos Syndrome 58 0.024
711
NWB001 Newborn Respiratory Distress Syndrome 58 0.024
712
P EPD003 Epidermolysis Bullosa Simplex 58 0.024
713
P OPT009 Optic Neuritis 57 0.024
714
c CHL119 Cholangitis, Primary Sclerosing 57 0.024
715
P PLY041 Polymyositis 57 0.024
716
MBS002 Moebius Syndrome 57 0.024
717
THY022 Thymic Carcinoma 57 0.024
718
CMM005 Common Cold 57 0.024
719
CYT008 Cytomegalovirus Infection 57 0.024
720
JPN002 Japanese Encephalitis 57 0.024
721
HYP266 Hypoxia 57 0.024
722
P PYL005 Pyelonephritis 56 0.024
723
DNN002 Donnai-Barrow Syndrome 56 0.024
724
P MLT074 Multiple Endocrine Neoplasia 56 0.024
725
ALL006 Allergic Asthma 56 0.024
726
PRS047 Prostatitis 56 0.024
727
OVR012 Ovarian Serous Cystadenocarcinoma 56 0.024
728
c MCR256 Microphthalmia, Syndromic 9 56 0.024
729
INT030 Intracranial Aneurysm 56 0.024
730
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.024
731
HPT022 Hepatoblastoma 56 0.024
732
BRN012 Bronchiolitis Obliterans 55 0.024
733
ADR008 Adrenal Adenoma 55 0.024
734
NRG002 Neurogenic Bladder 55 0.024
735
P TWN003 Townes-Brocks Syndrome 55 0.024
736
P STR020 Strabismus 55 0.024
737
ACT058 Active Peptic Ulcer Disease 55 0.024
738
P VNS003 Venous Insufficiency 55 0.024
739
ESN011 Eisenmenger Syndrome 55 0.024
740
END040 Endogenous Depression 55 0.024
741
CLF004 Cleft Lip/palate 54 0.024
742
FRN039 Frank-Ter Haar Syndrome 54 0.024
743
NCR004 Nocardiosis 54 0.024
744
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.024
745
P RST001 Restless Legs Syndrome 54 0.024
746
BRN014 Bronchopneumonia 54 0.024
747
HMS001 Hemosiderosis 54 0.024
748
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 54 0.024
749
MYM001 Myoma 54 0.024
750
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 0.024
751
NNL006 Non-Alcoholic Steatohepatitis 54 0.024
752
c SPN294 Spinocerebellar Ataxia 1 53 0.024
753
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.024
754
HRT012 Heart Valve Disease 53 0.024
755
P MNC007 Monocytic Leukemia 53 0.024
756
MST005 Mastitis 53 0.024
757
CYS005 Cysticercosis 53 0.024
758
P HML001 Hemolytic-Uremic Syndrome 53 0.024
759
INT075 Intracranial Hypertension 53 0.024
760
NRT001 Neurotic Disorder 53 0.024
761
P PNC025 Panic Disorder 53 0.024
762
EXP004 Exophthalmos 52 0.024
763
CHR073 Choreatic Disease 52 0.024
764
P PRG013 Paraganglioma 52 0.024
765
P HYP730 Hypogonadotropic Hypogonadism 52 0.024
766
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.024
767
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.024
768
P THY032 Thyroiditis 52 0.024
769
PPT001 Peptic Esophagitis 52 0.024
770
THR004 Thrombocytosis 51 0.024
771
c ALB020 Albinism, Oculocutaneous, Type Iii 51 0.024
772
MYL001 Myelitis 51 0.024
773
LNG095 Lung Abscess 51 0.024
774
P PRM018 Primary Hypertrophic Osteoarthropathy 51 0.024
775
P MRR011 Mirror Movements 1 51 0.024
776
CYS014 Cystadenocarcinoma 51 0.024
777
ESP002 Esophageal Varix 51 0.024
778
TLR001 Tularemia 51 0.024
779
P HYP040 Hypospadias 51 0.024
780
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.024
781
INT071 Intestinal Perforation 51 0.024
782
CHR005 Chorioamnionitis 51 0.024
783
P MMB011 Membranous Nephropathy 50 0.024
784
PLR008 Pleurisy 50 0.024
785
RDC002 Radiculopathy 50 0.024
786
DDN011 Duodenal Atresia 50 0.024
787
PRN009 Paranoid Schizophrenia 50 0.024
788
BLS002 Blastomycosis 50 0.024
789
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.024
790
PPL021 Papilledema 49 0.024
791
RJS001 Ruijs-Aalfs Syndrome 49 0.024
792
VLV047 Volvulus of Midgut 49 0.024
793
CRD002 Cri-Du-Chat Syndrome 49 0.024
794
MNN009 Meningoencephalitis 49 0.024
795
BRN071 Brain Injury 49 0.024
796
URM002 Uremia 49 0.024
797
P BRS053 Breast Fibroadenoma 49 0.024
798
VCC001 Vaccinia 49 0.024
799
MLR002 Miliary Tuberculosis 49 0.024
800
CRY014 Cryptococcal Meningitis 48 0.024
801
INT067 Interstitial Nephritis 48 0.024
802
BBS001 Babesiosis 48 0.024
803
P SCL015 Scleritis 48 0.024
804
P GND004 Gonadal Dysgenesis 48 0.024
805
TBR011 Tuberculous Meningitis 48 0.024
806
VTM002 Vitamin B12 Deficiency 48 0.024
807
HPR003 Heparin-Induced Thrombocytopenia 48 0.024
808
CRN017 Coronary Thrombosis 47 0.024
809
c INH020 Inherited Metabolic Disorder 47 0.024
810
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.024
811
AML029 Ameloblastoma 46 0.024
812
RTN023 Retinitis 46 0.024
813
ASP004 Asphyxia Neonatorum 46 0.024
814
TST014 Testicular Cancer 46 0.024
815
SMT001 Somatization Disorder 46 0.024
816
MTS001 Mutism 46 0.024
817
ANK017 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate 46 0.024
818
P HRT035 Heart Block, Congenital 46 0.024
819
P PLL002 Pellagra 46 0.024
820
SPR010 Sporotrichosis 46 0.024
821
END031 Endometrial Stromal Sarcoma 46 0.024
822
VGN019 Vaginal Discharge 46 0.024
823
ANG018 Angiomyolipoma 46 0.024
824
c MLG068 Malignant Glioma 46 0.024
825
LGH003 Leigh Syndrome, French Canadian Type 45 0.024
826
c TRC022 Tricuspid Valve Insufficiency 45 0.024
827
HMR023 Hemorrhagic Cystitis 45 0.024
828
CRB004 Cerebral Artery Occlusion 45 0.024
829
P PRD021 Periodic Paralysis 45 0.024
830
GRN017 Granulocytopenia 44 0.024
831
c PCH010 Pachyonychia Congenita 3 44 0.024
832
c HYP272 Hypercholesterolemia, Familial, 3 44 0.024
833
VNC001 Von Economo's Disease 44 0.024
834
HSD004 Hsd10 Mitochondrial Disease 44 0.024
835
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.024
836
DPR002 Depersonalization Disorder 43 0.024
837
SPN369 Spinal Disease 43 0.024
838
RFR003 Refractive Error 43 0.024
839
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.024
840
LWC001 Low Compliance Bladder 43 0.024
841
DYS032 Dystrophinopathies 43 0.024
842
P CRN035 Cranial Nerve Palsy 42 0.024
843
MNN017 Mononeuropathy 42 0.024
844
ATX019 Ataxia with Vitamin E Deficiency 42 0.024
845
NRR001 Neuroretinitis 42 0.024
846
MCH006 Mechanical Strabismus 42 0.024
847
MNN002 Mononeuritis Multiplex 41 0.024
848
ELP001 Elephantiasis 41 0.024
849
P RRH023 Rare Hereditary Hemochromatosis 41 0.024
850
OGD001 Ogden Syndrome 41 0.024
851
WLL039 Well-Differentiated Liposarcoma 41 0.024
852
RDN001 Reading Disorder 40 0.024
853
BDY001 Body Dysmorphic Disorder 40 0.024
854
P DYS005 Dyslexia 40 0.024
855
CRB086 Cerebral Aneurysms 40 0.024
856
MNK002 Monkeypox 39 0.024
857
DSS010 Dissociative Disorder 39 0.024
858
MCK029 Meckel Diverticulum 38 0.024
859
TRC005 Tracheal Stenosis 38 0.024
860
PSD016 Pseudosarcomatous Fibromatosis 37 0.024
861
PNB004 Panbronchiolitis, Diffuse 37 0.024
862
WNC001 Winchester Syndrome 36 0.024
863
P MXL015 Maxillary Sinusitis 36 0.024
864
BRK012 Broken Heart Syndrome 35 0.024
865
c TYP024 Type Ii Mixed Cryoglobulinemia 34 0.024
866
SPR006 Sparganosis 34 0.024
867
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.024
868
PPL052 Papillomatosis, Confluent and Reticulated 33 0.024
869
BNN005 Bunion 33 0.024
870
TXC020 Toxic Oil Syndrome 33 0.024
871
OTD001 Otodental Dysplasia 33 0.024
872
RMB001 Rombo Syndrome 31 0.024
873
SDD002 Sudden Infant Death with Dysgenesis of the Testes Syndrome 31 0.024
874
URC003 Urachal Adenocarcinoma 31 0.024
875
BRS057 Breast Mucinous Carcinoma 30 0.024
876
MTG001 Metagonimiasis 29 0.024
877
FTL064 Fetal Methylmercury Syndrome 26 0.024
878
CRT028 Cor Triatriatum 26 0.024
879
VRL002 Variola Minor 25 0.024
880
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.024
881
SPN356 Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia 21 0.024
882
NWN001 New-Onset Refractory Status Epilepticus 21 0.024
883
MYC021 Mycobacterium Xenopi 20 0.024
884
BLD153 Blood Group--Swann System 17 0.024
885
BRM001 Barmah Forest Virus Disease 14 0.024
886
VRB002 Variably Protease-Sensitive Prionopathy 13 0.024
887
YTB001 Yt Blood Group Antigen 9 0.024
888
c HRD112 Hereditary Thrombocytopenia with Normal Platelets 8 0.024
889
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.020
890
c FNC027 Fanconi Anemia, Complementation Group a 81 0.020
891
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.020
892
P RTN008 Retinitis Pigmentosa 79 0.020
893
PFF001 Pfeiffer Syndrome 79 0.020
894
P PRK057 Parkinson Disease, Late-Onset 78 0.020
895
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.020
896
KPS004 Kaposi Sarcoma 75 0.020
897
PHN003 Phenylketonuria 75 0.020
898
ADR007 Adrenoleukodystrophy 75 0.020
899
BRN028 Brain Cancer 74 0.020
900
BSL036 Basal Cell Nevus Syndrome 73 0.020
901
P FML018 Familial Mediterranean Fever 73 0.020
902
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.020
903
FBR012 Fabry Disease 72 0.020
904
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.020
905
P BRG001 Brugada Syndrome 71 0.020
906
MLT157 Multiple System Atrophy 1 70 0.020
907
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.020
908
ADN011 Adenoid Cystic Carcinoma 70 0.020
909
c PNC108 Pancreatitis, Hereditary 70 0.020
910
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.020
911
c BSL007 Basal Cell Carcinoma 68 0.020
912
GST092 Gastroesophageal Reflux 67 0.020
913
c INF071 Inflammatory Bowel Disease 1 67 0.020
914
FCT007 Factor Vii Deficiency 67 0.020
915
BRK010 Burkitt Lymphoma 67 0.020
916
ALL003 Allergic Rhinitis 67 0.020
917
c HMP029 Hemophilia a 67 0.020
918
P TRN020 Turner Syndrome 67 0.020
919
MYC006 Mycosis Fungoides 66 0.020
921
P LYS001 Loeys-Dietz Syndrome 65 0.020
922
P ART005 Arteriovenous Malformation 65 0.020
923
P AGM001 Agammaglobulinemia 65 0.020
924
ACR006 Aceruloplasminemia 65 0.020
925
P VNW001 Von Willebrand's Disease 65 0.020
926
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.020
927
c ART101 Aortic Valve Disease 2 65 0.020
928
c WLM013 Wilms Tumor 1 65 0.020
929
CLN015 Colon Adenocarcinoma 65 0.020
930
CRB011 Cerebrotendinous Xanthomatosis 65 0.020
931
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.020
932
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.020
933
MSC007 Muscle Hypertrophy 64 0.020
934
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.020
935
HYP020 Hyperprolactinemia 64 0.020
936
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.020
937
KRN002 Kearns-Sayre Syndrome 63 0.020
938
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.020
939
P GCH001 Gaucher's Disease 63 0.020
940
c MLG084 Malignant Fibrous Histiocytoma 63 0.020
941
P SHR029 Short Syndrome 63 0.020
942
ERL001 Early Myoclonic Encephalopathy 62 0.020
943
PRM126 Primary Peritoneal Carcinoma 62 0.020
944
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.020
945
HYD038 Hydrops Fetalis, Nonimmune 62 0.020
946
P BCK002 Beckwith-Wiedemann Syndrome 62 0.020
947
LSC001 Lesch-Nyhan Syndrome 62 0.020
948
PHL006 Phelan-Mcdermid Syndrome 62 0.020
949
P ACR001 Aicardi-Goutieres Syndrome 62 0.020
950
ESP020 Esophageal Atresia 62 0.020
951
c WLM018 Wilms Tumor 5 61 0.020
952
VRL011 Viral Infectious Disease 61 0.020
953
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.020
954
DCB001 Decubitus Ulcer 61 0.020
955
BTN003 Biotinidase Deficiency 60 0.020
956
c LPM012 Lipomatosis, Multiple 60 0.020
957
TRG002 Trigeminal Neuralgia 60 0.020
958
CRD223 Cardiac Arrhythmia 60 0.020
959
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.020
960
DNG002 Dengue Hemorrhagic Fever 60 0.020
961
P SNS001 Sensorineural Hearing Loss 60 0.020
962
P OCL002 Oculocutaneous Albinism 60 0.020
963
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.020
964
ANT009 Antithrombin Iii Deficiency 59 0.020
965
PRT058 Pure Autonomic Failure 59 0.020
966
P PRD006 Prader-Willi Syndrome 59 0.020
967
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.020
968
P BRS044 Breast Adenocarcinoma 59 0.020
969
GRD007 Grade Iii Astrocytoma 59 0.020
970
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.020
971
P DNG005 Dengue Virus 59 0.020
972
P ADM011 Adams-Oliver Syndrome 59 0.020
973
MNK003 Muenke Syndrome 59 0.020
974
INC002 Inclusion Body Myositis 58 0.020
975
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.020
976
P ANP001 Anaplastic Large Cell Lymphoma 58 0.020
977
P PGT001 Paget's Disease of Bone 58 0.020
978
ERY003 Erythema Multiforme 58 0.020
979
LYM027 Lymphopenia 58 0.020
980
EXT034 Extrinsic Allergic Alveolitis 58 0.020
981
PMP006 Pemphigus Vulgaris, Familial 57 0.020
982
P ESP035 Esophagitis, Eosinophilic, 1 57 0.020
983
P PLV020 Pelvic Organ Prolapse 57 0.020
984
c VSC019 Vesicoureteral Reflux 1 57 0.020
985
P MYM013 Moyamoya Disease 1 57 0.020
986
CHR003 Cherubism 57 0.020
987
CHK001 Chikungunya 57 0.020
988
APH001 Aphthous Stomatitis 57 0.020
989
c ART061 Arthrogryposis, Distal, Type 2a 57 0.020
990
TNS005 Tonsillitis 57 0.020
991
P CRD246 Cardiovascular System Disease 57 0.020
992
P FTL001 Fetal Alcohol Syndrome 57 0.020
993
VSC002 Vascular Dementia 57 0.020
994
c LKM070 Leukemia, Acute Monocytic 57 0.020
995
INT303 Intracranial Hypertension, Idiopathic 57 0.020
996
AYM001 Ayme-Gripp Syndrome 57 0.020
997
c LSS005 Lissencephaly 1 56 0.020
998
TCK001 Tick-Borne Encephalitis 56 0.020
999
P PNL012 Penile Cancer 56 0.020
1000
SFT003 Soft Tissue Sarcoma 56 0.020
1001
ISL001 Islet Cell Tumor 56 0.020
1002
ANN002 Anencephaly 56 0.020
1003
EMB004 Embryonal Carcinoma 56 0.020
1004
MCR141 Mucormycosis 56 0.020
1005
PRP082 Porphyria, Congenital Erythropoietic 56 0.020
1006
P PNM006 Pneumoconiosis 56 0.020
1007
P PLY019 Polyneuropathy 56 0.020
1008
ANS023 Anus, Imperforate 56 0.020
1009
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.020
1010
HST011 Histoplasmosis 55 0.020
1011
FDB001 Foodborne Botulism 55 0.020
1012
ZLL002 Zollinger-Ellison Syndrome 55 0.020
1013
PLV003 Pelvic Inflammatory Disease 55 0.020
1014
MMB001 Membranoproliferative Glomerulonephritis 55 0.020
1015
P MLN007 Male Infertility 55 0.020
1016
NPH009 Nephrolithiasis 55 0.020
1018
P PMP001 Pemphigus 54 0.020
1019
MNN032 Meningococcal Meningitis 54 0.020
1020
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.020
1021
FCL014 Focal Epilepsy 54 0.020
1022
MWT001 Mowat-Wilson Syndrome 54 0.020
1023
TND005 Tendinitis 54 0.020
1024
LYM040 Lymphoblastic Lymphoma 54 0.020
1025
HLL004 Hellp Syndrome 54 0.020
1026
SNS003 Sensory Peripheral Neuropathy 54 0.020
1027
CLR030 Clear Cell Renal Cell Carcinoma 53 0.020
1028
PLM012 Pulmonary Sarcoidosis 53 0.020
1029
P LCH002 Lichen Planus 53 0.020
1030
P END047 Endophthalmitis 53 0.020
1031
FRZ001 Frozen Shoulder 53 0.020
1032
CRY001 Cryptogenic Organizing Pneumonia 53 0.020
1033
RHM028 Rheumatic Heart Disease 53 0.020
1034
PRP036 Peripheral T-Cell Lymphoma 53 0.020
1035
BRD004 Borderline Personality Disorder 53 0.020
1036
P SHR001 Short Bowel Syndrome 53 0.020
1037
P HMR003 Hemorrhagic Disease 53 0.020
1038
FNG017 Fungal Infectious Disease 53 0.020
1039
HYP063 Hypersplenism 53 0.020
1040
GSG001 Gas Gangrene 53 0.020
1041
ERD001 Erdheim-Chester Disease 53 0.020
1042
IRD001 Iridocyclitis 53 0.020
1043
TRC008 Trachoma 53 0.020
1044
P RTN018 Retinal Disease 53 0.020
1045
STT041 Stuttering 52 0.020
1046
DRM011 Dermatophytosis 52 0.020
1047
MGC002 Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 52 0.020
1048
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 52 0.020
1049
P DDN001 Duodenal Ulcer 52 0.020
1050
MRG003 Marginal Zone B-Cell Lymphoma 52 0.020
1051
P PRR016 Pierre Robin Syndrome 52 0.020
1052
P DNT011 Dentinogenesis Imperfecta 52 0.020
1053
PTH003 Pathologic Nystagmus 52 0.020
1054
APR001 Apraxia 52 0.020
1055
ACT200 Acute Monoblastic Leukemia 52 0.020
1056
P PLG001 Pelger-Huet Anomaly 51 0.020
1057
UNV001 Unverricht-Lundborg Syndrome 51 0.020
1058
c PNC106 Pancreatic Agenesis 1 51 0.020
1059
P LSS002 Lissencephaly 51 0.020
1060
CLB002 Clubfoot 51 0.020
1061
SPN019 Spondylolisthesis 51 0.020
1062
SPL004 Splenic Marginal Zone Lymphoma 51 0.020
1063
P THR015 Thrombophilia 51 0.020
1064
BLL003 Bell's Palsy 51 0.020
1065
ACH005 Achalasia 51 0.020
1066
HND002 Hand, Foot and Mouth Disease 51 0.020
1067
TNG007 Tongue Carcinoma 51 0.020
1068
ASP003 Aseptic Meningitis 51 0.020
1069
c VRL007 Viral Encephalitis 51 0.020
1070
P AST007 Astrocytoma 51 0.020
1071
P RNL007 Renal Tubular Acidosis 51 0.020
1072
URC002 Urea Cycle Disorder 51 0.020
1073
IRN008 Iron Overload in Africa 51 0.020
1074
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.020
1075
SCB001 Scabies 50 0.020
1076
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.020
1077
P 46X052 46,xx Sex Reversal 1 50 0.020
1078
c HNT004 Huntington Disease-Like 2 50 0.020
1079
PST021 Postpartum Depression 50 0.020
1080
CRN030 Coronary Stenosis 50 0.020
1081
c EPL025 Epileptic Encephalopathy, Early Infantile, 2 50 0.020
1082
ATR002 Atransferrinemia 50 0.020
1083
CHL122 Cholesteatoma of Middle Ear 50 0.020
1084
ASC010 Ascaris Lumbricoides Infection 50 0.020
1085
THY125 Thyroid Gland Medullary Carcinoma 50 0.020
1086
P TMP001 Temporal Lobe Epilepsy 50 0.020
1087
c LRG001 Large Cell Carcinoma 50 0.020
1088
TRP002 Tropical Spastic Paraparesis 50 0.020
1089
c INF023 Inflammatory Breast Carcinoma 50 0.020
1090
P ATR005 Atrophic Gastritis 50 0.020
1091
RNL011 Renal Osteodystrophy 50 0.020
1092
P KLN006 Koolen-De Vries Syndrome 49 0.020
1093