Search results for proc

964 hits were found for proc

# Family MCID Name MIFTS Score
1
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 38 73.865
2
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 29 72.289
3
PRT011 Protein C Deficiency 47 47.164
4
P THR015 Thrombophilia 51 24.549
5
c THR092 Thrombophilia Due to Thrombin Defect 74 24.068
6
THR024 Thrombosis 56 23.277
7
P PRP034 Purpura Fulminans 41 20.999
8
c THR082 Thrombophilia Due to Activated Protein C Resistance 59 20.199
9
PRP030 Purpura 54 19.256
10
PRT014 Protein S Deficiency 41 14.096
11
PLM033 Pulmonary Embolism 58 13.020
12
PLC007 Placental Abruption 47 12.116
13
P THR014 Thrombocytopenia 66 11.001
14
P VND001 Vein Disease 42 10.838
15
PRT018 Portal Vein Thrombosis 50 10.445
16
P HRD209 Hereditary Angioedema with Normal C1inh 30 8.987
17
NNT024 Neonatal Stroke 33 8.349
18
BLD051 Blood Coagulation Disease 53 7.779
19
THR016 Thrombophlebitis 50 7.386
20
P NRN021 Neuronal Ceroid Lipofuscinosis 65 7.386
21
P HMR003 Hemorrhagic Disease 59 7.386
22
MNN021 Meningococcemia 34 7.386
23
CTS005 Catastrophic Antiphospholipid Syndrome 43 7.386
24
HLX001 Helix Syndrome 48 4.398
25
P OVR042 Ovarian Cancer 88 3.814
27
HMN044 Human Immunodeficiency Virus Type 1 78 3.022
28
P HRP006 Herpes Simplex 65 2.782
29
PRT037 Pertussis 65 2.457
30
VCC001 Vaccinia 47 2.425
31
STM007 Stomatitis 54 2.425
32
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.225
33
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 1.967
34
P NRB001 Neuroblastoma 66 1.967
35
DSS009 Disseminated Intravascular Coagulation 57 1.908
36
c PRC016 Pre-Eclampsia 65 1.888
37
HLL004 Hellp Syndrome 53 1.888
38
ACT098 Acute Erythroid Leukemia 55 1.887
39
47X002 47,xyy 48 1.887
40
CHL014 Cholera 62 1.887
41
P LVR013 Liver Disease 69 1.821
42
IMM167 Immune Deficiency Disease 78 1.803
43
HRW001 Hair Whorl 35 1.759
44
P CRD246 Cardiovascular System Disease 56 1.749
45
PLC008 Placenta Disease 49 1.672
46
c SVR005 Severe Pre-Eclampsia 50 1.672
47
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.622
48
SVR004 Severe Combined Immunodeficiency 72 1.622
49
c ANG045 Angioedema, Hereditary, Type Iii 30 1.601
50
P ALZ034 Alzheimer Disease 87 1.574
51
PLY150 Polykaryocytosis Inducer 29 1.574
52
BRK010 Burkitt Lymphoma 66 1.574
53
P NTR004 Neutropenia 63 1.574
54
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.574
55
c LKM005 Leukemia, T-Cell, Chronic 34 1.574
56
AGN016 Aging 54 1.524
57
P HNT016 Huntington Disease 73 1.524
58
48X005 48,xyyy 39 1.524
59
GLM045 Glioma 63 1.524
60
END057 Endometrial Cancer 72 1.495
61
ATS010 Autosomal Recessive Disease 42 1.495
62
EXT007 Extracutaneous Mastocytoma 38 1.495
63
MST004 Mast Cell Neoplasm 42 1.495
64
SCR011 Scrapie 39 1.472
65
DPH001 Diphtheria 59 1.472
66
P DRR001 Diarrhea 55 1.472
67
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.418
68
GLL048 Glial Tumor 52 1.418
69
SPN035 Spindle Cell Sarcoma 54 1.418
70
P END046 Endometritis 46 1.418
71
SRC014 Sarcoma 65 1.418
72
OVR094 Ovarian Epithelial Cancer 39 1.418
73
CHR431 Chronic Venous Insufficiency 48 1.389
74
c VRL010 Viral Hepatitis 53 1.389
75
P SYP003 Syphilis 59 1.389
76
P VNS003 Venous Insufficiency 55 1.389
77
VTM033 Vitamin K Deficiency Bleeding 48 1.389
78
P PHC003 Pheochromocytoma 69 1.363
79
c HPT073 Hepatitis C Virus 71 1.363
80
P RTN024 Retinoblastoma 73 1.363
81
OST159 Osteogenic Sarcoma 66 1.363
82
HND015 Hand Skill, Relative 30 1.363
83
ATH013 Atherosclerosis Susceptibility 63 1.305
84
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.305
85
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.305
86
ADR040 Adrenal Gland Pheochromocytoma 46 1.305
87
P BPL003 Bipolar Disorder 56 1.305
88
P PLY006 Polydactyly 59 1.264
89
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.264
90
P PNC035 Pancreatic Cancer 86 1.255
91
P PRS040 Prostate Cancer 95 1.255
92
INS024 Insulin-Like Growth Factor I 78 1.244
93
CYS001 Cystic Fibrosis 78 1.244
94
c MJR022 Major Affective Disorder 8 38 1.244
95
c MJR024 Major Affective Disorder 9 41 1.244
96
TRT001 Teratocarcinoma 42 1.244
97
P FBR017 Fibrosarcoma 56 1.244
98
P MLN008 Melanoma 76 1.244
99
P ADN016 Adenocarcinoma 63 1.244
100
TTN003 Tetanus 65 1.244
101
EMB004 Embryonal Carcinoma 56 1.244
102
c HPT016 Hepatitis B 62 1.244
103
HMP009 Haemophilus Influenzae 41 1.244
104
ANX004 Anoxia 40 1.180
105
P GLM040 Glioma Susceptibility 1 71 1.180
106
PST092 Posttransplant Acute Limbic Encephalitis 28 1.180
107
P SKN015 Skin Carcinoma 71 1.180
108
VGN019 Vaginal Discharge 47 1.180
109
P PRN023 Prion Disease 60 1.180
110
P BRS047 Breast Cancer 98 1.130
111
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.113
112
MSC007 Muscle Hypertrophy 64 1.113
113
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.113
114
KPS004 Kaposi Sarcoma 77 1.113
116
CRH001 Crohn's Disease 80 1.113
117
P BCL017 B-Cell Lymphoma 59 1.113
118
P INF038 Influenza 68 1.113
119
P LTR001 Lateral Sclerosis 58 1.113
120
CLN015 Colon Adenocarcinoma 65 1.113
121
P RHN004 Rhinitis 57 1.113
123
P MYC007 Myocardial Infarction 70 1.101
124
PRC003 Proctitis 49 1.101
125
RHM001 Rheumatic Fever 59 1.101
126
P THL005 Thalassemia 56 1.041
127
ALL003 Allergic Rhinitis 67 1.041
128
ALC007 Alcohol Dependence 66 1.041
129
c HYP836 Hypercholesterolemia, Familial, 1 73 1.041
130
c HPT003 Hepatitis a 63 1.041
131
P AMY004 Amyloidosis 70 1.041
132
MTH009 Mouth Disease 57 1.041
133
INT078 Intracranial Thrombosis 50 1.041
134
P LNG064 Lung Cancer Susceptibility 3 70 1.041
135
P LKM002 Leukemia 67 1.041
136
PPL022 Papilloma 53 1.041
137
SQM002 Squamous Cell Papilloma 46 1.041
138
MLG169 Malignant Astrocytoma 57 1.041
139
P HRT032 Heart Disease 81 1.041
140
RBS001 Rabies 58 1.041
141
LPD008 Lipid Metabolism Disorder 62 1.041
142
P CHR345 Chronic Pain 50 1.041
143
PTT037 Pituitary Tumors 44 1.041
144
SPN186 Spinal Cord Injury 61 0.964
145
P RTN008 Retinitis Pigmentosa 80 0.964
146
P ADL017 Adult T-Cell Leukemia 56 0.964
147
P ANP001 Anaplastic Large Cell Lymphoma 61 0.964
148
MLR004 Malaria 80 0.964
149
c BTT014 Beta-Thalassemia 72 0.964
150
DFF005 Diffuse Large B-Cell Lymphoma 54 0.964
151
P LYM118 Lymphoma 67 0.964
152
LTN004 Late-Onset Retinal Degeneration 60 0.964
153
c SML038 Small Cell Cancer of the Lung 69 0.964
154
DSS032 Disease by Infectious Agent 55 0.964
155
NRR001 Neuroretinitis 42 0.964
156
MDD018 Middle East Respiratory Syndrome 44 0.964
157
RTN023 Retinitis 46 0.964
158
CLF001 Cleft Lip 53 0.964
159
CHC001 Chickenpox 57 0.964
160
P BRS044 Breast Adenocarcinoma 58 0.964
161
P CTR002 Cataract 60 0.964
162
ALL029 Allergic Disease 59 0.964
163
LYM040 Lymphoblastic Lymphoma 53 0.964
164
CRD001 Cardiac Tamponade 43 0.964
165
MTR002 Mitral Valve Insufficiency 52 0.964
166
PLG002 Plague 58 0.964
167
LYS002 Lysosomal Storage Disease 51 0.964
168
P ENC004 Encephalitis 61 0.964
169
CYT002 Cytokine Deficiency 43 0.964
170
MSL001 Measles 61 0.964
171
P LNG032 Lung Cancer 98 0.880
172
P NSP012 Nasopharyngeal Carcinoma 61 0.880
173
P MYC084 Mycobacterium Tuberculosis 1 68 0.880
174
P SCH015 Schizophrenia 74 0.880
175
PPL052 Papillomatosis, Confluent and Reticulated 34 0.880
176
ATM095 Autoimmune Disease 61 0.880
177
P FML011 Familial Adenomatous Polyposis 71 0.880
178
P EXN002 Exanthem 58 0.880
179
PRT251 Proteinuria, Chronic Benign 57 0.880
180
CLT003 Colitis 63 0.880
181
c BRN108 Branchiootic Syndrome 1 62 0.880
182
SCK003 Sickle Cell Anemia 74 0.880
183
MYL069 Myeloma, Multiple 77 0.880
184
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.880
185
ARG004 Argyria 26 0.880
186
c HPT001 Hepatitis C 62 0.880
187
P RTN016 Retinal Degeneration 52 0.880
188
BRN028 Brain Cancer 74 0.880
189
P HYD006 Hydrocephalus 61 0.880
190
CHL123 Chlamydia 58 0.880
191
NWC001 Newcastle Disease 47 0.880
192
DPR016 Depression 65 0.880
193
c HMC039 Hemochromatosis, Type 1 73 0.787
194
P BLD134 Bladder Cancer 79 0.787
195
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.787
196
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.787
197
OBN001 Ouabain Resistance 16 0.787
198
RTC012 Reticuloendotheliosis, X-Linked 35 0.787
199
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.787
200
P LPR021 Leprosy 3 71 0.787
201
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.787
202
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.787
203
P DRM053 Dermatitis, Atopic 65 0.787
204
BRT054 Brittle Bone Disorder 74 0.787
205
ANX010 Anxiety 70 0.787
206
OBS002 Obsessive-Compulsive Disorder 68 0.787
207
P LKM071 Leukemia, Chronic Lymphocytic 75 0.787
208
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.787
209
DFC004 Deficiency Anemia 74 0.787
210
P CHN012 Chondrosarcoma 57 0.787
211
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.787
212
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.787
213
P GST053 Gastric Cancer 83 0.787
214
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.787
215
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.787
216
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.787
217
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.787
218
c TYP009 Type 2 Diabetes Mellitus 92 0.787
219
FBR054 Fibroma 44 0.787
220
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.787
221
c ACT073 Acute Leukemia 58 0.787
222
P PRK039 Parkinsonism 55 0.787
223
TRM010 Traumatic Brain Injury 51 0.787
224
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.787
225
P LPS004 Lupus Erythematosus 61 0.787
226
P MYP004 Myopathy 67 0.787
227
P RHB003 Rhabdomyosarcoma 66 0.787
228
P DBT009 Diabetes Mellitus 67 0.787
229
P MYL006 Myeloid Leukemia 61 0.787
230
FTT001 Fatty Liver Disease 62 0.787
231
P HML002 Hemolytic Anemia 62 0.787
232
HMG002 Hemoglobinuria 50 0.787
233
P TRM003 Tremor 48 0.787
234
P ALP008 Alopecia 54 0.787
235
P MSC005 Muscular Dystrophy 67 0.787
236
FDL002 Food Allergy 47 0.787
237
MNT002 Mental Depression 57 0.787
238
ANT024 Anthrax Disease 58 0.787
239
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.787
240
DNT012 Dental Caries 53 0.787
241
SNS003 Sensory Peripheral Neuropathy 52 0.787
242
P GCH001 Gaucher's Disease 70 0.787
243
P HPT021 Hepatitis 69 0.787
244
CNG034 Congestive Heart Failure 69 0.787
245
P KDN017 Kidney Cancer 61 0.787
246
MDD011 Mood Disorder 62 0.787
247
GST045 Gastroenteritis 58 0.787
248
c FML021 Familial Hypercholesterolemia 72 0.787
249
P ADL010 Adult Respiratory Distress Syndrome 71 0.787
250
APH001 Aphthous Stomatitis 58 0.787
251
P NRF002 Neurofibromatosis 57 0.787
252
HNS001 Hansen's Disease 32 0.787
253
WLL004 Wallerian Degeneration 38 0.787
254
P ENC018 Encephalopathy 62 0.787
255
HDN002 Head Injury 44 0.787
256
P SCK005 Sickle Cell Disease 56 0.787
257
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.787
258
GRW007 Growth Hormone Deficiency 46 0.708
259
SPP011 Suppression of Tumorigenicity 12 61 0.708
260
CRB132 Cerebral Sinovenous Thrombosis 30 0.708
261
c ACT075 Acute Myocardial Infarction 56 0.708
262
OVR063 Overnutrition 42 0.708
263
CRV040 Cervix Carcinoma 50 0.708
264
P ATS364 Autism 69 0.681
265
c TYP008 Type 1 Diabetes Mellitus 70 0.681
266
PLY100 Polyploidy 36 0.681
267
INT358 Intestinal Polyposis Syndrome 25 0.681
268
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 0.681
269
P OVR082 Overgrowth Syndrome 49 0.681
270
P CRN300 Coronary Heart Disease 1 73 0.681
271
c THY107 Thymoma, Familial 42 0.681
272
P FRG001 Fragile X Syndrome 70 0.681
273
MSC157 Muscular Dystrophy, Duchenne Type 79 0.681
274
P AST005 Asthma 76 0.681
275
STR067 Stroke, Ischemic 80 0.681
276
P RHM011 Rheumatoid Arthritis 82 0.681
277
MLN071 Melanoma Tumor Antigen Gp90 17 0.681
278
c SYS001 Systemic Lupus Erythematosus 87 0.681
279
c ATR087 Atrial Standstill 1 74 0.681
280
c MGR028 Migraine with or Without Aura 1 64 0.681
281
PRP027 Peripheral Vascular Disease 71 0.681
282
FDB001 Foodborne Botulism 55 0.681
283
c ATS007 Autism Spectrum Disorder 72 0.681
284
MLD018 Mild Cognitive Impairment 48 0.681
285
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.681
286
c LKM061 Leukemia, Acute Myeloid 83 0.681
287
NRL016 Neural Tube Defects 81 0.681
288
HXS001 Hexosaminidase C 11 0.681
289
PLM059 Pulmonary Atresia with Ventricular Septal Defect 29 0.681
290
c HNT011 Huntington Disease-Like 3 34 0.681
291
c PCH010 Pachyonychia Congenita 3 43 0.681
292
P MJR001 Major Depressive Disorder 68 0.681
293
WST005 West Nile Virus 57 0.681
294
OCL069 Ocular Motor Apraxia 57 0.681
295
P TTR001 Tetralogy of Fallot 69 0.681
296
P SPP010 Suppressor of Tumorigenicity 3 51 0.681
297
P MJR007 Major Affective Disorder 1 42 0.681
298
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.681
299
P HYP750 Hypertriglyceridemia, Familial 62 0.681
300
PNG002 Pain Agnosia 51 0.681
301
URM002 Uremia 47 0.681
302
P VSC011 Vasculitis 61 0.681
303
ULC004 Ulcerative Colitis 74 0.681
304
CHR074 Choriocarcinoma 46 0.681
305
HPT022 Hepatoblastoma 54 0.681
306
YLL002 Yellow Fever 61 0.681
307
P VNT002 Ventricular Septal Defect 58 0.681
308
HRT011 Heart Septal Defect 49 0.681
309
SVR001 Severe Acute Respiratory Syndrome 67 0.681
310
ACQ007 Acquired Immunodeficiency Syndrome 59 0.681
311
OST012 Osteoarthritis 77 0.681
312
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.681
313
SWN001 Swine Influenza 46 0.681
314
P DNG005 Dengue Virus 56 0.681
315
P DMN002 Dementia 66 0.681
316
CHG001 Chagas Disease 66 0.681
317
P HYP061 Hypertrophic Cardiomyopathy 69 0.681
318
c BPL002 Bipolar I Disorder 47 0.681
319
CCC002 Coccidiosis 50 0.681
320
HGH043 High Grade Glioma 45 0.681
321
P ECL001 Eclampsia 52 0.681
322
GST033 Gestational Diabetes 61 0.681
323
MST005 Mastitis 53 0.681
324
MCR013 Microphthalmia 60 0.681
325
P CNJ013 Conjunctivitis 66 0.681
326
PLM031 Poliomyelitis 63 0.681
327
P OVR046 Ovarian Cyst 46 0.681
328
P INF032 Infertility 57 0.681
329
P THY023 Thymoma 64 0.681
330
P BNG032 Benign Mesothelioma 53 0.681
331
DMY004 Demyelinating Disease 50 0.681
332
P EHL001 Ehlers-Danlos Syndrome 58 0.681
333
ENT004 Enthesopathy 51 0.681
334
HYP014 Hyperuricemia 51 0.681
335
SQM006 Squamous Cell Carcinoma 60 0.681
336
CRB037 Cerebral Palsy 67 0.681
337
HYP060 Hyperinsulinism 54 0.681
338
SNL007 Senile Cataract 40 0.681
339
HRP004 Herpes Zoster 61 0.681
340
SPL018 Splenomegaly 49 0.681
341
HYP266 Hypoxia 57 0.681
342
CHR178 Chromosomal Triplication 34 0.681
343
ALL014 Allergic Encephalomyelitis 34 0.681
344
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.556
345
VNZ002 Venezuelan Equine Encephalitis 46 0.556
346
ADR022 Adrenomyeloneuropathy 39 0.556
347
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.556
348
SPS019 Spastic Paraparesis 38 0.556
349
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.556
350
RST023 Resting Heart Rate, Variation in 40 0.556
351
FRN006 Frontotemporal Dementia 68 0.556
352
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 0.556
353
ADR007 Adrenoleukodystrophy 73 0.556
354
TNG002 Tangier Disease 64 0.556
355
ANN002 Anencephaly 57 0.556
356
ART002 Arts Syndrome 66 0.556
357
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.556
358
c LSS005 Lissencephaly 1 57 0.556
359
ALZ029 Alzheimer Disease Mitochondrial 24 0.556
360
P KLZ004 Kala-Azar 1 41 0.556
361
RTN017 Retinal Detachment 60 0.556
362
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.556
363
MRF001 Marfan Syndrome 76 0.556
364
P OST002 Osteoporosis 76 0.556
365
PHS027 Phosphoglycoprotein 1 15 0.556
366
NND010 Nondisjunction 34 0.556
367
CLF027 Cleft Palate, Isolated 64 0.556
368
CRT072 Creutzfeldt-Jakob Disease 68 0.556
369
P CLR023 Colorectal Cancer 100 0.556
370
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.556
371
c OST080 Osteogenesis Imperfecta, Type Ii 56 0.556
372
ASP002 Aspartylglucosaminuria 58 0.556
373
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.556
374
ANG054 Angina Pectoris 66 0.556
375
OPP004 Oppositional Defiant Disorder 49 0.556
376
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.556
377
c MCR115 Microvascular Complications of Diabetes 5 65 0.556
378
c MCR130 Microvascular Complications of Diabetes 6 41 0.556
379
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 0.556
380
MYL009 Myelodysplastic Syndrome 67 0.556
381
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.556
382
CHK001 Chikungunya 60 0.556
383
P MCL001 Mucolipidosis 49 0.556
384
HMN047 Human Cytomegalovirus Infection 57 0.556
385
UMB002 Umbilical Hernia 47 0.556
386
SXL003 Sexual Disorder 49 0.556
387
P SML001 Small Cell Carcinoma 52 0.556
388
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.556
389
BTT017 Beta-Thalassemia Major 51 0.556
390
KRT019 Keratitis, Hereditary 66 0.556
391
ALV005 Alveolar Soft Part Sarcoma 61 0.556
392
P LKM062 Leukemia, Acute Lymphoblastic 69 0.556
393
c MCR120 Microvascular Complications of Diabetes 7 47 0.556
394
CVT001 Cavitary Optic Disc Anomalies 37 0.556
395
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.556
396
P MNN019 Mannosidosis, Beta a, Lysosomal 49 0.556
397
CYS013 Cystinuria 66 0.556
398
DWN001 Down Syndrome 70 0.556
399
PHN003 Phenylketonuria 76 0.556
400
LRN002 Laron Syndrome 63 0.556
401
c NMN015 Niemann-Pick Disease, Type C1 68 0.556
402
TBC004 Tobacco Addiction 63 0.556
403
DYS192 Dystonia, Dopa-Responsive 55 0.556
404
THY111 Thyroid Carcinoma, Familial Medullary 67 0.556
405
MYL057 Myelopathy, Htlv-1-Associated 38 0.556
406
c NRF024 Neurofibromatosis, Type I 72 0.556
407
OCL052 Ocular Dominance 40 0.556
408
PCK003 Pick Disease of Brain 69 0.556
409
P HPT023 Hepatocellular Carcinoma 96 0.556
410
ARB004 Arbitrary Restriction Polymorphism 1 14 0.556
411
P HMN032 Human Herpesvirus 8 48 0.556
412
P FLL037 Follicular Lymphoma 74 0.556
413
THY029 Thyroid Carcinoma 51 0.556
414
P VNW001 Von Willebrand's Disease 65 0.556
415
P MYP006 Myopia 56 0.556
416
CWP001 Cowpox 45 0.556
417
P ZLL001 Zellweger Syndrome 65 0.556
418
PRX001 Peroxisomal Disease 46 0.556
419
P MSC003 Muscular Atrophy 52 0.556
420
AVN001 Avian Influenza 61 0.556
421
SCH012 Schizoaffective Disorder 50 0.556
422
P DYS154 Dystonia 64 0.556
423
INT007 Intermediate Coronary Syndrome 54 0.556
424
CRV002 Cervix Uteri Carcinoma in Situ 47 0.556
425
LSH001 Leishmaniasis 64 0.556
426
VRL011 Viral Infectious Disease 61 0.556
427
P RRH023 Rare Hereditary Hemochromatosis 54 0.556
428
SKN016 Skin Disease 63 0.556
429
PLM001 Pulmonary Tuberculosis 69 0.556
430
P ANT006 Antiphospholipid Syndrome 55 0.556
431
P OLG002 Oligodendroglioma 66 0.556
432
P CHR012 Chronic Granulomatous Disease 69 0.556
433
DSS008 Disease of Mental Health 74 0.556
434
P PLM036 Pulmonary Fibrosis 66 0.556
435
INS001 Insulinoma 59 0.556
436
P GST044 Gastritis 55 0.556
437
ART016 Aortic Aneurysm 68 0.556
438
GST040 Gastric Adenocarcinoma 67 0.556
439
THY125 Thyroid Gland Medullary Carcinoma 48 0.556
440
PLS011 Plasmacytoma 56 0.556
441
LNG039 Lung Squamous Cell Carcinoma 57 0.556
442
P PNC025 Panic Disorder 52 0.556
443
ADN018 Adenoma 59 0.556
444
PRT036 Peritonitis 65 0.556
445
ACT084 Acute Stress Disorder 54 0.556
446
LYM027 Lymphopenia 56 0.556
447
P PRD008 Periodontitis 64 0.556
448
P INT070 Intestinal Obstruction 57 0.556
449
CMB007 Combined Immunodeficiency 57 0.556
450
SPP007 Suppression Amblyopia 38 0.556
451
AMB002 Amblyopia 50 0.556
452
RCK004 Rickets 68 0.556
453
P GRF003 Graft-Versus-Host Disease 71 0.556
454
c MCR113 Microvascular Complications of Diabetes 3 52 0.556
455
c MCR133 Microvascular Complications of Diabetes 4 41 0.556
456
LMB002 Lambert-Eaton Myasthenic Syndrome 52 0.556
457
TCK001 Tick-Borne Encephalitis 59 0.556
458
HMS001 Hemosiderosis 48 0.556
459
TXC005 Toxic Shock Syndrome 62 0.556
460
IMP005 Impotence 52 0.556
461
P DDN001 Duodenal Ulcer 53 0.556
462
RTN020 Retinal Vascular Disease 46 0.556
463
DMP001 Dumping Syndrome 43 0.556
464
NRT004 Neuritis 53 0.556
465
c HPT015 Hepatitis D 49 0.556
466
P HYP086 Hypothyroidism 69 0.556
467
KRT009 Keratosis 53 0.556
468
SCH014 Schistosomiasis 56 0.556
469
HMG005 Hemoglobinopathy 56 0.556
470
P BND020 Bone Disease 59 0.556
471
LPR001 Lepromatous Leprosy 49 0.556
472
SPS004 Spastic Quadriplegia 40 0.556
473
HMP005 Hemiplegia 54 0.556
474
P RSP003 Respiratory Failure 74 0.556
475
LYM017 Lyme Disease 62 0.556
476
WST002 Western Equine Encephalitis 40 0.556
477
KRT002 Keratomalacia 55 0.556
478
P END033 Endocarditis 58 0.556
479
c VRL005 Viral Pneumonia 53 0.556
480
P SHR001 Short Bowel Syndrome 53 0.556
481
P DYS005 Dyslexia 41 0.556
482
LVR012 Liver Cirrhosis 63 0.556
483
P TRT010 Teratoma 51 0.556
484
P ART021 Arteriosclerosis 54 0.556
485
DRM006 Dermatitis 62 0.556
486
TRP002 Tropical Spastic Paraparesis 49 0.556
487
ORL005 Oral Candidiasis 56 0.556
488
TYP007 Typhoid Fever 64 0.556
489
LST001 Listeriosis 59 0.556
490
SPS003 Spastic Diplegia 53 0.556
491
QDR001 Quadriplegia 50 0.556
492
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.556
493
RCT020 Rectum Adenocarcinoma 48 0.556
494
HYP080 Hypogonadism 50 0.556
495
PST028 Post-Traumatic Stress Disorder 59 0.556
496
P MYT002 Myotonic Dystrophy 51 0.556
497
P INS002 in Situ Carcinoma 53 0.556
498
P MNN013 Meningitis 65 0.556
499
c ACT135 Acute Graft Versus Host Disease 51 0.556
500
ORP003 Oropharynx Cancer 55 0.556
501
HYP056 Hypoglycemia 65 0.556
502
HRP011 Herpes Zoster Ophthalmicus 24 0.556
503
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.556
504
PST053 Postherpetic Neuralgia 40 0.556
505
BCK006 Back Pain 47 0.556
506
ANR040 Aneurysm 61 0.556
507
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.556
508
CRV045 Cervical Intraepithelial Neoplasia 39 0.556
509
MYC019 Mycobacterium Marinum 29 0.556
510
EXN003 Exencephaly 30 0.556
511
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.556
512
SPN050 Spinocerebellar Degeneration 39 0.393
513
P PRG139 Progeroid Syndrome 27 0.393
514
CMP097 Complex Chromosomal Rearrangement 23 0.393
515
PST021 Postpartum Depression 50 0.393
516
c BCT007 Bacterial Meningitis 55 0.393
517
P DBT005 Diabetes Insipidus 54 0.393
518
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.393
519
MTC005 Mitochondrial Metabolism Disease 45 0.393
520
BNG077 Benign Idiopathic Neonatal Seizures 23 0.393
521
CNC014 Cancer-Associated Retinopathy 42 0.393
522
STP007 Staphylococcal Scarlet Fever 16 0.393
523
P SZR006 Seizure Disorder 70 0.393
524
SNK001 Snakebite Envenomation 22 0.393
525
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.393
526
STP004 Staphylococcal Toxic Shock Syndrome 45 0.393
527
SPS057 Spasticity 42 0.393
528
MTH086 Methotrexate Toxicity 32 0.393
530
c ACT134 Acute Liver Failure 59 0.393
531
CLS049 Classic Phenylketonuria 41 0.393
532
PFF001 Pfeiffer Syndrome 77 0.393
533
c ALZ049 Alzheimer Disease 2 48 0.393
534
c STC015 Stickler Syndrome, Type I 51 0.393
535
c EPS035 Episodic Ataxia, Type 2 63 0.393
536
P MCH002 Machado-Joseph Disease 62 0.393
537
P BLR024 Biliary Cirrhosis, Primary, 1 28 0.393
538
NCL008 Nuclear Ribonucleic Acid 15 0.393
539
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 0.393
540
P RTT002 Rett Syndrome 79 0.393
541
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.393
542
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.393
543
P MYS003 Myasthenia Gravis 68 0.393
544
SMT004 Smith-Lemli-Opitz Syndrome 70 0.393
545
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.393
546
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.393
547
HMT020 Hematopoietic Stem Cell Kinetics, Control of 8 0.393
548
SDD001 Sudden Infant Death Syndrome 60 0.393
549
VCT004 Vacterl Association with Hydrocephalus 32 0.393
550
P LSS036 Lissencephaly, X-Linked, 1 47 0.393
551
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.393
552
CRD223 Cardiac Arrhythmia 63 0.393
553
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.393
554
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.393
555
c MCL046 Mucolipidosis Iii Alpha/beta 60 0.393
556
c MCL016 Mucolipidosis Iii Gamma 50 0.393
557
c CRP023 Carpenter Syndrome 1 59 0.393
558
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.393
559
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 0.393
560
FBR012 Fabry Disease 70 0.393
561
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.393
562
c SCH051 Schizophrenia 4 32 0.393
563
BDD001 Budd-Chiari Syndrome 62 0.393
564
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.393
565
CRV035 Cervical Cancer 73 0.393
566
c RBN018 Robinow Syndrome, Autosomal Dominant 1 50 0.393
567
P LFR001 Li-Fraumeni Syndrome 73 0.393
568
P MLN069 Melanoma, Uveal 61 0.393
569
PRP090 Peripheral Dysostosis 22 0.393
570
PRN011 Pernicious Anemia 53 0.393
571
P EST010 Esterase B 13 0.393
572
P BCK002 Beckwith-Wiedemann Syndrome 62 0.393
573
FCT001 Factor Viii Deficiency 60 0.393
574
c SPN225 Spondyloarthropathy 1 70 0.393
575
GST092 Gastroesophageal Reflux 61 0.393
576
ABT001 Abetalipoproteinemia 68 0.393
577
c MST023 Mesothelioma, Malignant 56 0.393
578
c OST135 Osteogenesis Imperfecta, Type I 53 0.393
579
OTT002 Otitis Media 71 0.393
580
P PRK057 Parkinson Disease, Late-Onset 80 0.393
581
c FNC027 Fanconi Anemia, Complementation Group a 81 0.393
582
c LKM063 Leukemia, Chronic Myeloid 71 0.393
583
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.393
584
P APL001 Aplastic Anemia 73 0.393
585
P LSS002 Lissencephaly 50 0.393
586
EPD015 Epidemic Typhus 44 0.393
587
P ADV001 Advanced Sleep Phase Syndrome 41 0.393
588
P OCL002 Oculocutaneous Albinism 59 0.393
589
P SLP006 Sleep Apnea 69 0.393
590
FTL006 Fetal Alcohol Spectrum Disorder 43 0.393
591
MYX005 Myxoid Liposarcoma 65 0.393
592
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.393
593
c RTN134 Retinitis Pigmentosa 40 33 0.393
594
c CRN110 Cranioectodermal Dysplasia 3 27 0.393
595
VRL003 Variola Major 43 0.393
596
c SVR003 Severe Congenital Neutropenia 59 0.393
597
TTH002 Tooth Agenesis 61 0.393
598
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.393
599
c RTN106 Retinitis Pigmentosa 51 36 0.393
600
LPP008 Lipoprotein Quantitative Trait Locus 65 0.393
601
c SLV029 Silver-Russell Syndrome 2 26 0.393
602
c ATM101 Autoimmune Gastritis 40 0.393
603
CVD001 Covid-19 57 0.393
604
P ERY036 Erythema Nodosum 49 0.393
605
P URN019 Urinary Tract Infection 49 0.393
606
INF034 Infective Endocarditis 54 0.393
607
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.393
608
WTH001 Withdrawal Disorder 48 0.393
609
BDY001 Body Dysmorphic Disorder 41 0.393
610
P ATR011 Atrial Fibrillation 66 0.393
611
ECT026 Ectopic Pregnancy 48 0.393
612
RSP021 Respiratory Allergy 41 0.393
613
P LYM033 Lymphoproliferative Syndrome 59 0.393
614
P SLM003 Salmonellosis 54 0.393
615
c ERL056 Early-Onset Parkinson's Disease 40 0.393
616
PHY002 Physical Disorder 41 0.393
617
MNN032 Meningococcal Meningitis 53 0.393
618
HPT046 Hepatic Veno-Occlusive Disease 62 0.393
619
P FML023 Familial Hemiplegic Migraine 53 0.393
620
CRH005 Crohn's Colitis 53 0.393
621
P BRC006 Brachydactyly 51 0.393
622
c FML001 Familial Atrial Fibrillation 65 0.393
623
P FTL001 Fetal Alcohol Syndrome 55 0.393
624
ZLL002 Zollinger-Ellison Syndrome 55 0.393
625
CLR108 Colorectal Adenoma 64 0.393
626
PMP004 Pemphigus Foliaceus 43 0.393
627
TTH032 Tooth Size 35 0.393
628
NRF008 Neurofibromatosis-Noonan Syndrome 55 0.393
629
ACT088 Acute Insulin Response 39 0.393
630
BLL001 Baller-Gerold Syndrome 58 0.393
631
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.393
632
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 38 0.393
633
P TYS001 Tay-Sachs Disease 69 0.393
634
c GRV008 Graves Disease 1 54 0.393
635
c TYR012 Tyrosinemia, Type I 61 0.393
636
WRN001 Werner Syndrome 69 0.393
637
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.393
638
SPN360 Spondylometaphyseal Dysplasia, Corner Fracture Type 38 0.393
639
CNT105 Central Core Disease of Muscle 59 0.393
640
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.393
641
P PRP003 Porphyria Cutanea Tarda 66 0.393
642
IGR001 Ige Responsiveness, Atopic 59 0.393
643
c SPN309 Spinocerebellar Ataxia 6 58 0.393
644
P PRD006 Prader-Willi Syndrome 61 0.393
645
c PRG020 Paragangliomas 3 39 0.393
646
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.393
647
MCR025 Microhydranencephaly 33 0.393
648
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.393
649
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.393
650
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.393
651
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.393
652
ANL018 Analbuminemia 53 0.393
653
HYP110 Hyperproinsulinemia 37 0.393
654
CHP002 Chops Syndrome 47 0.393
655
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.393
656
EWN003 Ewing Sarcoma 70 0.393
657
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.393
658
ACD008 Acid-Labile Subunit Deficiency 52 0.393
659
PRC054 Perching Syndrome 33 0.393
660
HMM004 Hamamy Syndrome 39 0.393
661
c MCR312 Microphthalmia, Syndromic 10 40 0.393
662
c MJR006 Major Affective Disorder 5 32 0.393
663
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 0.393
664
ACT119 Acute Promyelocytic Leukemia 62 0.393
665
c LPD035 Lipodystrophy, Congenital Generalized, Type 4 45 0.393
666
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.393
667
c MJR003 Major Affective Disorder 6 32 0.393
668
c GLY043 Glycogen Storage Disease Xii 30 0.393
669
c CLR080 Colorectal Cancer 5 25 0.393
670
c PSD048 Pseudo-Von Willebrand Disease 39 0.393
671
c SCH079 Schizophrenia 1 44 0.393
672
GLT038 Glutamyl Ribose-5-Phosphate Storage Disease 8 0.393
673
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.393
674
PLY068 Polysubstance Abuse 41 0.393
675
c ALB019 Albinism, Oculocutaneous, Type Iv 48 0.393
676
c RTN036 Retinal Cone Dystrophy 4 35 0.393
677
c HMP029 Hemophilia a 68 0.393
679
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.393
680
c LFR007 Li-Fraumeni Syndrome 2 46 0.393
681
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.393
682
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 0.393
683
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.393
684
PLS030 Plasminogen Deficiency, Type I 51 0.393
685
DYS179 Dyssegmental Dysplasia, Rolland-Desbuquois Type 25 0.393
686
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.393
687
VRC005 Varicose Veins 60 0.393
688
c WLM013 Wilms Tumor 1 66 0.393
689
BTT016 Batten-Turner Congenital Myopathy 53 0.393
690
SBC001 Subacute Sclerosing Panencephalitis 53 0.393
691
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.393
692
VTR016 Vater/vacterl Association 49 0.393
693
VLC001 Velocardiofacial Syndrome 57 0.393
694
YST001 Yeast Factor 6 0.393
695
P SCL057 Scoliosis, Isolated 1 40 0.393
696
c NRB010 Neuroblastoma 1 59 0.393
697
PTR032 Peters-Plus Syndrome 63 0.393
698
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.393
699
c INF071 Inflammatory Bowel Disease 1 65 0.393
700
c TBR025 Tuberous Sclerosis 1 84 0.393
701
P UTR058 Uterine Anomalies 46 0.393
702
HYP732 Hyperalphalipoproteinemia 1 52 0.393
703
c MLG147 Malignant Hyperthermia 1 45 0.393
704
DFC006 Defective Interfering Particle Induction, Control of 15 0.393
705
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.393
706
c EXS020 Exostoses, Multiple, Type Ii 38 0.393
707
HYP042 Hypochondroplasia 59 0.393
708
c CND033 Candidiasis, Familial, 1 27 0.393
709
CLB010 Coloboma of Macula 53 0.393
710
PPL048 Papillorenal Syndrome 58 0.393
711
DRM046 Dermal Ridges-off-the-End 20 0.393
712
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 33 0.393
713
EPD023 Epidermolysis Bullosa Simplex with Mottled Pigmentation 45 0.393
714
c EXS019 Exostoses, Multiple, Type I 54 0.393
715
P NNN008 Noonan Syndrome 1 77 0.393
716
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.393
717
PMP006 Pemphigus Vulgaris, Familial 58 0.393
718
PLT016 Platelet Adenylate Cyclase Activity 16 0.393
719
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.393
720
c MGR032 Migraine, Familial Hemiplegic, 1 54 0.393
721
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 42 0.393
722
c FTL065 Fetal Hemoglobin Quantitative Trait Locus 5 16 0.393
723
c FTL036 Fetal Hemoglobin Quantitative Trait Locus 2 16 0.393
724
ACH004 Achondroplasia 66 0.393
725
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.393
726
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 31 0.393
727
APN008 Apnea, Obstructive Sleep 67 0.393
728
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.393
729
MMM006 Mammographic Density 39 0.393
730
c OST125 Osteopetrosis, Autosomal Dominant 1 34 0.393
731
PNT009 Pontine Tegmental Cap Dysplasia 35 0.393
732
c EHL085 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2 46 0.393
733
HYP020 Hyperprolactinemia 63 0.393
734
c RBN017 Robinow Syndrome, Autosomal Dominant 2 45 0.393
735
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.393
736
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.393
737
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.393
738
P SCL018 Scoliosis 57 0.393
739
RNL077 Renal Fibrosis 46 0.393
740
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 0.393
741
OPT010 Optic Papillitis 38 0.393
742
BCT022 Bacterial Infectious Disease 56 0.393
743
GLC003 Glucose Intolerance 54 0.393
744
PRM329 Premature Aging 36 0.393
745
P HYP730 Hypogonadotropic Hypogonadism 53 0.393
746
LBR036 Leber Plus Disease 66 0.393
747
c HMP004 Hemophilia B 68 0.393
748
c MLT095 Multiple Sclerosis 4 18 0.393
749
c CRN111 Cranioectodermal Dysplasia 4 31 0.393
750
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.393
751
PMP014 Pemphigoid 51 0.393
752
P MTP001 Metaphyseal Dysplasia 38 0.393
753
SPN250 Spondyloepimetaphyseal Dysplasia 36 0.393
754
CTN007 Cutaneous Leishmaniasis 62 0.393
755
TRC020 Tracheitis 43 0.393
756
DVR002 Diverticulitis 46 0.393
757
c CHR684 Chronic Kidney Disease 69 0.393
758
PLM014 Pleomorphic Adenoma 51 0.393
759
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.393
760
GST030 Gastrinoma 45 0.393
761
P KDN018 Kidney Disease 72 0.393
762
BRN018 Borna Disease 36 0.393
763
URT010 Ureteral Obstruction 45 0.393
764
CRC021 Carcinosarcoma 64 0.393
765
NRM001 Neuromyelitis Optica 61 0.393
766
SKN019 Skin Melanoma 71 0.393
767
VSC003 Visceral Leishmaniasis 55 0.393
768
P PMP001 Pemphigus 55 0.393
769
P HMC002 Homocystinuria 53 0.393
770
P TYR004 Tyrosinemia 50 0.393
771
c BRS049 Breast Carcinoma in Situ 50 0.393
772
P PSR002 Psoriasis 63 0.393
773
ALL006 Allergic Asthma 56 0.393
774
P NRP001 Neuropathy 60 0.393
775
P MLG056 Malignant Hyperthermia 66 0.393
776
SML019 Smallpox 55 0.393
777
ADN001 Adenosine Deaminase Deficiency 59 0.393
778
ADG002 Audiogenic Seizures 25 0.393
779
NM001 Noma 38 0.393
780
P HYP098 Hypereosinophilic Syndrome 66 0.393
781
c FML191 Familial Long Qt Syndrome 55 0.393
782
P MTH008 Methylmalonic Acidemia 52 0.393
783
P ALC033 Alcohol Use Disorder 61 0.393
784
P CYS018 Cystitis 59 0.393
785
PNC129 Pancreatic Adenocarcinoma 65 0.393
786
IGG001 Iga Glomerulonephritis 50 0.393
787
GLB002 Glioblastoma 67 0.393
788
P EPL164 Epilepsy 68 0.393
789
P OPT006 Optic Nerve Disease 58 0.393
790
DYS018 Dysostosis 44 0.393
791
P TRN020 Turner Syndrome 67 0.393
792
P CNT009 Central Core Myopathy 43 0.393
793
P CND004 Candidiasis 58 0.393
794
P LCT001 Lactic Acidosis 51 0.393
795
ADR005 Adrenal Carcinoma 62 0.393
796
CLL014 Cll/sll 45 0.393
797
PST011 Pustulosis of Palm and Sole 52 0.393
798
HYP005 Hypokalemia 55 0.393
799
END086 End Stage Renal Disease 52 0.393
800
NPH009 Nephrolithiasis 54 0.393
801
AGR002 Agoraphobia 45 0.393
802
FBR047 Fibromyalgia 58 0.393
803
SPN051 Spondylitis 51 0.393
804
P CRN028 Corneal Ulcer 47 0.393
805
P ART022 Arthritis 71 0.393
806
LNG099 Lung Disease 62 0.393
807
c FML253 Familial Cold Autoinflammatory Syndrome 3 49 0.393
808
P HRD001 Hereditary Multiple Exostoses 48 0.393
809
P NGH001 Night Blindness 52 0.393
810
BLL006 Bullous Pemphigoid 61 0.393
811
P MNC007 Monocytic Leukemia 47 0.393
812
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.393
814
SLP001 Sleeping Sickness 56 0.393
815
TRY001 Trypanosomiasis 50 0.393
816
CRB004 Cerebral Artery Occlusion 45 0.393
817
SLC006 Silicosis 56 0.393
818
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.393
819
INH001 Inhalation Anthrax 42 0.393
820
P MGR003 Migraine with Aura 52 0.393
821
THY006 Thymus Lymphoma 27 0.393
822
PLR008 Pleurisy 50 0.393
823
P CHR071 Charcot-Marie-Tooth Disease 64 0.393
824
P MLT007 Multiple Epiphyseal Dysplasia 56 0.393
825
c DLT002 Dilated Cardiomyopathy 78 0.393
826
GT001 Gout 64 0.393
827
LYM009 Lymphocytic Choriomeningitis 46 0.393
828
P MLN007 Male Infertility 56 0.393
829
P OPT009 Optic Neuritis 57 0.393
830
INF009 Inflammatory Spondylopathy 30 0.393
831
GTR002 Goiter 53 0.393
832
PRN009 Paranoid Schizophrenia 49 0.393
833
LWC001 Low Compliance Bladder 45 0.393
834
PRM236 Primary Biliary Cholangitis 60 0.393
835
ALC006 Alcoholic Hepatitis 61 0.393
836
P SPN046 Spinal Muscular Atrophy 63 0.393
837
PRV004 Periventricular Leukomalacia 52 0.393
838
c ACT068 Acute Cystitis 61 0.393
839
HRY003 Hairy Cell Leukemia 61 0.393
840
c ACT027 Acute Pancreatitis 60 0.393
841
P HYP069 Hyperparathyroidism 62 0.393
842
CHN002 Chancroid 36 0.393
843
P VSC007 Vascular Disease 63 0.393
844
P HYP035 Hypophosphatasia 62 0.393
845
PSY004 Psychotic Disorder 66 0.393
846
P NMN002 Niemann-Pick Disease 60 0.393
847
P BRS053 Breast Fibroadenoma 49 0.393
848
P CRN037 Craniosynostosis 68 0.393
849
GLS001 Gliosarcoma 64 0.393
850
P TBR001 Tuberous Sclerosis 69 0.393
851
HYP081 Hypolipoproteinemia 49 0.393
852
P INT143 Interstitial Cystitis 60 0.393
853
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.393
854
TRN018 Transitional Cell Carcinoma 56 0.393
855
P LNG028 Long Qt Syndrome 64 0.393
856
ATN004 Autonomic Neuropathy 42 0.393
857
HYD002 Hydronephrosis 58 0.393
858
P CRD119 Cardiac Arrest 67 0.393
859
ING001 Inguinal Hernia 59 0.393
860
SPN369 Spinal Disease 44 0.393
861
HYP041 Hypochondrogenesis 35 0.393
862
P STC001 Stickler Syndrome 60 0.393
863
P MCR010 Microcephaly 60 0.393
864
TTH006 Tooth Disease 51 0.393
865
EST003 Eastern Equine Encephalitis 38 0.393
866
QFV001 Q Fever 62 0.393
867
c PRM005 Primary Hyperparathyroidism 59 0.393
868
P PLY011 Polycystic Ovary Syndrome 57 0.393
869
P NNT058 Neonatal Diabetes 52 0.393
870
TBR006 Tuberculoid Leprosy 43 0.393
871
CYS010 Cystinosis 62 0.393
872
BRN024 Bronchitis 67 0.393
873
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.393
874
c INH020 Inherited Metabolic Disorder 48 0.393
875
c HPT007 Hepatitis E 51 0.393
876
P BRT004 Bartter Disease 58 0.393
877
P END047 Endophthalmitis 53 0.393
878
MXD026 Mixed Glioma 45 0.393
879
P PNC044 Pancreatitis 61 0.393
880
TST018 Testicular Yolk Sac Tumor 39 0.393
881
ART017 Aortic Disease 49 0.393
882
URN010 Urinary Tract Obstruction 55 0.393
883
P PRP019 Peripheral Nervous System Disease 58 0.393
884
P PNM007 Pneumonia 67 0.393
885
P RTN018 Retinal Disease 53 0.393
886
ANP009 Anaplastic Oligodendroglioma 41 0.393
887
PRR001 Periarthritis 34 0.393
888
BRS099 Breast Ductal Carcinoma 61 0.393
889
c ACT071 Acute Kidney Failure 60 0.393
890
ANP005 Anaplastic Astrocytoma 57 0.393
891
MSN004 Mesenchymal Cell Neoplasm 42 0.393
892
P LPS002 Liposarcoma 64 0.393
893
P MTR014 Motor Neuron Disease 65 0.393
894
NCR004 Nocardiosis 53 0.393
895
P HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.393
896
P TMP001 Temporal Lobe Epilepsy 49 0.393
897
P GLM007 Glomerulonephritis 60 0.393
898
P OBS001 Obstructive Jaundice 48 0.393
899
IDP070 Idiopathic Scoliosis 42 0.393
900
P PRP029 Porphyria 60 0.393
901
KLB003 Klebsiella Pneumonia 50 0.393
902
P GND004 Gonadal Dysgenesis 47 0.393
903
HMN048 Human Papillomavirus Infectious Disease 46 0.393
904
PLS007 Plasmodium Falciparum Malaria 52 0.393
905
ALL009 Allergic Conjunctivitis 51 0.393
906
APP010 Appendix Cancer 45 0.393
907
VCT001 Vacterl Association 47 0.393
908
HND002 Hand, Foot and Mouth Disease 50 0.393
909
AMN003 Amnestic Disorder 54 0.393
910
CHR073 Choreatic Disease 54 0.393
911
LGP001 Lagophthalmos 30 0.393
912
IRN002 Iron Metabolism Disease 57 0.393
913
P END039 Endodermal Sinus Tumor 41 0.393
914
GST052 Gestational Choriocarcinoma 35 0.393
915
END028 Endemic Goiter 41 0.393
916
UPP004 Upper Respiratory Tract Disease 33 0.393
917
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.393
918
ALB002 Albinism 47 0.393
919
ISL099 Isolated Methylmalonic Acidemia 36 0.393
920
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 0.393
921
c ALM001 Al Amyloidosis 54 0.393
922
P CLL015 Collagen Disease 48 0.393
923
GRM010 Germ Cells Tumors 33 0.393
924
GRN017 Granulocytopenia 42 0.393
925
PTH003 Pathologic Nystagmus 52 0.393
926
PRS037 Periostitis 40 0.393
927
NRF007 Neurofibroma 64 0.393
928
P EPS003 Episodic Ataxia 59 0.393
929
TRC023 Trichinosis 53 0.393
930
P HMP007 Hemophilia 52 0.393
931
c PSD047 Pseudo-Turner Syndrome 52 0.393
932
SFT003 Soft Tissue Sarcoma 57 0.393
933
TRC096 Trichothiodystrophy 55 0.393
934
P HDC001 Headache 57 0.393
935
CMP083 Complete Plasminogen Activator Inhibitor 1 Deficiency 27 0.393
936
HRD104 Hereditary Multiple Osteochondromas 43 0.393
937
P MTC069 Mitochondrial Disorders 57 0.393
939
CRB086 Cerebral Aneurysms 40 0.393
940
P HYP265 Hypotonia 42 0.393
941
ATN005 Autonomic Dysfunction 46 0.393
943
SRF006 Surfactant Dysfunction 33 0.393
944
P NNS072 Nonsyndromic Hearing Loss 40 0.393
945
DYS073 Dysphagia 53 0.393
946
BWN006 Bowen's Disease 32 0.393
947
CHL078 Childhood-Onset Schizophrenia 29 0.393
948
CRT033 Corticobasal Degeneration 47 0.393
949
P FML187 Familial Hypertension 34 0.393
950
LKP003 Leukoplakia 39 0.393
951
P OGC005 Oguchi Disease 45 0.393