Search results for Ferrous glycine sulfate

656 hits were found for Ferrous glycine sulfate

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 56 37.183
2
DFC004 Deficiency Anemia 74 32.759
3
IRN001 Iron Deficiency Anemia 58 26.353
4
RPD005 Rapidly Involuting Congenital Hemangioma 48 20.086
5
CLT003 Colitis 63 19.814
6
OST012 Osteoarthritis 77 14.786
7
P INF037 Inflammatory Bowel Disease 53 13.144
8
c CHR684 Chronic Kidney Disease 73 12.875
9
AGN016 Aging 53 12.451
10
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 12.409
11
HLX001 Helix Syndrome 47 12.407
12
HMN044 Human Immunodeficiency Virus Type 1 76 12.332
13
NTR005 Nutritional Deficiency Disease 60 11.940
14
ULC004 Ulcerative Colitis 74 11.814
15
P DRR001 Diarrhea 55 11.633
16
c PRC016 Pre-Eclampsia 64 11.395
17
P KDN018 Kidney Disease 71 10.712
18
HMN014 Human Immunodeficiency Virus Infectious Disease 54 10.317
19
48X005 48,xyyy 39 10.249
20
P ECL001 Eclampsia 52 10.093
21
P NRB001 Neuroblastoma 66 9.843
22
P ENC018 Encephalopathy 62 9.544
23
LYM019 Lymphosarcoma 46 9.359
24
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 9.242
25
CRH001 Crohn's Disease 80 9.191
26
P LYM118 Lymphoma 66 9.112
27
P CLR023 Colorectal Cancer 100 8.901
28
P CHR345 Chronic Pain 50 8.846
29
IMM167 Immune Deficiency Disease 76 8.581
30
CYS001 Cystic Fibrosis 77 8.375
31
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 8.330
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 8.308
33
DWN001 Down Syndrome 70 8.304
34
P SZR006 Seizure Disorder 69 8.286
35
ADL002 Adult Syndrome 69 8.205
36
P TRN020 Turner Syndrome 67 8.204
37
P HRP006 Herpes Simplex 65 8.029
38
P BRS047 Breast Cancer 97 7.991
39
HYP266 Hypoxia 56 7.909
40
c TYP009 Type 2 Diabetes Mellitus 91 7.836
41
CNS004 Constipation 56 7.756
42
CHL068 Cholestasis 61 7.680
43
ACQ007 Acquired Immunodeficiency Syndrome 58 7.638
44
P LKM002 Leukemia 65 7.607
45
MLR004 Malaria 77 7.587
46
MTH071 Methane Production 24 7.405
47
PRT251 Proteinuria, Chronic Benign 58 7.329
48
HMS001 Hemosiderosis 48 7.290
49
P RRH023 Rare Hereditary Hemochromatosis 52 7.272
50
P LKM062 Leukemia, Acute Lymphoblastic 69 7.270
51
KRT002 Keratomalacia 54 7.185
52
P HYP086 Hypothyroidism 68 7.154
53
ISC004 Ischemia 61 7.064
54
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 7.036
55
PLM129 Pulmonary Disease, Chronic Obstructive 74 6.955
56
GLM045 Glioma 62 6.914
57
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 6.843
58
CNT047 Contact Dermatitis 56 6.820
59
GLL048 Glial Tumor 51 6.755
60
P LVR013 Liver Disease 68 6.723
61
DRM006 Dermatitis 61 6.710
62
P PRD008 Periodontitis 63 6.695
63
SVR001 Severe Acute Respiratory Syndrome 68 6.598
64
P ALC033 Alcohol Use Disorder 67 6.554
65
P MLN008 Melanoma 75 6.553
66
DPR016 Depression 64 6.533
67
MNT002 Mental Depression 56 6.457
68
P CYS018 Cystitis 58 6.376
69
END086 End Stage Renal Disease 54 6.374
70
SPN186 Spinal Cord Injury 60 6.370
71
HYP066 Hyperglycemia 60 6.355
72
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.331
73
P ANR048 Aniridia 1 66 6.207
74
RHB024 Rhabdomyosarcoma 2 65 6.188
75
c HYP836 Hypercholesterolemia, Familial, 1 73 6.149
76
P LTR001 Lateral Sclerosis 57 6.105
77
P ALZ034 Alzheimer Disease 87 6.102
78
P INT143 Interstitial Cystitis 59 6.073
79
c AMY091 Amyotrophic Lateral Sclerosis 1 87 6.044
80
P GLM040 Glioma Susceptibility 1 70 6.015
81
P BCL017 B-Cell Lymphoma 57 6.008
82
PRT037 Pertussis 49 5.948
83
c PNS012 Paine Syndrome 60 5.947
84
47X002 47,xyy 47 5.942
85
GLB002 Glioblastoma 67 5.914
86
CHL014 Cholera 62 5.881
87
c EPS039 Episodic Pain Syndrome, Familial, 1 42 5.835
88
P ATS364 Autism 72 5.820
89
P PRK039 Parkinsonism 55 5.808
90
STM007 Stomatitis 52 5.797
91
P CRN300 Coronary Heart Disease 1 73 5.780
92
STR067 Stroke, Ischemic 79 5.727
93
P HYP265 Hypotonia 42 5.720
94
BRT054 Brittle Bone Disorder 74 5.713
95
P PHC003 Pheochromocytoma 70 5.688
96
ADR040 Adrenal Gland Pheochromocytoma 45 5.688
97
P DBT009 Diabetes Mellitus 67 5.658
98
ATH013 Atherosclerosis Susceptibility 63 5.655
99
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.645
100
P INT068 Intestinal Disease 53 5.598
101
BRN071 Brain Injury 50 5.595
102
OST062 Osteoarthritis with Mild Chondrodysplasia 46 5.571
103
P HPT021 Hepatitis 68 5.564
104
P VSC007 Vascular Disease 62 5.563
105
P LNG032 Lung Cancer 98 5.531
106
ALL029 Allergic Disease 61 5.463
107
c ACT071 Acute Kidney Failure 60 5.442
108
CVD001 Covid-19 59 5.426
109
FTT001 Fatty Liver Disease 61 5.416
110
LNG099 Lung Disease 62 5.414
111
CYT002 Cytokine Deficiency 43 5.412
112
HYP005 Hypokalemia 55 5.406
113
BCT022 Bacterial Infectious Disease 55 5.384
114
ANT039 Antisynthetase Syndrome 55 5.378
115
URM002 Uremia 47 5.352
116
TXC005 Toxic Shock Syndrome 61 5.301
117
PRT036 Peritonitis 65 5.293
118
P MYC033 Myoclonus 46 5.274
119
P MJR001 Major Depressive Disorder 68 5.274
120
c MCR120 Microvascular Complications of Diabetes 7 47 5.247
121
P AMY004 Amyloidosis 69 5.225
122
P CNJ013 Conjunctivitis 66 5.223
123
ANX004 Anoxia 40 5.205
124
P ART022 Arthritis 70 5.202
125
PPL052 Papillomatosis, Confluent and Reticulated 34 5.197
126
P PLY011 Polycystic Ovary Syndrome 57 5.192
127
P ATT013 Attention Deficit-Hyperactivity Disorder 65 5.149
128
ATS010 Autosomal Recessive Disease 42 5.126
129
TRM010 Traumatic Brain Injury 50 5.122
130
AND005 Androgen Insensitivity Syndrome, Mild 21 5.114
131
ALL010 Allergic Contact Dermatitis 55 5.113
132
P HPT023 Hepatocellular Carcinoma 95 5.103
133
P GST044 Gastritis 55 5.100
134
MYL069 Myeloma, Multiple 76 5.070
135
LVR012 Liver Cirrhosis 62 5.053
136
BRN024 Bronchitis 67 5.029
137
HYP781 Hypoascorbemia 52 4.965
138
c MCR133 Microvascular Complications of Diabetes 4 41 4.915
139
c MCR113 Microvascular Complications of Diabetes 3 52 4.915
140
c MCR130 Microvascular Complications of Diabetes 6 41 4.915
141
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 4.907
142
LPD008 Lipid Metabolism Disorder 61 4.889
143
P ADN016 Adenocarcinoma 63 4.850
144
P OVR042 Ovarian Cancer 88 4.844
145
P HRT032 Heart Disease 84 4.840
146
P NRP001 Neuropathy 59 4.819
147
P PLM037 Pulmonary Hypertension 69 4.813
148
HRW001 Hair Whorl 35 4.812
149
c DRR009 Diarrhea 6 46 4.805
150
c ATS007 Autism Spectrum Disorder 71 4.801
151
OCL069 Ocular Motor Apraxia 57 4.769
152
P PLM036 Pulmonary Fibrosis 65 4.680
153
VCC001 Vaccinia 49 4.653
154
c HPT003 Hepatitis a 63 4.642
155
P MSC005 Muscular Dystrophy 66 4.639
156
HYP056 Hypoglycemia 65 4.626
157
SKN016 Skin Disease 63 4.611
158
PPT005 Peptic Ulcer Disease 58 4.609
159
BRN004 Brain Edema 54 4.608
160
INS024 Insulin-Like Growth Factor I 77 4.607
161
TTN003 Tetanus 64 4.603
162
P ANP001 Anaplastic Large Cell Lymphoma 59 4.597
163
BNR002 Bone Resorption Disease 47 4.566
164
HMP009 Haemophilus Influenzae 41 4.563
165
c SYS001 Systemic Lupus Erythematosus 85 4.550
166
P GLM007 Glomerulonephritis 59 4.526
167
P HDC001 Headache 56 4.526
168
LPP008 Lipoprotein Quantitative Trait Locus 65 4.514
169
ARG004 Argyria 26 4.514
170
OST159 Osteogenic Sarcoma 66 4.508
171
RCK004 Rickets 64 4.505
172
GLS018 Glass Syndrome 60 4.497
173
P FBR017 Fibrosarcoma 55 4.495
174
HRL003 Hurler Syndrome 66 4.481
175
CRV035 Cervical Cancer 72 4.473
176
PSY004 Psychotic Disorder 66 4.467
177
P PRP029 Porphyria 60 4.442
178
P MYC084 Mycobacterium Tuberculosis 1 68 4.428
179
P LPS004 Lupus Erythematosus 61 4.418
180
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.405
181
P EHL001 Ehlers-Danlos Syndrome 57 4.381
182
CLN015 Colon Adenocarcinoma 64 4.380
183
P PNC035 Pancreatic Cancer 87 4.356
184
CHL123 Chlamydia 58 4.348
185
MLG169 Malignant Astrocytoma 57 4.325
186
c MGR028 Migraine with or Without Aura 1 63 4.287
187
GST045 Gastroenteritis 58 4.275
188
NPH009 Nephrolithiasis 54 4.271
189
P RSP003 Respiratory Failure 73 4.271
190
P PRS040 Prostate Cancer 95 4.248
191
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 4.228
192
CNG034 Congestive Heart Failure 69 4.226
193
P EPL164 Epilepsy 70 4.216
194
ART140 Arteries, Anomalies of 52 4.187
195
P TRM003 Tremor 50 4.169
196
P THL005 Thalassemia 56 4.162
197
URL001 Urolithiasis 45 4.135
198
P PRP019 Peripheral Nervous System Disease 57 4.111
199
c LKM061 Leukemia, Acute Myeloid 83 4.074
200
P DNG005 Dengue Virus 55 4.036
201
P CLC063 Celiac Disease 1 65 4.024
202
SPS057 Spasticity 43 4.000
203
P ART023 Arthropathy 59 3.985
204
CRH005 Crohn's Colitis 53 3.978
205
P ADL010 Adult Respiratory Distress Syndrome 70 3.963
206
P PNC044 Pancreatitis 61 3.958
207
P DMN002 Dementia 65 3.955
208
THY029 Thyroid Carcinoma 55 3.915
209
ACT011 Acute Contagious Conjunctivitis 41 3.882
210
c ACT068 Acute Cystitis 60 3.874
211
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 3.862
212
P THR014 Thrombocytopenia 66 3.850
213
MTB004 Metabolic Acidosis 48 3.843
214
c ACT027 Acute Pancreatitis 60 3.835
215
PST011 Pustulosis of Palm and Sole 52 3.826
216
P PSR002 Psoriasis 63 3.817
217
PST092 Posttransplant Acute Limbic Encephalitis 29 3.799
218
P ESP024 Esophagitis 60 3.784
219
c HPT073 Hepatitis C Virus 70 3.779
220
DPH001 Diphtheria 59 3.755
221
GST023 Gastric Ulcer 52 3.749
222
GLC003 Glucose Intolerance 53 3.744
223
P RTN024 Retinoblastoma 72 3.728
224
P MVM001 Movement Disease 61 3.724
225
P GRF003 Graft-Versus-Host Disease 71 3.708
226
P URN019 Urinary Tract Infection 48 3.694
227
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.690
228
MST004 Mast Cell Neoplasm 41 3.673
229
EXT007 Extracutaneous Mastocytoma 38 3.673
230
P SLP005 Sleep Disorder 61 3.672
231
P INF032 Infertility 60 3.660
232
LPT014 Leptin Deficiency or Dysfunction 77 3.660
233
IRR003 Irritant Dermatitis 47 3.660
234
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.657
235
P SCK005 Sickle Cell Disease 56 3.657
236
MDD011 Mood Disorder 61 3.651
237
HMC014 Homocysteinemia 52 3.649
238
ENT011 Enterocolitis 55 3.640
239
GST050 Gastrointestinal System Disease 55 3.632
240
BRN002 Bronchiolitis 57 3.629
241
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.628
242
STT001 Status Epilepticus 58 3.594
243
P RST001 Restless Legs Syndrome 52 3.584
244
PLS009 Plasma Cell Neoplasm 64 3.562
245
P DRM053 Dermatitis, Atopic 65 3.558
246
PLM001 Pulmonary Tuberculosis 69 3.552
247
P MYL006 Myeloid Leukemia 60 3.548
248
P EXN002 Exanthem 58 3.530
249
P SCL018 Scoliosis 57 3.517
250
P BNG032 Benign Mesothelioma 53 3.514
251
P KLZ004 Kala-Azar 1 41 3.510
252
LSH001 Leishmaniasis 63 3.510
253
LYS002 Lysosomal Storage Disease 51 3.509
254
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.499
255
P PNM007 Pneumonia 64 3.497
256
PLC008 Placenta Disease 48 3.489
257
OST017 Osteomyelitis 63 3.481
258
CRB039 Cerebrovascular Disease 65 3.475
259
P CTR002 Cataract 59 3.470
260
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.467
261
P RHN004 Rhinitis 56 3.450
262
P RHM011 Rheumatoid Arthritis 81 3.450
263
P RCT021 Rectum Cancer 54 3.430
264
P HML002 Hemolytic Anemia 62 3.428
265
PRN019 Perinatal Necrotizing Enterocolitis 60 3.425
266
CHL065 Cholangiocarcinoma 57 3.408
267
INT079 Intrahepatic Cholangiocarcinoma 51 3.408
268
c TYP008 Type 1 Diabetes Mellitus 77 3.407
269
c SML038 Small Cell Cancer of the Lung 68 3.375
270
P PRK057 Parkinson Disease, Late-Onset 79 3.353
271
P PRN023 Prion Disease 60 3.351
272
ALL006 Allergic Asthma 55 3.351
273
DFF005 Diffuse Large B-Cell Lymphoma 55 3.343
274
SCR011 Scrapie 39 3.333
275
P BND020 Bone Disease 60 3.321
276
VRC005 Varicose Veins 59 3.316
277
SKN019 Skin Melanoma 70 3.309
278
ALL014 Allergic Encephalomyelitis 34 3.306
279
P CRD246 Cardiovascular System Disease 55 3.292
280
LMY002 Leiomyoma 51 3.278
281
PLY150 Polykaryocytosis Inducer 29 3.269
282
DSS032 Disease by Infectious Agent 55 3.266
283
c LKM005 Leukemia, T-Cell, Chronic 33 3.248
284
DSS008 Disease of Mental Health 74 3.222
285
HPT004 Hepatic Coma 43 3.208
286
P END044 Endometriosis 62 3.206
287
c HPT001 Hepatitis C 61 3.200
288
c PRD040 Periodontitis, Chronic 52 3.196
289
ATM095 Autoimmune Disease 61 3.195
290
BRK010 Burkitt Lymphoma 65 3.189
291
HPT019 Hepatic Encephalopathy 59 3.189
292
HYP043 Hyperandrogenism 47 3.187
293
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.176
294
NRL016 Neural Tube Defects 80 3.174
295
c BRN108 Branchiootic Syndrome 1 63 3.172
296
BLR008 Bilirubin Metabolic Disorder 57 3.158
297
c BLD140 Blood Group, I System 47 3.131
298
P HYP750 Hypertriglyceridemia, Familial 61 3.108
299
TLN003 Telangiectasis 51 3.106
300
P GST053 Gastric Cancer 82 3.099
301
VGN023 Vaginitis 56 3.096
302
THR024 Thrombosis 56 3.095
303
c THR092 Thrombophilia Due to Thrombin Defect 74 3.080
304
GST033 Gestational Diabetes 60 3.072
305
MCR018 Microcytic Anemia 46 3.057
306
P ACN011 Acne 55 3.056
307
ANX010 Anxiety 70 3.041
308
P LCT001 Lactic Acidosis 50 3.040
309
c BTT014 Beta-Thalassemia 72 3.039
310
P HMP007 Hemophilia 52 3.033
311
P THY032 Thyroiditis 56 3.020
313
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.999
314
c HMP029 Hemophilia a 69 2.998
315
P BLD134 Bladder Cancer 79 2.998
316
P ALP008 Alopecia 53 2.998
317
P OST002 Osteoporosis 76 2.997
318
P MDL005 Medulloblastoma 75 2.994
319
c ACT073 Acute Leukemia 59 2.986
320
P HMR005 Hemorrhoid 49 2.980
321
P MYC007 Myocardial Infarction 69 2.978
322
P BRS044 Breast Adenocarcinoma 58 2.965
323
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.964
324
PPL022 Papilloma 53 2.960
325
DYS073 Dysphagia 53 2.947
326
CHL079 Children's Interstitial Lung Disease 25 2.944
327
SQM002 Squamous Cell Papilloma 45 2.933
328
P PLY018 Polycythemia 56 2.929
329
NNL006 Non-Alcoholic Steatohepatitis 54 2.904
330
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.893
331
c ACT075 Acute Myocardial Infarction 55 2.884
332
c PCH010 Pachyonychia Congenita 3 43 2.883
333
P HMC002 Homocystinuria 52 2.878
334
P HNT016 Huntington Disease 73 2.874
335
HDN002 Head Injury 44 2.851
336
PLM033 Pulmonary Embolism 58 2.820
337
RTN017 Retinal Detachment 60 2.809
338
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.802
339
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.802
340
GT001 Gout 63 2.782
341
P SBS003 Substance Abuse 54 2.778
342
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.777
343
ANG054 Angina Pectoris 65 2.763
344
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.752
345
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.744
346
P DDN001 Duodenal Ulcer 52 2.743
347
P NSP012 Nasopharyngeal Carcinoma 60 2.706
348
CYN002 Cyanosis, Transient Neonatal 43 2.690
349
CMM005 Common Cold 55 2.685
350
c VRL010 Viral Hepatitis 52 2.681
351
CRB090 Cerebral Hypoxia 42 2.681
352
P PRP003 Porphyria Cutanea Tarda 66 2.673
353
ACT098 Acute Erythroid Leukemia 55 2.643
354
GTR002 Goiter 52 2.631
355
P LNG064 Lung Cancer Susceptibility 3 69 2.629
356
P CRV039 Cervicitis 52 2.629
357
PRP030 Purpura 54 2.619
358
CLF027 Cleft Palate, Isolated 64 2.588
359
KRT009 Keratosis 52 2.579
360
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.564
361
HYP017 Hypophosphatemia 49 2.557
362
P SKN015 Skin Carcinoma 71 2.555
363
OTT002 Otitis Media 70 2.545
364
SCK003 Sickle Cell Anemia 74 2.534
365
PLS007 Plasmodium Falciparum Malaria 52 2.526
366
CHG001 Chagas Disease 65 2.499
367
P OBS001 Obstructive Jaundice 49 2.488
368
DSS009 Disseminated Intravascular Coagulation 56 2.476
369
PYL006 Pyloric Stenosis 48 2.471
370
P NTR004 Neutropenia 62 2.471
371
SQM006 Squamous Cell Carcinoma 59 2.470
372
P RTN016 Retinal Degeneration 52 2.458
373
ENT004 Enthesopathy 51 2.448
374
ESP021 Esophageal Cancer 84 2.444
375
c WLM013 Wilms Tumor 1 65 2.428
376
VSC002 Vascular Dementia 59 2.406
377
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 2.404
378
CHR073 Choreatic Disease 53 2.404
379
DNT012 Dental Caries 53 2.404
380
PRT038 Protein-Energy Malnutrition 53 2.391
381
INT323 Intraocular Pressure Quantitative Trait Locus 63 2.389
382
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.380
383
SCH014 Schistosomiasis 56 2.380
384
c HMC039 Hemochromatosis, Type 1 73 2.337
385
DYS015 Dysentery 49 2.325
386
ORL011 Oral Cancer 60 2.322
387
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.314
388
P SYS005 Systemic Scleroderma 73 2.291
389
THY030 Thyroid Gland Disease 50 2.290
390
EWN003 Ewing Sarcoma 69 2.289
391
FBR047 Fibromyalgia 57 2.269
392
SYN007 Synovitis 54 2.268
393
PLC002 Plica Syndrome 35 2.268
394
c ACT134 Acute Liver Failure 57 2.249
395
P EYD002 Eye Disease 57 2.245
396
P SDR003 Sideroblastic Anemia 49 2.228
397
CHR178 Chromosomal Triplication 33 2.223
398
c MST023 Mesothelioma, Malignant 56 2.199
399
PRS047 Prostatitis 57 2.192
400
CLR109 Colorectal Adenocarcinoma 50 2.170
401
ALV005 Alveolar Soft Part Sarcoma 61 2.167
402
c ATR087 Atrial Standstill 1 74 2.154
403
P VSC011 Vasculitis 61 2.149
404
c EXD008 Exudative Vitreoretinopathy 1 71 2.140
405
PSD088 Pseudobulbar Affect 33 2.140
406
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.137
407
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.137
408
MYM001 Myoma 54 2.136
409
STN013 Stenotrophomonas Maltophilia Infection 26 2.131
410
BNG077 Benign Idiopathic Neonatal Seizures 23 2.130
411
INT066 Interstitial Lung Disease 60 2.122
412
c RST012 Restless Legs Syndrome 1 33 2.099
413
P RTN018 Retinal Disease 53 2.089
414
P OPT006 Optic Nerve Disease 57 2.081
415
P URT039 Urticaria 57 2.061
416
CNG506 Congenital Amyoplasia 27 2.049
417
c OVR114 Ovarian Cancer 1 60 2.044
418
NRR001 Neuroretinitis 42 2.043
419
RTN023 Retinitis 45 2.043
420
c SCL052 Scleroderma, Familial Progressive 60 2.031
421
HNT002 Hantavirus Pulmonary Syndrome 55 2.028
422
GST092 Gastroesophageal Reflux 59 2.015
423
ANT024 Anthrax Disease 57 2.011
424
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.002
425
DNG003 Dengue Disease 65 1.962
426
P MYS003 Myasthenia Gravis 67 1.957
427
AMN001 Amenorrhea 53 1.949
428
P MTH007 Methemoglobinemia 46 1.943
429
P MNC007 Monocytic Leukemia 48 1.921
430
c ACT135 Acute Graft Versus Host Disease 51 1.921
431
MNN043 Meningioma, Familial 79 1.906
432
c DLT002 Dilated Cardiomyopathy 79 1.904
433
P PLY014 Polycystic Kidney Disease 71 1.899
434
PRM329 Premature Aging 36 1.893
435
P SYP003 Syphilis 59 1.886
436
PNC129 Pancreatic Adenocarcinoma 64 1.883
437
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.874
438
SCR001 Secretory Meningioma 40 1.874
439
INT395 Intracranial Meningioma 47 1.874
440
HLC007 Helicobacter Pylori Infection 67 1.870
441
c ATM101 Autoimmune Gastritis 40 1.866
442
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.861
443
MYL009 Myelodysplastic Syndrome 67 1.850
444
P SLM003 Salmonellosis 54 1.829
445
SPL018 Splenomegaly 47 1.823
446
CHR100 Chronic Ulcer of Skin 57 1.821
447
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.804
448
P SHR001 Short Bowel Syndrome 53 1.799
449
c DWL002 Dowling-Degos Disease 1 58 1.785
450
P SPP010 Suppressor of Tumorigenicity 3 50 1.785
451
LMY014 Leiomyoma, Uterine 55 1.781
452
P PTS002 Ptosis 52 1.776
453
PLY001 Polycythemia Vera 69 1.775
454
FCL014 Focal Epilepsy 53 1.770
455
P PRV006 Pervasive Developmental Disorder 52 1.768
456
CHD004 Chudley-Mccullough Syndrome 47 1.767
457
HVY002 Heavy Metal Poisoning 22 1.765
458
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.755
459
P SDR002 Siderosis 42 1.755
460
P THR015 Thrombophilia 51 1.753
461
PLG002 Plague 58 1.745
462
P KRT007 Keratoconus 49 1.739
463
P MLN007 Male Infertility 56 1.729
464
MGL001 Megaloblastic Anemia 59 1.729
465
MRF001 Marfan Syndrome 76 1.720
466
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 1.713
467
P END047 Endophthalmitis 53 1.710
468
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.693
469
MYF001 Myofibroma 42 1.688
470
P TXP001 Toxoplasmosis 59 1.679
471
ORL015 Oral Squamous Cell Carcinoma 43 1.674
472
MLD018 Mild Cognitive Impairment 48 1.673
473
SLC006 Silicosis 55 1.668
474
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 1.662
475
WLL004 Wallerian Degeneration 38 1.654
476
FNG017 Fungal Infectious Disease 54 1.653
478
HYP014 Hyperuricemia 51 1.643
479
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.638
480
GRW007 Growth Hormone Deficiency 47 1.638
481
SYN036 Syncope 44 1.633
482
MSL001 Measles 61 1.616
483
c LKM063 Leukemia, Chronic Myeloid 70 1.610
484
IMP005 Impotence 52 1.607
485
P RBL001 Rubella 58 1.602
486
PRN011 Pernicious Anemia 52 1.593
487
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.588
488
IGR001 Ige Responsiveness, Atopic 58 1.587
489
OCC001 Occupational Dermatitis 27 1.574
490
P CRN037 Craniosynostosis 67 1.561
491
ANT018 Anthracosis 50 1.553
492
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.550
493
P GLL018 Gallbladder Cancer 59 1.534
494
CLF001 Cleft Lip 54 1.534
495
P SLP006 Sleep Apnea 69 1.532
496
KWS001 Kwashiorkor 44 1.527
497
ACT003 Acute Kidney Tubular Necrosis 46 1.527
498
PRP083 Porphyria, Acute Intermittent 64 1.526
499
P HYP069 Hyperparathyroidism 62 1.523
500
WLS001 Wilson Disease 70 1.522
501
TLR001 Tularemia 56 1.519
502
P PNM006 Pneumoconiosis 55 1.511
503
PST021 Postpartum Depression 50 1.510
504
MYL005 Myelofibrosis 70 1.497
505
BRC012 Brucellosis 66 1.465
506
c PSR023 Psoriasis 1 52 1.457
507
INT007 Intermediate Coronary Syndrome 53 1.447
508
P UVT001 Uveitis 57 1.443
509
SLP001 Sleeping Sickness 56 1.439
510
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 1.436
511
c PRG106 Progressive Muscular Dystrophy 31 1.425
512
PPL002 Papillary Carcinoma 46 1.424
513
FCL012 Facial Paralysis 49 1.421
514
TRN015 Transient Cerebral Ischemia 62 1.420
515
BCT004 Bacteriuria 48 1.412
516
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.402
517
MNG007 Manganese Poisoning 28 1.387
518
c PSR028 Psoriasis 7 42 1.387
519
c PSR017 Psoriasis 2 53 1.387
520
c PSR018 Psoriasis 13 40 1.387
521
c PSR032 Psoriasis 11 47 1.387
522
VTM002 Vitamin B12 Deficiency 48 1.385
523
CRC021 Carcinosarcoma 62 1.371
524
DBT010 Diabetic Neuropathy 54 1.367
525
P MRC003 Mercury Poisoning 48 1.366
526
P STR020 Strabismus 56 1.357
527
CRN027 Corneal Neovascularization 47 1.357
528
INS001 Insulinoma 59 1.331
529
HMG005 Hemoglobinopathy 55 1.327
530
P HYP083 Hypopituitarism 51 1.323
531
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.318
532
PSR001 Psoriatic Arthritis 61 1.313
533
HNS001 Hansen's Disease 32 1.305
534
PHN003 Phenylketonuria 76 1.304
535
P LPR021 Leprosy 3 71 1.299
536
ACR041 Acromelic Frontonasal Dysostosis 53 1.298
537
OST011 Osteomalacia 52 1.287
538
OVR094 Ovarian Epithelial Cancer 39 1.278
539
HYP025 Hyperphosphatemia 47 1.276
540
HYP001 Hypochromic Microcytic Anemia 36 1.273
541
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 1.269
542
PRP080 Peripheral Artery Disease 54 1.264
543
TRG002 Trigeminal Neuralgia 61 1.237
544
ESP002 Esophageal Varix 51 1.233
545
VSC003 Visceral Leishmaniasis 54 1.230
546
P FNC004 Fanconi Syndrome 60 1.223
547
GRD001 Giardiasis 46 1.214
548
FBR054 Fibroma 44 1.209
549
LSC001 Lesch-Nyhan Syndrome 62 1.196
550
P OLG002 Oligodendroglioma 66 1.175
551
P END033 Endocarditis 58 1.172
552
IRR002 Irritable Bowel Syndrome 64 1.167
553
P HLP001 Holoprosencephaly 68 1.163
554
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.153
555
CND006 Candida Glabrata 29 1.147
556
P PSD087 Pseudoxanthoma Elasticum 66 1.147
557
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 1.121
558
P CHN059 Chondrocalcinosis 51 1.102
559
TRC003 Trichomoniasis 53 1.099
560
c ALP101 Alpha-Thalassemia 62 1.085
561
c CRN278 Craniosynostosis 1 55 1.085
562
P TYR004 Tyrosinemia 49 1.079
563
P ATR005 Atrophic Gastritis 50 1.077
564
P CHR012 Chronic Granulomatous Disease 69 1.068
565
c SPN225 Spondyloarthropathy 1 70 1.065
566
MYC019 Mycobacterium Marinum 29 1.064
567
P BRB001 Beriberi 44 1.049
568
EXT006 Extrahepatic Cholestasis 41 1.046
569
PRM020 Premenstrual Tension 39 1.038
570
P HMR003 Hemorrhagic Disease 59 1.037
571
ANC001 Ancylostomiasis 39 1.036
572
HML018 Homologous Wasting Disease 21 1.026
573
HMG002 Hemoglobinuria 50 1.021
574
c GRV008 Graves Disease 1 54 1.021
575
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 1.016
576
VLV047 Volvulus of Midgut 55 1.001
577
P ART005 Arteriovenous Malformation 64 1.000
578
MTR002 Mitral Valve Insufficiency 51 1.000
579
LGN006 Legionnaire Disease 52 0.995
580
HST011 Histoplasmosis 54 0.969
581
GRN017 Granulocytopenia 42 0.954
582
c VSC019 Vesicoureteral Reflux 1 56 0.944
583
P MTC069 Mitochondrial Disorders 57 0.940
584
NNT012 Neonatal Jaundice 53 0.934
585
FND002 Fundus Dystrophy 54 0.931
586
P AXN001 Axonal Neuropathy 33 0.926
587
CCC002 Coccidiosis 50 0.910
588
LST001 Listeriosis 59 0.904
589
INF034 Infective Endocarditis 53 0.889
590
BCT002 Bacterial Vaginosis 52 0.884
591
ETN001 Eating Disorder 59 0.881
592
P DYS193 Dystonia 11, Myoclonic 55 0.877
593
P ERY036 Erythema Nodosum 49 0.857
594
PNC001 Pancytopenia 52 0.854
595
ASB001 Asbestosis 47 0.837
596
ASB003 Asbestos Intoxication 32 0.837
597
PTY002 Pityriasis Versicolor 38 0.836
598
CLF004 Cleft Lip/palate 56 0.818
599
OCC016 Occupational Asthma 33 0.809
600
CYN003 Cyanide Poisoning 22 0.803
601
LCH001 Leech Infestation 37 0.794
602
MCH006 Mechanical Strabismus 40 0.785
603
GSG001 Gas Gangrene 52 0.778
604
P ESS003 Essential Thrombocythemia 68 0.772
605
KLB003 Klebsiella Pneumonia 49 0.770
606
OLG001 Oligospermia 45 0.766
607
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.758
608
ACT119 Acute Promyelocytic Leukemia 62 0.753
609
c INH030 Inherited Retinal Disorder 28 0.752
610
THR016 Thrombophlebitis 50 0.731
611
MLT006 Multidrug-Resistant Tuberculosis 47 0.731
612
P ECT006 Ectodermal Dysplasia 62 0.723
613
PLV003 Pelvic Inflammatory Disease 54 0.723
614
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.711
615
CPR004 Coproporphyria, Hereditary 57 0.700
616
c PRG020 Paragangliomas 3 39 0.676
617
c SPR086 Spermatogenic Failure 3 47 0.672
618
RFR010 Refractory Anemia 49 0.672
619
MRS001 Marasmus 41 0.638
620
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.637
621
APN008 Apnea, Obstructive Sleep 66 0.629
622
PRT013 Portal Hypertension 59 0.584
623
P MTR003 Mitral Valve Stenosis 53 0.581
624
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.576
625
MLD001 Melioidosis 67 0.528
626
HMP005 Hemiplegia 53 0.522
627
PCD001 Pica Disease 38 0.508
628
THR004 Thrombocytosis 52 0.497
629
FLR002 Filariasis 55 0.482
630
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.454
631
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.449
632
P FRD001 Friedreich Ataxia 62 0.449
633
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.435
634
BTT017 Beta-Thalassemia Major 54 0.433
635
HSH003 Hashimoto Thyroiditis 60 0.412
636
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.412
637
P PRR002 Pure Red-Cell Aplasia 46 0.402
638
CRD137 Cardiogenic Shock 56 0.383
639
XLN067 X-Linked Protoporphyria 19 0.372
640
MCR017 Macrocytic Anemia 44 0.358
641
EHR002 Ehrlichiosis 39 0.349
642
FLR001 Filarial Elephantiasis 59 0.349
643
ORL004 Oral Submucous Fibrosis 56 0.320
644
SRT004 Serotonin Syndrome 54 0.320
645
c DRM040 Dermatitis Herpetiformis, Familial 35 0.318
646
GLN002 Glanders 38 0.318
647
P DRM007 Dermatitis Herpetiformis 54 0.318
648
P LCT002 Lactose Intolerance 51 0.306
649
DDN006 Duodenitis 49 0.297
650
ALK013 Alkaptonuria 58 0.289
651
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.289
652
NPH018 Nephrogenic Systemic Fibrosis 48 0.270
653
FBR099 Fibromuscular Dysplasia, Arterial 23 0.268
654
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.241
655
HRN029 Hearing Loss, Noise-Induced 37 0.241
656
DDN010 Duodenum Cancer 51 0.241
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