Search results for ACADS

954 hits were found for ACADS

# Family MCID Name MIFTS Score
1
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 55 88.795
2
P MYP004 Myopathy 67 17.188
3
P DBT009 Diabetes Mellitus 67 13.200
4
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 11.531
5
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 10.614
6
ENC055 Encephalopathy, Ethylmalonic 51 10.218
7
ISV001 Isovaleric Acidemia 54 10.218
8
RBF001 Riboflavin Deficiency 49 10.218
9
ORG002 Organic Acidemia 44 10.218
10
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 9.669
11
P PRD006 Prader-Willi Syndrome 61 8.017
12
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 7.621
13
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 52 7.621
14
P MLG056 Malignant Hyperthermia 66 7.621
15
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 37 7.225
16
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 7.225
17
FZL002 Fazio-Londe Disease 39 7.225
18
CRN239 Carnitine Deficiency, Systemic Primary 61 7.225
19
c SHR067 Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly 44 7.225
20
P SPN202 Spinocerebellar Ataxia, X-Linked 1 41 7.225
21
c SPN403 Spinocerebellar Ataxia, X-Linked 2 20 7.225
22
MTC027 Mitochondrial Trifunctional Protein Deficiency 57 7.225
23
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 7.225
24
XLN076 X-Linked Cerebellar Ataxia 21 7.225
25
MSC193 Muscular Lipidosis 22 7.225
26
INF065 Infantile Hypotonia 21 7.225
27
HLX001 Helix Syndrome 48 4.445
28
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 4.233
29
HMN044 Human Immunodeficiency Virus Type 1 78 3.041
30
LPP008 Lipoprotein Quantitative Trait Locus 65 3.016
31
ART140 Arteries, Anomalies of 53 2.937
32
P HRP006 Herpes Simplex 65 2.828
33
HYP056 Hypoglycemia 65 2.575
34
PRT037 Pertussis 65 2.535
35
IMM167 Immune Deficiency Disease 78 2.489
36
VCC001 Vaccinia 47 2.441
37
STM007 Stomatitis 54 2.441
38
P ENC018 Encephalopathy 62 2.398
39
MTB004 Metabolic Acidosis 48 2.351
40
P HYP265 Hypotonia 42 2.351
41
c TYP009 Type 2 Diabetes Mellitus 92 2.331
42
ATS010 Autosomal Recessive Disease 42 2.252
43
GLM045 Glioma 63 2.137
44
HPT004 Hepatic Coma 43 2.090
45
HPT019 Hepatic Encephalopathy 59 2.090
46
47X002 47,xyy 48 1.980
47
P NRB001 Neuroblastoma 66 1.940
48
c INH020 Inherited Metabolic Disorder 48 1.906
49
ACT098 Acute Erythroid Leukemia 55 1.899
50
CHL014 Cholera 62 1.899
51
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.815
52
ART002 Arts Syndrome 66 1.807
53
P GLM040 Glioma Susceptibility 1 71 1.776
54
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 1.726
55
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.688
56
HRW001 Hair Whorl 35 1.680
57
CLT003 Colitis 63 1.603
58
P HNT016 Huntington Disease 73 1.584
59
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.584
60
c LKM005 Leukemia, T-Cell, Chronic 34 1.584
61
P ALZ034 Alzheimer Disease 87 1.534
62
PLY150 Polykaryocytosis Inducer 29 1.534
63
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.534
64
ULC004 Ulcerative Colitis 74 1.510
65
CNT047 Contact Dermatitis 57 1.510
66
DRM006 Dermatitis 62 1.510
67
KPS004 Kaposi Sarcoma 77 1.482
68
SPN035 Spindle Cell Sarcoma 54 1.482
69
SRC014 Sarcoma 65 1.482
70
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.428
71
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.428
72
SCR011 Scrapie 39 1.428
73
FTT001 Fatty Liver Disease 62 1.428
74
DPH001 Diphtheria 59 1.428
75
CHL123 Chlamydia 58 1.428
76
ACT088 Acute Insulin Response 39 1.404
77
PMP014 Pemphigoid 51 1.404
78
EXT007 Extracutaneous Mastocytoma 38 1.404
79
MST004 Mast Cell Neoplasm 42 1.404
80
P PHC003 Pheochromocytoma 69 1.372
81
P RTN024 Retinoblastoma 73 1.372
82
HND015 Hand Skill, Relative 30 1.372
83
LPD008 Lipid Metabolism Disorder 62 1.372
84
P OVR042 Ovarian Cancer 88 1.343
85
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.313
86
c HPT073 Hepatitis C Virus 71 1.313
87
ADR040 Adrenal Gland Pheochromocytoma 46 1.313
88
PST092 Posttransplant Acute Limbic Encephalitis 28 1.313
89
GLL048 Glial Tumor 52 1.313
90
P SKN015 Skin Carcinoma 71 1.313
91
CRT016 Carotid Artery Disease 52 1.313
92
c MGR028 Migraine with or Without Aura 1 64 1.278
93
BLL006 Bullous Pemphigoid 61 1.278
94
ATH013 Atherosclerosis Susceptibility 63 1.252
95
ANG054 Angina Pectoris 66 1.252
96
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.252
97
OST159 Osteogenic Sarcoma 66 1.252
98
TRT001 Teratocarcinoma 42 1.252
99
P FBR017 Fibrosarcoma 56 1.252
100
P PRN023 Prion Disease 60 1.252
101
SVR004 Severe Combined Immunodeficiency 72 1.252
102
EMB004 Embryonal Carcinoma 56 1.252
103
P PNC035 Pancreatic Cancer 86 1.237
104
P OLG002 Oligodendroglioma 66 1.216
105
ANX004 Anoxia 40 1.188
106
P THL005 Thalassemia 56 1.188
107
P MYC084 Mycobacterium Tuberculosis 1 68 1.188
108
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.188
109
BRK010 Burkitt Lymphoma 66 1.188
110
CYS001 Cystic Fibrosis 78 1.188
111
P FRD001 Friedreich Ataxia 61 1.188
113
c HYP836 Hypercholesterolemia, Familial, 1 73 1.188
114
P SPS008 Spastic Ataxia 41 1.188
115
P BPL003 Bipolar Disorder 56 1.188
116
P LTR001 Lateral Sclerosis 58 1.188
117
PPL022 Papilloma 53 1.188
118
c HPT016 Hepatitis B 62 1.188
119
48X005 48,xyyy 39 1.188
120
HMP009 Haemophilus Influenzae 41 1.188
121
P LNG032 Lung Cancer 98 1.120
122
INS024 Insulin-Like Growth Factor I 78 1.120
123
c MJR022 Major Affective Disorder 8 38 1.120
124
c BTT014 Beta-Thalassemia 72 1.120
125
c MJR024 Major Affective Disorder 9 41 1.120
126
2MT003 2-Methylbutyryl-Coa Dehydrogenase Deficiency 39 1.120
127
c HPT003 Hepatitis a 63 1.120
128
CHL147 Chlamydia Pneumonia 47 1.120
129
SQM002 Squamous Cell Papilloma 46 1.120
130
P STR020 Strabismus 56 1.114
131
PMP006 Pemphigus Vulgaris, Familial 58 1.114
132
P HPT023 Hepatocellular Carcinoma 96 1.114
133
P PMP001 Pemphigus 55 1.114
134
MCH006 Mechanical Strabismus 40 1.114
135
P BRS047 Breast Cancer 98 1.111
136
P BCK002 Beckwith-Wiedemann Syndrome 62 1.111
137
AGN016 Aging 54 1.048
138
ADR041 Adrenal Cortical Adenoma 49 1.048
139
MTC151 Mitochondrial Complex I Deficiency, Nuclear Type 20 36 1.048
140
P VSC011 Vasculitis 61 1.048
141
P INF038 Influenza 68 1.048
142
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.048
143
P LKM002 Leukemia 67 1.048
144
CRT013 Carotid Stenosis 51 1.048
145
CLN015 Colon Adenocarcinoma 65 1.048
146
MLG169 Malignant Astrocytoma 57 1.048
147
TTN003 Tetanus 65 1.048
148
MDD011 Mood Disorder 62 1.048
149
P ENC004 Encephalitis 61 1.048
150
P NSP012 Nasopharyngeal Carcinoma 61 0.970
151
P FRG001 Fragile X Syndrome 70 0.970
152
P ADL017 Adult T-Cell Leukemia 56 0.970
153
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.970
154
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.970
155
MDD018 Middle East Respiratory Syndrome 44 0.970
156
P AMY004 Amyloidosis 70 0.970
157
P DYS154 Dystonia 64 0.970
158
P TRM003 Tremor 48 0.970
159
MTH009 Mouth Disease 57 0.970
160
LNG039 Lung Squamous Cell Carcinoma 57 0.970
161
P CTR002 Cataract 60 0.970
162
P MLN008 Melanoma 76 0.970
163
RBS001 Rabies 58 0.970
164
PLM031 Poliomyelitis 63 0.970
165
LYS002 Lysosomal Storage Disease 51 0.970
166
P SCK005 Sickle Cell Disease 56 0.970
167
PTT037 Pituitary Tumors 44 0.970
168
MSL001 Measles 61 0.970
169
SPN186 Spinal Cord Injury 61 0.885
170
P BLD134 Bladder Cancer 79 0.885
171
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.885
172
P RTN008 Retinitis Pigmentosa 80 0.885
173
P SCH015 Schizophrenia 74 0.885
174
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.885
175
ATM095 Autoimmune Disease 61 0.885
176
P FML011 Familial Adenomatous Polyposis 71 0.885
177
MLR004 Malaria 80 0.885
178
DFC004 Deficiency Anemia 74 0.885
179
SCK003 Sickle Cell Anemia 74 0.885
180
DWN001 Down Syndrome 70 0.885
181
DSS032 Disease by Infectious Agent 55 0.885
182
NRR001 Neuroretinitis 42 0.885
183
P PRK039 Parkinsonism 55 0.885
184
CRN030 Coronary Stenosis 50 0.885
185
RTN023 Retinitis 46 0.885
186
P EPL164 Epilepsy 68 0.885
187
ADN018 Adenoma 59 0.885
188
P RTN016 Retinal Degeneration 52 0.885
189
P LNG064 Lung Cancer Susceptibility 3 70 0.885
190
PLG002 Plague 58 0.885
191
NWC001 Newcastle Disease 47 0.885
192
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.885
193
P ATS364 Autism 69 0.792
194
c HMC039 Hemochromatosis, Type 1 73 0.792
195
OBN001 Ouabain Resistance 16 0.792
196
RTC012 Reticuloendotheliosis, X-Linked 35 0.792
197
ANX010 Anxiety 70 0.792
198
PPL052 Papillomatosis, Confluent and Reticulated 34 0.792
199
MYL009 Myelodysplastic Syndrome 67 0.792
200
P CHN012 Chondrosarcoma 57 0.792
201
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.792
202
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.792
203
KWS002 Kawasaki Disease 65 0.792
204
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.792
205
CRN270 Coronary Artery Dissection, Spontaneous 32 0.792
206
FBR054 Fibroma 44 0.792
207
c ACT073 Acute Leukemia 58 0.792
208
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.792
209
P RHB003 Rhabdomyosarcoma 66 0.792
210
P MYL006 Myeloid Leukemia 61 0.792
211
P HML002 Hemolytic Anemia 62 0.792
212
SKN016 Skin Disease 63 0.792
213
P LVR013 Liver Disease 69 0.792
214
c HPT001 Hepatitis C 62 0.792
215
MNT002 Mental Depression 57 0.792
216
MRK001 Merkel Cell Carcinoma 64 0.792
217
ANT024 Anthrax Disease 58 0.792
218
BRN028 Brain Cancer 74 0.792
219
CHG001 Chagas Disease 66 0.792
220
ALL029 Allergic Disease 59 0.792
221
MLN003 Melancholia 41 0.792
222
P ADN016 Adenocarcinoma 63 0.792
223
BRC012 Brucellosis 66 0.792
224
P RSP003 Respiratory Failure 74 0.792
225
ISC004 Ischemia 61 0.792
226
P SBS003 Substance Abuse 54 0.792
227
P KDN017 Kidney Cancer 61 0.792
228
c FML021 Familial Hypercholesterolemia 72 0.792
229
SQM006 Squamous Cell Carcinoma 60 0.792
230
WLL004 Wallerian Degeneration 38 0.792
231
P CRN074 Coronary Artery Aneurysm 42 0.792
232
VRL003 Variola Major 43 0.718
233
CVD001 Covid-19 57 0.718
234
PNG002 Pain Agnosia 51 0.718
235
c CHR708 Chronic Urticaria 42 0.718
236
SML019 Smallpox 55 0.718
237
IRR003 Irritant Dermatitis 47 0.718
238
P URT039 Urticaria 58 0.718
239
c TYP008 Type 1 Diabetes Mellitus 70 0.686
240
PLY100 Polyploidy 36 0.686
241
INT358 Intestinal Polyposis Syndrome 25 0.686
242
P OVR082 Overgrowth Syndrome 49 0.686
243
P MCH002 Machado-Joseph Disease 62 0.686
244
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.686
245
P LPR021 Leprosy 3 71 0.686
246
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.686
247
MSC157 Muscular Dystrophy, Duchenne Type 79 0.686
248
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.686
249
BRT054 Brittle Bone Disorder 74 0.686
250
MLN071 Melanoma Tumor Antigen Gp90 17 0.686
251
P LKM071 Leukemia, Chronic Lymphocytic 75 0.686
252
c ATR087 Atrial Standstill 1 74 0.686
253
FBR032 Fibromuscular Dysplasia 48 0.686
254
WLL001 Williams-Beuren Syndrome 61 0.686
255
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.686
256
ADR016 Adrenal Cortical Carcinoma 62 0.686
257
P EXN002 Exanthem 58 0.686
258
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 0.686
259
P INF037 Inflammatory Bowel Disease 53 0.686
260
MSC007 Muscle Hypertrophy 64 0.686
261
END062 Endometrial Hyperplasia 48 0.686
262
NNL006 Non-Alcoholic Steatohepatitis 54 0.686
263
c LKM061 Leukemia, Acute Myeloid 83 0.686
264
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.686
265
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.686
266
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.686
267
c BRN108 Branchiootic Syndrome 1 62 0.686
268
c HNT011 Huntington Disease-Like 3 34 0.686
269
P GST053 Gastric Cancer 83 0.686
270
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.686
271
c PCH010 Pachyonychia Congenita 3 43 0.686
272
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.686
273
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.686
274
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.686
275
OCL069 Ocular Motor Apraxia 57 0.686
276
PHN003 Phenylketonuria 76 0.686
277
P SPP010 Suppressor of Tumorigenicity 3 51 0.686
278
P PRS040 Prostate Cancer 95 0.686
279
HMF008 Hemifacial Atrophy, Progressive 38 0.686
280
P HMN032 Human Herpesvirus 8 48 0.686
281
BCT022 Bacterial Infectious Disease 56 0.686
282
ARG004 Argyria 26 0.686
283
THY029 Thyroid Carcinoma 51 0.686
284
TRM010 Traumatic Brain Injury 51 0.686
285
CRH001 Crohn's Disease 80 0.686
286
P PSR002 Psoriasis 63 0.686
287
CHC001 Chickenpox 57 0.686
288
CHR074 Choriocarcinoma 46 0.686
289
HPT022 Hepatoblastoma 54 0.686
290
P ALP008 Alopecia 54 0.686
291
P MSC005 Muscular Dystrophy 67 0.686
292
P ALC033 Alcohol Use Disorder 61 0.686
293
ADR004 Adrenal Cortical Adenocarcinoma 38 0.686
294
c VRL010 Viral Hepatitis 53 0.686
295
P BRS044 Breast Adenocarcinoma 58 0.686
296
P LCT001 Lactic Acidosis 51 0.686
297
P SYS005 Systemic Scleroderma 74 0.686
298
ACQ007 Acquired Immunodeficiency Syndrome 59 0.686
299
P ACN011 Acne 57 0.686
300
PST011 Pustulosis of Palm and Sole 52 0.686
301
c LCL006 Localized Scleroderma 65 0.686
302
FCL003 Facial Hemiatrophy 29 0.686
303
P PRD008 Periodontitis 64 0.686
304
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.686
305
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.686
306
P DNG005 Dengue Virus 56 0.686
307
P CHR071 Charcot-Marie-Tooth Disease 64 0.686
308
P HYP061 Hypertrophic Cardiomyopathy 69 0.686
309
CNN003 Conn's Syndrome 79 0.686
310
c ACT027 Acute Pancreatitis 60 0.686
311
SNS003 Sensory Peripheral Neuropathy 52 0.686
312
c BSL007 Basal Cell Carcinoma 68 0.686
313
P GCH001 Gaucher's Disease 70 0.686
314
KRT009 Keratosis 53 0.686
315
P HPT021 Hepatitis 69 0.686
316
HGH043 High Grade Glioma 45 0.686
317
TTH006 Tooth Disease 51 0.686
318
CNG034 Congestive Heart Failure 69 0.686
319
CRB039 Cerebrovascular Disease 66 0.686
320
LVR012 Liver Cirrhosis 63 0.686
321
P PNC044 Pancreatitis 61 0.686
322
P OVR046 Ovarian Cyst 46 0.686
323
GST045 Gastroenteritis 58 0.686
324
P BNG032 Benign Mesothelioma 53 0.686
325
DMY004 Demyelinating Disease 50 0.686
326
P PTS002 Ptosis 52 0.686
327
P DRR001 Diarrhea 55 0.686
328
ENT004 Enthesopathy 51 0.686
329
PST028 Post-Traumatic Stress Disorder 59 0.686
330
P RCT021 Rectum Cancer 54 0.686
331
SNL007 Senile Cataract 40 0.686
332
P NRF002 Neurofibromatosis 57 0.686
333
HNS001 Hansen's Disease 32 0.686
334
SPL018 Splenomegaly 49 0.686
335
HYP266 Hypoxia 57 0.686
336
BRK012 Broken Heart Syndrome 42 0.686
337
CHR178 Chromosomal Triplication 34 0.686
338
LNR005 Linear Scleroderma 21 0.686
339
ALL014 Allergic Encephalomyelitis 34 0.686
340
c GLM047 Glioma Susceptibility 3 33 0.656
341
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.656
342
c GLM025 Glioma Susceptibility 2 30 0.656
343
c GLM043 Glioma Susceptibility 9 30 0.656
344
MNN043 Meningioma, Familial 79 0.656
345
VNZ002 Venezuelan Equine Encephalitis 46 0.560
346
ADR022 Adrenomyeloneuropathy 39 0.560
347
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.560
348
SPS019 Spastic Paraparesis 38 0.560
349
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 0.560
350
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.560
351
P ALP061 Alopecia, Androgenetic, 1 49 0.560
352
FRN006 Frontotemporal Dementia 68 0.560
353
c DWL002 Dowling-Degos Disease 1 58 0.560
354
P MYS003 Myasthenia Gravis 68 0.560
355
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 0.560
356
ADR007 Adrenoleukodystrophy 73 0.560
357
c THY107 Thymoma, Familial 42 0.560
358
SDD001 Sudden Infant Death Syndrome 60 0.560
359
TNG002 Tangier Disease 64 0.560
360
c LSS005 Lissencephaly 1 57 0.560
361
ALZ029 Alzheimer Disease Mitochondrial 24 0.560
362
P DRM053 Dermatitis, Atopic 65 0.560
363
END057 Endometrial Cancer 72 0.560
364
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.560
365
MRF001 Marfan Syndrome 76 0.560
366
OBS002 Obsessive-Compulsive Disorder 68 0.560
367
PHS027 Phosphoglycoprotein 1 15 0.560
368
NND010 Nondisjunction 34 0.560
369
CLF027 Cleft Palate, Isolated 64 0.560
370
CRT072 Creutzfeldt-Jakob Disease 68 0.560
371
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.560
372
ALC007 Alcohol Dependence 66 0.560
373
ABT001 Abetalipoproteinemia 68 0.560
374
c OST080 Osteogenesis Imperfecta, Type Ii 56 0.560
375
P PRK057 Parkinson Disease, Late-Onset 80 0.560
376
ASP002 Aspartylglucosaminuria 58 0.560
377
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.560
378
FDB001 Foodborne Botulism 55 0.560
379
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 36 0.560
380
WST001 West Syndrome 59 0.560
381
P MCL001 Mucolipidosis 49 0.560
382
c ATS007 Autism Spectrum Disorder 72 0.560
383
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.560
384
AND014 Androgenic Alopecia 47 0.560
385
KRN002 Kearns-Sayre Syndrome 63 0.560
386
HLC007 Helicobacter Pylori Infection 67 0.560
387
NRL016 Neural Tube Defects 81 0.560
388
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.560
389
P PRP003 Porphyria Cutanea Tarda 66 0.560
390
LTN004 Late-Onset Retinal Degeneration 60 0.560
391
CVT001 Cavitary Optic Disc Anomalies 37 0.560
392
CYS013 Cystinuria 66 0.560
393
NTH001 Netherton Syndrome 61 0.560
394
LRN002 Laron Syndrome 63 0.560
395
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.560
396
c NMN015 Niemann-Pick Disease, Type C1 68 0.560
397
P MJR007 Major Affective Disorder 1 42 0.560
398
P HYP750 Hypertriglyceridemia, Familial 62 0.560
399
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.560
400
DYS192 Dystonia, Dopa-Responsive 55 0.560
401
THY111 Thyroid Carcinoma, Familial Medullary 67 0.560
402
MYL057 Myelopathy, Htlv-1-Associated 38 0.560
403
c NRF024 Neurofibromatosis, Type I 72 0.560
404
OCL052 Ocular Dominance 40 0.560
405
PCK003 Pick Disease of Brain 69 0.560
406
ARB004 Arbitrary Restriction Polymorphism 1 14 0.560
407
CHR431 Chronic Venous Insufficiency 48 0.560
408
P FLL037 Follicular Lymphoma 74 0.560
409
P VNW001 Von Willebrand's Disease 65 0.560
410
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.560
411
CWP001 Cowpox 45 0.560
412
P ZLL001 Zellweger Syndrome 65 0.560
413
PRX001 Peroxisomal Disease 46 0.560
414
P BCL017 B-Cell Lymphoma 59 0.560
415
P MSC003 Muscular Atrophy 52 0.560
416
AVN001 Avian Influenza 61 0.560
417
DRM011 Dermatophytosis 52 0.560
418
P LCH002 Lichen Planus 54 0.560
419
VRL011 Viral Infectious Disease 61 0.560
420
P RRH023 Rare Hereditary Hemochromatosis 54 0.560
421
P MTH008 Methylmalonic Acidemia 52 0.560
422
ALL010 Allergic Contact Dermatitis 56 0.560
423
NRN001 Neuroendocrine Carcinoma 47 0.560
424
P CHR012 Chronic Granulomatous Disease 69 0.560
425
P GST044 Gastritis 55 0.560
426
ART016 Aortic Aneurysm 68 0.560
427
GST040 Gastric Adenocarcinoma 67 0.560
428
THY125 Thyroid Gland Medullary Carcinoma 48 0.560
429
PLS011 Plasmacytoma 56 0.560
430
CNN005 Connective Tissue Disease 67 0.560
431
PRT036 Peritonitis 65 0.560
432
OCC001 Occupational Dermatitis 28 0.560
433
END086 End Stage Renal Disease 52 0.560
434
ACT084 Acute Stress Disorder 54 0.560
435
SCB001 Scabies 50 0.560
436
CMB007 Combined Immunodeficiency 57 0.560
437
P VNS003 Venous Insufficiency 55 0.560
438
P GRF003 Graft-Versus-Host Disease 71 0.560
439
TCK001 Tick-Borne Encephalitis 59 0.560
440
SWN001 Swine Influenza 46 0.560
441
c DLT002 Dilated Cardiomyopathy 78 0.560
442
P DMN002 Dementia 66 0.560
443
HMS001 Hemosiderosis 48 0.560
444
P NTR004 Neutropenia 63 0.560
445
PCD001 Pica Disease 38 0.560
446
P HMN010 Hemangioma 62 0.560
447
P VSC007 Vascular Disease 63 0.560
448
IMP005 Impotence 52 0.560
449
RTN020 Retinal Vascular Disease 46 0.560
450
NRT004 Neuritis 53 0.560
451
c HPT015 Hepatitis D 49 0.560
452
P ECT006 Ectodermal Dysplasia 63 0.560
453
SCH014 Schistosomiasis 56 0.560
454
P HRT032 Heart Disease 81 0.560
455
LPR001 Lepromatous Leprosy 49 0.560
456
P MCR010 Microcephaly 60 0.560
457
LYM017 Lyme Disease 62 0.560
458
WST002 Western Equine Encephalitis 40 0.560
459
QFV001 Q Fever 62 0.560
460
KRT002 Keratomalacia 55 0.560
461
P END033 Endocarditis 58 0.560
462
P DYS005 Dyslexia 41 0.560
463
P TRT010 Teratoma 51 0.560
464
P THY023 Thymoma 64 0.560
465
P MTR014 Motor Neuron Disease 65 0.560
466
P ART021 Arteriosclerosis 54 0.560
467
CRY004 Cryoglobulinemia 48 0.560
468
TRP002 Tropical Spastic Paraparesis 49 0.560
469
TYP007 Typhoid Fever 64 0.560
470
P PRP029 Porphyria 60 0.560
471
P ADL010 Adult Respiratory Distress Syndrome 71 0.560
472
LST001 Listeriosis 59 0.560
473
P CRD246 Cardiovascular System Disease 56 0.560
474
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.560
475
HYP014 Hyperuricemia 51 0.560
476
HYP060 Hyperinsulinism 54 0.560
477
P MYT002 Myotonic Dystrophy 51 0.560
478
ISL099 Isolated Methylmalonic Acidemia 36 0.560
479
GRN017 Granulocytopenia 42 0.560
480
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.560
481
MLT028 Multiminicore Disease 43 0.560
482
ANR040 Aneurysm 61 0.560
483
CHL078 Childhood-Onset Schizophrenia 29 0.560
484
CYT002 Cytokine Deficiency 43 0.560
485
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.560
486
MYC019 Mycobacterium Marinum 29 0.560
487
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.560
489
ETN001 Eating Disorder 59 0.560
490
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.396
491
SPN050 Spinocerebellar Degeneration 39 0.396
492
P PRG139 Progeroid Syndrome 27 0.396
493
CMP097 Complex Chromosomal Rearrangement 23 0.396
494
PST021 Postpartum Depression 50 0.396
495
P DBT005 Diabetes Insipidus 54 0.396
496
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.396
497
SLP010 Slipped Capital Femoral Epiphysis 38 0.396
498
MTC005 Mitochondrial Metabolism Disease 45 0.396
499
CNN002 Cannabis Abuse 45 0.396
500
CNC014 Cancer-Associated Retinopathy 42 0.396
501
STP007 Staphylococcal Scarlet Fever 16 0.396
502
CYT017 Cytophagic Histiocytic Panniculitis 18 0.396
503
P SZR006 Seizure Disorder 70 0.396
504
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.396
505
OST115 Osteonecrosis of the Jaw 41 0.396
506
P AVS003 Avascular Necrosis 41 0.396
507
STP004 Staphylococcal Toxic Shock Syndrome 45 0.396
508
SPS057 Spasticity 42 0.396
509
MTH086 Methotrexate Toxicity 32 0.396
511
c ACT134 Acute Liver Failure 59 0.396
512
CLS049 Classic Phenylketonuria 41 0.396
513
THY128 Thyroid Tumor 35 0.396
514
PFF001 Pfeiffer Syndrome 77 0.396
515
c ALZ049 Alzheimer Disease 2 48 0.396
516
c EPS035 Episodic Ataxia, Type 2 63 0.396
517
P BLR024 Biliary Cirrhosis, Primary, 1 28 0.396
518
RST023 Resting Heart Rate, Variation in 40 0.396
519
P CRN300 Coronary Heart Disease 1 73 0.396
520
NCL008 Nuclear Ribonucleic Acid 15 0.396
521
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 0.396
522
P RTT002 Rett Syndrome 79 0.396
523
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.396
524
SMT004 Smith-Lemli-Opitz Syndrome 70 0.396
525
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.396
526
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.396
527
HMT020 Hematopoietic Stem Cell Kinetics, Control of 8 0.396
528
P LSS036 Lissencephaly, X-Linked, 1 47 0.396
529
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.396
530
CRD223 Cardiac Arrhythmia 63 0.396
531
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.396
532
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.396
533
c MCL046 Mucolipidosis Iii Alpha/beta 60 0.396
534
c MCL016 Mucolipidosis Iii Gamma 50 0.396
535
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.396
536
ANN002 Anencephaly 57 0.396
537
FBR012 Fabry Disease 70 0.396
538
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.396
539
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.396
540
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.396
541
c SCH051 Schizophrenia 4 32 0.396
542
P MTR004 Maturity-Onset Diabetes of the Young 68 0.396
543
P KLZ004 Kala-Azar 1 41 0.396
544
c RBN018 Robinow Syndrome, Autosomal Dominant 1 50 0.396
545
P LFR001 Li-Fraumeni Syndrome 73 0.396
546
LPM012 Lipomatosis, Multiple 60 0.396
547
MCR037 Macroglossia 44 0.396
548
P MLN066 Melanoma, Cutaneous Malignant 1 66 0.396
549
PRN011 Pernicious Anemia 53 0.396
550
LNT004 Lentigines 46 0.396
551
c SYS001 Systemic Lupus Erythematosus 87 0.396
552
CRD002 Cri-Du-Chat Syndrome 49 0.396
553
P EST010 Esterase B 13 0.396
554
P CLR023 Colorectal Cancer 100 0.396
555
FCT001 Factor Viii Deficiency 60 0.396
556
GLL008 Gilles De La Tourette Syndrome 65 0.396
557
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.396
558
c MST023 Mesothelioma, Malignant 56 0.396
559
c OST135 Osteogenesis Imperfecta, Type I 53 0.396
560
OTT002 Otitis Media 71 0.396
561
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 0.396
562
HYP781 Hypoascorbemia 52 0.396
563
c LKM063 Leukemia, Chronic Myeloid 71 0.396
564
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.396
565
P APL001 Aplastic Anemia 73 0.396
566
CHR100 Chronic Ulcer of Skin 57 0.396
567
PRP027 Peripheral Vascular Disease 71 0.396
568
P LSS002 Lissencephaly 50 0.396
569
EPD015 Epidemic Typhus 44 0.396
570
P ADV001 Advanced Sleep Phase Syndrome 41 0.396
571
P OCL002 Oculocutaneous Albinism 59 0.396
572
FTL006 Fetal Alcohol Spectrum Disorder 43 0.396
573
OPP004 Oppositional Defiant Disorder 49 0.396
574
c MCR115 Microvascular Complications of Diabetes 5 65 0.396
575
c MCR130 Microvascular Complications of Diabetes 6 41 0.396
576
MYX005 Myxoid Liposarcoma 65 0.396
577
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.396
578
c RTN134 Retinitis Pigmentosa 40 33 0.396
579
c CRN110 Cranioectodermal Dysplasia 3 27 0.396
580
HYP003 Hypermethioninemia 51 0.396
581
P HRD021 Hereditary Sensory Neuropathy 48 0.396
582
c SVR003 Severe Congenital Neutropenia 59 0.396
583
DFF005 Diffuse Large B-Cell Lymphoma 54 0.396
584
TRC010 Trichotillomania 50 0.396
585
c RTN106 Retinitis Pigmentosa 51 36 0.396
586
PMP013 Pemphigus Gestationis 19 0.396
587
CHK001 Chikungunya 60 0.396
588
c SLV029 Silver-Russell Syndrome 2 26 0.396
589
PRT251 Proteinuria, Chronic Benign 57 0.396
590
c ATM101 Autoimmune Gastritis 40 0.396
591
P ERY036 Erythema Nodosum 49 0.396
592
P URN019 Urinary Tract Infection 49 0.396
593
INF034 Infective Endocarditis 54 0.396
594
AMS001 Amusia 24 0.396
595
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.396
596
HMN047 Human Cytomegalovirus Infection 57 0.396
597
WTH001 Withdrawal Disorder 48 0.396
598
P CTN015 Cutaneous T Cell Lymphoma 48 0.396
599
APR001 Apraxia 52 0.396
600
RSP021 Respiratory Allergy 41 0.396
601
BNR002 Bone Resorption Disease 47 0.396
602
P SLM003 Salmonellosis 54 0.396
603
c ERL056 Early-Onset Parkinson's Disease 40 0.396
604
PHY002 Physical Disorder 41 0.396
605
MNN032 Meningococcal Meningitis 53 0.396
606
P FML023 Familial Hemiplegic Migraine 53 0.396
607
CRH005 Crohn's Colitis 53 0.396
608
PRL013 Paralytic Poliomyelitis 30 0.396
609
c FML001 Familial Atrial Fibrillation 65 0.396
610
P FTL001 Fetal Alcohol Syndrome 55 0.396
611
ZLL002 Zollinger-Ellison Syndrome 55 0.396
612
URL001 Urolithiasis 46 0.396
613
BTT017 Beta-Thalassemia Major 51 0.396
614
PMP004 Pemphigus Foliaceus 43 0.396
615
c RTN041 Retinitis Pigmentosa 11 42 0.396
616
DDN011 Duodenal Atresia 48 0.396
617
TRD006 Tardive Dyskinesia 53 0.396
618
P TYS001 Tay-Sachs Disease 69 0.396
619
c TYR012 Tyrosinemia, Type I 61 0.396
620
WRN001 Werner Syndrome 69 0.396
621
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.396
622
LGH007 Leigh Syndrome 70 0.396
623
SPN360 Spondylometaphyseal Dysplasia, Corner Fracture Type 38 0.396
624
CNT105 Central Core Disease of Muscle 59 0.396
625
c SPN309 Spinocerebellar Ataxia 6 58 0.396
626
c PRG020 Paragangliomas 3 39 0.396
627
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.396
628
ALV005 Alveolar Soft Part Sarcoma 61 0.396
629
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.396
630
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.396
631
AST006 Astigmatism 47 0.396
632
P LKM062 Leukemia, Acute Lymphoblastic 69 0.396
633
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.396
634
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.396
635
ANL018 Analbuminemia 53 0.396
636
HYP110 Hyperproinsulinemia 37 0.396
637
c LYM150 Lymphatic Malformation 7 38 0.396
638
EWN003 Ewing Sarcoma 70 0.396
639
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.396
640
P MJR001 Major Depressive Disorder 68 0.396
641
HMM004 Hamamy Syndrome 39 0.396
642
c MCR312 Microphthalmia, Syndromic 10 40 0.396
643
c MJR006 Major Affective Disorder 5 32 0.396
644
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 0.396
645
ACT119 Acute Promyelocytic Leukemia 62 0.396
646
c MCR120 Microvascular Complications of Diabetes 7 47 0.396
647
HRN029 Hearing Loss, Noise-Induced 37 0.396
648
c LPD035 Lipodystrophy, Congenital Generalized, Type 4 45 0.396
649
ALP103 Alpha-1-Antitrypsin Deficiency 68 0.396
650
c MJR003 Major Affective Disorder 6 32 0.396
651
c GLY043 Glycogen Storage Disease Xii 30 0.396
652
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.396
653
WST005 West Nile Virus 57 0.396
654
c PSD048 Pseudo-Von Willebrand Disease 39 0.396
655
c SCH079 Schizophrenia 1 44 0.396
656
TBL029 Tubulin, Beta 28 0.396
657
GLT038 Glutamyl Ribose-5-Phosphate Storage Disease 8 0.396
658
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.396
659
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.396
660
PLY068 Polysubstance Abuse 41 0.396
661
c ALB019 Albinism, Oculocutaneous, Type Iv 48 0.396
662
c RTN036 Retinal Cone Dystrophy 4 35 0.396
664
ALS001 Alstrom Syndrome 65 0.396
665
c HMP029 Hemophilia a 68 0.396
666
INC021 Incontinentia Pigmenti 63 0.396
667
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.396
668
c LFR007 Li-Fraumeni Syndrome 2 46 0.396
669
c PLN018 Peeling Skin Syndrome 2 38 0.396
670
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 0.396
671
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.396
672
PLS030 Plasminogen Deficiency, Type I 51 0.396
673
DYS179 Dyssegmental Dysplasia, Rolland-Desbuquois Type 25 0.396
674
P GLC113 Galactosemia I 66 0.396
675
c WLM013 Wilms Tumor 1 66 0.396
676
BTT016 Batten-Turner Congenital Myopathy 53 0.396
677
c PRD040 Periodontitis, Chronic 52 0.396
678
EPL131 Epilepsy, Pyridoxine-Dependent 45 0.396
679
c PNC106 Pancreatic Agenesis 1 51 0.396
680
SBC001 Subacute Sclerosing Panencephalitis 53 0.396
681
P IMR002 Imerslund-Grasbeck Syndrome 1 42 0.396
682
VLC001 Velocardiofacial Syndrome 57 0.396
683
YST001 Yeast Factor 6 0.396
684
P SRC025 Sarcoidosis 1 71 0.396
685
KRT071 Keratosis, Seborrheic 56 0.396
686
c NRB010 Neuroblastoma 1 59 0.396
687
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.396
688
c INF071 Inflammatory Bowel Disease 1 65 0.396
689
TBC004 Tobacco Addiction 63 0.396
690
c TBR025 Tuberous Sclerosis 1 84 0.396
691
HYP732 Hyperalphalipoproteinemia 1 52 0.396
692
c MLG147 Malignant Hyperthermia 1 45 0.396
693
DFC006 Defective Interfering Particle Induction, Control of 15 0.396
694
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.396
695
c EXS020 Exostoses, Multiple, Type Ii 38 0.396
696
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.396
697
HYP042 Hypochondroplasia 59 0.396
698
c CND033 Candidiasis, Familial, 1 27 0.396
699
CLB010 Coloboma of Macula 53 0.396
700
PPL048 Papillorenal Syndrome 58 0.396
701
DRM046 Dermal Ridges-off-the-End 20 0.396
702
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 33 0.396
703
EPD023 Epidermolysis Bullosa Simplex with Mottled Pigmentation 45 0.396
704
c EXS019 Exostoses, Multiple, Type I 54 0.396
705
NVS017 Nevus, Epidermal 66 0.396
706
PLT016 Platelet Adenylate Cyclase Activity 16 0.396
707
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.396
708
c MGR032 Migraine, Familial Hemiplegic, 1 54 0.396
709
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 42 0.396
710
c FTL065 Fetal Hemoglobin Quantitative Trait Locus 5 16 0.396
711
c FTL036 Fetal Hemoglobin Quantitative Trait Locus 2 16 0.396
712
ACH004 Achondroplasia 66 0.396
713
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.396
714
ADP007 Adie Pupil 40 0.396
715
c OST125 Osteopetrosis, Autosomal Dominant 1 34 0.396
716
P MYC007 Myocardial Infarction 70 0.396
717
c EHL085 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2 46 0.396
718
HYP020 Hyperprolactinemia 63 0.396
719
c RBN017 Robinow Syndrome, Autosomal Dominant 2 45 0.396
720
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.396
721
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.396
722
P PTN014 Patent Ductus Arteriosus 1 59 0.396
723
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 0.396
724
GLC003 Glucose Intolerance 54 0.396
725
PRM329 Premature Aging 36 0.396
726
MLD011 Mild Hyperphenylalaninemia 24 0.396
727
P PLN008 Peeling Skin Syndrome 43 0.396
728
P HYP730 Hypogonadotropic Hypogonadism 53 0.396
729
LBR036 Leber Plus Disease 66 0.396
730
c HMP004 Hemophilia B 68 0.396
731
c MLT095 Multiple Sclerosis 4 18 0.396
732
c CRN111 Cranioectodermal Dysplasia 4 31 0.396
733
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.396
734
LTX001 Latex Allergy 42 0.396
735
SPN250 Spondyloepimetaphyseal Dysplasia 36 0.396
736
P LPS004 Lupus Erythematosus 61 0.396
737
c ACT075 Acute Myocardial Infarction 56 0.396
738
CTN004 Cutaneous Fibrous Histiocytoma 39 0.396
739
CLC001 Calciphylaxis 51 0.396
740
ANG016 Angiokeratoma 37 0.396
741
GST030 Gastrinoma 45 0.396
742
SCH012 Schizoaffective Disorder 50 0.396
743
LCN001 Lice Infestation 41 0.396
744
BRN018 Borna Disease 36 0.396
745
URT010 Ureteral Obstruction 45 0.396
746
CRC021 Carcinosarcoma 64 0.396
747
MLL001 Molluscum Contagiosum 48 0.396
748
NRM001 Neuromyelitis Optica 61 0.396
749
SKN019 Skin Melanoma 71 0.396
750
P NRC002 Narcolepsy 56 0.396
751
CRV002 Cervix Uteri Carcinoma in Situ 47 0.396
752
VSC003 Visceral Leishmaniasis 55 0.396
753
P HMC002 Homocystinuria 53 0.396
754
P TYR004 Tyrosinemia 50 0.396
755
c BRS049 Breast Carcinoma in Situ 50 0.396
756
P ACT008 Actinic Keratosis 54 0.396
757
KRT006 Keratoconjunctivitis 53 0.396
758
P NRP001 Neuropathy 60 0.396
759
LRN003 Learning Disability 49 0.396
760
LSH001 Leishmaniasis 64 0.396
761
P VND001 Vein Disease 42 0.396
762
P MVM001 Movement Disease 61 0.396
763
ADN001 Adenosine Deaminase Deficiency 59 0.396
764
ADG002 Audiogenic Seizures 25 0.396
765
NM001 Noma 38 0.396
766
YLL002 Yellow Fever 61 0.396
767
P HYP098 Hypereosinophilic Syndrome 66 0.396
768
SYN036 Syncope 45 0.396
769
c FML191 Familial Long Qt Syndrome 55 0.396
770
IMM206 Immune Complex Mediated Vasculitis 13 0.396
771
MNG007 Manganese Poisoning 28 0.396
772
P PRS038 Personality Disorder 65 0.396
773
P PTT006 Pituitary Adenoma 55 0.396
774
PNC129 Pancreatic Adenocarcinoma 65 0.396
775
SVR001 Severe Acute Respiratory Syndrome 67 0.396
776
P ANT006 Antiphospholipid Syndrome 55 0.396
777
CHR001 Churg-Strauss Syndrome 61 0.396
778
GLB002 Glioblastoma 67 0.396
779
CNN001 Cannabis Dependence 38 0.396
780
P BRD002 Bardet-Biedl Syndrome 66 0.396
781
CLL003 Cellulitis 53 0.396
782
P TRN020 Turner Syndrome 67 0.396
783
P CNT009 Central Core Myopathy 43 0.396
784
P CND004 Candidiasis 58 0.396
785
END040 Endogenous Depression 55 0.396
786
P PLM036 Pulmonary Fibrosis 66 0.396
787
INS001 Insulinoma 59 0.396
788
SMN006 Seminal Vesicle Tumor 19 0.396
789
ADR005 Adrenal Carcinoma 62 0.396
790
BLD131 Bladder Urothelial Carcinoma 60 0.396
791
TCK004 Tick Infestation 30 0.396
792
P PNC025 Panic Disorder 52 0.396
793
CLL014 Cll/sll 45 0.396
794
NPH009 Nephrolithiasis 54 0.396
795
ESP023 Esophageal Disease 52 0.396
796
CYC005 Cyclothymic Disorder 40 0.396
797
OST012 Osteoarthritis 77 0.396
798
SBC011 Sebaceous Adenocarcinoma 43 0.396
799
TNC002 Tinea Capitis 42 0.396
800
P HRD001 Hereditary Multiple Exostoses 48 0.396
801
P INT070 Intestinal Obstruction 57 0.396
802
P NGH001 Night Blindness 52 0.396
803
P MNC007 Monocytic Leukemia 47 0.396
805
SLP001 Sleeping Sickness 56 0.396
806
TRY001 Trypanosomiasis 50 0.396
807
CRB004 Cerebral Artery Occlusion 45 0.396
808
PLM005 Pleomorphic Lipoma 40 0.396
809
P DRM010 Dermatomyositis 61 0.396
810
RCK004 Rickets 68 0.396
811
c MCR113 Microvascular Complications of Diabetes 3 52 0.396
812
c MCR133 Microvascular Complications of Diabetes 4 41 0.396
813
LMB002 Lambert-Eaton Myasthenic Syndrome 52 0.396
814
INH001 Inhalation Anthrax 42 0.396
815
P MGR003 Migraine with Aura 52 0.396
816
OST003 Osteonecrosis 61 0.396
817
c PRC016 Pre-Eclampsia 65 0.396
818
GT001 Gout 64 0.396
819
TNC003 Tinea Corporis 40 0.396
820
LYM009 Lymphocytic Choriomeningitis 46 0.396
821
P MLN007 Male Infertility 56 0.396
822
P ESP024 Esophagitis 60 0.396
823
P OPT009 Optic Neuritis 57 0.396
824
SHG001 Shigellosis 63 0.396
825
PRM236 Primary Biliary Cholangitis 60 0.396
826
ALC006 Alcoholic Hepatitis 61 0.396
827
P SPN046 Spinal Muscular Atrophy 63 0.396
828
PRV004 Periventricular Leukomalacia 52 0.396
829
c ACT068 Acute Cystitis 61 0.396
830
P WST004 West Nile Encephalitis 44 0.396
831
WST003 West Nile Fever 40 0.396
832
HRY003 Hairy Cell Leukemia 61 0.396
833
CRD003 Cardiac Sarcoidosis 44 0.396
834
P HYP069 Hyperparathyroidism 62 0.396
835
CHN002 Chancroid 36 0.396
836
TXC005 Toxic Shock Syndrome 62 0.396
837
P HYP035 Hypophosphatasia 62 0.396
838
PSY004 Psychotic Disorder 66 0.396
839
P NMN002 Niemann-Pick Disease 60 0.396
840
PMP002 Pemphigoid Gestationis 38 0.396
841
P BRS053 Breast Fibroadenoma 49 0.396
842
PPL002 Papillary Carcinoma 46 0.396
843
P TBR001 Tuberous Sclerosis 69 0.396
844
HYP081 Hypolipoproteinemia 49 0.396
845
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.396
846
TRN018 Transitional Cell Carcinoma 56 0.396
847
P LNG028 Long Qt Syndrome 64 0.396
848
HMG005 Hemoglobinopathy 56 0.396
849
P HYD006 Hydrocephalus 61 0.396
850
HYD002 Hydronephrosis 58 0.396
851
P CRD119 Cardiac Arrest 67 0.396
852
SPN369 Spinal Disease 44 0.396
853
P BND020 Bone Disease 59 0.396
854
HYP041 Hypochondrogenesis 35 0.396
855
MCS002 Mucositis 56 0.396
856
PRT013 Portal Hypertension 59 0.396
857
CCT002 Cicatricial Pemphigoid 53 0.396
858
EST003 Eastern Equine Encephalitis 38 0.396
859
BRD004 Borderline Personality Disorder 53 0.396
860
ANH002 Anhidrosis 46 0.396
861
c PRM005 Primary Hyperparathyroidism 59 0.396
862
P HRN001 Horner's Syndrome 46 0.396
863
P NNT058 Neonatal Diabetes 52 0.396
864
TBR006 Tuberculoid Leprosy 43 0.396
865
c VRL005 Viral Pneumonia 53 0.396
866
MCR013 Microphthalmia 60 0.396
867
CYS010 Cystinosis 62 0.396
868
BRN024 Bronchitis 67 0.396
869
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.396
870
c HPT007 Hepatitis E 51 0.396
871
P BRT004 Bartter Disease 58 0.396
872
TST018 Testicular Yolk Sac Tumor 39 0.396
873
ART017 Aortic Disease 49 0.396
874
P INF032 Infertility 57 0.396
875
P PRP019 Peripheral Nervous System Disease 58 0.396
876
CHS002 Chiasmal Syndrome 24 0.396
877
P RTN018 Retinal Disease 53 0.396
878
ANP009 Anaplastic Oligodendroglioma 41 0.396
879
CCN002 Cocaine Abuse 49 0.396
880
PRP030 Purpura 54 0.396
881
BRS099 Breast Ductal Carcinoma 61 0.396
882
GNG013 Gingivitis 59 0.396
883
ANP005 Anaplastic Astrocytoma 57 0.396
884
RCT009 Rectosigmoid Cancer 37 0.396
885
MSN004 Mesenchymal Cell Neoplasm 42 0.396
886
P LPS002 Liposarcoma 64 0.396
887
NCR004 Nocardiosis 53 0.396
888
PNC034 Pancreas Disease 50 0.396
889
P HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.396
890
NCR002 Necrobiosis Lipoidica 38 0.396
891
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.396
892
KLB003 Klebsiella Pneumonia 50 0.396
893
P GND004 Gonadal Dysgenesis 47 0.396
894
HMN048 Human Papillomavirus Infectious Disease 46 0.396
895
P EHL001 Ehlers-Danlos Syndrome 58 0.396
896
PLS007 Plasmodium Falciparum Malaria 52 0.396
897
GNG003 Gingival Recession 49 0.396
898
PNN001 Panniculitis 52 0.396
899
RHM001 Rheumatic Fever 59 0.396
900
HND002 Hand, Foot and Mouth Disease 50 0.396
901
AMN003 Amnestic Disorder 54 0.396
902
GNR004 Generalized Anxiety Disorder 55 0.396
903
IRN002 Iron Metabolism Disease 57 0.396
904
P END039 Endodermal Sinus Tumor 41 0.396
905
HYP080 Hypogonadism 50 0.396
906
GST052 Gestational Choriocarcinoma 35 0.396
907
P ICH004 Ichthyosis 56 0.396
908
UPP004 Upper Respiratory Tract Disease 33 0.396
909
SBS004 Substance Dependence 47 0.396
910
HYP141 Hyperphenylalaninemia 42 0.396
911
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.396
912
ALB002 Albinism 47 0.396
913
P INS002 in Situ Carcinoma 53 0.396
914
INV005 Inverted Follicular Keratosis 32 0.396
915
c ACT135 Acute Graft Versus Host Disease 51 0.396
916
ADS004 Aids Dementia Complex 40 0.396
917
P CLL015 Collagen Disease 48 0.396
918
GRM010 Germ Cells Tumors 33 0.396
919
NRF007 Neurofibroma 64 0.396
920
P EPS003 Episodic Ataxia 59 0.396
921
TRC023 Trichinosis 53 0.396
922
P HMP007 Hemophilia 52 0.396
923
TTR005 Tetrahydrobiopterin Deficiency 48 0.396
924
MYX011 Myxozoa 18 0.396
925
NSS002 Neisseria Meningitidis Infection 47 0.396
926
TRC096 Trichothiodystrophy 55 0.396
927
DPR016 Depression 65 0.396
928
CMP083 Complete Plasminogen Activator Inhibitor 1 Deficiency 27 0.396
929
HRD104 Hereditary Multiple Osteochondromas 43 0.396
930
P MTC069 Mitochondrial Disorders 57 0.396
932
P CRB088 Cerebral Atrophy 33 0.396
933
P CHR345 Chronic Pain 50 0.396
934
TRP014 Triploidy 38 0.396
935
WLL006 Wells Syndrome 49 0.396
937
SRF006 Surfactant Dysfunction 33 0.396
938
CNG069 Congenital Cytomegalovirus 51 0.396
939
ALL012 Allergic Angiitis 24 0.396
940
CRV045 Cervical Intraepithelial Neoplasia 39 0.396
941
CRT033 Corticobasal Degeneration 47 0.396
942
P OGC005 Oguchi Disease 45 0.396
943
PRS119 Persistent Genital Arousal Disorder 18 0.396
944
c RNG024 Ring Chromosome 8 28 0.396
945
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.396
946
EXN003 Exencephaly 30 0.396
947
c HMG029 Hemoglobin Se Disease 40 0.396
948
AMN006 Aminoaciduria 37 0.396
949
DWR001 Dwarfism 44 0.396
950
c FML053 Familial Colorectal Cancer 48 0.396
951
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.396
952