Search results for FAD

880 hits were found for FAD

# Family MCID Name MIFTS Score
1
P FTL069 Fetal Akinesia Deformation Sequence 1 63 34.333
2
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 19.896
3
P ALZ034 Alzheimer Disease 87 15.045
4
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 14.550
5
c FTL070 Fetal Akinesia Deformation Sequence 2 36 11.689
6
c FTL071 Fetal Akinesia Deformation Sequence 3 30 6.602
7
RBF001 Riboflavin Deficiency 49 5.732
8
P CHR012 Chronic Granulomatous Disease 69 4.861
9
HLX001 Helix Syndrome 48 4.786
10
DRM006 Dermatitis 62 4.772
11
CNG506 Congenital Amyoplasia 27 4.604
12
DWN001 Down Syndrome 70 4.480
13
P NRB001 Neuroblastoma 66 4.303
14
ETN001 Eating Disorder 59 4.063
15
P MYP004 Myopathy 67 4.061
16
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 4.010
17
P DMN002 Dementia 66 3.886
19
P AMY004 Amyloidosis 70 3.657
20
P MYC033 Myoclonus 47 3.657
21
P DST002 Distal Arthrogryposis 65 3.425
22
c ALZ056 Alzheimer Disease 3 55 3.351
23
MLD018 Mild Cognitive Impairment 48 3.262
24
CHR178 Chromosomal Triplication 34 3.219
25
P DRM053 Dermatitis, Atopic 65 3.205
26
CLF027 Cleft Palate, Isolated 64 3.196
27
P MJR001 Major Depressive Disorder 68 3.042
28
MNT002 Mental Depression 57 3.009
29
AGN016 Aging 54 2.912
30
P CNG001 Congenital Myasthenic Syndrome 68 2.906
31
IRN002 Iron Metabolism Disease 57 2.873
32
SPS019 Spastic Paraparesis 38 2.871
33
PRT037 Pertussis 65 2.871
34
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.834
35
P MTH007 Methemoglobinemia 46 2.763
36
ATS010 Autosomal Recessive Disease 42 2.753
37
FRN006 Frontotemporal Dementia 68 2.751
38
SKN016 Skin Disease 63 2.726
39
ART140 Arteries, Anomalies of 53 2.705
40
LPP008 Lipoprotein Quantitative Trait Locus 65 2.705
41
DPR016 Depression 65 2.688
42
c ALZ063 Alzheimer's Disease 1 31 2.628
43
APH002 Aphasia 56 2.610
44
c MJR022 Major Affective Disorder 8 38 2.569
45
c MJR024 Major Affective Disorder 9 41 2.569
46
P PRK039 Parkinsonism 55 2.569
47
P BPL003 Bipolar Disorder 56 2.569
48
PLY012 Polyhydramnios 46 2.560
49
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.534
50
ISC004 Ischemia 61 2.444
51
NRL016 Neural Tube Defects 81 2.433
52
HYP266 Hypoxia 57 2.433
53
c INH020 Inherited Metabolic Disorder 48 2.400
54
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.388
55
c DLT002 Dilated Cardiomyopathy 78 2.388
56
LPD008 Lipid Metabolism Disorder 62 2.337
57
CHL014 Cholera 62 2.309
58
CHG001 Chagas Disease 66 2.283
59
P MYC008 Myocarditis 59 2.283
60
c 2HY001 2-Hydroxyglutaric Aciduria 38 2.262
61
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.262
62
P CTR002 Cataract 60 2.228
63
HMC014 Homocysteinemia 52 2.214
64
P HNT016 Huntington Disease 73 2.214
65
CRN048 Craniofacial-Deafness-Hand Syndrome 52 2.214
66
47X002 47,xyy 48 2.214
67
P SYP003 Syphilis 59 2.214
68
HYP060 Hyperinsulinism 54 2.214
69
FTT001 Fatty Liver Disease 62 2.171
70
P ENC018 Encephalopathy 62 2.171
71
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.164
72
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.164
73
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.164
74
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.164
75
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.164
76
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.164
77
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.164
78
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.164
79
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.164
80
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.164
81
PPL052 Papillomatosis, Confluent and Reticulated 34 2.112
82
c CNG223 Congenital Methemoglobinemia 39 2.112
83
P PSR002 Psoriasis 63 2.111
84
PST011 Pustulosis of Palm and Sole 52 2.111
85
IRR002 Irritable Bowel Syndrome 65 2.085
86
BCK006 Back Pain 47 2.076
87
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 2.068
88
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 2.059
89
ARG004 Argyria 26 2.059
90
GLB002 Glioblastoma 67 2.059
91
RST011 Restrictive Dermopathy, Lethal 51 2.059
92
c L2H001 L-2-Hydroxyglutaric Aciduria 49 2.004
93
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 22 2.004
94
P MSC003 Muscular Atrophy 52 2.004
95
ALL014 Allergic Encephalomyelitis 34 2.004
96
ALL029 Allergic Disease 59 1.987
97
c ATR087 Atrial Standstill 1 74 1.982
98
CNG065 Congenital Contractures 25 1.982
99
MTB004 Metabolic Acidosis 48 1.946
100
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.946
101
MLR009 Miliaria 33 1.946
102
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.946
103
MLR001 Miliaria Rubra 32 1.946
104
NRN004 Neuroendocrine Tumor 59 1.946
105
CRC006 Carcinoid Syndrome 55 1.946
106
c ALZ054 Alzheimer Disease 4 43 1.945
107
TRM010 Traumatic Brain Injury 51 1.945
108
PRN009 Paranoid Schizophrenia 49 1.945
109
P AST005 Asthma 76 1.913
110
CND006 Candida Glabrata 30 1.913
111
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 1.902
112
APR001 Apraxia 52 1.902
113
P BRS053 Breast Fibroadenoma 49 1.902
114
KRT009 Keratosis 53 1.902
115
ANR007 Anorexia Nervosa 60 1.859
116
P HYP069 Hyperparathyroidism 62 1.859
117
STN013 Stenotrophomonas Maltophilia Infection 26 1.824
118
CYN002 Cyanosis, Transient Neonatal 43 1.824
119
ANT003 Antley-Bixler Syndrome 49 1.824
120
P HMC002 Homocystinuria 53 1.824
121
c ALZ049 Alzheimer Disease 2 48 1.768
122
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.768
123
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.768
124
P LTR001 Lateral Sclerosis 58 1.768
125
P PRS040 Prostate Cancer 95 1.759
126
PRT038 Protein-Energy Malnutrition 53 1.758
127
CYS002 Cystic Lymphangioma 45 1.758
128
HYP056 Hypoglycemia 65 1.758
129
c FTL072 Fetal Akinesia Deformation Sequence 4 37 1.749
130
VRG001 Variegate Porphyria 56 1.721
131
TCK004 Tick Infestation 30 1.721
132
PSY004 Psychotic Disorder 66 1.721
133
P PRP029 Porphyria 60 1.721
134
c MCR115 Microvascular Complications of Diabetes 5 65 1.689
135
c TYP009 Type 2 Diabetes Mellitus 92 1.689
136
BCT022 Bacterial Infectious Disease 56 1.689
137
c ACT076 Acute Myocarditis 47 1.689
138
END086 End Stage Renal Disease 52 1.689
139
P SPN046 Spinal Muscular Atrophy 63 1.689
140
P SCL018 Scoliosis 57 1.673
141
ADN018 Adenoma 59 1.672
142
VSC002 Vascular Dementia 60 1.672
143
BRN071 Brain Injury 50 1.672
144
MSC193 Muscular Lipidosis 22 1.622
145
PST028 Post-Traumatic Stress Disorder 59 1.622
146
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 1.615
147
P TRM004 Trimethylaminuria 45 1.615
148
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.615
149
P DBT009 Diabetes Mellitus 67 1.615
150
P EPL164 Epilepsy 68 1.615
151
DNT012 Dental Caries 53 1.615
152
INS024 Insulin-Like Growth Factor I 78 1.571
153
P MYC084 Mycobacterium Tuberculosis 1 68 1.571
154
P BRS047 Breast Cancer 98 1.571
155
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.571
156
P AGN002 Agnosia 54 1.571
157
P HYP265 Hypotonia 42 1.571
158
P INF037 Inflammatory Bowel Disease 53 1.535
159
AMN003 Amnestic Disorder 54 1.535
160
STM007 Stomatitis 54 1.535
161
P THL005 Thalassemia 56 1.518
162
P BRW001 Brown-Vialetto-Van Laere Syndrome 50 1.518
163
MNC011 Minicore Myopathy with External Ophthalmoplegia 37 1.518
164
CRH001 Crohn's Disease 80 1.518
165
FLL031 Follicular Adenoma 40 1.518
166
NRM005 Neuromuscular Disease 63 1.518
167
P LYM118 Lymphoma 67 1.499
168
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 1.499
169
LYM019 Lymphosarcoma 46 1.499
170
P RCT021 Rectum Cancer 54 1.468
171
P SCH015 Schizophrenia 74 1.462
172
HLT001 Holt-Oram Syndrome 66 1.462
173
c VRL010 Viral Hepatitis 53 1.462
174
GTR002 Goiter 53 1.462
175
P CRD246 Cardiovascular System Disease 56 1.462
176
P ATS364 Autism 69 1.448
177
CVD001 Covid-19 57 1.448
178
CVT001 Cavitary Optic Disc Anomalies 37 1.448
179
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 1.448
180
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 1.448
181
HYP748 Hypertelorism 46 1.448
182
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 1.448
183
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 26 1.448
184
THY029 Thyroid Carcinoma 51 1.448
185
CRV002 Cervix Uteri Carcinoma in Situ 47 1.448
186
GRD001 Giardiasis 46 1.448
187
CRV045 Cervical Intraepithelial Neoplasia 39 1.448
188
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.405
189
EPD002 Epidermolytic Hyperkeratosis 56 1.405
190
HMR039 Hemorrhage, Intracerebral 57 1.405
191
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 1.405
192
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 1.405
193
48X005 48,xyyy 39 1.405
194
P CRB088 Cerebral Atrophy 33 1.405
195
PSD088 Pseudobulbar Affect 33 1.405
196
P CRN300 Coronary Heart Disease 1 73 1.353
197
P MYS003 Myasthenia Gravis 68 1.353
198
HYD038 Hydrops Fetalis, Nonimmune 59 1.353
199
PRT251 Proteinuria, Chronic Benign 57 1.353
200
RSP021 Respiratory Allergy 41 1.353
201
NPH009 Nephrolithiasis 54 1.353
202
PTH002 Pathological Gambling 48 1.353
203
PRM209 Primary Trimethylaminuria 19 1.353
204
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.345
205
P KLZ004 Kala-Azar 1 41 1.345
206
AVN001 Avian Influenza 61 1.345
207
LSH001 Leishmaniasis 64 1.345
208
DSS008 Disease of Mental Health 74 1.345
209
P HYP076 Hyperthyroidism 53 1.345
210
ORL011 Oral Cancer 60 1.345
211
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.339
212
BLM002 Bulimia Nervosa 57 1.283
213
DFC004 Deficiency Anemia 74 1.283
214
ORL015 Oral Squamous Cell Carcinoma 43 1.283
215
P RTN016 Retinal Degeneration 52 1.283
216
P THY032 Thyroiditis 57 1.283
217
MLT028 Multiminicore Disease 43 1.283
218
CRT033 Corticobasal Degeneration 47 1.283
219
DBT006 Diabetic Macular Edema 48 1.260
220
MCL006 Macular Retinal Edema 57 1.260
221
CNG538 Congenital Arthrogryposis with Anterior Horn Cell Disease 32 1.247
222
P MTR004 Maturity-Onset Diabetes of the Young 68 1.244
223
P CLR023 Colorectal Cancer 100 1.244
224
ANG054 Angina Pectoris 66 1.244
225
P GST053 Gastric Cancer 83 1.244
226
PHN003 Phenylketonuria 76 1.244
227
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.244
228
P PRS038 Personality Disorder 65 1.244
229
P LVR013 Liver Disease 69 1.244
230
FDL002 Food Allergy 47 1.244
231
MLT010 Multiple Personality Disorder 29 1.244
232
URN010 Urinary Tract Obstruction 55 1.244
233
KWS001 Kwashiorkor 45 1.244
234
LPT001 Leptospirosis 66 1.244
235
HYP014 Hyperuricemia 51 1.244
236
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 1.244
237
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 1.244
238
c HMC039 Hemochromatosis, Type 1 73 1.217
239
ATH013 Atherosclerosis Susceptibility 63 1.217
240
NND010 Nondisjunction 34 1.217
241
c LKM061 Leukemia, Acute Myeloid 83 1.217
243
SNL009 Senile Plaque Formation 29 1.217
244
c HYP836 Hypercholesterolemia, Familial, 1 73 1.217
245
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 21 1.217
246
P HYP086 Hypothyroidism 69 1.217
247
HMG005 Hemoglobinopathy 56 1.217
248
IRN001 Iron Deficiency Anemia 58 1.217
249
P HYD006 Hydrocephalus 61 1.217
250
c PRM005 Primary Hyperparathyroidism 59 1.217
251
P NML001 Nemaline Myopathy 48 1.217
252
P CLC063 Celiac Disease 1 66 1.171
253
CHR081 Choroideremia 58 1.171
254
c TYP008 Type 1 Diabetes Mellitus 70 1.147
255
WRT005 Warty Dyskeratoma 16 1.147
256
MTH047 Methanol Poisoning 37 1.147
257
c MYS052 Myasthenic Syndrome, Congenital, 10 43 1.147
258
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 1.147
259
ANX010 Anxiety 70 1.147
260
PRN011 Pernicious Anemia 53 1.147
261
HSH003 Hashimoto Thyroiditis 60 1.147
262
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.147
264
DYS004 Dyscalculia 35 1.147
265
PRT019 Protein-Losing Enteropathy 45 1.147
266
P KDN018 Kidney Disease 72 1.147
267
ULC004 Ulcerative Colitis 74 1.147
268
P ALP008 Alopecia 54 1.147
269
P HRM001 Hermansky-Pudlak Syndrome 65 1.147
270
CNN003 Conn's Syndrome 79 1.147
271
P VSC007 Vascular Disease 63 1.147
272
PPL002 Papillary Carcinoma 46 1.147
273
GST033 Gestational Diabetes 61 1.147
274
PLC008 Placenta Disease 49 1.147
275
MCR017 Macrocytic Anemia 44 1.147
276
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 1.147
277
HDN002 Head Injury 44 1.147
278
CRB090 Cerebral Hypoxia 42 1.147
279
ART002 Arts Syndrome 66 1.115
280
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 1.115
281
c ATS007 Autism Spectrum Disorder 72 1.115
282
LGH007 Leigh Syndrome 70 1.115
283
MYL069 Myeloma, Multiple 77 1.115
284
c HYP595 Hypertension, Essential 85 1.115
285
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.115
286
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 1.115
287
P PLY011 Polycystic Ovary Syndrome 57 1.115
288
CNT047 Contact Dermatitis 57 1.115
289
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 1.073
290
CLT003 Colitis 63 1.073
291
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.073
292
NMN001 Nominal Aphasia 40 1.073
293
VSC003 Visceral Leishmaniasis 55 1.073
294
P LCT001 Lactic Acidosis 51 1.073
295
DLS001 Delusional Disorder 45 1.073
296
CRB004 Cerebral Artery Occlusion 45 1.073
297
P LNG064 Lung Cancer Susceptibility 3 70 1.073
298
TLN003 Telangiectasis 51 1.073
299
TRN015 Transient Cerebral Ischemia 63 1.073
300
P EYD002 Eye Disease 57 1.073
301
P SBS003 Substance Abuse 54 1.073
302
MDD011 Mood Disorder 62 1.073
303
NDL007 Nodular Goiter 48 1.073
304
GRV012 Grover's Disease 29 0.993
305
P OVR042 Ovarian Cancer 88 0.993
306
c MGR028 Migraine with or Without Aura 1 64 0.993
307
P PTY003 Pityriasis Rubra Pilaris 57 0.993
308
KRN002 Kearns-Sayre Syndrome 63 0.993
309
c ALZ050 Alzheimer Disease 5 33 0.993
310
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.993
311
P MYC007 Myocardial Infarction 70 0.993
312
STR095 Structural Heart Defects and Renal Anomalies Syndrome 20 0.993
313
PRM329 Premature Aging 36 0.993
314
MTC004 Mitochondrial Encephalomyopathy 42 0.993
315
HYP066 Hyperglycemia 61 0.993
316
MTH009 Mouth Disease 57 0.993
317
ACT084 Acute Stress Disorder 54 0.993
318
LYM027 Lymphopenia 56 0.993
319
c ACT004 Acute Diarrhea 40 0.993
320
c PRC016 Pre-Eclampsia 65 0.993
321
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.993
322
P DRR001 Diarrhea 55 0.993
323
SQM006 Squamous Cell Carcinoma 60 0.993
324
GRN017 Granulocytopenia 42 0.993
325
DYS073 Dysphagia 53 0.993
326
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.993
327
HMP009 Haemophilus Influenzae 41 0.993
328
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.947
329
OTT002 Otitis Media 71 0.947
330
P EXN002 Exanthem 58 0.947
331
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.947
332
P SPP010 Suppressor of Tumorigenicity 3 51 0.947
333
P FLL037 Follicular Lymphoma 74 0.947
334
OBS082 Obstructive Nephropathy 41 0.947
335
P LPS004 Lupus Erythematosus 61 0.947
336
SKN019 Skin Melanoma 71 0.947
337
ALL010 Allergic Contact Dermatitis 56 0.947
338
P ACN011 Acne 57 0.947
339
MLK006 Milk Allergy 47 0.947
340
MTC166 Mitochondrial Complex I Deficiency, Nuclear Type 19 23 0.947
341
STT001 Status Epilepticus 59 0.947
342
P MYT002 Myotonic Dystrophy 51 0.947
343
P CHR345 Chronic Pain 50 0.947
344
FML304 Familial Isolated Dilated Cardiomyopathy 49 0.907
345
ANX004 Anoxia 40 0.907
346
NRM022 Neurometabolic Disease 24 0.907
347
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 55 0.907
348
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.907
349
P RTN008 Retinitis Pigmentosa 80 0.907
350
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.907
351
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.907
352
P MLT020 Multiple Sclerosis 79 0.907
353
FZL002 Fazio-Londe Disease 39 0.907
354
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.907
355
c CRD113 Cardiomyopathy, Dilated, 1v 24 0.907
356
LMB062 Limb Ischemia 55 0.907
357
PLY166 Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1 8 0.907
358
P FRD001 Friedreich Ataxia 61 0.907
359
GLT035 Glutaric Acidemia I 57 0.907
360
ORG002 Organic Acidemia 44 0.907
361
NRR001 Neuroretinitis 42 0.907
362
GLC003 Glucose Intolerance 54 0.907
364
RTN023 Retinitis 46 0.907
365
ART014 Articulation Disorder 34 0.907
366
ASP007 Aspiration Pneumonia 49 0.907
367
GT001 Gout 64 0.907
368
SCH014 Schistosomiasis 56 0.907
369
P RSP003 Respiratory Failure 74 0.907
370
CHL123 Chlamydia 58 0.907
371
P PRN023 Prion Disease 60 0.907
372
SVR004 Severe Combined Immunodeficiency 72 0.907
373
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.907
374
P TXP001 Toxoplasmosis 60 0.907
375
CCN001 Cocaine Dependence 48 0.907
376
LKP003 Leukoplakia 39 0.907
377
IDP022 Idiopathic Spinal Cord Herniation 17 0.907
378
P LNG032 Lung Cancer 98 0.811
379
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.811
380
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.811
381
SMN008 Semantic Dementia 47 0.811
382
SDD001 Sudden Infant Death Syndrome 60 0.811
383
CMB017 Combined Oxidative Phosphorylation Deficiency 6 41 0.811
384
P MYS005 Myositis 56 0.811
385
OBS002 Obsessive-Compulsive Disorder 68 0.811
386
P ATX030 Ataxia-Telangiectasia 80 0.811
387
ISV001 Isovaleric Acidemia 54 0.811
388
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.811
389
OPP004 Oppositional Defiant Disorder 49 0.811
390
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.811
391
P ATR011 Atrial Fibrillation 66 0.811
392
CRP032 Corpus Callosum, Agenesis of 49 0.811
393
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.811
394
CNT105 Central Core Disease of Muscle 59 0.811
395
IGR001 Ige Responsiveness, Atopic 59 0.811
396
DMT001 Dimethylglycine Dehydrogenase Deficiency 27 0.811
397
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.811
398
c MCR312 Microphthalmia, Syndromic 10 40 0.811
399
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 35 0.811
400
OST159 Osteogenic Sarcoma 66 0.811
401
P HYP750 Hypertriglyceridemia, Familial 62 0.811
402
HRW001 Hair Whorl 35 0.811
403
c CRT081 Cortical Dysplasia, Complex, with Other Brain Malformations 7 31 0.811
404
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.811
405
P MLG056 Malignant Hyperthermia 66 0.811
406
P MYL006 Myeloid Leukemia 61 0.811
407
P TRM003 Tremor 48 0.811
408
MCR099 Microlissencephaly 37 0.811
409
SVR001 Severe Acute Respiratory Syndrome 67 0.811
410
P KRT005 Keratoacanthoma 47 0.811
411
OVR063 Overnutrition 42 0.811
412
HYP005 Hypokalemia 55 0.811
413
ANT007 Anterior Horn Cell Disease 31 0.811
414
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.811
415
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.811
416
CHL004 Cholelithiasis 49 0.811
417
OLG003 Oligohydramnios 51 0.811
418
CRT015 Carotid Artery Occlusion 45 0.811
419
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.811
420
PLR005 Pleuropneumonia 33 0.811
421
PLS007 Plasmodium Falciparum Malaria 52 0.811
422
P ART005 Arteriovenous Malformation 65 0.811
423
NNT010 Nontoxic Goiter 32 0.811
424
SNL007 Senile Cataract 40 0.811
425
TBL023 Tubulinopathies 31 0.811
426
PLY024 Polymicrogyria 47 0.811
427
P HDC001 Headache 57 0.811
428
P HYP120 Hypoaldosteronism 35 0.811
429
PRN039 Paraneoplastic Syndromes 37 0.766
430
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.719
431
c DRM054 Dermatitis, Atopic, 2 46 0.719
432
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.719
433
MTC005 Mitochondrial Metabolism Disease 45 0.702
434
P SZR006 Seizure Disorder 70 0.702
435
c DWL002 Dowling-Degos Disease 1 58 0.702
436
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.702
437
MSC157 Muscular Dystrophy, Duchenne Type 79 0.702
438
DSM002 Desmosterolosis 39 0.702
439
ACR020 Acropectorovertebral Dysplasia 23 0.702
440
ALC007 Alcohol Dependence 66 0.702
441
P PRK057 Parkinson Disease, Late-Onset 80 0.702
442
P FML011 Familial Adenomatous Polyposis 71 0.702
443
MLR004 Malaria 80 0.702
444
P HYP111 Hyperprolinemia 45 0.702
445
P PLY014 Polycystic Kidney Disease 69 0.702
446
HMN047 Human Cytomegalovirus Infection 57 0.702
447
SBJ001 Subjective Cognitive Decline 30 0.702
448
c RHZ004 Rhizomelic Chondrodysplasia Punctata, Type 3 42 0.702
449
PRL023 Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome 46 0.702
450
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.702
451
P PNC035 Pancreatic Cancer 86 0.702
453
KRT019 Keratitis, Hereditary 66 0.702
454
c SPN284 Spinocerebellar Ataxia 38 40 0.702
455
P ASP006 Aspergillosis 72 0.702
456
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 47 0.702
457
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.702
458
DMN031 Dementia, Lewy Body 65 0.702
459
PCK003 Pick Disease of Brain 69 0.702
460
c NMN014 Niemann-Pick Disease, Type C2 49 0.702
461
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.702
462
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.702
463
P ZLL001 Zellweger Syndrome 65 0.702
464
P BCL017 B-Cell Lymphoma 59 0.702
465
c CHR684 Chronic Kidney Disease 69 0.702
466
URM002 Uremia 47 0.702
467
P HRP006 Herpes Simplex 65 0.702
468
P MSC005 Muscular Dystrophy 67 0.702
469
P MTH008 Methylmalonic Acidemia 52 0.702
470
P ALC033 Alcohol Use Disorder 61 0.702
471
VCC001 Vaccinia 47 0.702
472
LCL004 Localized Osteosarcoma 34 0.702
473
P SKN015 Skin Carcinoma 71 0.702
474
END040 Endogenous Depression 55 0.702
475
SPN035 Spindle Cell Sarcoma 54 0.702
476
P INF038 Influenza 68 0.702
477
LNG099 Lung Disease 62 0.702
478
TRY001 Trypanosomiasis 50 0.702
479
P DNG005 Dengue Virus 56 0.702
480
P KLP003 Klippel-Feil Syndrome 47 0.702
481
P NTR004 Neutropenia 63 0.702
482
c SCN007 Secondary Hyperparathyroidism 51 0.702
483
c ACT027 Acute Pancreatitis 60 0.702
484
THY122 Thyroid Gland Cancer 59 0.702
485
CLB002 Clubfoot 51 0.702
486
CCC002 Coccidiosis 50 0.702
487
P ECL001 Eclampsia 52 0.702
488
SRC014 Sarcoma 65 0.702
489
P HYP040 Hypospadias 51 0.702
490
P HYP024 Hypoparathyroidism 55 0.702
491
HYD001 Hydranencephaly 43 0.702
492
PLG002 Plague 58 0.702
493
CRB033 Cerebral Degeneration 39 0.702
494
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.702
495
KRT008 Keratopathy 46 0.702
496
CRB037 Cerebral Palsy 67 0.702
497
P INS002 in Situ Carcinoma 53 0.702
498
HRN003 Heroin Dependence 44 0.702
499
P SCK005 Sickle Cell Disease 56 0.702
500
ERY069 Erythrokeratoderma ''en Cocardes'' 27 0.702
501
ADR022 Adrenomyeloneuropathy 39 0.574
502
PLY100 Polyploidy 36 0.574
503
P AVS003 Avascular Necrosis 41 0.574
504
CHR696 Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia 32 0.574
505
P RTT002 Rett Syndrome 79 0.574
506
ADR007 Adrenoleukodystrophy 73 0.574
507
LSC001 Lesch-Nyhan Syndrome 62 0.574
508
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.574
509
P FRG001 Fragile X Syndrome 70 0.574
510
SRC015 Sarcosinemia 38 0.574
511
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.574
512
c CTR132 Cataract 3, Multiple Types 42 0.574
513
BRT054 Brittle Bone Disorder 74 0.574
514
CRV035 Cervical Cancer 73 0.574
515
END057 Endometrial Cancer 72 0.574
516
CRT072 Creutzfeldt-Jakob Disease 68 0.574
517
GRS011 Gerstmann-Straussler Disease 56 0.574
518
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.574
519
CRN287 Carnitine Deficiency, Myopathic 17 0.574
520
CYS001 Cystic Fibrosis 78 0.574
521
c GLY007 Glycogen Storage Disease Iv 58 0.574
522
CHR100 Chronic Ulcer of Skin 57 0.574
523
P LSS002 Lissencephaly 50 0.574
524
FML037 Female Breast Cancer 51 0.574
525
VTM002 Vitamin B12 Deficiency 48 0.574
526
c BTT014 Beta-Thalassemia 72 0.574
527
DFF005 Diffuse Large B-Cell Lymphoma 54 0.574
528
NNL006 Non-Alcoholic Steatohepatitis 54 0.574
529
AGR018 Agraphia 37 0.574
530
SXL003 Sexual Disorder 49 0.574
531
c CNG006 Congenital Hypothyroidism 63 0.574
532
CLR108 Colorectal Adenoma 64 0.574
533
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 0.574
534
IMM167 Immune Deficiency Disease 78 0.574
535
c GRV008 Graves Disease 1 54 0.574
536
PRN056 Parana Hard-Skin Syndrome 17 0.574
537
c SPH013 Spherocytosis, Type 1 42 0.574
538
PRS012 Pars Planitis 47 0.574
539
c BRN108 Branchiootic Syndrome 1 62 0.574
540
P LKM062 Leukemia, Acute Lymphoblastic 69 0.574
541
LPT014 Leptin Deficiency or Dysfunction 78 0.574
542
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 0.574
543
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.574
544
MYP163 Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay 27 0.574
545
P DVL012 Developmental Dysplasia of the Hip 1 46 0.574
546
c CRB098 Cerebrooculofacioskeletal Syndrome 2 30 0.574
547
c CRB100 Cerebrooculofacioskeletal Syndrome 4 33 0.574
548
P CRB101 Cerebrooculofacioskeletal Syndrome 1 53 0.574
549
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 53 0.574
550
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 33 0.574
551
BTT016 Batten-Turner Congenital Myopathy 53 0.574
552
MYL005 Myelofibrosis 71 0.574
553
OCL069 Ocular Motor Apraxia 57 0.574
554
TLC001 Telecanthus 35 0.574
555
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.574
556
P SRC025 Sarcoidosis 1 71 0.574
557
P SCL057 Scoliosis, Isolated 1 40 0.574
558
RFS006 Refsum Disease, Classic 63 0.574
559
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.574
560
P PTN014 Patent Ductus Arteriosus 1 59 0.574
561
OST017 Osteomyelitis 63 0.574
562
P PNT019 Pontocerebellar Hypoplasia 46 0.574
563
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.574
564
c CHR697 Charcot-Marie-Tooth Disease X-Linked Recessive 4 31 0.574
565
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.574
566
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.574
567
HPT004 Hepatic Coma 43 0.574
568
BLS002 Blastomycosis 47 0.574
569
IDP073 Idiopathic Hypercalciuria 40 0.574
570
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.574
571
DYS003 Dysgraphia 35 0.574
572
SCH012 Schizoaffective Disorder 50 0.574
573
P DYS154 Dystonia 64 0.574
574
VLK001 Volkmann Contracture 23 0.574
575
P MVM001 Movement Disease 61 0.574
576
P HML002 Hemolytic Anemia 62 0.574
577
HMG002 Hemoglobinuria 50 0.574
578
GLL048 Glial Tumor 52 0.574
579
P HMR005 Hemorrhoid 49 0.574
580
GLY078 Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency 38 0.574
581
P THR014 Thrombocytopenia 66 0.574
582
P BRS044 Breast Adenocarcinoma 58 0.574
583
ART016 Aortic Aneurysm 68 0.574
584
P SYS005 Systemic Scleroderma 74 0.574
585
MTS001 Mutism 44 0.574
586
c SBC007 Subacute Thyroiditis 43 0.574
587
INH003 Inhibited Female Orgasm 27 0.574
588
P SNS001 Sensorineural Hearing Loss 59 0.574
589
SLP001 Sleeping Sickness 56 0.574
590
RCK004 Rickets 68 0.574
591
MYP164 Myopathy, Congenital, with Diaphragmatic Defects, Respiratory Insufficiency, and Dysmorphic Facies 24 0.574
592
P UVT001 Uveitis 57 0.574
593
BRN028 Brain Cancer 74 0.574
594
MRS001 Marasmus 42 0.574
595
P GRV001 Graves' Disease 55 0.574
596
PCD001 Pica Disease 38 0.574
597
ATY001 Atypical Depressive Disorder 45 0.574
598
P GLL022 Guillain-Barre Syndrome 60 0.574
599
IMP005 Impotence 52 0.574
600
c BSL007 Basal Cell Carcinoma 68 0.574
601
NRT004 Neuritis 53 0.574
602
NNT012 Neonatal Jaundice 53 0.574
603
P ADN016 Adenocarcinoma 63 0.574
604
MGL001 Megaloblastic Anemia 58 0.574
605
HYP030 Hypoactive Sexual Desire Disorder 41 0.574
606
P GLY013 Glycogen Storage Disease 60 0.574
607
P END044 Endometriosis 62 0.574
608
P HRT032 Heart Disease 81 0.574
609
PRM013 Premature Menopause 58 0.574
610
BRD004 Borderline Personality Disorder 53 0.574
611
MNN009 Meningoencephalitis 48 0.574
612
P PNC044 Pancreatitis 61 0.574
613
P INF032 Infertility 57 0.574
614
P RTN018 Retinal Disease 53 0.574
615
P AXN001 Axonal Neuropathy 35 0.574
616
P PRM002 Primary Hyperoxaluria 65 0.574
617
P KDN017 Kidney Cancer 61 0.574
618
P MTR014 Motor Neuron Disease 65 0.574
619
PHM001 Phimosis 38 0.574
620
BRS051 Breast Disease 58 0.574
621
DMY004 Demyelinating Disease 50 0.574
622
IDP070 Idiopathic Scoliosis 42 0.574
623
LST001 Listeriosis 59 0.574
624
CHR073 Choreatic Disease 54 0.574
625
P HRD011 Hereditary Spherocytosis 64 0.574
626
CND002 Conduct Disorder 51 0.574
627
HST011 Histoplasmosis 55 0.574
628
SBS004 Substance Dependence 47 0.574
629
P TRC031 Trichorhinophalangeal Syndrome 38 0.574
630
DCB001 Decubitus Ulcer 62 0.574
631
FSC004 Fasciitis 49 0.574
632
PRL005 Proliferative Fasciitis 20 0.574
633
ISC003 Ischemic Fasciitis 28 0.574
634
MYP017 Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay 14 0.574
635
GB1002 Gbe1 Adult Polyglucosan Body Disease 7 0.574
636
ANR040 Aneurysm 61 0.574
637
BRN056 Bronchopulmonary Dysplasia 56 0.574
638
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.574
639
CCC003 Coccygodynia 18 0.574
640
GLM045 Glioma 63 0.574
641
SPT023 Septate Uterus 30 0.541
642
URM005 Uremic Pruritus 45 0.541
643
c DRM040 Dermatitis Herpetiformis, Familial 35 0.541
644
ATM095 Autoimmune Disease 61 0.541
645
P RST001 Restless Legs Syndrome 52 0.541
646
P CRP001 Carpal Tunnel Syndrome 66 0.541
647
c PCH010 Pachyonychia Congenita 3 43 0.541
648
PLY105 Polycystic Ovary Syndrome 1 39 0.541
649
c CWD006 Cowden Syndrome 1 78 0.541
650
P VSC011 Vasculitis 61 0.541
651
CHR066 Chronic Fatigue Syndrome 60 0.541
652
WHT017 Wheat Allergy 31 0.541
653
CHR001 Churg-Strauss Syndrome 61 0.541
654
APP008 Appendicitis 62 0.541
655
PPT005 Peptic Ulcer Disease 58 0.541
656
P DRM007 Dermatitis Herpetiformis 54 0.541
657
P VNS003 Venous Insufficiency 55 0.541
658
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.541
659
TBS001 Tabes Dorsalis 31 0.541
660
CNS004 Constipation 56 0.541
661
P CWD010 Cowden Syndrome 70 0.541
662
FLL008 Folliculitis 46 0.541
663
P SLP005 Sleep Disorder 61 0.541
664
P ADL010 Adult Respiratory Distress Syndrome 71 0.541
665
PTL002 Patellofemoral Pain Syndrome 34 0.541
666
ALL012 Allergic Angiitis 24 0.541
667
P CLS010 Cluster Headache 42 0.541
668
ESN016 Eosinophilic Pustular Folliculitis 24 0.541
669
MCR088 Microscopic Polyangiitis 51 0.541
670
ANC002 Anca-Associated Vasculitis 44 0.541
671
c GRN062 Granulomatous Disease, Chronic, Autosomal Recessive, 1 46 0.406
672
PST021 Postpartum Depression 50 0.406
673
DMN026 Dementia Pugilistica 27 0.406
674
RFR010 Refractory Anemia 49 0.406
675
SNK001 Snakebite Envenomation 22 0.406
676
CYN003 Cyanide Poisoning 22 0.406
677
OST115 Osteonecrosis of the Jaw 41 0.406
678
SPS057 Spasticity 42 0.406
679
ARG006 Aregenerative Anemia 28 0.406
680
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.406
681
c STC015 Stickler Syndrome, Type I 51 0.406
682
P BLD134 Bladder Cancer 79 0.406
683
P NSP012 Nasopharyngeal Carcinoma 61 0.406
684
GND001 Gonadoblastoma 43 0.406
685
MRD002 Marden-Walker Syndrome 56 0.406
686
FRG010 Fragile X Tremor/ataxia Syndrome 44 0.406
687
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.406
688
MND023 Mend Syndrome 49 0.406
689
MST021 Meester-Loeys Syndrome 42 0.406
690
P LPR021 Leprosy 3 71 0.406
691
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 0.406
692
ALL003 Allergic Rhinitis 67 0.406
693
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.406
694
STR067 Stroke, Ischemic 80 0.406
695
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.406
696
P PHC003 Pheochromocytoma 69 0.406
697
c SYS001 Systemic Lupus Erythematosus 87 0.406
698
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.406
699
PLY150 Polykaryocytosis Inducer 29 0.406
700
P CNR004 Cone-Rod Dystrophy 2 74 0.406
701
CRD002 Cri-Du-Chat Syndrome 49 0.406
702
c FNC027 Fanconi Anemia, Complementation Group a 81 0.406
703
HYP781 Hypoascorbemia 52 0.406
704
PLL017 Pallister-Hall-Like Syndrome 37 0.406
705
c LKM063 Leukemia, Chronic Myeloid 71 0.406
706
EPD015 Epidemic Typhus 44 0.406
707
END014 Endemic Typhus 32 0.406
708
CNZ001 Coenzyme Q10 Deficiency Disease 41 0.406
709
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 0.406
710
DLY008 Delayed Sleep Phase Disorder 44 0.406
711
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 26 0.406
712
INV001 Invasive Aspergillosis 49 0.406
713
P URN019 Urinary Tract Infection 49 0.406
714
ALX002 Alexithymia 37 0.406
715
ASS001 Associative Agnosia 24 0.406
716
MCR191 Microscopic Colitis 46 0.406
717
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.406
718
LWG006 Low Grade Glioma 41 0.406
719
P CTN015 Cutaneous T Cell Lymphoma 48 0.406
720
CRH005 Crohn's Colitis 53 0.406
721
FSR001 Fusariosis 45 0.406
722
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.406
723
P HYP768 Hyperlipoproteinemia, Type I 67 0.406
724
GST108 Gist-Plus Syndrome 22 0.406
725
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.406
726
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.406
727
SCK003 Sickle Cell Anemia 74 0.406
728
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.406
729
HMM004 Hamamy Syndrome 39 0.406
730
ACT119 Acute Promyelocytic Leukemia 62 0.406
731
TBL029 Tubulin, Beta 28 0.406
732
P MPL001 Maple Syrup Urine Disease 70 0.406
733
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.406
734
MTC207 Mitochondrial Complex Ii Deficiency, Nuclear Type 1 55 0.406
735
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.406
736
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 35 0.406
737
c HYD064 Hydrocephalus, Congenital, 1 51 0.406
738
c HYP248 Hyperprolinemia, Type I 42 0.406
739
VRC005 Varicose Veins 60 0.406
740
VLC001 Velocardiofacial Syndrome 57 0.406
741
RTN179 Retinal Arteries, Tortuosity of 41 0.406
742
KRT071 Keratosis, Seborrheic 56 0.406
743
P STR020 Strabismus 56 0.406
744
DGR001 Digeorge Syndrome 62 0.406
745
CRN238 Corneal Dystrophy, Epithelial Basement Membrane 32 0.406
746
P MJR007 Major Affective Disorder 1 42 0.406
747
MLT157 Multiple System Atrophy 1 69 0.406
748
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 42 0.406
749
P ANG001 Angelman Syndrome 65 0.406
750
ANT078 Antipyrine Metabolism 23 0.406
751
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.406
752
c MYP118 Myopathy, Myofibrillar, 8 30 0.406
753
PNG002 Pain Agnosia 51 0.406
754
GST019 Gastrointestinal Stromal Tumor 78 0.406
755
CLR109 Colorectal Adenocarcinoma 50 0.406
756
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.406
757
ADR040 Adrenal Gland Pheochromocytoma 46 0.406
758
BLP004 Blepharophimosis 36 0.406
759
P LCT002 Lactose Intolerance 52 0.406
760
ADN072 Adenoma of Pancreas 17 0.406
761
c CHR695 Chronic Primary Adrenal Insufficiency 15 0.406
762
P PRN026 Porencephaly 55 0.406
763
MTC151 Mitochondrial Complex I Deficiency, Nuclear Type 20 36 0.406
764
PRC002 Paracoccidioidomycosis 54 0.406
765
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.406
766
c ACT073 Acute Leukemia 58 0.406
767
P MYP006 Myopia 56 0.406
768
FSC002 Fascioliasis 44 0.406
769
P SDR003 Sideroblastic Anemia 51 0.406
770
PRX001 Peroxisomal Disease 46 0.406
771
P HYP083 Hypopituitarism 52 0.406
772
NTR005 Nutritional Deficiency Disease 61 0.406
773
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.406
774
INT075 Intracranial Hypertension 53 0.406
775
GSG001 Gas Gangrene 52 0.406
776
MCH006 Mechanical Strabismus 40 0.406
777
P NRP001 Neuropathy 60 0.406
778
AMB001 Amebiasis 57 0.406
779
P MTC133 Mitochondrial Myopathy 50 0.406
780
PST092 Posttransplant Acute Limbic Encephalitis 28 0.406
781
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.406
782
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 22 0.406
783
YLL002 Yellow Fever 61 0.406
784
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 26 0.406
785
PNC129 Pancreatic Adenocarcinoma 65 0.406
786
c HPT001 Hepatitis C 62 0.406
787
SYS004 Systemic Mastocytosis 63 0.406
788
P TRN020 Turner Syndrome 67 0.406
789
P MST009 Mastocytosis 64 0.406
790
AVD001 Avoidant Personality Disorder 49 0.406
791
P GST044 Gastritis 55 0.406
792
ACQ007 Acquired Immunodeficiency Syndrome 59 0.406
793
ILS001 Ileus 50 0.406
794
CLR030 Clear Cell Renal Cell Carcinoma 54 0.406
795
ANT024 Anthrax Disease 58 0.406
796
CHL061 Childhood Leukemia 47 0.406
797
P PLL002 Pellagra 46 0.406
798
P ART022 Arthritis 71 0.406
799
P RTN014 Retinal Artery Occlusion 47 0.406
800
P MNC007 Monocytic Leukemia 47 0.406
801
ASY002 Asymptomatic Neurosyphilis 41 0.406
802
SLC006 Silicosis 56 0.406
803
CMM005 Common Cold 56 0.406
804
c SPR162 Spermatogenic Failure 50 42 0.406
805
CHL147 Chlamydia Pneumonia 47 0.406
806
STR103 Streptococcus Pneumonia 47 0.406
807
OST003 Osteonecrosis 61 0.406
808
DNG003 Dengue Disease 65 0.406
809
P MLN007 Male Infertility 56 0.406
810
P ESP024 Esophagitis 60 0.406
811
SYN005 Synostosis 43 0.406
812
P LKM002 Leukemia 67 0.406
813
BRN026 Branch Retinal Artery Occlusion 41 0.406
814
PPL022 Papilloma 53 0.406
815
BLR008 Bilirubin Metabolic Disorder 57 0.406
816
P BRB001 Beriberi 44 0.406
817
SQM002 Squamous Cell Papilloma 46 0.406
818
TXC005 Toxic Shock Syndrome 62 0.406
819
P MLN008 Melanoma 76 0.406
820
RTN020 Retinal Vascular Disease 46 0.406
821
P NPH012 Nephrotic Syndrome 60 0.406
822
P CRN037 Craniosynostosis 68 0.406
823
HPT014 Hepatorenal Syndrome 49 0.406
824
P MCR010 Microcephaly 60 0.406
825
RBS001 Rabies 58 0.406
826
SPT005 Spotted Fever 49 0.406
827
KRT002 Keratomalacia 55 0.406
828
TTN003 Tetanus 65 0.406
829
HYP006 Hypertensive Heart Disease 49 0.406
830
P RHN004 Rhinitis 57 0.406
831
THY030 Thyroid Gland Disease 50 0.406
832
ADJ001 Adjustment Disorder 47 0.406
833
P PRP019 Peripheral Nervous System Disease 58 0.406
834
PRM020 Premenstrual Tension 39 0.406
835
GNG013 Gingivitis 59 0.406
836
c CNT035 Central Nervous System Disease 54 0.406
837
GST045 Gastroenteritis 58 0.406
838
P ART021 Arteriosclerosis 54 0.406
839
P THR015 Thrombophilia 51 0.406
840
c FML021 Familial Hypercholesterolemia 72 0.406
841
P PLY019 Polyneuropathy 52 0.406
842
TYP007 Typhoid Fever 64 0.406
843
ERY004 Erysipelas 47 0.406
844
CHL035 Cholinergic Urticaria 29 0.406
845
P GND004 Gonadal Dysgenesis 47 0.406
846
NCR001 Necrotizing Ulcerative Gingivitis 26 0.406
847
PLM010 Pulmonary Edema 55 0.406
848
GNG011 Gingival Disease 54 0.406
849
P URT039 Urticaria 58 0.406
850
AZS001 Azoospermia 45 0.406
851
HDR002 Hidradenitis Suppurativa 54 0.406
852
P BNC003 Bone Cancer 58 0.406
853
c SVR005 Severe Pre-Eclampsia 50 0.406
854
DVL001 Developmental Coordination Disorder 34 0.406
855
P MNN013 Meningitis 65 0.406
856
INV005 Inverted Follicular Keratosis 32 0.406
857
P ACT105 Acute Mountain Sickness 52 0.406
858
ADS004 Aids Dementia Complex 40 0.406
859
P ENC004 Encephalitis 61 0.406
860
ATS301 Autosomal Dominant Epilepsy with Auditory Features 36 0.406
861
HNS001 Hansen's Disease 32 0.406
862
MNN020 Meningococcal Infection 45 0.406
863
NNT017 Neonatal Adrenoleukodystrophy 54 0.406
864
ORL012 Oral Leukoplakia 36 0.406
865
WLL004 Wallerian Degeneration 38 0.406
866
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 0.406
867
DSR002 Disorders of Intracellular Cobalamin Metabolism 29 0.406
868
P MTC069 Mitochondrial Disorders 57 0.406
869
CRB086 Cerebral Aneurysms 40 0.406
870
DVL005 Developmental Dyspraxia 22 0.406
871
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.406
872
CYT002 Cytokine Deficiency 43 0.406
873
P ADT009 Auditory Neuropathy Spectrum Disorder 34 0.406
874
EXR007 Exercise-Induced Anaphylaxis 23 0.406
875
NRS003 Neurosyphilis 45 0.406
876
PNC049 Pancreatic Adenoma 14 0.406
877
PST046 Post-Transplant Lymphoproliferative Disease 53 0.406
878
DWR001 Dwarfism 44 0.406
879
MSL001 Measles 61 0.406
880
P NRV007 Nervous System Disease 67 0.406
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