Search results for FAD

904 hits were found for FAD

# Family MCID Name MIFTS Score
1
P FTL069 Fetal Akinesia Deformation Sequence 1 63 30.543
2
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 14.293
3
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 11.661
4
c FTL070 Fetal Akinesia Deformation Sequence 2 36 6.391
5
P ALZ034 Alzheimer Disease 87 6.167
6
c FTL071 Fetal Akinesia Deformation Sequence 3 29 3.943
7
RBF001 Riboflavin Deficiency 49 2.424
8
DRM006 Dermatitis 61 2.417
9
c ALZ056 Alzheimer Disease 3 56 2.300
10
FRN006 Frontotemporal Dementia 68 2.139
11
P CHR012 Chronic Granulomatous Disease 69 2.116
12
CNG506 Congenital Amyoplasia 27 2.058
13
PCK003 Pick Disease of Brain 70 2.007
14
P ACN016 Acne Inversa, Familial, 3 28 1.957
15
HLX001 Helix Syndrome 47 1.893
16
ETN001 Eating Disorder 59 1.822
17
P DRM053 Dermatitis, Atopic 65 1.743
18
P MYP004 Myopathy 67 1.583
19
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 1.583
20
ART140 Arteries, Anomalies of 52 1.565
21
LPP008 Lipoprotein Quantitative Trait Locus 65 1.565
22
P LYM118 Lymphoma 66 1.501
23
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 1.501
24
LYM019 Lymphosarcoma 46 1.501
25
CLF027 Cleft Palate, Isolated 64 1.498
26
P NRB001 Neuroblastoma 66 1.448
27
P DST002 Distal Arthrogryposis 63 1.426
28
P DMN002 Dementia 65 1.353
29
PLY012 Polyhydramnios 46 1.340
30
BCK006 Back Pain 43 1.328
32
P AMY004 Amyloidosis 69 1.315
33
P MYC033 Myoclonus 46 1.315
34
AGN016 Aging 53 1.288
35
IRN002 Iron Metabolism Disease 56 1.288
36
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.279
37
MCL006 Macular Retinal Edema 56 1.260
38
DBT006 Diabetic Macular Edema 48 1.260
39
ATS010 Autosomal Recessive Disease 42 1.258
40
IRR002 Irritable Bowel Syndrome 64 1.221
41
MLD018 Mild Cognitive Impairment 48 1.217
42
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.204
43
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.204
44
PRT037 Pertussis 49 1.202
45
c DLT002 Dilated Cardiomyopathy 79 1.168
46
P MJR001 Major Depressive Disorder 68 1.162
47
LPD008 Lipid Metabolism Disorder 61 1.155
48
MNT002 Mental Depression 56 1.154
49
RST011 Restrictive Dermopathy, Lethal 51 1.145
50
CHG001 Chagas Disease 65 1.142
51
P MYC008 Myocarditis 59 1.142
52
P CNG001 Congenital Myasthenic Syndrome 68 1.128
53
P CTR002 Cataract 59 1.128
54
SPS019 Spastic Paraparesis 38 1.120
55
FTT001 Fatty Liver Disease 61 1.114
56
P ENC018 Encephalopathy 62 1.114
57
DWN001 Down Syndrome 70 1.113
58
P SCL018 Scoliosis 57 1.099
59
PST011 Pustulosis of Palm and Sole 52 1.099
60
P PSR002 Psoriasis 63 1.099
61
P MTH007 Methemoglobinemia 46 1.093
62
SKN016 Skin Disease 63 1.083
63
DPR016 Depression 64 1.074
64
c FTL072 Fetal Akinesia Deformation Sequence 4 37 1.068
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.067
66
c ATR087 Atrial Standstill 1 74 1.067
67
CNG065 Congenital Contractures 27 1.067
68
APH002 Aphasia 55 1.055
69
P AST005 Asthma 75 1.050
70
CND006 Candida Glabrata 29 1.050
71
c MJR022 Major Affective Disorder 8 37 1.045
72
c MJR024 Major Affective Disorder 9 40 1.045
73
P PRK039 Parkinsonism 55 1.045
74
P BPL003 Bipolar Disorder 56 1.045
75
ISC004 Ischemia 61 1.013
76
P PRS040 Prostate Cancer 95 1.011
77
c INH020 Inherited Metabolic Disorder 47 1.003
78
CHL014 Cholera 62 0.980
79
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.968
80
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.968
81
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.956
82
HMC014 Homocysteinemia 52 0.956
83
c CNG223 Congenital Methemoglobinemia 39 0.956
84
P HNT016 Huntington Disease 73 0.956
85
HYP060 Hyperinsulinism 53 0.956
86
GLB002 Glioblastoma 67 0.956
87
P SYP003 Syphilis 59 0.956
88
CNG538 Congenital Arthrogryposis with Anterior Horn Cell Disease 32 0.944
89
P RCT021 Rectum Cancer 54 0.939
90
PPL052 Papillomatosis, Confluent and Reticulated 34 0.931
91
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.931
92
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.931
93
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.931
94
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.931
95
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.931
96
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.931
97
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.931
98
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.931
99
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.931
100
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.918
101
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.918
102
ARG004 Argyria 26 0.918
103
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.904
104
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 22 0.904
105
P MSC003 Muscular Atrophy 52 0.904
106
ALL014 Allergic Encephalomyelitis 34 0.904
107
MTB004 Metabolic Acidosis 48 0.890
108
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.890
109
MLR009 Miliaria 33 0.890
110
NRN004 Neuroendocrine Tumor 55 0.890
111
P EPL164 Epilepsy 70 0.890
112
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.890
113
MLR001 Miliaria Rubra 32 0.890
114
CRC006 Carcinoid Syndrome 55 0.890
115
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.875
116
P CLC063 Celiac Disease 1 65 0.865
117
CHR081 Choroideremia 58 0.865
118
CYN002 Cyanosis, Transient Neonatal 43 0.859
119
ANT003 Antley-Bixler Syndrome 50 0.859
120
P HMC002 Homocystinuria 52 0.859
121
STN013 Stenotrophomonas Maltophilia Infection 26 0.859
122
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.843
123
CYS002 Cystic Lymphangioma 45 0.843
124
PRT038 Protein-Energy Malnutrition 53 0.843
125
HYP056 Hypoglycemia 65 0.843
126
c MCR115 Microvascular Complications of Diabetes 5 65 0.826
127
P SPN046 Spinal Muscular Atrophy 62 0.826
128
BCT022 Bacterial Infectious Disease 55 0.826
129
c ACT076 Acute Myocarditis 46 0.826
130
END086 End Stage Renal Disease 54 0.826
131
47X002 47,xyy 47 0.826
132
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.807
133
c TYP009 Type 2 Diabetes Mellitus 91 0.807
134
P TRM004 Trimethylaminuria 45 0.807
135
DNT012 Dental Caries 53 0.807
136
CHR178 Chromosomal Triplication 33 0.800
137
AMN003 Amnestic Disorder 53 0.788
138
STM007 Stomatitis 52 0.788
139
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.766
140
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.766
141
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 0.766
142
ALP089 Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality 26 0.766
143
HYP748 Hypertelorism 46 0.766
144
CVT001 Cavitary Optic Disc Anomalies 38 0.766
145
GRD001 Giardiasis 46 0.766
146
CRV002 Cervix Uteri Carcinoma in Situ 48 0.766
147
CRV045 Cervical Intraepithelial Neoplasia 38 0.766
148
THY029 Thyroid Carcinoma 55 0.766
149
PRN039 Paraneoplastic Syndromes 37 0.765
150
PRT251 Proteinuria, Chronic Benign 58 0.742
151
P CRN300 Coronary Heart Disease 1 73 0.742
152
HYD038 Hydrops Fetalis, Nonimmune 57 0.742
153
c LYM150 Lymphatic Malformation 7 43 0.742
154
P MYS003 Myasthenia Gravis 67 0.742
155
RSP021 Respiratory Allergy 41 0.742
156
PTH002 Pathological Gambling 48 0.742
157
NPH009 Nephrolithiasis 54 0.742
158
PRM209 Primary Trimethylaminuria 19 0.742
159
c DRM054 Dermatitis, Atopic, 2 47 0.719
160
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.719
161
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.719
162
P MTR004 Maturity-Onset Diabetes of the Young 66 0.715
163
P ATS364 Autism 72 0.715
164
LGH007 Leigh Syndrome 70 0.715
165
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.715
166
P CLR023 Colorectal Cancer 100 0.715
167
ANG054 Angina Pectoris 65 0.715
168
P GST053 Gastric Cancer 82 0.715
169
PHN003 Phenylketonuria 76 0.715
170
MLT010 Multiple Personality Disorder 29 0.715
171
FDL002 Food Allergy 47 0.715
172
HYP014 Hyperuricemia 51 0.715
173
KWS001 Kwashiorkor 44 0.715
174
URN010 Urinary Tract Obstruction 55 0.715
175
LPT001 Leptospirosis 65 0.715
176
P LVR013 Liver Disease 68 0.715
177
P PRS038 Personality Disorder 65 0.715
178
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.715
179
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.715
180
c ATS007 Autism Spectrum Disorder 71 0.683
181
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.683
182
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.683
183
ART002 Arts Syndrome 66 0.683
184
MYL069 Myeloma, Multiple 76 0.683
185
c HYP595 Hypertension, Essential 84 0.683
186
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.683
187
CNT047 Contact Dermatitis 56 0.683
188
P PLY011 Polycystic Ovary Syndrome 57 0.683
189
c ALZ063 Alzheimer's Disease 1 32 0.653
190
c ALZ054 Alzheimer Disease 4 44 0.645
191
MTC166 Mitochondrial Complex I Deficiency, Nuclear Type 19 23 0.641
192
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.641
193
PNG002 Pain Agnosia 51 0.641
194
P INF037 Inflammatory Bowel Disease 53 0.641
195
OTT002 Otitis Media 70 0.641
196
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.641
197
P EXN002 Exanthem 58 0.641
198
P SPP010 Suppressor of Tumorigenicity 3 50 0.641
199
OBS082 Obstructive Nephropathy 41 0.641
200
P FLL037 Follicular Lymphoma 66 0.641
201
P ACN011 Acne 55 0.641
202
STT001 Status Epilepticus 58 0.641
203
MLK006 Milk Allergy 47 0.641
204
ALL010 Allergic Contact Dermatitis 55 0.641
205
P MYT002 Myotonic Dystrophy 51 0.641
206
SKN019 Skin Melanoma 70 0.641
207
P LPS004 Lupus Erythematosus 61 0.641
208
P CHR345 Chronic Pain 50 0.641
209
NRL016 Neural Tube Defects 80 0.605
210
HYP266 Hypoxia 56 0.605
211
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.541
212
c DRM040 Dermatitis Herpetiformis, Familial 35 0.541
213
P RST001 Restless Legs Syndrome 52 0.541
214
P CRP001 Carpal Tunnel Syndrome 65 0.541
215
PLY105 Polycystic Ovary Syndrome 1 39 0.541
216
c PCH010 Pachyonychia Congenita 3 43 0.541
217
ATM095 Autoimmune Disease 61 0.541
218
TBS001 Tabes Dorsalis 30 0.541
219
P VNS003 Venous Insufficiency 54 0.541
220
CHR001 Churg-Strauss Syndrome 61 0.541
221
WHT017 Wheat Allergy 30 0.541
222
FLL008 Folliculitis 45 0.541
223
CNS004 Constipation 56 0.541
224
P ADL010 Adult Respiratory Distress Syndrome 70 0.541
225
PTL002 Patellofemoral Pain Syndrome 34 0.541
226
P DRM007 Dermatitis Herpetiformis 54 0.541
227
P SLP005 Sleep Disorder 61 0.541
228
P CWD010 Cowden Syndrome 70 0.541
229
P VSC011 Vasculitis 61 0.541
230
ANC002 Anca-Associated Vasculitis 44 0.541
231
PPT005 Peptic Ulcer Disease 58 0.541
232
APP008 Appendicitis 62 0.541
233
CHR066 Chronic Fatigue Syndrome 59 0.541
234
P CLS010 Cluster Headache 42 0.541
235
MCR088 Microscopic Polyangiitis 51 0.541
236
ALL012 Allergic Angiitis 24 0.541
237
SPT023 Septate Uterus 31 0.541
238
ESN016 Eosinophilic Pustular Folliculitis 25 0.541
239
URM005 Uremic Pruritus 46 0.541
240
MLT163 Multiple Pterygium Syndrome, Escobar Variant 62 0.514
241
P BRS053 Breast Fibroadenoma 48 0.504
242
NRM005 Neuromuscular Disease 62 0.494
243
ALL029 Allergic Disease 61 0.494
244
BRN071 Brain Injury 50 0.494
245
PRN009 Paranoid Schizophrenia 49 0.483
246
TRM010 Traumatic Brain Injury 50 0.483
247
APR001 Apraxia 51 0.473
248
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.473
249
KRT009 Keratosis 52 0.473
250
ANR007 Anorexia Nervosa 59 0.462
251
P HYP069 Hyperparathyroidism 62 0.462
252
c ALZ049 Alzheimer Disease 2 48 0.439
253
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.439
254
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.439
255
P LTR001 Lateral Sclerosis 57 0.439
256
VRG001 Variegate Porphyria 55 0.428
257
P PRP029 Porphyria 60 0.428
258
TCK004 Tick Infestation 29 0.428
259
PSY004 Psychotic Disorder 66 0.428
260
P MYC084 Mycobacterium Tuberculosis 1 68 0.416
261
VSC002 Vascular Dementia 59 0.416
262
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.403
263
P BRS047 Breast Cancer 97 0.403
264
PST028 Post-Traumatic Stress Disorder 58 0.403
265
MSC193 Muscular Lipidosis 23 0.403
266
INS024 Insulin-Like Growth Factor I 77 0.390
267
P BRW001 Brown-Vialetto-Van Laere Syndrome 49 0.390
268
ADN018 Adenoma 58 0.390
269
P AGN002 Agnosia 53 0.390
270
P HYP265 Hypotonia 42 0.390
271
MNC011 Minicore Myopathy with External Ophthalmoplegia 38 0.377
272
CNT105 Central Core Disease of Muscle 59 0.377
273
FLL031 Follicular Adenoma 40 0.377
274
GTR002 Goiter 52 0.377
275
P THL005 Thalassemia 56 0.377
276
HLT001 Holt-Oram Syndrome 66 0.363
277
c VRL010 Viral Hepatitis 52 0.363
278
P CRD246 Cardiovascular System Disease 55 0.363
279
CRH001 Crohn's Disease 80 0.363
280
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.349
281
HMR039 Hemorrhage, Intracerebral 57 0.349
282
EPD002 Epidermolytic Hyperkeratosis 55 0.349
283
CYT014 Cytochrome P450 Oxidoreductase Deficiency 35 0.349
284
48X005 48,xyyy 39 0.349
285
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 37 0.349
286
PSD088 Pseudobulbar Affect 33 0.349
287
P CRB088 Cerebral Atrophy 32 0.349
288
ORL015 Oral Squamous Cell Carcinoma 43 0.334
289
P SCH015 Schizophrenia 74 0.334
290
ATH013 Atherosclerosis Susceptibility 63 0.334
291
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.334
292
P KLZ004 Kala-Azar 1 41 0.334
293
AVN001 Avian Influenza 61 0.334
294
LSH001 Leishmaniasis 63 0.334
295
P HYP076 Hyperthyroidism 53 0.334
296
ORL011 Oral Cancer 60 0.334
297
DFC004 Deficiency Anemia 74 0.319
298
BLM002 Bulimia Nervosa 56 0.319
299
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.319
300
P TMR010 Tumor Predisposition Syndrome 69 0.319
301
P HYP086 Hypothyroidism 68 0.319
302
P CNT009 Central Core Myopathy 44 0.319
303
P RTN016 Retinal Degeneration 52 0.319
304
P THY032 Thyroiditis 56 0.319
305
MLT028 Multiminicore Disease 44 0.319
306
CRT033 Corticobasal Degeneration 48 0.319
307
INH023 Inherited Cancer-Predisposing Syndrome 53 0.319
308
MTC207 Mitochondrial Complex Ii Deficiency, Nuclear Type 1 57 0.302
310
c LKM061 Leukemia, Acute Myeloid 83 0.302
311
SNL009 Senile Plaque Formation 28 0.302
312
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 21 0.302
313
c HMC039 Hemochromatosis, Type 1 73 0.302
314
c HYP836 Hypercholesterolemia, Familial, 1 73 0.302
315
NND010 Nondisjunction 34 0.302
316
P NML001 Nemaline Myopathy 49 0.302
317
DSS008 Disease of Mental Health 74 0.302
318
IRN001 Iron Deficiency Anemia 58 0.302
319
HMG005 Hemoglobinopathy 55 0.302
320
P HYD006 Hydrocephalus 62 0.302
321
c PRM005 Primary Hyperparathyroidism 59 0.302
322
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.285
324
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.285
325
PRN011 Pernicious Anemia 52 0.285
326
ANX010 Anxiety 70 0.285
327
c TYP008 Type 1 Diabetes Mellitus 77 0.285
328
HSH003 Hashimoto Thyroiditis 60 0.285
329
c MYS052 Myasthenic Syndrome, Congenital, 10 46 0.285
330
c PRG094 Paragangliomas 5 29 0.285
331
PRT019 Protein-Losing Enteropathy 44 0.285
332
PPL002 Papillary Carcinoma 46 0.285
333
P VSC007 Vascular Disease 62 0.285
334
P HRM001 Hermansky-Pudlak Syndrome 65 0.285
335
P KDN018 Kidney Disease 71 0.285
336
MCR017 Macrocytic Anemia 44 0.285
337
GST033 Gestational Diabetes 60 0.285
338
DYS004 Dyscalculia 35 0.285
339
PLC008 Placenta Disease 48 0.285
340
ULC004 Ulcerative Colitis 74 0.285
341
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.285
342
P ALP008 Alopecia 53 0.285
343
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 0.285
344
CRB090 Cerebral Hypoxia 42 0.285
345
HDN002 Head Injury 44 0.285
346
MTH047 Methanol Poisoning 37 0.285
347
WRT005 Warty Dyskeratoma 16 0.285
348
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.267
349
MYS057 Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency 38 0.267
350
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 40 0.267
351
P LNG064 Lung Cancer Susceptibility 3 69 0.267
352
NMN001 Nominal Aphasia 40 0.267
353
P EYD002 Eye Disease 57 0.267
354
TRN015 Transient Cerebral Ischemia 62 0.267
355
MDD011 Mood Disorder 61 0.267
356
P SBS003 Substance Abuse 54 0.267
357
NDL007 Nodular Goiter 48 0.267
358
CRB004 Cerebral Artery Occlusion 45 0.267
359
TLN003 Telangiectasis 51 0.267
360
P LCT001 Lactic Acidosis 50 0.267
361
VSC003 Visceral Leishmaniasis 54 0.267
362
DLS001 Delusional Disorder 44 0.267
363
CLT003 Colitis 63 0.247
364
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.247
365
c MGR028 Migraine with or Without Aura 1 63 0.247
366
P OVR042 Ovarian Cancer 88 0.247
367
P PTY003 Pityriasis Rubra Pilaris 57 0.247
368
c ALZ050 Alzheimer Disease 5 35 0.247
369
STR095 Structural Heart Defects and Renal Anomalies Syndrome 20 0.247
370
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.247
371
c ACT004 Acute Diarrhea 40 0.247
372
P MYC007 Myocardial Infarction 69 0.247
373
c NML025 Nemaline Myopathy 8 36 0.247
374
KRN002 Kearns-Sayre Syndrome 62 0.247
375
SQM006 Squamous Cell Carcinoma 59 0.247
376
P DRR001 Diarrhea 55 0.247
377
LYM027 Lymphopenia 56 0.247
378
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.247
379
MTH009 Mouth Disease 57 0.247
380
HYP066 Hyperglycemia 60 0.247
381
c PRC016 Pre-Eclampsia 64 0.247
382
ACT084 Acute Stress Disorder 53 0.247
383
MTC004 Mitochondrial Encephalomyopathy 42 0.247
384
GRN017 Granulocytopenia 42 0.247
385
HMP009 Haemophilus Influenzae 41 0.247
386
GRV012 Grover's Disease 30 0.247
387
c SVR040 Severe Congenital Nemaline Myopathy 37 0.247
388
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.247
389
DYS073 Dysphagia 53 0.247
390
PRM329 Premature Aging 36 0.247
391
ORG002 Organic Acidemia 43 0.225
392
MLR004 Malaria 77 0.225
393
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.225
394
MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 37 0.225
395
ASP007 Aspiration Pneumonia 49 0.225
396
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.225
397
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.225
398
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.225
399
c NML003 Nemaline Myopathy 2 51 0.225
400
GLT035 Glutaric Acidemia I 57 0.225
401
P MLT020 Multiple Sclerosis 79 0.225
402
P D2H002 D-2-Hydroxyglutaric Aciduria 1 53 0.225
403
PLY166 Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1 8 0.225
404
MYP163 Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay 27 0.225
405
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.225
406
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.225
407
FZL002 Fazio-Londe Disease 39 0.225
408
P RTN008 Retinitis Pigmentosa 79 0.225
409
c CRD113 Cardiomyopathy, Dilated, 1v 23 0.225
410
P FRD001 Friedreich Ataxia 62 0.225
411
P RSP003 Respiratory Failure 73 0.225
412
CHL123 Chlamydia 58 0.225
413
LMB062 Limb Ischemia 55 0.225
414
SVR004 Severe Combined Immunodeficiency 70 0.225
415
NRR001 Neuroretinitis 42 0.225
416
ART014 Articulation Disorder 34 0.225
417
GLC003 Glucose Intolerance 53 0.225
418
SCH014 Schistosomiasis 56 0.225
419
GT001 Gout 63 0.225
420
P PRN023 Prion Disease 60 0.225
421
RTN023 Retinitis 45 0.225
422
P DBT009 Diabetes Mellitus 67 0.225
423
P TXP001 Toxoplasmosis 59 0.225
424
IDP022 Idiopathic Spinal Cord Herniation 17 0.225
425
P SZR006 Seizure Disorder 69 0.225
426
ANX004 Anoxia 40 0.225
427
CCN001 Cocaine Dependence 47 0.225
428
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.225
429
FML304 Familial Isolated Dilated Cardiomyopathy 50 0.225
431
NRM022 Neurometabolic Disease 24 0.225
432
LKP003 Leukoplakia 39 0.225
433
MYP017 Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay 14 0.225
434
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.202
435
P ATR011 Atrial Fibrillation 66 0.202
436
DMT001 Dimethylglycine Dehydrogenase Deficiency 27 0.202
437
OPP004 Oppositional Defiant Disorder 48 0.202
438
CRP032 Corpus Callosum, Agenesis of 49 0.202
439
OBS002 Obsessive-Compulsive Disorder 67 0.202
440
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.202
441
OST159 Osteogenic Sarcoma 66 0.202
442
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.202
443
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.202
444
c MCR312 Microphthalmia, Syndromic 10 39 0.202
445
CMB017 Combined Oxidative Phosphorylation Deficiency 6 41 0.202
446
P ATX030 Ataxia-Telangiectasia 80 0.202
447
P HYP750 Hypertriglyceridemia, Familial 61 0.202
448
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.202
449
ISV001 Isovaleric Acidemia 54 0.202
450
SDD001 Sudden Infant Death Syndrome 60 0.202
451
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.202
452
P MYS005 Myositis 55 0.202
453
HRW001 Hair Whorl 35 0.202
454
IGR001 Ige Responsiveness, Atopic 58 0.202
455
c CRT081 Cortical Dysplasia, Complex, with Other Brain Malformations 7 31 0.202
456
TBL035 Tubulinopathy 34 0.202
457
MCR099 Microlissencephaly 39 0.202
458
P LKM002 Leukemia 65 0.202
459
P KRT005 Keratoacanthoma 47 0.202
460
OVR063 Overnutrition 42 0.202
461
HYP005 Hypokalemia 55 0.202
462
ANT007 Anterior Horn Cell Disease 31 0.202
463
c ACT027 Acute Pancreatitis 60 0.202
464
P ART005 Arteriovenous Malformation 64 0.202
465
CVD001 Covid-19 59 0.202
466
OLG003 Oligohydramnios 50 0.202
467
PLS007 Plasmodium Falciparum Malaria 52 0.202
468
PLR005 Pleuropneumonia 33 0.202
469
NNT010 Nontoxic Goiter 32 0.202
470
CHL004 Cholelithiasis 48 0.202
471
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.202
472
PLY024 Polymicrogyria 48 0.202
473
SNL007 Senile Cataract 40 0.202
474
P MLG056 Malignant Hyperthermia 65 0.202
475
P HYP120 Hypoaldosteronism 33 0.202
476
P SCK005 Sickle Cell Disease 56 0.202
477
CRT015 Carotid Artery Occlusion 45 0.202
478
P TRM003 Tremor 50 0.202
479
SMN008 Semantic Dementia 46 0.202
480
P HDC001 Headache 56 0.202
481
c NMN014 Niemann-Pick Disease, Type C2 49 0.175
482
PRL023 Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome 48 0.175
483
DMN031 Dementia, Lewy Body 65 0.175
484
c DWL002 Dowling-Degos Disease 1 58 0.175
485
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.175
486
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 48 0.175
487
MSC157 Muscular Dystrophy, Duchenne Type 78 0.175
488
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 63 0.175
489
ALC007 Alcohol Dependence 65 0.175
490
c BRN108 Branchiootic Syndrome 1 63 0.175
491
DSM002 Desmosterolosis 39 0.175
492
c CNG006 Congenital Hypothyroidism 63 0.175
493
P FML011 Familial Adenomatous Polyposis 70 0.175
494
P PNC035 Pancreatic Cancer 87 0.175
495
KRT019 Keratitis, Hereditary 66 0.175
497
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 34 0.175
498
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.175
499
P DNG005 Dengue Virus 55 0.175
500
P ASP006 Aspergillosis 71 0.175
501
ACR020 Acropectorovertebral Dysplasia 24 0.175
502
P PRK057 Parkinson Disease, Late-Onset 79 0.175
503
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.175
504
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.175
505
c RHZ004 Rhizomelic Chondrodysplasia Punctata, Type 3 41 0.175
506
P SNS001 Sensorineural Hearing Loss 60 0.175
507
TRY001 Trypanosomiasis 50 0.175
508
HMN047 Human Cytomegalovirus Infection 59 0.175
509
SBJ001 Subjective Cognitive Decline 29 0.175
510
P PLY014 Polycystic Kidney Disease 71 0.175
511
P HYP111 Hyperprolinemia 44 0.175
512
END040 Endogenous Depression 54 0.175
513
KRT008 Keratopathy 46 0.175
514
VCC001 Vaccinia 49 0.175
515
CCC002 Coccidiosis 50 0.175
516
THY122 Thyroid Gland Cancer 59 0.175
517
CRB037 Cerebral Palsy 66 0.175
518
HMS001 Hemosiderosis 48 0.175
519
P KLP003 Klippel-Feil Syndrome 47 0.175
520
c SPN284 Spinocerebellar Ataxia 38 40 0.175
521
P ALC033 Alcohol Use Disorder 67 0.175
522
P ECL001 Eclampsia 52 0.175
523
CRB033 Cerebral Degeneration 36 0.175
524
SVR001 Severe Acute Respiratory Syndrome 68 0.175
525
SPN035 Spindle Cell Sarcoma 51 0.175
526
LCL004 Localized Osteosarcoma 35 0.175
527
c SCN007 Secondary Hyperparathyroidism 50 0.175
528
P SKN015 Skin Carcinoma 71 0.175
529
HYD001 Hydranencephaly 42 0.175
530
URM002 Uremia 47 0.175
531
CLB002 Clubfoot 50 0.175
532
P HYP040 Hypospadias 51 0.175
533
P HYP024 Hypoparathyroidism 55 0.175
534
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.175
535
P NTR004 Neutropenia 62 0.175
536
P MTH008 Methylmalonic Acidemia 52 0.175
537
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.175
538
SRC014 Sarcoma 64 0.175
539
PLG002 Plague 58 0.175
540
MTC005 Mitochondrial Metabolism Disease 44 0.175
541
P MYL006 Myeloid Leukemia 60 0.175
542
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.175
543
P ZLL001 Zellweger Syndrome 65 0.175
544
P BCL017 B-Cell Lymphoma 57 0.175
545
P INF038 Influenza 68 0.175
546
LNG099 Lung Disease 62 0.175
547
P INS002 in Situ Carcinoma 52 0.175
548
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.175
549
P HRP006 Herpes Simplex 65 0.175
550
P MSC005 Muscular Dystrophy 66 0.175
551
HRN003 Heroin Dependence 44 0.175
552
P RRH023 Rare Hereditary Hemochromatosis 52 0.175
553
P RRT020 Rare Tumor 39 0.175
554
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.175
555
IDP070 Idiopathic Scoliosis 41 0.143
556
c CRB098 Cerebrooculofacioskeletal Syndrome 2 30 0.143
557
SXL003 Sexual Disorder 49 0.143
558
AGR018 Agraphia 37 0.143
559
P PNT019 Pontocerebellar Hypoplasia 45 0.143
560
P CRB101 Cerebrooculofacioskeletal Syndrome 1 53 0.143
561
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 53 0.143
562
CYS001 Cystic Fibrosis 77 0.143
563
P SRC025 Sarcoidosis 1 70 0.143
564
P SCL057 Scoliosis, Isolated 1 40 0.143
565
c SPH013 Spherocytosis, Type 1 42 0.143
566
c GLY007 Glycogen Storage Disease Iv 58 0.143
567
BTT016 Batten-Turner Congenital Myopathy 54 0.143
568
OCL069 Ocular Motor Apraxia 57 0.143
569
GRS011 Gerstmann-Straussler Disease 56 0.143
570
TLC001 Telecanthus 34 0.143
571
CHR696 Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia 32 0.143
572
P RTT002 Rett Syndrome 79 0.143
573
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.143
574
RFS006 Refsum Disease, Classic 63 0.143
575
ADR007 Adrenoleukodystrophy 73 0.143
576
LSC001 Lesch-Nyhan Syndrome 62 0.143
577
c CTR132 Cataract 3, Multiple Types 41 0.143
578
BRT054 Brittle Bone Disorder 74 0.143
579
SRC015 Sarcosinemia 38 0.143
580
P PTN014 Patent Ductus Arteriosus 1 59 0.143
581
CHR100 Chronic Ulcer of Skin 57 0.143
582
FML037 Female Breast Cancer 51 0.143
583
VTM002 Vitamin B12 Deficiency 48 0.143
584
c CRB100 Cerebrooculofacioskeletal Syndrome 4 33 0.143
585
MYP164 Myopathy, Congenital, with Diaphragmatic Defects, Respiratory Insufficiency, and Dysmorphic Facies 24 0.143
586
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.143
587
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.143
588
P LSS002 Lissencephaly 52 0.143
589
CRN287 Carnitine Deficiency, Myopathic 17 0.143
590
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.143
591
P LNG032 Lung Cancer 98 0.143
592
P DVL012 Developmental Dysplasia of the Hip 1 45 0.143
593
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.143
594
IMM167 Immune Deficiency Disease 76 0.143
595
MYL005 Myelofibrosis 70 0.143
596
PRN056 Parana Hard-Skin Syndrome 17 0.143
597
c GRV008 Graves Disease 1 54 0.143
598
P FRG001 Fragile X Syndrome 70 0.143
599
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.143
600
P LKM062 Leukemia, Acute Lymphoblastic 69 0.143
601
c PNT034 Pontocerebellar Hypoplasia, Type 2e 53 0.143
602
LPT014 Leptin Deficiency or Dysfunction 77 0.143
603
c BTT014 Beta-Thalassemia 72 0.143
604
CRT072 Creutzfeldt-Jakob Disease 67 0.143
605
PRS012 Pars Planitis 47 0.143
606
CRV035 Cervical Cancer 72 0.143
607
END057 Endometrial Cancer 76 0.143
608
DFF005 Diffuse Large B-Cell Lymphoma 55 0.143
609
OST017 Osteomyelitis 63 0.143
610
NNL006 Non-Alcoholic Steatohepatitis 54 0.143
611
CLR108 Colorectal Adenoma 63 0.143
612
HYP030 Hypoactive Sexual Desire Disorder 40 0.143
613
PHM001 Phimosis 37 0.143
614
c BSL007 Basal Cell Carcinoma 67 0.143
615
P PRM002 Primary Hyperoxaluria 65 0.143
616
P GLY013 Glycogen Storage Disease 59 0.143
617
NNT012 Neonatal Jaundice 53 0.143
618
NRT004 Neuritis 53 0.143
619
IMP005 Impotence 52 0.143
620
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.143
621
c CHR697 Charcot-Marie-Tooth Disease X-Linked Recessive 4 33 0.143
622
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.143
623
DYS003 Dysgraphia 35 0.143
624
P MVM001 Movement Disease 61 0.143
625
VLK001 Volkmann Contracture 23 0.143
626
SCH012 Schizoaffective Disorder 49 0.143
627
P DYS154 Dystonia 64 0.143
628
P MTR014 Motor Neuron Disease 65 0.143
629
P HRT032 Heart Disease 84 0.143
630
MGL001 Megaloblastic Anemia 59 0.143
631
P KDN017 Kidney Cancer 60 0.143
632
P END044 Endometriosis 62 0.143
633
P ADN016 Adenocarcinoma 63 0.143
634
P SYS005 Systemic Scleroderma 73 0.143
635
MTS001 Mutism 44 0.143
636
DMY004 Demyelinating Disease 50 0.143
637
P BRS044 Breast Adenocarcinoma 58 0.143
638
ART016 Aortic Aneurysm 68 0.143
639
P PNC044 Pancreatitis 61 0.143
640
MRS001 Marasmus 41 0.143
641
P GRV001 Graves' Disease 54 0.143
642
LST001 Listeriosis 59 0.143
643
MNN009 Meningoencephalitis 47 0.143
644
CHR073 Choreatic Disease 53 0.143
645
RCK004 Rickets 64 0.143
646
BRD004 Borderline Personality Disorder 53 0.143
647
BLS002 Blastomycosis 47 0.143
648
P GLL022 Guillain-Barre Syndrome 59 0.143
649
P HRD011 Hereditary Spherocytosis 63 0.143
650
P UVT001 Uveitis 57 0.143
651
PRM013 Premature Menopause 57 0.143
652
PCD001 Pica Disease 38 0.143
653
P THR014 Thrombocytopenia 66 0.143
654
HST011 Histoplasmosis 54 0.143
655
CND002 Conduct Disorder 50 0.143
656
SLP001 Sleeping Sickness 56 0.143
657
ATY001 Atypical Depressive Disorder 45 0.143
658
HPT004 Hepatic Coma 43 0.143
659
BRN028 Brain Cancer 73 0.143
660
P RTN018 Retinal Disease 53 0.143
661
HMG002 Hemoglobinuria 50 0.143
662
P HML002 Hemolytic Anemia 62 0.143
663
BRS051 Breast Disease 58 0.143
664
P AXN001 Axonal Neuropathy 33 0.143
665
INH003 Inhibited Female Orgasm 29 0.143
666
DCB001 Decubitus Ulcer 61 0.143
667
AMN002 Amino Acid Metabolic Disorder 40 0.143
668
SBS004 Substance Dependence 46 0.143
669
P TRC031 Trichorhinophalangeal Syndrome 37 0.143
670
ADR022 Adrenomyeloneuropathy 38 0.143
671
BRN056 Bronchopulmonary Dysplasia 57 0.143
672
FSC004 Fasciitis 49 0.143
673
PRL005 Proliferative Fasciitis 22 0.143
674
CCC003 Coccygodynia 18 0.143
675
GLM045 Glioma 62 0.143
676
ISC003 Ischemic Fasciitis 31 0.143
677
P HMR005 Hemorrhoid 49 0.143
678
GB1002 Gbe1 Adult Polyglucosan Body Disease 7 0.143
679
c SBC007 Subacute Thyroiditis 43 0.143
680
c CHR684 Chronic Kidney Disease 73 0.143
681
ANR040 Aneurysm 60 0.143
682
P AVS003 Avascular Necrosis 41 0.143
683
PLY100 Polyploidy 36 0.143
684
IDP073 Idiopathic Hypercalciuria 41 0.143
685
GLY078 Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency 38 0.143
686
GLL048 Glial Tumor 51 0.143
687
P RNL123 Renal Agenesis, Bilateral 37 0.143
688
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.143
689
ASS001 Associative Agnosia 24 0.101
690
HMM004 Hamamy Syndrome 39 0.101
691
ACT119 Acute Promyelocytic Leukemia 62 0.101
692
c MYP118 Myopathy, Myofibrillar, 8 31 0.101
693
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.101
694
ALL003 Allergic Rhinitis 66 0.101
695
ALX002 Alexithymia 36 0.101
696
MCR191 Microscopic Colitis 46 0.101
697
CRH005 Crohn's Colitis 53 0.101
698
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.101
699
P CTN015 Cutaneous T Cell Lymphoma 48 0.101
700
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.101
701
P PRN026 Porencephaly 54 0.101
702
VLC001 Velocardiofacial Syndrome 57 0.101
703
VRC005 Varicose Veins 59 0.101
704
c SYS001 Systemic Lupus Erythematosus 85 0.101
705
P MJR007 Major Affective Disorder 1 42 0.101
706
KRT071 Keratosis, Seborrheic 56 0.101
707
RTN179 Retinal Arteries, Tortuosity of 42 0.101
708
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.101
709
c GRN062 Granulomatous Disease, Chronic, Autosomal Recessive, 1 46 0.101
710
c HYD064 Hydrocephalus, Congenital, 1 51 0.101
711
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.101
712
PLY150 Polykaryocytosis Inducer 29 0.101
713
CRN238 Corneal Dystrophy, Epithelial Basement Membrane 32 0.101
714
CRD002 Cri-Du-Chat Syndrome 50 0.101
715
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 43 0.101
716
P HYP768 Hyperlipoproteinemia, Type I 67 0.101
717
P MPL001 Maple Syrup Urine Disease 69 0.101
718
MRD002 Marden-Walker Syndrome 56 0.101
719
DGR001 Digeorge Syndrome 62 0.101
720
c FNC027 Fanconi Anemia, Complementation Group a 80 0.101
721
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.101
722
c STC015 Stickler Syndrome, Type I 50 0.101
723
P BLD134 Bladder Cancer 79 0.101
724
STR067 Stroke, Ischemic 79 0.101
725
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.101
726
SCK003 Sickle Cell Anemia 74 0.101
727
NRL018 Neural Tube Defects, Folate-Sensitive 46 0.101
728
GND001 Gonadoblastoma 42 0.101
729
P NSP012 Nasopharyngeal Carcinoma 60 0.101
730
CNZ001 Coenzyme Q10 Deficiency Disease 41 0.101
731
MTC151 Mitochondrial Complex I Deficiency, Nuclear Type 20 37 0.101
732
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.101
733
IFP003 Ifap Syndrome 2 41 0.101
734
c SPR162 Spermatogenic Failure 50 42 0.101
735
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 0.101
736
FSR001 Fusariosis 45 0.101
737
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 57 0.101
738
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.101
739
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 37 0.101
740
c HYP248 Hyperprolinemia, Type I 43 0.101
741
HYP781 Hypoascorbemia 52 0.101
742
P LPR021 Leprosy 3 71 0.101
743
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.101
744
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.101
745
MND023 Mend Syndrome 49 0.101
746
MST021 Meester-Loeys Syndrome 37 0.101
747
TBL029 Tubulin, Beta 28 0.101
748
P STR020 Strabismus 56 0.101
749
DLY008 Delayed Sleep Phase Disorder 44 0.101
750
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.101
751
GST019 Gastrointestinal Stromal Tumor 78 0.101
752
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.101
753
c LKM063 Leukemia, Chronic Myeloid 70 0.101
754
CNZ008 Coenzyme Q10 Deficiency, Primary, 6 34 0.101
755
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 0.101
756
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 26 0.101
757
P ANG001 Angelman Syndrome 64 0.101
758
ANT078 Antipyrine Metabolism 24 0.101
759
P CNR004 Cone-Rod Dystrophy 2 74 0.101
760
MLT157 Multiple System Atrophy 1 69 0.101
761
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.101
762
P PHC003 Pheochromocytoma 70 0.101
763
GST108 Gist-Plus Syndrome 22 0.101
764
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 36 0.101
765
EPD015 Epidemic Typhus 44 0.101
766
END014 Endemic Typhus 32 0.101
767
INV001 Invasive Aspergillosis 48 0.101
768
ADR040 Adrenal Gland Pheochromocytoma 45 0.101
769
OST003 Osteonecrosis 60 0.101
770
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 22 0.101
771
RBS001 Rabies 57 0.101
772
ERY004 Erysipelas 47 0.101
773
LWG006 Low Grade Glioma 41 0.101
774
P NPH012 Nephrotic Syndrome 61 0.101
775
CLR109 Colorectal Adenocarcinoma 50 0.101
776
SLC006 Silicosis 55 0.101
777
BLP004 Blepharophimosis 36 0.101
778
ASY002 Asymptomatic Neurosyphilis 41 0.101
779
P LCT002 Lactose Intolerance 51 0.101
780
HDR002 Hidradenitis Suppurativa 54 0.101
781
P CRN037 Craniosynostosis 67 0.101
782
P ART021 Arteriosclerosis 53 0.101
783
BLR008 Bilirubin Metabolic Disorder 57 0.101
784
P THR015 Thrombophilia 51 0.101
785
PPL022 Papilloma 53 0.101
786
RTN020 Retinal Vascular Disease 45 0.101
787
P BNC003 Bone Cancer 58 0.101
788
P BRB001 Beriberi 44 0.101
789
P MLN007 Male Infertility 56 0.101
790
CHL147 Chlamydia Pneumonia 47 0.101
791
STR103 Streptococcus Pneumonia 47 0.101
792
ADJ001 Adjustment Disorder 46 0.101
793
SYS004 Systemic Mastocytosis 62 0.101
794
P TRN020 Turner Syndrome 67 0.101
795
CLR030 Clear Cell Renal Cell Carcinoma 53 0.101
796
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.101
797
P PRP019 Peripheral Nervous System Disease 57 0.101
798
NTR005 Nutritional Deficiency Disease 60 0.101
799
c CNT035 Central Nervous System Disease 53 0.101
800
CNG034 Congestive Heart Failure 69 0.101
801
P HPT021 Hepatitis 68 0.101
802
GST045 Gastroenteritis 58 0.101
803
HYP006 Hypertensive Heart Disease 48 0.101
804
HPT014 Hepatorenal Syndrome 49 0.101
805
P MYP006 Myopia 55 0.101
806
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.101
807
P URN019 Urinary Tract Infection 48 0.101
808
c HPT001 Hepatitis C 61 0.101
809
P ESP024 Esophagitis 60 0.101
810
c FML021 Familial Hypercholesterolemia 71 0.101
811
P PLY019 Polyneuropathy 52 0.101
812
SQM002 Squamous Cell Papilloma 45 0.101
813
TYP007 Typhoid Fever 63 0.101
814
P RHN004 Rhinitis 56 0.101
815
THY030 Thyroid Gland Disease 50 0.101
816
P GST044 Gastritis 55 0.101
817
PNC129 Pancreatic Adenocarcinoma 64 0.101
818
NCR001 Necrotizing Ulcerative Gingivitis 26 0.101
819
GNG013 Gingivitis 59 0.101
820
SYN005 Synostosis 43 0.101
821
CNN003 Conn's Syndrome 77 0.101
822
PLM010 Pulmonary Edema 54 0.101
823
c ACT073 Acute Leukemia 59 0.101
824
SPT005 Spotted Fever 49 0.101
825
KRT002 Keratomalacia 54 0.101
826
TTN003 Tetanus 64 0.101
827
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.101
828
PRC002 Paracoccidioidomycosis 53 0.101
829
CMM005 Common Cold 55 0.101
830
P MCR010 Microcephaly 59 0.101
831
TXC005 Toxic Shock Syndrome 61 0.101
832
CHL035 Cholinergic Urticaria 29 0.101
833
AVD001 Avoidant Personality Disorder 49 0.101
834
P GND004 Gonadal Dysgenesis 46 0.101
835
AZS001 Azoospermia 45 0.101
836
GNG011 Gingival Disease 53 0.101
837
P URT039 Urticaria 57 0.101
838
DNG003 Dengue Disease 65 0.101
839
BRN026 Branch Retinal Artery Occlusion 41 0.101
840
c SVR005 Severe Pre-Eclampsia 49 0.101
841
P MLN008 Melanoma 75 0.101
842
P INF032 Infertility 60 0.101
843
P MST009 Mastocytosis 64 0.101
844
ACQ007 Acquired Immunodeficiency Syndrome 58 0.101
845
INV005 Inverted Follicular Keratosis 31 0.101
846
ANT024 Anthrax Disease 57 0.101
847
CHL061 Childhood Leukemia 47 0.101
848
ILS001 Ileus 49 0.101
849
FSC002 Fascioliasis 43 0.101
850
P MTC133 Mitochondrial Myopathy 51 0.101
851
GSG001 Gas Gangrene 52 0.101
852
PRM020 Premenstrual Tension 39 0.101
853
DVL001 Developmental Coordination Disorder 34 0.101
854
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 0.101
855
PRX001 Peroxisomal Disease 46 0.101
856
P ENC004 Encephalitis 61 0.101
857
AMB001 Amebiasis 56 0.101
858
MCH006 Mechanical Strabismus 40 0.101
859
YLL002 Yellow Fever 61 0.101
860
P SDR003 Sideroblastic Anemia 49 0.101
861
P HYP083 Hypopituitarism 51 0.101
862
P PLL002 Pellagra 46 0.101
863
P RTN014 Retinal Artery Occlusion 46 0.101
864
P MNC007 Monocytic Leukemia 48 0.101
865
CYT002 Cytokine Deficiency 43 0.101
866
HNS001 Hansen's Disease 32 0.101
867
MNN020 Meningococcal Infection 44 0.101
868
MTH021 Methylmalonic Acidemia with Homocystinuria 44 0.101
869
PST021 Postpartum Depression 50 0.101
870
MSL001 Measles 61 0.101
871
P NRV007 Nervous System Disease 65 0.101
872
P NRP001 Neuropathy 59 0.101
873
ATS301 Autosomal Dominant Epilepsy with Auditory Features 41 0.101
874
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 0.101
875
P MTC069 Mitochondrial Disorders 57 0.101
876
NRS003 Neurosyphilis 45 0.101
877
P MNN013 Meningitis 65 0.101
878
WLL004 Wallerian Degeneration 38 0.101
879
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.101
880
HRD180 Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome 26 0.101
881
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.101
882
INT075 Intracranial Hypertension 52 0.101
883
ORL012 Oral Leukoplakia 35 0.101
884
PNC049 Pancreatic Adenoma 14 0.101
885
NNT017 Neonatal Adrenoleukodystrophy 51 0.101
886
P ACT105 Acute Mountain Sickness 52 0.101
887
ADS004 Aids Dementia Complex 39 0.101
888
P ADT009 Auditory Neuropathy Spectrum Disorder 34 0.101
889
SNK001 Snakebite Envenomation 22 0.101
890
CYN003 Cyanide Poisoning 22 0.101
891
DMN026 Dementia Pugilistica 27 0.101
892
RFR010 Refractory Anemia 49 0.101
893
ARG006 Aregenerative Anemia 28 0.101
894
OST115 Osteonecrosis of the Jaw 40 0.101
895
ADN072 Adenoma of Pancreas 17 0.101
896
DWR001 Dwarfism 44 0.101
897
EXR007 Exercise-Induced Anaphylaxis 24 0.101
898
PST046 Post-Transplant Lymphoproliferative Disease 53 0.101
899
CRB086 Cerebral Aneurysms 40 0.101
900
DVL005 Developmental Dyspraxia 22 0.101
901
SPS057 Spasticity 43 0.101
902
PST092 Posttransplant Acute Limbic Encephalitis 29 0.101
903
c CHR695 Chronic Primary Adrenal Insufficiency 15 0.101
904
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.101
Content
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