Search results for Nicotinamide

838 hits were found for Nicotinamide

# Family MCID Name MIFTS Score
1
HYP066 Hyperglycemia 61 0.180
2
P SKN015 Skin Carcinoma 66 0.144
3
c NRF023 Neurofibromatosis, Type Ii 80 0.127
4
FTT001 Fatty Liver Disease 61 0.118
5
CRB004 Cerebral Artery Occlusion 45 0.118
6
c DBT099 Diabetes Mellitus, Type I 65 0.116
7
AGN016 Aging 56 0.116
8
P DBT009 Diabetes Mellitus 64 0.111
9
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.108
10
DPH001 Diphtheria 60 0.108
11
GLC003 Glucose Intolerance 54 0.108
12
P KDN018 Kidney Disease 72 0.106
13
P LVR013 Liver Disease 68 0.106
14
c MCR113 Microvascular Complications of Diabetes 3 52 0.106
15
c MCR120 Microvascular Complications of Diabetes 7 47 0.106
16
P PLL002 Pellagra 46 0.106
17
c MCR130 Microvascular Complications of Diabetes 6 41 0.106
18
c MCR133 Microvascular Complications of Diabetes 4 41 0.106
19
BRN071 Brain Injury 49 0.103
20
P BLD134 Bladder Cancer 79 0.100
21
c CHR684 Chronic Kidney Disease 70 0.100
22
P NRP001 Neuropathy 56 0.100
23
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.100
24
ISC004 Ischemia 58 0.097
25
HYP025 Hyperphosphatemia 48 0.097
26
P ALZ034 Alzheimer Disease 88 0.094
27
P NRB001 Neuroblastoma 72 0.091
28
P MLN008 Melanoma 69 0.091
29
HYP056 Hypoglycemia 66 0.091
30
BLL006 Bullous Pemphigoid 62 0.091
31
48X005 48,xyyy 39 0.091
32
P CHR012 Chronic Granulomatous Disease 67 0.088
33
LPD008 Lipid Metabolism Disorder 62 0.088
34
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.085
35
GLB015 Glioblastoma Multiforme 75 0.085
36
c PRC016 Pre-Eclampsia 63 0.085
37
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.085
38
HYP266 Hypoxia 57 0.085
39
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.085
40
TRM010 Traumatic Brain Injury 51 0.085
41
WLL004 Wallerian Degeneration 39 0.085
42
P PRP019 Peripheral Nervous System Disease 58 0.082
43
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.082
44
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.078
45
P PRK057 Parkinson Disease, Late-Onset 78 0.078
46
c ATR087 Atrial Standstill 1 75 0.078
47
P MYP004 Myopathy 70 0.078
48
P DRM053 Dermatitis, Atopic 66 0.078
49
SKN016 Skin Disease 63 0.078
50
SQM006 Squamous Cell Carcinoma 60 0.078
51
ADN018 Adenoma 59 0.078
52
P CRD246 Cardiovascular System Disease 57 0.078
53
P LNG032 Lung Cancer 98 0.075
54
P HNT016 Huntington Disease 72 0.075
55
P VSC007 Vascular Disease 63 0.075
56
P PSR002 Psoriasis 62 0.075
57
P PMP001 Pemphigus 54 0.075
58
PST011 Pustulosis of Palm and Sole 52 0.075
59
END086 End Stage Renal Disease 51 0.075
60
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.075
61
HMP009 Haemophilus Influenzae 43 0.075
62
P CLR023 Colorectal Cancer 99 0.071
63
c HYP595 Hypertension, Essential 84 0.071
64
P HRT032 Heart Disease 75 0.071
65
ATH013 Atherosclerosis Susceptibility 65 0.071
66
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.071
67
ATM095 Autoimmune Disease 62 0.071
68
P OVR042 Ovarian Cancer 88 0.067
69
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.067
70
P SCH015 Schizophrenia 74 0.067
71
CNG034 Congestive Heart Failure 69 0.067
72
c SML038 Small Cell Cancer of the Lung 65 0.067
73
P ADN016 Adenocarcinoma 64 0.067
74
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
75
DRM006 Dermatitis 61 0.067
76
P ENC018 Encephalopathy 61 0.067
77
THY029 Thyroid Carcinoma 59 0.067
78
VSL002 Visual Epilepsy 59 0.067
79
FML063 Familial Glucocorticoid Deficiency 58 0.067
80
P MTC069 Mitochondrial Disorders 56 0.067
81
P SZR006 Seizure Disorder 56 0.067
82
HYP060 Hyperinsulinism 54 0.067
83
DBT010 Diabetic Neuropathy 54 0.067
84
NNL006 Non-Alcoholic Steatohepatitis 54 0.067
85
CYT002 Cytokine Deficiency 42 0.067
86
ANX004 Anoxia 40 0.067
87
P HPT023 Hepatocellular Carcinoma 100 0.062
88
STR067 Stroke, Ischemic 81 0.062
89
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.062
90
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
91
P MYC084 Mycobacterium Tuberculosis 1 68 0.062
92
P DMN002 Dementia 66 0.062
93
KHL003 Kohlschutter-Tonz Syndrome 65 0.062
94
c SVR001 Severe Acute Respiratory Syndrome 62 0.062
95
ALL026 Allergic Hypersensitivity Disease 62 0.062
96
CHL014 Cholera 59 0.062
97
RSC001 Rosacea 54 0.062
98
P LCT001 Lactic Acidosis 51 0.062
99
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.062
100
ORL015 Oral Squamous Cell Carcinoma 43 0.062
101
c DLT002 Dilated Cardiomyopathy 79 0.058
102
P MYC007 Myocardial Infarction 70 0.058
103
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.058
104
ART016 Aortic Aneurysm 69 0.058
105
c BSL007 Basal Cell Carcinoma 68 0.058
106
SKN019 Skin Melanoma 68 0.058
107
RCK004 Rickets 68 0.058
108
P THR014 Thrombocytopenia 67 0.058
109
P NRV007 Nervous System Disease 66 0.058
110
P FRD001 Friedreich Ataxia 64 0.058
111
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.058
112
INS001 Insulinoma 60 0.058
113
P MYC008 Myocarditis 59 0.058
114
ART140 Arteries, Anomalies of 52 0.058
115
P ECL001 Eclampsia 50 0.058
116
P SCK005 Sickle Cell Disease 50 0.058
117
P PRC031 Preeclampsia/eclampsia 1 38 0.058
118
P BRS047 Breast Cancer 97 0.053
119
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.053
120
c SYS001 Systemic Lupus Erythematosus 86 0.053
121
P PNC035 Pancreatic Cancer 84 0.053
122
P LKM071 Leukemia, Chronic Lymphocytic 79 0.053
123
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.053
124
DFC004 Deficiency Anemia 70 0.053
125
P PLM037 Pulmonary Hypertension 67 0.053
126
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.053
127
PRT037 Pertussis 65 0.053
128
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.053
129
LPP008 Lipoprotein Quantitative Trait Locus 62 0.053
130
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.053
131
P LPS004 Lupus Erythematosus 61 0.053
132
P BCL017 B-Cell Lymphoma 58 0.053
133
c DWL002 Dowling-Degos Disease 1 58 0.053
134
P FBR017 Fibrosarcoma 56 0.053
135
P DRR001 Diarrhea 55 0.053
136
P GRV001 Graves' Disease 55 0.053
137
P INF037 Inflammatory Bowel Disease 54 0.053
138
c PSR017 Psoriasis 2 53 0.053
139
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.053
140
c PSR023 Psoriasis 1 52 0.053
141
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.053
142
P MTC133 Mitochondrial Myopathy 49 0.053
143
MTC005 Mitochondrial Metabolism Disease 49 0.053
144
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.053
145
c PSR032 Psoriasis 11 47 0.053
146
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.053
147
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.053
148
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.053
149
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.053
150
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.053
151
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.053
152
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.053
153
c PSR028 Psoriasis 7 42 0.053
154
c PSR018 Psoriasis 13 41 0.053
155
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.053
156
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.053
157
P PRS040 Prostate Cancer 97 0.047
159
P GST053 Gastric Cancer 83 0.047
160
CRV035 Cervical Cancer 76 0.047
161
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.047
162
ULC004 Ulcerative Colitis 73 0.047
163
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.047
164
c LKM063 Leukemia, Chronic Myeloid 72 0.047
165
P SLP006 Sleep Apnea 69 0.047
166
P LYM118 Lymphoma 68 0.047
167
CRB039 Cerebrovascular Disease 67 0.047
168
ACR006 Aceruloplasminemia 65 0.047
169
MSC007 Muscle Hypertrophy 64 0.047
170
P HYP069 Hyperparathyroidism 63 0.047
171
NTR005 Nutritional Deficiency Disease 62 0.047
172
CHR066 Chronic Fatigue Syndrome 61 0.047
173
GST033 Gestational Diabetes 61 0.047
174
P MYL006 Myeloid Leukemia 60 0.047
175
SPN186 Spinal Cord Injury 60 0.047
176
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.047
177
ORL011 Oral Cancer 60 0.047
178
c ACT071 Acute Kidney Failure 60 0.047
179
ANR040 Aneurysm 59 0.047
180
ERY029 Erythermalgia, Primary 58 0.047
181
CNS004 Constipation 58 0.047
182
P INF032 Infertility 57 0.047
183
P EXN002 Exanthem 57 0.047
184
P HDC001 Headache 57 0.047
185
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.047
186
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.047
187
P HYP076 Hyperthyroidism 55 0.047
188
P LRY044 Larynx Cancer 55 0.047
189
SNS003 Sensory Peripheral Neuropathy 54 0.047
190
P CTN003 Cutaneous Lupus Erythematosus 53 0.047
191
GTR002 Goiter 53 0.047
192
HMC014 Homocysteinemia 53 0.047
193
P ACT008 Actinic Keratosis 53 0.047
194
IMP005 Impotence 52 0.047
195
KRT009 Keratosis 51 0.047
196
CCT002 Cicatricial Pemphigoid 51 0.047
197
HYP017 Hypophosphatemia 50 0.047
198
47X002 47,xyy 49 0.047
199
HLX001 Helix Syndrome 47 0.047
200
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.047
201
DBT002 Diabetic Autonomic Neuropathy 41 0.047
202
ALL014 Allergic Encephalomyelitis 38 0.047
203
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 35 0.047
204
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.047
205
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.047
206
c LKM061 Leukemia, Acute Myeloid 84 0.041
207
OST012 Osteoarthritis 78 0.041
208
P LNG064 Lung Cancer Susceptibility 3 78 0.041
209
AST005 Asthma 76 0.041
210
P RSP003 Respiratory Failure 74 0.041
211
SCK003 Sickle Cell Anemia 74 0.041
212
SVR004 Severe Combined Immunodeficiency 73 0.041
213
P MLT020 Multiple Sclerosis 72 0.041
214
PRP027 Peripheral Vascular Disease 71 0.041
215
DWN001 Down Syndrome 70 0.041
216
P LPR021 Leprosy 3 69 0.041
217
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.041
218
P TRN020 Turner Syndrome 67 0.041
219
FLL027 Fallopian Tube Carcinoma 67 0.041
220
OST159 Osteogenic Sarcoma 66 0.041
221
P MCR115 Microvascular Complications of Diabetes 5 66 0.041
222
P PLM036 Pulmonary Fibrosis 65 0.041
223
SRC014 Sarcoma 65 0.041
224
c JVN010 Juvenile Rheumatoid Arthritis 64 0.041
225
P PRD008 Periodontitis 64 0.041
226
KRN002 Kearns-Sayre Syndrome 63 0.041
227
LSH001 Leishmaniasis 63 0.041
228
CLT003 Colitis 62 0.041
229
P PLY014 Polycystic Kidney Disease 62 0.041
230
LVR012 Liver Cirrhosis 62 0.041
231
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.041
232
P KDN017 Kidney Cancer 60 0.041
233
c JVN061 Juvenile Arthritis 60 0.041
234
LNG099 Lung Disease 60 0.041
235
P CTR002 Cataract 60 0.041
236
P BRS044 Breast Adenocarcinoma 59 0.041
237
c CHL140 Chilblain Lupus 1 58 0.041
238
PMP006 Pemphigus Vulgaris, Familial 57 0.041
239
P BPL003 Bipolar Disorder 56 0.041
240
c BSL024 Basal Cell Carcinoma 1 56 0.041
241
P PLY011 Polycystic Ovary Syndrome 56 0.041
242
c ACT134 Acute Liver Failure 56 0.041
243
BCT022 Bacterial Infectious Disease 56 0.041
244
MCS002 Mucositis 56 0.041
245
BRN004 Brain Edema 56 0.041
246
P PLY019 Polyneuropathy 56 0.041
247
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.041
248
P MLN007 Male Infertility 55 0.041
249
NPH009 Nephrolithiasis 55 0.041
250
P ART021 Arteriosclerosis 54 0.041
251
P LTR001 Lateral Sclerosis 54 0.041
252
CLR030 Clear Cell Renal Cell Carcinoma 53 0.041
253
P INS002 in Situ Carcinoma 53 0.041
254
P RTN016 Retinal Degeneration 53 0.041
255
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.041
256
SPN035 Spindle Cell Sarcoma 53 0.041
257
PRP080 Peripheral Artery Disease 53 0.041
258
LNG031 Lung Benign Neoplasm 51 0.041
259
c SCN007 Secondary Hyperparathyroidism 51 0.041
260
SKN013 Skin Benign Neoplasm 51 0.041
261
HYP781 Hypoascorbemia 51 0.041
262
HYP081 Hypolipoproteinemia 51 0.041
263
P OVR082 Overgrowth Syndrome 50 0.041
264
HRT031 Hartnup Disorder 50 0.041
265
SYS003 Systolic Heart Failure 49 0.041
266
P OPN001 Open-Angle Glaucoma 49 0.041
267
HYP043 Hyperandrogenism 48 0.041
268
c HRD026 Hereditary Ataxia 48 0.041
269
ATS010 Autosomal Recessive Disease 48 0.041
270
SPL018 Splenomegaly 48 0.041
271
PRD004 Prediabetes Syndrome 47 0.041
272
RNL077 Renal Fibrosis 47 0.041
273
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.041
274
c PCH010 Pachyonychia Congenita 3 44 0.041
275
P MTC004 Mitochondrial Encephalomyopathy 44 0.041
276
c HYP272 Hypercholesterolemia, Familial, 3 44 0.041
277
CVD001 Covid-19 44 0.041
278
TRP009 Triple X Syndrome 42 0.041
279
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.041
280
P KLZ004 Kala-Azar 1 41 0.041
281
RST023 Resting Heart Rate, Variation in 41 0.041
282
c MJR024 Major Affective Disorder 9 41 0.041
283
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.041
284
SPR126 Superior Semicircular Canal Dehiscence 40 0.041
285
c HMG029 Hemoglobin Se Disease 39 0.041
286
c OVR114 Ovarian Cancer 1 38 0.041
287
c SYS043 Systemic Lupus Erythematosus 1 38 0.041
288
c MJR022 Major Affective Disorder 8 38 0.041
289
HNS001 Hansen's Disease 34 0.041
290
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.041
291
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.041
292
MYL069 Myeloma, Multiple 85 0.033
293
NRL016 Neural Tube Defects 82 0.033
294
P ATX030 Ataxia-Telangiectasia 82 0.033
295
IMM167 Immune Deficiency Disease 78 0.033
296
c THR092 Thrombophilia Due to Thrombin Defect 73 0.033
297
P CNR004 Cone-Rod Dystrophy 2 73 0.033
298
ANX010 Anxiety 73 0.033
299
P LFR001 Li-Fraumeni Syndrome 72 0.033
300
HMN044 Human Immunodeficiency Virus Type 1 71 0.033
301
P EPL164 Epilepsy 71 0.033
302
P ATS364 Autism 70 0.033
303
MYL005 Myelofibrosis 70 0.033
304
PLM001 Pulmonary Tuberculosis 69 0.033
305
P ART022 Arthritis 69 0.033
306
LYM133 Lymphoma, Hodgkin, Classic 69 0.033
307
P HYP086 Hypothyroidism 69 0.033
308
P LKM002 Leukemia 68 0.033
309
BRN024 Bronchitis 68 0.033
310
c ATS007 Autism Spectrum Disorder 67 0.033
311
c MGR028 Migraine with or Without Aura 1 67 0.033
312
c RHB024 Rhabdomyosarcoma 2 67 0.033
313
ANG054 Angina Pectoris 66 0.033
314
P NSP012 Nasopharyngeal Carcinoma 66 0.033
315
c MCR129 Microvascular Complications of Diabetes 1 66 0.033
316
CHG001 Chagas Disease 66 0.033
317
P CCK001 Cockayne Syndrome 66 0.033
318
c MCL013 Mucolipidosis Iv 66 0.033
319
P MTR014 Motor Neuron Disease 65 0.033
320
P RHB003 Rhabdomyosarcoma 63 0.033
321
P GLM045 Glioma 63 0.033
322
P ANR048 Aniridia 1 63 0.033
323
P CRN300 Coronary Heart Disease 1 63 0.033
324
P MVM001 Movement Disease 63 0.033
325
c ACT068 Acute Cystitis 63 0.033
326
TRN015 Transient Cerebral Ischemia 63 0.033
327
DPR016 Depression 63 0.033
328
c GLC092 Glaucoma, Primary Open Angle 62 0.033
329
P HYP750 Hypertriglyceridemia, Familial 62 0.033
330
LSC001 Lesch-Nyhan Syndrome 62 0.033
331
CRC021 Carcinosarcoma 62 0.033
332
BLD131 Bladder Urothelial Carcinoma 62 0.033
333
ACQ007 Acquired Immunodeficiency Syndrome 60 0.033
334
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 0.033
335
P OPT006 Optic Nerve Disease 60 0.033
336
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.033
337
P BND020 Bone Disease 59 0.033
338
c HPT016 Hepatitis B 59 0.033
339
P SLP005 Sleep Disorder 59 0.033
340
P CYS018 Cystitis 59 0.033
341
FBR047 Fibromyalgia 58 0.033
342
P URT039 Urticaria 58 0.033
343
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.033
344
GLS018 Glass Syndrome 57 0.033
345
BRN056 Bronchopulmonary Dysplasia 57 0.033
346
P RHN004 Rhinitis 57 0.033
347
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.033
348
c FML035 Familial Hyperlipidemia 55 0.033
349
HYP005 Hypokalemia 55 0.033
350
P SCK002 Sick Sinus Syndrome 55 0.033
351
MCL006 Macular Retinal Edema 55 0.033
352
P DRM007 Dermatitis Herpetiformis 55 0.033
353
AMN003 Amnestic Disorder 54 0.033
354
PRT038 Protein-Energy Malnutrition 54 0.033
355
PLM010 Pulmonary Edema 54 0.033
356
AMN001 Amenorrhea 54 0.033
357
P LCH002 Lichen Planus 53 0.033
358
GLC042 Glucocorticoid Deficiency 1 53 0.033
359
GST023 Gastric Ulcer 53 0.033
360
c GLL024 Gallbladder Disease 1 53 0.033
361
PRP016 Paraplegia 52 0.033
362
ACR041 Acromelic Frontonasal Dysostosis 52 0.033
363
NRT004 Neuritis 52 0.033
364
DYS015 Dysentery 52 0.033
365
TLN003 Telangiectasis 52 0.033
366
LMY002 Leiomyoma 52 0.033
367
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.033
368
c PRM108 Primary Progressive Multiple Sclerosis 51 0.033
369
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.033
370
RTN003 Retinal Ischemia 50 0.033
371
VTR016 Vater/vacterl Association 50 0.033
372
PLC008 Placenta Disease 50 0.033
373
P OBS001 Obstructive Jaundice 50 0.033
374
DBT004 Diabetic Polyneuropathy 49 0.033
375
ENT004 Enthesopathy 49 0.033
376
P END046 Endometritis 49 0.033
377
CHL004 Cholelithiasis 49 0.033
378
P CTN015 Cutaneous T Cell Lymphoma 49 0.033
379
BLD044 Bladder Disease 48 0.033
380
DGN001 Degenerative Disc Disease 48 0.033
381
SXL003 Sexual Disorder 47 0.033
382
KRT002 Keratomalacia 47 0.033
383
CHR074 Choriocarcinoma 47 0.033
384
P OVR046 Ovarian Cyst 47 0.033
385
P MTH007 Methemoglobinemia 46 0.033
386
GLL048 Glial Tumor 45 0.033
387
c LFR007 Li-Fraumeni Syndrome 2 45 0.033
388
ATN004 Autonomic Neuropathy 45 0.033
389
GRD001 Giardiasis 45 0.033
390
MYF001 Myofibroma 45 0.033
391
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.033
392
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.033
393
P HYP265 Hypotonia 43 0.033
394
PMP004 Pemphigus Foliaceus 43 0.033
395
VCT001 Vacterl Association 42 0.033
396
URM005 Uremic Pruritus 42 0.033
397
LRY017 Laryngeal Disease 42 0.033
398
ACT088 Acute Insulin Response 41 0.033
399
PMP002 Pemphigoid Gestationis 39 0.033
400
c PLY105 Polycystic Ovary Syndrome 1 38 0.033
401
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 38 0.033
402
HRN029 Hearing Loss, Noise-Induced 37 0.033
403
c DRM040 Dermatitis Herpetiformis, Familial 35 0.033
404
CND006 Candida Glabrata 32 0.033
405
PLR005 Pleuropneumonia 31 0.033
406
PMP008 Pemphigus Vegetans 27 0.033
407
STN013 Stenotrophomonas Maltophilia Infection 25 0.033
408
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.033
409
PMP013 Pemphigus Gestationis 19 0.033
410
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.033
411
c PLL014 Pellagra-Like Syndrome 18 0.033
412
MLR004 Malaria 81 0.024
413
CYS001 Cystic Fibrosis 81 0.024
414
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.024
415
P RTN008 Retinitis Pigmentosa 79 0.024
416
GST019 Gastrointestinal Stromal Tumor 78 0.024
417
c TBR025 Tuberous Sclerosis 1 77 0.024
418
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.024
419
PHN003 Phenylketonuria 75 0.024
420
c ART115 Aortic Valve Disease 1 75 0.024
421
END057 Endometrial Cancer 74 0.024
422
LPT014 Leptin Deficiency or Dysfunction 74 0.024
423
P OST002 Osteoporosis 74 0.024
424
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.024
425
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.024
426
P GRF003 Graft-Versus-Host Disease 72 0.024
427
P PHC003 Pheochromocytoma 71 0.024
428
ACR007 Acromegaly 71 0.024
429
P SRC025 Sarcoidosis 1 70 0.024
430
LGH007 Leigh Syndrome 70 0.024
431
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.024
432
ADN011 Adenoid Cystic Carcinoma 70 0.024
433
P TTR001 Tetralogy of Fallot 70 0.024
434
ADL002 Adult Syndrome 70 0.024
435
P TBR001 Tuberous Sclerosis 70 0.024
436
P ASP006 Aspergillosis 69 0.024
437
PLY001 Polycythemia Vera 69 0.024
438
CRB037 Cerebral Palsy 69 0.024
439
EWN003 Ewing Sarcoma 69 0.024
440
P LKM062 Leukemia, Acute Lymphoblastic 69 0.024
441
MNT001 Mantle Cell Lymphoma 69 0.024
442
c MYT021 Myotonic Dystrophy 1 69 0.024
443
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.024
444
P PNM007 Pneumonia 68 0.024
445
OBS002 Obsessive-Compulsive Disorder 68 0.024
446
P ESS003 Essential Thrombocythemia 68 0.024
447
P MJR001 Major Depressive Disorder 68 0.024
448
PNC129 Pancreatic Adenocarcinoma 68 0.024
449
P HPT021 Hepatitis 67 0.024
450
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.024
451
c INF071 Inflammatory Bowel Disease 1 67 0.024
452
P FLL037 Follicular Lymphoma 67 0.024
453
ALL003 Allergic Rhinitis 67 0.024
454
PSY004 Psychotic Disorder 67 0.024
455
P HYP098 Hypereosinophilic Syndrome 67 0.024
456
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.024
457
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.024
458
c FML021 Familial Hypercholesterolemia 66 0.024
459
P MSC005 Muscular Dystrophy 66 0.024
460
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.024
461
P ATR011 Atrial Fibrillation 66 0.024
462
P MNN013 Meningitis 66 0.024
463
MYL031 Myeloproliferative Neoplasm 66 0.024
464
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.024
465
P DYS154 Dystonia 65 0.024
466
PPL049 Papillon-Lefevre Syndrome 65 0.024
467
TNG002 Tangier Disease 65 0.024
468
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.024
469
PND002 Pendred Syndrome 65 0.024
470
c ART101 Aortic Valve Disease 2 65 0.024
471
IRR002 Irritable Bowel Syndrome 65 0.024
472
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.024
473
P PRS038 Personality Disorder 65 0.024
474
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.024
475
P CHR071 Charcot-Marie-Tooth Disease 65 0.024
476
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.024
477
APN008 Apnea, Obstructive Sleep 64 0.024
478
GT001 Gout 64 0.024
479
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.024
480
BRC012 Brucellosis 64 0.024
481
ART002 Arts Syndrome 64 0.024
482
P FTL069 Fetal Akinesia Deformation Sequence 1 64 0.024
483
OST017 Osteomyelitis 64 0.024
484
P HML002 Hemolytic Anemia 63 0.024
485
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.024
486
P THR117 Three M Syndrome 1 63 0.024
487
CHN016 Cohen Syndrome 63 0.024
488
P LMY004 Leiomyosarcoma 63 0.024
489
c OPT053 Optic Atrophy 1 63 0.024
490
c ALP101 Alpha-Thalassemia 62 0.024
491
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.024
492
HMT002 Hematologic Cancer 62 0.024
493
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.024
494
c HPT001 Hepatitis C 62 0.024
495
c HPT003 Hepatitis a 62 0.024
496
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.024
497
HYD038 Hydrops Fetalis, Nonimmune 62 0.024
498
P VSC011 Vasculitis 62 0.024
499
PHL006 Phelan-Mcdermid Syndrome 62 0.024
500
MDD011 Mood Disorder 62 0.024
501
MSL001 Measles 62 0.024
502
P DRM010 Dermatomyositis 61 0.024
504
OST003 Osteonecrosis 61 0.024
505
INT002 Intermittent Claudication 61 0.024
506
c PNS012 Paine Syndrome 61 0.024
507
ALC006 Alcoholic Hepatitis 61 0.024
508
WLD007 Waldenstroem's Macroglobulinemia 61 0.024
509
P PNC044 Pancreatitis 61 0.024
510
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.024
511
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.024
512
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.024
513
STT001 Status Epilepticus 60 0.024
514
P THL005 Thalassemia 60 0.024
515
P MCR010 Microcephaly 59 0.024
516
IDP011 Idiopathic Interstitial Pneumonia 59 0.024
517
CHL123 Chlamydia 59 0.024
518
P MLN069 Melanoma, Uveal 59 0.024
519
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.024
520
IRN001 Iron Deficiency Anemia 59 0.024
521
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.024
522
P PLY006 Polydactyly 59 0.024
523
PPT005 Peptic Ulcer Disease 59 0.024
524
INC002 Inclusion Body Myositis 58 0.024
525
P PLY017 Polyarteritis Nodosa 58 0.024
526
P ANP001 Anaplastic Large Cell Lymphoma 58 0.024
527
ANT024 Anthrax Disease 58 0.024
528
PST028 Post-Traumatic Stress Disorder 58 0.024
529
P HYP726 Hypercalcemia, Infantile, 1 58 0.024
530
c BNG091 Benign Chronic Pemphigus 58 0.024
531
P ALC033 Alcohol Use Disorder 58 0.024
532
CNT047 Contact Dermatitis 58 0.024
533
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.024
534
EYD002 Eye Disease 58 0.024
535
DSS008 Disease of Mental Health 58 0.024
536
CRV038 Cervical Squamous Cell Carcinoma 58 0.024
537
MNT002 Mental Depression 58 0.024
538
CHL028 Childhood Type Dermatomyositis 58 0.024
539
APP015 Apparent Mineralocorticoid Excess 58 0.024
540
LYM027 Lymphopenia 58 0.024
541
P CND004 Candidiasis 58 0.024
542
P GLM007 Glomerulonephritis 57 0.024
543
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.024
544
IRN002 Iron Metabolism Disease 57 0.024
545
MNR012 Meniere Disease 57 0.024
546
DSS009 Disseminated Intravascular Coagulation 57 0.024
547
THY122 Thyroid Gland Cancer 57 0.024
548
THR024 Thrombosis 57 0.024
549
c MYT020 Myotonic Dystrophy 2 57 0.024
550
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.024
551
P FTL001 Fetal Alcohol Syndrome 57 0.024
552
CHR177 Chromophobe Renal Cell Carcinoma 57 0.024
553
BLR008 Bilirubin Metabolic Disorder 57 0.024
554
VSC002 Vascular Dementia 57 0.024
555
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.024
556
P PYL005 Pyelonephritis 56 0.024
557
P MYS005 Myositis 56 0.024
558
P PLY018 Polycythemia 56 0.024
559
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.024
560
CMR002 Coumarin Resistance 56 0.024
561
LST001 Listeriosis 56 0.024
562
TRN018 Transitional Cell Carcinoma 56 0.024
563
LBL001 Lobular Neoplasia 56 0.024
564
LMY014 Leiomyoma, Uterine 56 0.024
565
ERY051 Erythroleukemia, Familial 56 0.024
566
SFT003 Soft Tissue Sarcoma 56 0.024
567
SCH003 Schizophreniform Disorder 56 0.024
568
HMG005 Hemoglobinopathy 56 0.024
569
P NRF002 Neurofibromatosis 56 0.024
570
GST050 Gastrointestinal System Disease 56 0.024
571
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.024
572
P GST044 Gastritis 56 0.024
573
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.024
574
ATR057 Atrioventricular Block 55 0.024
575
NRN004 Neuroendocrine Tumor 55 0.024
576
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.024
577
ORL004 Oral Submucous Fibrosis 55 0.024
578
LMB062 Limb Ischemia 55 0.024
579
DFF005 Diffuse Large B-Cell Lymphoma 55 0.024
580
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.024
581
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.024
582
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.024
583
P SBS003 Substance Abuse 55 0.024
584
HDR002 Hidradenitis Suppurativa 55 0.024
585
BRN045 Brunner Syndrome 55 0.024
586
c ATM024 Autoimmune Pancreatitis 55 0.024
587
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.024
588
END040 Endogenous Depression 55 0.024
589
INT007 Intermediate Coronary Syndrome 55 0.024
590
P SLM003 Salmonellosis 55 0.024
591
ACD008 Acid-Labile Subunit Deficiency 54 0.024
592
SJG002 Sjogren-Larsson Syndrome 54 0.024
593
PRT082 Preterm Premature Rupture of the Membranes 54 0.024
594
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.024
595
P CYS039 Cystic Kidney Disease 54 0.024
596
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.024
597
HMS001 Hemosiderosis 54 0.024
598
LYM040 Lymphoblastic Lymphoma 54 0.024
599
SLP001 Sleeping Sickness 54 0.024
600
c SPN294 Spinocerebellar Ataxia 1 53 0.024
601
c CNT016 Central Retinal Vein Occlusion 53 0.024
602
HRT012 Heart Valve Disease 53 0.024
603
P MNC007 Monocytic Leukemia 53 0.024
604
PRP036 Peripheral T-Cell Lymphoma 53 0.024
605
OCL006 Ocular Hypertension 53 0.024
606
MST005 Mastitis 53 0.024
607
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.024
608
CLF001 Cleft Lip 53 0.024
609
c HRM017 Hermansky-Pudlak Syndrome 2 53 0.024
610
NNT012 Neonatal Jaundice 53 0.024
611
NRT001 Neurotic Disorder 53 0.024
612
TXC002 Toxic Encephalopathy 53 0.024
613
PRN011 Pernicious Anemia 53 0.024
614
P RTN022 Retinal Vein Occlusion 53 0.024
615
c HYP740 Hyperlipoproteinemia, Type V 53 0.024
616
c HPT007 Hepatitis E 53 0.024
617
TRC008 Trachoma 53 0.024
618
EXP004 Exophthalmos 52 0.024
619
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.024
620
DRM011 Dermatophytosis 52 0.024
621
c VRL010 Viral Hepatitis 52 0.024
622
c SPN291 Spinocerebellar Ataxia 7 52 0.024
623
CRT016 Carotid Artery Disease 52 0.024
624
THY030 Thyroid Gland Disease 52 0.024
625
P MSC003 Muscular Atrophy 52 0.024
626
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.024
627
BWN001 Bowen-Conradi Syndrome 52 0.024
628
LGN006 Legionnaire Disease 52 0.024
629
HYP014 Hyperuricemia 52 0.024
630
c ACT135 Acute Graft Versus Host Disease 52 0.024
631
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.024
632
SPS003 Spastic Diplegia 51 0.024
634
OCL069 Ocular Motor Apraxia 51 0.024
635
AVD001 Avoidant Personality Disorder 51 0.024
636
FDL002 Food Allergy 51 0.024
637
PLS009 Plasma Cell Neoplasm 51 0.024
638
THR016 Thrombophlebitis 51 0.024
639
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.024
640
SCH012 Schizoaffective Disorder 50 0.024
641
PLR008 Pleurisy 50 0.024
642
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.024
643
PST021 Postpartum Depression 50 0.024
644
CRT013 Carotid Stenosis 50 0.024
645
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.024
646
TRY001 Trypanosomiasis 50 0.024
647
NTR046 Neutrophil Migration 50 0.024
648
MTB004 Metabolic Acidosis 50 0.024
649
OPT003 Opiate Dependence 50 0.024
650
LPR001 Lepromatous Leprosy 50 0.024
651
HYP080 Hypogonadism 50 0.024
652
RNL011 Renal Osteodystrophy 50 0.024
653
ONC007 Oncocytoma 49 0.024
654
PLP001 Pulpitis 49 0.024
655
HDR003 Hidradenitis 49 0.024
656
SLD003 Sialadenitis 49 0.024
657
MCR004 Macroglobulinemia 49 0.024
658
DYS009 Dysthymic Disorder 49 0.024
659
IMP004 Impetigo 49 0.024
660
ACT029 Acute Interstitial Pneumonia 49 0.024
661
PTH002 Pathological Gambling 49 0.024
662
URM002 Uremia 49 0.024
663
VCC001 Vaccinia 49 0.024
664
ADR016 Adrenal Cortical Carcinoma 48 0.024
665
c ACT150 Acute Adrenal Insufficiency 48 0.024
666
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.024
667
SBS004 Substance Dependence 48 0.024
668
CLC006 Calcinosis 48 0.024
669
VTM033 Vitamin K Deficiency Bleeding 48 0.024
670
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.024
671
DBT006 Diabetic Macular Edema 48 0.024
672
RCT020 Rectum Adenocarcinoma 48 0.024
673
P KRT005 Keratoacanthoma 48 0.024
674
ART004 Aortic Atherosclerosis 47 0.024
675
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 47 0.024
676
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.024
677
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.024
678
P RNL015 Renal Hypertension 47 0.024
679
ACT084 Acute Stress Disorder 47 0.024
680
ANT011 Antisocial Personality Disorder 47 0.024
681
KHN001 Kuhnt-Junius Degeneration 47 0.024
682
LYM012 Lymphoplasmacytic Lymphoma 47 0.024
683
TTR011 Tetraploidy 47 0.024
684
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.024
685
HYP082 Hypopharynx Cancer 47 0.024
686
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.024
687
c PRM093 Premature Ovarian Failure 7 47 0.024
688
LYM019 Lymphosarcoma 46 0.024
689
P PRC019 Precocious Puberty 46 0.024
690
RTN023 Retinitis 46 0.024
691
P VTR007 Vitreoretinopathy 46 0.024
692
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.024
693
LPD009 Lipid Storage Disease 46 0.024
694
RTN020 Retinal Vascular Disease 46 0.024
695
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.024
696
TTH006 Tooth Disease 46 0.024
697
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 46 0.024
698
KRT013 Keratolytic Winter Erythema 46 0.024
699
OBS003 Obsessive-Compulsive Personality Disorder 46 0.024
700
c SCH079 Schizophrenia 1 46 0.024
701
GRW007 Growth Hormone Deficiency 46 0.024
702
GST010 Gestational Trophoblastic Neoplasm 46 0.024
703
OPD001 Opioid Abuse 46 0.024
704
c DRR009 Diarrhea 6 46 0.024
705
P HYP733 Hypercalciuria, Absorptive, 2 45 0.024
706
URT010 Ureteral Obstruction 45 0.024
707
TRT001 Teratocarcinoma 45 0.024
708
CYN002 Cyanosis, Transient Neonatal 45 0.024
709
DST006 Diastolic Heart Failure 45 0.024
711
CLC017 Calcification of Joints and Arteries 45 0.024
712
MLN073 Melanosis, Neurocutaneous 45 0.024
713
P SBR004 Seborrheic Dermatitis 45 0.024
714
CNT017 Central Nervous System Origin Vertigo 45 0.024
715
SPS057 Spasticity 45 0.024
716
ASP026 Asplenia, Isolated Congenital 44 0.024
717
RTR001 Retrograde Amnesia 44 0.024
718
c DRM054 Dermatitis, Atopic, 2 44 0.024
719
CNN002 Cannabis Abuse 44 0.024
720
DWR001 Dwarfism 44 0.024
721
CRB008 Cerebral Atherosclerosis 44 0.024
722
OVR063 Overnutrition 44 0.024
723
FML091 Familial Tumoral Calcinosis 44 0.024
724
SYR002 Syringocystadenoma Papilliferum 44 0.024
725
P BNG095 Benign Giant Cell Tumor 44 0.024
726
c PRM038 Primary Agammaglobulinemia 44 0.024
727
P HYP121 Hypoalphalipoproteinemia 43 0.024
728
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.024
729
SBC012 Subcorneal Pustular Dermatosis 43 0.024
730
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.024
731
P MJR007 Major Affective Disorder 1 43 0.024
732
PHY002 Physical Disorder 42 0.024
733
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.024
734
ALC010 Alcoholic Cardiomyopathy 42 0.024
735
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.024
736
c GRN050 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii 42 0.024
737
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.024
738
MNN017 Mononeuropathy 42 0.024
739
BCK006 Back Pain 42 0.024
740
ATX019 Ataxia with Vitamin E Deficiency 42 0.024
741
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.024
742
OBS082 Obstructive Nephropathy 42 0.024
743
MYF002 Myofascial Pain Syndrome 42 0.024
744
NRR001 Neuroretinitis 42 0.024
745
PSD001 Pseudobulbar Palsy 42 0.024
746
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.024
747
CRB025 Carbohydrate Metabolic Disorder 41 0.024
748
MMM006 Mammographic Density 41 0.024
749
PRS063 Paresthesia 41 0.024
750
P RRH023 Rare Hereditary Hemochromatosis 41 0.024
751
KLB003 Klebsiella Pneumonia 41 0.024
752
c MCR112 Microvascular Complications of Diabetes 2 41 0.024
753
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.024
754
RDN001 Reading Disorder 40 0.024
755
P MLG074 Malignant Mesenchymoma 40 0.024
756
LNR006 Linear Iga Disease 40 0.024
757
CLD014 Cole Disease 40 0.024
758
GLC008 Glucose Metabolism Disease 40 0.024
759
P PRG092 Pregnancy Loss, Recurrent 1 40 0.024
760
SCH011 Schizotypal Personality Disorder 40 0.024
761
PLY100 Polyploidy 40 0.024
762
CNN001 Cannabis Dependence 40 0.024
763
CHL045 Choline Deficiency Disease 39 0.024
764
LNG030 Lung Adenoma 39 0.024
765
CRV045 Cervical Intraepithelial Neoplasia 39 0.024
766
ADR004 Adrenal Cortical Adenocarcinoma 39 0.024
767
BLL012 Bullous Impetigo 39 0.024
768
HYP344 Hyperthyroidism, Familial Gestational 39 0.024
769
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.024
770
AML001 Amelanotic Melanoma 39 0.024
771
c CHR682 Chronic Bilirubin Encephalopathy 39 0.024
772
NCR002 Necrobiosis Lipoidica 38 0.024
773
OVR094 Ovarian Epithelial Cancer 38 0.024
774
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.024
775
c SCH051 Schizophrenia 4 37 0.024
776
DBT081 Diabetic Encephalopathy 37 0.024
777
c LPR022 Leprosy 2 37 0.024
778
c CHR020 Chronic Interstitial Cystitis 37 0.024
779
c CNG223 Congenital Methemoglobinemia 36 0.024
780
HRW001 Hair Whorl 36 0.024
782
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.024
783
HYP114 Hypertensive Nephropathy 36 0.024
784
FST010 Fasting Hypoglycemia 35 0.024
785
NRD001 Neurodermatitis 35 0.024
786
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.024
787
c MJR008 Major Affective Disorder 2 35 0.024
788
MYT011 Myotonia 34 0.024
789
PYR009 Pyridoxine Deficiency Anemia 34 0.024
790
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 0.024
791
LCH013 Lichen Planus Pemphigoides 34 0.024
792
c MJR023 Major Affective Disorder 7 33 0.024
793
PPL052 Papillomatosis, Confluent and Reticulated 33 0.024
794
c CHR064 Chronic Monocytic Leukemia 33 0.024
795
c SCH083 Schizophrenia 7 33 0.024
796
c MJR003 Major Affective Disorder 6 33 0.024
797
c MJR006 Major Affective Disorder 5 33 0.024
798
c PRS136 Prostate Cancer, Hereditary, 6 33 0.024
799
c SCH085 Schizophrenia 2 33 0.024
800
c PRS130 Prostate Cancer, Hereditary, 8 32 0.024
801
KDN013 Kidney Hypertrophy 32 0.024
802
NTR011 Neutrophil-Specific Granule Deficiency 32 0.024
803
ANN011 Annular Erythema 32 0.024
804
c SCH080 Schizophrenia 3 32 0.024
805
PRX097 Paroxysmal Dystonia 32 0.024
806
SPC026 Specific Granule Deficiency 1 31 0.024
807
c SCH082 Schizophrenia 5 31 0.024
808
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 0.024
809
ADR001 Adrenal Rest Tumor 30 0.024
810
CNJ001 Conjugate Gaze Palsy 29 0.024
811
CRD220 Cardiac Valvular Defect, Developmental 29 0.024
812
c HYP839 Hyperlipidemia, Familial Combined, 1 29 0.024
813
c MJR004 Major Affective Disorder 4 28 0.024
814
c SCH084 Schizophrenia 8 28 0.024
815
P OVR096 Overlap Myositis 27 0.024
816
HYD030 Hydroxykynureninuria 27 0.024
817
ARG004 Argyria 27 0.024
818
DMN026 Dementia Pugilistica 27 0.024
819
MLR020 Malaria, Mild 27 0.024
820
CHL079 Children's Interstitial Lung Disease 26 0.024
821
c RNG015 Ring Chromosome 2 26 0.024
822
ACT162 Acute Sensory Ataxic Neuropathy 26 0.024
823
MTH071 Methane Production 26 0.024
824
ADG002 Audiogenic Seizures 25 0.024
825
NNT021 Neonatal Meningitis 25 0.024
826
TXC004 Toxic Diffuse Goiter 24 0.024
827
INT074 Intracranial Arteriosclerosis 23 0.024
828
HDG004 Hodgkin's Granuloma 23 0.024
829
HDG006 Hodgkin's Paragranuloma 22 0.024
830
c RNG019 Ring Chromosome 3 22 0.024
831
HML018 Homologous Wasting Disease 22 0.024
832
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.024
833
P RRN010 Rare Neurodegenerative Disease 20 0.024
834
BLD065 Blue Diaper Syndrome 20 0.024
835
DFN191 Deafness, Congenital Heart Defects, and Posterior Embryotoxon 20 0.024
836
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 19 0.024
838
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.024
Content
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