Search results for Ergocalciferol

420 hits were found for Ergocalciferol

# Family MCID Name MIFTS Score
1
RCK004 Rickets 68 20.870
2
c CHR684 Chronic Kidney Disease 69 10.483
3
P KDN018 Kidney Disease 72 9.895
4
P HYP069 Hyperparathyroidism 62 9.583
5
c SCN007 Secondary Hyperparathyroidism 51 8.864
6
END086 End Stage Renal Disease 52 5.182
7
OST011 Osteomalacia 52 4.995
8
P BND020 Bone Disease 59 4.861
9
KRT002 Keratomalacia 55 4.611
10
CYS001 Cystic Fibrosis 78 4.516
11
HYP025 Hyperphosphatemia 48 4.391
12
P HYP024 Hypoparathyroidism 55 3.692
13
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 3.439
14
RNL011 Renal Osteodystrophy 49 3.421
15
NPH009 Nephrolithiasis 54 3.402
16
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.149
17
P OST002 Osteoporosis 76 3.123
18
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.123
19
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.123
20
CLC006 Calcinosis 47 2.882
21
PRT251 Proteinuria, Chronic Benign 57 2.795
22
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.689
23
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.689
24
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.689
25
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.689
26
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.689
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.689
28
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.689
29
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.689
30
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.689
31
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.689
32
BNR002 Bone Resorption Disease 47 2.686
33
P ALZ034 Alzheimer Disease 87 2.517
34
LPT014 Leptin Deficiency or Dysfunction 78 2.473
35
HYP017 Hypophosphatemia 49 2.391
36
IRN002 Iron Metabolism Disease 57 2.368
37
P HRD086 Hereditary Hypophosphatemic Rickets 40 2.305
38
c TYP009 Type 2 Diabetes Mellitus 92 2.292
39
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.277
40
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.243
41
URM005 Uremic Pruritus 45 2.207
42
GLC086 Glucocorticoid-Induced Osteoporosis 43 2.207
43
c PRM005 Primary Hyperparathyroidism 59 2.156
44
P HYP733 Hypercalciuria, Absorptive, 2 45 2.059
45
P DBT009 Diabetes Mellitus 67 1.876
46
P INF037 Inflammatory Bowel Disease 53 1.843
47
LVR012 Liver Cirrhosis 63 1.843
48
48X005 48,xyyy 39 1.755
49
END072 Endotheliitis 36 1.714
50
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.714
51
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.714
52
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 1.714
53
ART140 Arteries, Anomalies of 53 1.697
54
LPP008 Lipoprotein Quantitative Trait Locus 65 1.697
55
P SRC025 Sarcoidosis 1 71 1.697
56
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.693
57
OST003 Osteonecrosis 61 1.693
58
ALC009 Alcoholic Liver Cirrhosis 54 1.693
59
P MLT020 Multiple Sclerosis 79 1.657
60
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.592
61
HYP057 Hypervitaminosis D 37 1.592
62
P OVR042 Ovarian Cancer 88 1.514
63
TTH002 Tooth Agenesis 61 1.514
64
EXC002 Exocrine Pancreatic Insufficiency 42 1.514
65
CHR710 Chronic Spontaneous Urticaria 45 1.502
66
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.497
67
c TBL032 Tubulointerstitial Kidney Disease, Autosomal Dominant, 2 33 1.497
68
URL001 Urolithiasis 46 1.497
69
c XNT010 Xanthinuria, Type I 52 1.497
70
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.497
71
ORT010 Orthostatic Hypotensive Disorder, Streeten Type 17 1.497
73
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 34 1.497
74
P MYC084 Mycobacterium Tuberculosis 1 68 1.464
75
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.464
76
P PRK057 Parkinson Disease, Late-Onset 80 1.392
77
PRT029 Parathyroid Adenoma 51 1.378
78
DRM006 Dermatitis 62 1.351
79
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 1.337
80
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.281
81
P TRN034 Transverse Myelitis 47 1.281
82
MYL001 Myelitis 50 1.281
83
CVD001 Covid-19 57 1.173
85
P HYP726 Hypercalcemia, Infantile, 1 58 1.173
86
GLC003 Glucose Intolerance 54 1.173
87
P LVR013 Liver Disease 69 1.173
88
SVR001 Severe Acute Respiratory Syndrome 67 1.173
89
OST012 Osteoarthritis 77 1.173
90
LPD008 Lipid Metabolism Disorder 62 1.173
91
P HYP058 Hypervitaminosis a 47 1.125
92
ADN018 Adenoma 59 1.125
93
PRP016 Paraplegia 52 1.125
94
P ART021 Arteriosclerosis 54 1.125
95
P URT039 Urticaria 58 1.125
96
P RHM011 Rheumatoid Arthritis 82 1.118
97
P ART022 Arthritis 71 1.118
98
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 45 0.980
99
ANR007 Anorexia Nervosa 60 0.975
100
P RTN024 Retinoblastoma 73 0.975
101
P MYP004 Myopathy 67 0.975
102
SKN016 Skin Disease 63 0.975
103
c ACT071 Acute Kidney Failure 60 0.975
104
CHL068 Cholestasis 61 0.975
105
P BRS047 Breast Cancer 98 0.972
106
BRD001 Brody Myopathy 55 0.972
107
BHR001 Behr Syndrome 51 0.972
108
CRD132 Cardiac Conduction Defect 60 0.939
109
P CLR023 Colorectal Cancer 100 0.939
110
NNL006 Non-Alcoholic Steatohepatitis 54 0.939
111
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.939
112
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.939
113
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.939
114
DSS032 Disease by Infectious Agent 55 0.939
115
THY029 Thyroid Carcinoma 51 0.939
116
c HPT003 Hepatitis a 63 0.939
117
P PRK039 Parkinsonism 55 0.939
118
P PSR002 Psoriasis 63 0.939
119
FTT001 Fatty Liver Disease 62 0.939
120
PLM001 Pulmonary Tuberculosis 69 0.939
121
PST011 Pustulosis of Palm and Sole 52 0.939
122
P THY032 Thyroiditis 57 0.939
123
P RSP003 Respiratory Failure 74 0.939
124
CNG034 Congestive Heart Failure 69 0.939
125
P SCK005 Sickle Cell Disease 56 0.939
126
c TYP008 Type 1 Diabetes Mellitus 70 0.901
127
P CRN300 Coronary Heart Disease 1 73 0.901
128
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.901
129
c BLD140 Blood Group, I System 46 0.901
130
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.901
131
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 0.901
132
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.901
133
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.901
134
c SRC023 Sarcoidosis 2 44 0.901
135
RHB024 Rhabdomyosarcoma 2 67 0.901
136
c HYP724 Hyperlipoproteinemia, Type Iii 67 0.901
137
ANT039 Antisynthetase Syndrome 55 0.901
138
P TRN020 Turner Syndrome 67 0.901
139
P SHR001 Short Bowel Syndrome 53 0.901
140
ISC004 Ischemia 61 0.901
141
P CRD246 Cardiovascular System Disease 56 0.901
142
CYT002 Cytokine Deficiency 43 0.901
143
c THR092 Thrombophilia Due to Thrombin Defect 74 0.796
144
P CLC063 Celiac Disease 1 66 0.796
145
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.796
146
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.796
147
P SCL018 Scoliosis 57 0.796
148
47X002 47,xyy 48 0.796
149
P RTN016 Retinal Degeneration 52 0.796
150
FBR047 Fibromyalgia 58 0.796
151
P VSC007 Vascular Disease 63 0.796
152
P FNC004 Fanconi Syndrome 60 0.796
153
P ADL010 Adult Respiratory Distress Syndrome 71 0.796
154
P HYP265 Hypotonia 42 0.796
155
P PTT014 Pitt-Hopkins Syndrome 64 0.596
156
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.563
157
OST115 Osteonecrosis of the Jaw 41 0.563
158
SPS057 Spasticity 42 0.563
159
P RRT020 Rare Tumor 39 0.563
160
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.563
161
PRS129 Prostatic Hyperplasia, Benign 49 0.563
162
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 0.563
163
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.563
164
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.563
165
HMC014 Homocysteinemia 52 0.563
166
END057 Endometrial Cancer 72 0.563
167
CLF027 Cleft Palate, Isolated 64 0.563
168
c MGR028 Migraine with or Without Aura 1 64 0.563
169
PRP027 Peripheral Vascular Disease 71 0.563
170
ART035 Arterial Calcification of Infancy 58 0.563
171
ATS010 Autosomal Recessive Disease 42 0.563
172
APR001 Apraxia 52 0.563
173
THR024 Thrombosis 56 0.563
174
c HYP293 Hypophosphatasia, Adult 51 0.563
175
IGR001 Ige Responsiveness, Atopic 59 0.563
176
TRG002 Trigeminal Neuralgia 61 0.563
177
FBR054 Fibroma 44 0.563
178
P LCT002 Lactose Intolerance 52 0.563
179
VSC064 Vascular Parkinsonism 21 0.563
180
MDD018 Middle East Respiratory Syndrome 44 0.563
181
NPH003 Nephrocalcinosis 49 0.563
182
P FML355 Familial Intrahepatic Cholestasis 42 0.563
183
P MSC003 Muscular Atrophy 52 0.563
184
URM002 Uremia 47 0.563
185
CLC001 Calciphylaxis 51 0.563
186
GTP001 Gait Apraxia 29 0.563
187
P ALP008 Alopecia 54 0.563
188
P PSD015 Pseudohypoparathyroidism 55 0.563
189
P GRF003 Graft-Versus-Host Disease 71 0.563
190
c DLT002 Dilated Cardiomyopathy 78 0.563
191
GT001 Gout 64 0.563
192
DNT012 Dental Caries 53 0.563
193
BLR008 Bilirubin Metabolic Disorder 57 0.563
194
PRS021 Prostatic Adenoma 43 0.563
195
P HYP035 Hypophosphatasia 62 0.563
196
P NPH012 Nephrotic Syndrome 60 0.563
197
GLS007 Glossitis 47 0.563
198
P HYP086 Hypothyroidism 69 0.563
199
FCL012 Facial Paralysis 49 0.563
200
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.563
201
P INT099 Intrahepatic Cholestasis of Pregnancy 62 0.563
202
HMP005 Hemiplegia 54 0.563
203
PRS045 Prostatic Hypertrophy 53 0.563
204
GST050 Gastrointestinal System Disease 55 0.563
205
OST004 Osteitis Fibrosa 38 0.563
206
BNN003 Bone Inflammation Disease 48 0.563
207
MMM001 Mammary Paget's Disease 53 0.563
208
KWS001 Kwashiorkor 45 0.563
209
P NRF002 Neurofibromatosis 57 0.563
210
PTH003 Pathologic Nystagmus 52 0.563
211
ATN005 Autonomic Dysfunction 46 0.563
212
BCK006 Back Pain 47 0.563
213
AMN006 Aminoaciduria 37 0.563
214
c CHR417 Chronic Graft Versus Host Disease 55 0.563
215
ONC003 Oncogenic Osteomalacia 42 0.563
216
P ANR048 Aniridia 1 64 0.524
217
P ATS364 Autism 69 0.377
218
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.377
219
GRW007 Growth Hormone Deficiency 46 0.377
220
ADR022 Adrenomyeloneuropathy 39 0.377
221
CHR682 Chronic Bilirubin Encephalopathy 37 0.377
222
PDT035 Pediatric Systemic Lupus Erythematosus 47 0.377
223
SPN186 Spinal Cord Injury 61 0.377
224
P THL005 Thalassemia 56 0.377
225
RST023 Resting Heart Rate, Variation in 40 0.377
226
ADR007 Adrenoleukodystrophy 73 0.377
227
P SJG008 Sjogren Syndrome 61 0.377
228
ART002 Arts Syndrome 66 0.377
229
ALL003 Allergic Rhinitis 67 0.377
230
AGN016 Aging 54 0.377
231
P AST005 Asthma 76 0.377
232
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.377
233
STR067 Stroke, Ischemic 80 0.377
234
P DRM053 Dermatitis, Atopic 65 0.377
235
BRT054 Brittle Bone Disorder 74 0.377
236
c ALP101 Alpha-Thalassemia 62 0.377
237
TRP008 Tropical Calcific Pancreatitis 46 0.377
238
P SCH015 Schizophrenia 74 0.377
239
c LKM070 Leukemia, Acute Monocytic 56 0.377
240
P FNG006 Feingold Syndrome 1 62 0.377
241
c PNC108 Pancreatitis, Hereditary 69 0.377
242
P CNR004 Cone-Rod Dystrophy 2 74 0.377
243
c ATR087 Atrial Standstill 1 74 0.377
244
ATM095 Autoimmune Disease 61 0.377
245
ALC007 Alcohol Dependence 66 0.377
246
BSL036 Basal Cell Nevus Syndrome 73 0.377
247
BWN001 Bowen-Conradi Syndrome 53 0.377
248
P APL001 Aplastic Anemia 73 0.377
249
HMN044 Human Immunodeficiency Virus Type 1 78 0.377
250
c MCR115 Microvascular Complications of Diabetes 5 65 0.377
251
c MCR130 Microvascular Complications of Diabetes 6 41 0.377
252
MYL009 Myelodysplastic Syndrome 67 0.377
253
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.377
254
MSC007 Muscle Hypertrophy 64 0.377
255
BRR014 Barrett Esophagus 66 0.377
256
DFC004 Deficiency Anemia 74 0.377
257
PYR010 Peyronie's Disease 50 0.377
258
CLT003 Colitis 63 0.377
259
CHL159 Childhood-Onset Asthma 30 0.377
260
C1N001 C1 Inhibitor Deficiency 43 0.377
261
P LYM118 Lymphoma 67 0.377
262
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.377
263
c LKM061 Leukemia, Acute Myeloid 83 0.377
264
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.377
265
VTM028 Vitamin E, Familial Isolated Deficiency of 53 0.377
266
c OST164 Osteoporosis, Juvenile 54 0.377
267
P PNC035 Pancreatic Cancer 86 0.377
268
LMY014 Leiomyoma, Uterine 56 0.377
269
c PSR028 Psoriasis 7 43 0.377
270
c BSL024 Basal Cell Carcinoma 1 55 0.377
271
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.377
272
c DRM054 Dermatitis, Atopic, 2 46 0.377
273
SCK003 Sickle Cell Anemia 74 0.377
274
P MCR129 Microvascular Complications of Diabetes 1 68 0.377
275
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.377
276
c PSR017 Psoriasis 2 53 0.377
277
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 0.377
278
P LKM062 Leukemia, Acute Lymphoblastic 69 0.377
279
LPT006 Leptin Receptor Deficiency 50 0.377
280
GLS018 Glass Syndrome 61 0.377
281
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.377
282
P MJR001 Major Depressive Disorder 68 0.377
283
c PRS136 Prostate Cancer, Hereditary, 6 33 0.377
284
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 0.377
285
c MCR120 Microvascular Complications of Diabetes 7 47 0.377
286
c PSR018 Psoriasis 13 52 0.377
287
PLY105 Polycystic Ovary Syndrome 1 39 0.377
288
c PSR023 Psoriasis 1 52 0.377
289
CHY002 Chylomicron Retention Disease 64 0.377
290
c CHL140 Chilblain Lupus 1 58 0.377
291
ATM052 Autoimmune Disease 1 36 0.377
292
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 48 0.377
293
P PRC031 Preeclampsia/eclampsia 1 43 0.377
294
DWN001 Down Syndrome 70 0.377
295
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.377
296
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.377
297
P PRS040 Prostate Cancer 95 0.377
298
c HYP595 Hypertension, Essential 85 0.377
299
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.377
300
P PHT010 Photoparoxysmal Response 1 46 0.377
301
ERY051 Erythroleukemia, Familial 37 0.377
302
P PYR039 Peyronie Disease 39 0.377
303
P HPT023 Hepatocellular Carcinoma 96 0.377
304
ADL002 Adult Syndrome 70 0.377
305
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.377
306
MMM006 Mammographic Density 39 0.377
307
c FML347 Familial Adenomatous Polyposis 2 55 0.377
308
NRR001 Neuroretinitis 42 0.377
309
AGG012 Aggressive Nk-Cell Leukemia 46 0.377
310
SPR126 Superior Semicircular Canal Dehiscence 41 0.377
311
c PRS130 Prostate Cancer, Hereditary, 8 32 0.377
312
c PSR032 Psoriasis 11 47 0.377
313
LMY002 Leiomyoma 51 0.377
314
c CHR708 Chronic Urticaria 42 0.377
315
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.377
316
ACT250 Acute Megakaryocytic Leukemia 60 0.377
317
NTR005 Nutritional Deficiency Disease 61 0.377
318
RTN023 Retinitis 46 0.377
319
SKN019 Skin Melanoma 71 0.377
320
KRT006 Keratoconjunctivitis 53 0.377
321
VRL011 Viral Infectious Disease 61 0.377
322
ULC004 Ulcerative Colitis 74 0.377
323
P MYL006 Myeloid Leukemia 61 0.377
324
P HML002 Hemolytic Anemia 62 0.377
325
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 38 0.377
326
PRS047 Prostatitis 58 0.377
327
P PRS038 Personality Disorder 65 0.377
328
P ALC033 Alcohol Use Disorder 61 0.377
329
HYP066 Hyperglycemia 61 0.377
330
FDL002 Food Allergy 47 0.377
331
c HPT001 Hepatitis C 62 0.377
332
END040 Endogenous Depression 55 0.377
333
MNT002 Mental Depression 57 0.377
334
GLC008 Glucose Metabolism Disease 40 0.377
335
MCR019 Microglandular Adenosis 44 0.377
336
ACQ007 Acquired Immunodeficiency Syndrome 59 0.377
337
CNN005 Connective Tissue Disease 67 0.377
338
PRT036 Peritonitis 65 0.377
339
MYF001 Myofibroma 42 0.377
340
PHT003 Phototoxic Dermatitis 28 0.377
341
LNG099 Lung Disease 62 0.377
342
P PRD008 Periodontitis 64 0.377
343
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.377
344
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.377
345
c MCR112 Microvascular Complications of Diabetes 2 42 0.377
346
c MCR113 Microvascular Complications of Diabetes 3 52 0.377
347
c MCR133 Microvascular Complications of Diabetes 4 41 0.377
348
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.377
349
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.377
350
P CTN003 Cutaneous Lupus Erythematosus 52 0.377
351
DRY001 Dry Eye Syndrome 50 0.377
352
c PRC016 Pre-Eclampsia 65 0.377
353
ALL029 Allergic Disease 59 0.377
354
P OPT009 Optic Neuritis 57 0.377
355
P LKM002 Leukemia 67 0.377
356
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.377
357
P END084 Endocrine System Disease 44 0.377
358
c ACT027 Acute Pancreatitis 60 0.377
359
PRM003 Premature Ejaculation 44 0.377
360
P MLN008 Melanoma 76 0.377
361
c BSL007 Basal Cell Carcinoma 68 0.377
362
NRT004 Neuritis 53 0.377
363
P ANG015 Angioedema 56 0.377
364
P HPT021 Hepatitis 69 0.377
365
P ADN016 Adenocarcinoma 63 0.377
366
P ECL001 Eclampsia 52 0.377
367
P END044 Endometriosis 62 0.377
368
P HRT032 Heart Disease 81 0.377
369
GST033 Gestational Diabetes 61 0.377
370
LYM040 Lymphoblastic Lymphoma 53 0.377
371
MCS002 Mucositis 56 0.377
372
VTM033 Vitamin K Deficiency Bleeding 48 0.377
373
P PLY011 Polycystic Ovary Syndrome 57 0.377
374
PRD004 Prediabetes Syndrome 52 0.377
375
c CNG027 Congenital Hemolytic Anemia 48 0.377
376
BRN024 Bronchitis 67 0.377
377
P CNJ013 Conjunctivitis 66 0.377
378
CRB039 Cerebrovascular Disease 66 0.377
379
P RHN004 Rhinitis 57 0.377
380
ALC005 Alcoholic Pancreatitis 38 0.377
381
P PNC044 Pancreatitis 61 0.377
382
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.377
383
P INT068 Intestinal Disease 53 0.377
384
NRT001 Neurotic Disorder 56 0.377
385
P EYD002 Eye Disease 57 0.377
386
P PNM007 Pneumonia 67 0.377
387
PLC008 Placenta Disease 49 0.377
388
GNG013 Gingivitis 59 0.377
389
MDD011 Mood Disorder 62 0.377
390
CLN045 Colonic Benign Neoplasm 48 0.377
391
BRS051 Breast Disease 58 0.377
392
BRN002 Bronchiolitis 57 0.377
393
ANS011 Anus Cancer 57 0.377
394
ACT011 Acute Contagious Conjunctivitis 42 0.377
395
RSP006 Respiratory System Disease 51 0.377
396
ACT017 Acute Chest Syndrome 50 0.377
397
KRT001 Keratoconjunctivitis Sicca 50 0.377
398
c HPT016 Hepatitis B 62 0.377
399
HYP080 Hypogonadism 50 0.377
400
P RCT021 Rectum Cancer 54 0.377
401
HLL004 Hellp Syndrome 53 0.377
402
P INS002 in Situ Carcinoma 53 0.377
403
49X006 49, Xxxxy Syndrome 40 0.377
404
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.377
405
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.377
406
ATX019 Ataxia with Vitamin E Deficiency 44 0.377
407
HRP008 Herpes Simiae 23 0.377
408
c JVN025 Juvenile Primary Osteoporosis 21 0.377
409
DPR016 Depression 65 0.377
410
P CHR345 Chronic Pain 50 0.377
411
DYS073 Dysphagia 53 0.377
412
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.377
413
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.377
414
BRN056 Bronchopulmonary Dysplasia 56 0.377
415
c HMG029 Hemoglobin Se Disease 40 0.377
416
LYM019 Lymphosarcoma 46 0.377
417
c PRM038 Primary Agammaglobulinemia 47 0.377
418
CHL079 Children's Interstitial Lung Disease 26 0.377
419
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.377
420
c CHR064 Chronic Monocytic Leukemia 36 0.377
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