Search results for Ferrous gluconate

478 hits were found for Ferrous gluconate

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 56 30.436
2
DFC004 Deficiency Anemia 74 25.496
3
IRN001 Iron Deficiency Anemia 58 20.501
4
c CHR684 Chronic Kidney Disease 73 8.298
5
P KDN018 Kidney Disease 71 8.199
6
NTR005 Nutritional Deficiency Disease 60 7.332
7
P INF037 Inflammatory Bowel Disease 53 5.510
8
HMS001 Hemosiderosis 48 5.241
9
P RRH023 Rare Hereditary Hemochromatosis 52 5.238
10
END086 End Stage Renal Disease 54 5.140
11
CNS004 Constipation 56 5.129
12
P PNM007 Pneumonia 64 5.078
13
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.075
14
P PRD008 Periodontitis 63 5.074
15
P TRN020 Turner Syndrome 67 5.073
16
AGN016 Aging 53 4.941
17
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.652
18
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 4.553
19
MLR004 Malaria 77 4.442
20
CYS001 Cystic Fibrosis 77 4.351
21
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 4.344
22
CRH001 Crohn's Disease 80 4.277
23
DWN001 Down Syndrome 70 4.277
24
CMM005 Common Cold 55 4.174
25
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.967
26
CNG034 Congestive Heart Failure 69 3.942
27
P ACN011 Acne 55 3.934
28
P KLZ004 Kala-Azar 1 41 3.890
29
LSH001 Leishmaniasis 63 3.890
30
48X005 48,xyyy 39 3.849
31
P DRR001 Diarrhea 55 3.847
32
HYP005 Hypokalemia 55 3.841
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.748
34
RHB024 Rhabdomyosarcoma 2 65 3.732
35
PRT036 Peritonitis 65 3.667
36
CLT003 Colitis 63 3.639
37
KRT002 Keratomalacia 54 3.604
38
ANT039 Antisynthetase Syndrome 55 3.549
39
VGN023 Vaginitis 56 3.537
40
DRM006 Dermatitis 61 3.516
41
ADL002 Adult Syndrome 69 3.507
42
c TYP009 Type 2 Diabetes Mellitus 91 3.410
43
P ALC033 Alcohol Use Disorder 67 3.364
44
DNT012 Dental Caries 53 3.353
45
c PRD040 Periodontitis, Chronic 52 3.330
46
P HRT032 Heart Disease 84 3.273
47
STR067 Stroke, Ischemic 79 3.238
48
BCT022 Bacterial Infectious Disease 55 3.232
49
VSC003 Visceral Leishmaniasis 54 3.225
50
AND005 Androgen Insensitivity Syndrome, Mild 21 3.220
51
OST012 Osteoarthritis 77 3.199
52
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.126
53
P BRS047 Breast Cancer 97 3.106
54
PRT251 Proteinuria, Chronic Benign 58 3.005
55
P EXN002 Exanthem 58 2.990
56
P PRP029 Porphyria 60 2.971
57
HLX001 Helix Syndrome 47 2.935
58
ULC004 Ulcerative Colitis 74 2.878
59
c ACT068 Acute Cystitis 60 2.869
60
STM007 Stomatitis 52 2.852
61
P URN019 Urinary Tract Infection 48 2.779
62
CNT047 Contact Dermatitis 56 2.734
63
SKN016 Skin Disease 63 2.711
64
PLS007 Plasmodium Falciparum Malaria 52 2.690
65
ALL029 Allergic Disease 61 2.659
66
HMN044 Human Immunodeficiency Virus Type 1 76 2.634
67
P CLR023 Colorectal Cancer 100 2.606
68
ISC004 Ischemia 61 2.586
69
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.561
70
ACQ007 Acquired Immunodeficiency Syndrome 58 2.559
71
P INT068 Intestinal Disease 53 2.510
72
P HDC001 Headache 56 2.510
73
P RSP003 Respiratory Failure 73 2.485
74
P PNC044 Pancreatitis 61 2.471
75
P DBT009 Diabetes Mellitus 67 2.468
76
CRV035 Cervical Cancer 72 2.467
77
P PRP003 Porphyria Cutanea Tarda 66 2.442
78
CRH005 Crohn's Colitis 53 2.438
79
P HYP086 Hypothyroidism 68 2.423
80
P ANR048 Aniridia 1 66 2.420
81
MYL069 Myeloma, Multiple 76 2.408
82
HRW001 Hair Whorl 35 2.384
83
DYS073 Dysphagia 53 2.328
84
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.280
85
GLS018 Glass Syndrome 60 2.276
86
P ANP001 Anaplastic Large Cell Lymphoma 59 2.225
87
HYP266 Hypoxia 56 2.222
88
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.195
89
SCH014 Schistosomiasis 56 2.195
90
P GRF003 Graft-Versus-Host Disease 71 2.144
91
HYP781 Hypoascorbemia 52 2.140
92
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.134
93
P OST002 Osteoporosis 76 2.134
94
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.134
95
THR024 Thrombosis 56 2.089
96
HYP066 Hyperglycemia 60 2.082
97
P DMN002 Dementia 65 2.079
98
P GLM040 Glioma Susceptibility 1 70 2.042
99
RCK004 Rickets 64 2.030
100
P LYM118 Lymphoma 66 1.990
101
LYM019 Lymphosarcoma 46 1.990
102
P KHL003 Kohlschutter-Tonz Syndrome 57 1.976
103
c ACT027 Acute Pancreatitis 60 1.969
104
c ACT073 Acute Leukemia 59 1.933
105
P INF032 Infertility 60 1.928
106
PLS009 Plasma Cell Neoplasm 64 1.926
107
HMP009 Haemophilus Influenzae 41 1.923
108
GLB002 Glioblastoma 67 1.873
109
c MGR028 Migraine with or Without Aura 1 63 1.847
110
BNR002 Bone Resorption Disease 47 1.841
111
c HMP029 Hemophilia a 69 1.839
112
ACT011 Acute Contagious Conjunctivitis 41 1.839
113
P CNJ013 Conjunctivitis 66 1.839
114
VSC002 Vascular Dementia 59 1.839
115
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.839
116
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.839
117
P ART022 Arthritis 70 1.827
118
BRN004 Brain Edema 54 1.807
119
P LKM062 Leukemia, Acute Lymphoblastic 69 1.791
120
P ESP024 Esophagitis 60 1.788
121
P GST044 Gastritis 55 1.766
122
P CLC063 Celiac Disease 1 65 1.752
123
P THL005 Thalassemia 56 1.751
124
CVD001 Covid-19 59 1.749
125
P ADL010 Adult Respiratory Distress Syndrome 70 1.720
126
P LKM002 Leukemia 65 1.717
127
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.716
128
P NRB001 Neuroblastoma 66 1.716
129
P MSC005 Muscular Dystrophy 66 1.715
130
c ACT071 Acute Kidney Failure 60 1.713
131
FTT001 Fatty Liver Disease 61 1.700
132
P LVR013 Liver Disease 68 1.694
133
P RST001 Restless Legs Syndrome 52 1.685
134
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.673
135
CHL079 Children's Interstitial Lung Disease 25 1.673
136
P HYP069 Hyperparathyroidism 62 1.664
137
ACT058 Active Peptic Ulcer Disease 55 1.649
138
GST023 Gastric Ulcer 52 1.636
139
WLS001 Wilson Disease 70 1.633
140
PRT037 Pertussis 49 1.633
141
CHL014 Cholera 62 1.616
142
P PNC035 Pancreatic Cancer 87 1.615
143
c HMC039 Hemochromatosis, Type 1 73 1.612
144
SVR001 Severe Acute Respiratory Syndrome 68 1.612
145
P CRN300 Coronary Heart Disease 1 73 1.592
146
IRR003 Irritant Dermatitis 47 1.581
147
SYN036 Syncope 44 1.581
148
P CRD246 Cardiovascular System Disease 55 1.575
149
c ATS007 Autism Spectrum Disorder 71 1.571
150
P ATS364 Autism 72 1.571
151
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.565
152
P RHM011 Rheumatoid Arthritis 81 1.562
153
ANX004 Anoxia 40 1.550
154
P ALP008 Alopecia 53 1.547
155
P PHC003 Pheochromocytoma 70 1.542
156
ADR040 Adrenal Gland Pheochromocytoma 45 1.542
157
P NRP001 Neuropathy 59 1.539
158
PLM033 Pulmonary Embolism 58 1.524
159
STN013 Stenotrophomonas Maltophilia Infection 26 1.523
160
ALV001 Alveolar Periostitis 34 1.520
161
P END044 Endometriosis 62 1.515
162
P SLM003 Salmonellosis 54 1.510
163
OST017 Osteomyelitis 63 1.492
164
P PRK039 Parkinsonism 55 1.486
165
P HPT023 Hepatocellular Carcinoma 95 1.478
166
GST045 Gastroenteritis 58 1.470
167
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.466
168
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.464
169
ALL010 Allergic Contact Dermatitis 55 1.445
170
c DRR009 Diarrhea 6 46 1.439
171
MNT002 Mental Depression 56 1.424
172
DPR016 Depression 64 1.424
173
PLM001 Pulmonary Tuberculosis 69 1.418
174
BRN071 Brain Injury 50 1.417
175
P OVR042 Ovarian Cancer 88 1.403
176
P HMR005 Hemorrhoid 49 1.401
177
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.399
178
c BLD140 Blood Group, I System 47 1.399
179
P THR014 Thrombocytopenia 66 1.387
180
ANX010 Anxiety 70 1.385
181
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.383
182
BRN024 Bronchitis 67 1.380
183
CHL068 Cholestasis 61 1.378
184
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.370
185
OST062 Osteoarthritis with Mild Chondrodysplasia 46 1.365
186
P MLN008 Melanoma 75 1.356
187
DSS032 Disease by Infectious Agent 55 1.349
188
P SHR001 Short Bowel Syndrome 53 1.315
190
TRM010 Traumatic Brain Injury 50 1.292
191
LVR012 Liver Cirrhosis 62 1.291
192
P SDR002 Siderosis 42 1.286
193
P HML002 Hemolytic Anemia 62 1.276
194
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 1.264
195
c EXD008 Exudative Vitreoretinopathy 1 71 1.259
196
CHL123 Chlamydia 58 1.247
197
P HRP006 Herpes Simplex 65 1.247
198
KRT009 Keratosis 52 1.246
199
ESP021 Esophageal Cancer 84 1.234
200
SPN186 Spinal Cord Injury 60 1.234
201
P VNS003 Venous Insufficiency 54 1.228
202
VGN019 Vaginal Discharge 33 1.223
203
c THR092 Thrombophilia Due to Thrombin Defect 74 1.219
204
P SCK005 Sickle Cell Disease 56 1.218
205
TTN003 Tetanus 64 1.217
206
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.213
207
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.213
208
ACR041 Acromelic Frontonasal Dysostosis 53 1.213
209
49X006 49, Xxxxy Syndrome 40 1.213
210
P URT039 Urticaria 57 1.205
211
PRS047 Prostatitis 57 1.191
212
SWL001 Swallowing Disorders 37 1.188
213
HLC007 Helicobacter Pylori Infection 67 1.186
214
NPH009 Nephrolithiasis 54 1.178
215
P HPT021 Hepatitis 68 1.170
216
P LNG032 Lung Cancer 98 1.164
217
TLN003 Telangiectasis 51 1.157
218
HYP006 Hypertensive Heart Disease 48 1.152
219
CRB039 Cerebrovascular Disease 65 1.151
220
P PRS040 Prostate Cancer 95 1.150
221
PST092 Posttransplant Acute Limbic Encephalitis 29 1.143
222
GST050 Gastrointestinal System Disease 55 1.138
223
SKN019 Skin Melanoma 70 1.134
224
CND006 Candida Glabrata 29 1.132
225
PPL052 Papillomatosis, Confluent and Reticulated 34 1.131
226
HYP017 Hypophosphatemia 49 1.128
227
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.126
228
P PLM037 Pulmonary Hypertension 69 1.117
229
c PRG106 Progressive Muscular Dystrophy 31 1.108
230
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.106
231
c PNS012 Paine Syndrome 60 1.106
232
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.106
233
OTT002 Otitis Media 70 1.104
234
P TRM003 Tremor 50 1.089
235
MTB004 Metabolic Acidosis 48 1.084
236
OST011 Osteomalacia 52 1.081
237
OCL069 Ocular Motor Apraxia 57 1.078
238
ART140 Arteries, Anomalies of 52 1.076
239
LPP008 Lipoprotein Quantitative Trait Locus 65 1.076
240
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.073
241
P BCL017 B-Cell Lymphoma 57 1.068
242
URM002 Uremia 47 1.067
243
c HPT003 Hepatitis a 63 1.065
244
RTR008 Root Resorption 44 1.058
245
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.033
246
GST033 Gestational Diabetes 60 1.024
247
TXC005 Toxic Shock Syndrome 61 1.022
248
HYP056 Hypoglycemia 65 1.021
249
PRP083 Porphyria, Acute Intermittent 64 0.981
250
ATM095 Autoimmune Disease 61 0.981
251
c MCR133 Microvascular Complications of Diabetes 4 41 0.977
252
c MCR113 Microvascular Complications of Diabetes 3 52 0.977
253
c MCR130 Microvascular Complications of Diabetes 6 41 0.977
254
c MCR120 Microvascular Complications of Diabetes 7 47 0.977
255
ENT011 Enterocolitis 55 0.973
256
URL001 Urolithiasis 45 0.971
257
c LKM061 Leukemia, Acute Myeloid 83 0.970
258
P ADN016 Adenocarcinoma 63 0.970
259
PSD088 Pseudobulbar Affect 33 0.969
260
P CHR345 Chronic Pain 50 0.969
261
P END047 Endophthalmitis 53 0.962
262
c PCH010 Pachyonychia Congenita 3 43 0.950
263
TRY001 Trypanosomiasis 50 0.947
264
SLP001 Sleeping Sickness 56 0.947
265
FCL012 Facial Paralysis 49 0.940
266
BLR008 Bilirubin Metabolic Disorder 57 0.939
267
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.928
268
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.920
269
PPT005 Peptic Ulcer Disease 58 0.919
270
CRB090 Cerebral Hypoxia 42 0.919
271
P DRM053 Dermatitis, Atopic 65 0.902
272
PRN019 Perinatal Necrotizing Enterocolitis 60 0.898
273
P FBR017 Fibrosarcoma 55 0.897
274
P PRP019 Peripheral Nervous System Disease 57 0.892
275
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.891
276
c SYS001 Systemic Lupus Erythematosus 85 0.887
277
P LPS004 Lupus Erythematosus 61 0.887
278
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 54 0.887
279
c HPT001 Hepatitis C 61 0.887
280
c VRL010 Viral Hepatitis 52 0.887
281
CLN015 Colon Adenocarcinoma 64 0.886
282
P ALZ034 Alzheimer Disease 87 0.883
283
c ACT075 Acute Myocardial Infarction 55 0.880
284
c ATR087 Atrial Standstill 1 74 0.875
285
CYT002 Cytokine Deficiency 43 0.875
286
GRN017 Granulocytopenia 42 0.874
287
P MYC007 Myocardial Infarction 69 0.869
288
P ECL001 Eclampsia 52 0.865
289
P MYS003 Myasthenia Gravis 67 0.859
290
P PLY011 Polycystic Ovary Syndrome 57 0.845
291
P NTR004 Neutropenia 62 0.839
292
P BND020 Bone Disease 60 0.836
293
GLS007 Glossitis 46 0.831
294
P PRV006 Pervasive Developmental Disorder 52 0.830
295
c BRN108 Branchiootic Syndrome 1 63 0.818
296
PST011 Pustulosis of Palm and Sole 52 0.815
297
P PSR002 Psoriasis 63 0.815
298
HYP025 Hyperphosphatemia 47 0.811
299
P SZR006 Seizure Disorder 69 0.805
300
P PTS002 Ptosis 52 0.798
301
P RHN004 Rhinitis 56 0.798
302
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.782
303
ALK024 Alkuraya-Kucinskas Syndrome 46 0.782
304
c PRM108 Primary Progressive Multiple Sclerosis 51 0.782
305
c ART144 Arthrogryposis, Distal, Type 1a 61 0.782
306
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.782
307
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.782
308
c VTM027 Vitamin D-Dependent Rickets, Type 2a 54 0.782
309
P SPP010 Suppressor of Tumorigenicity 3 50 0.782
310
P DST002 Distal Arthrogryposis 63 0.782
311
P CRV039 Cervicitis 52 0.782
312
PSY004 Psychotic Disorder 66 0.782
313
HNT002 Hantavirus Pulmonary Syndrome 55 0.782
314
NNN007 Non-Involuting Congenital Hemangioma 40 0.782
315
CNG506 Congenital Amyoplasia 27 0.782
316
CLC001 Calciphylaxis 50 0.756
317
P MVM001 Movement Disease 61 0.749
318
c SPN225 Spondyloarthropathy 1 70 0.740
319
P ENC018 Encephalopathy 62 0.732
320
P MJR001 Major Depressive Disorder 68 0.719
321
c PRC016 Pre-Eclampsia 64 0.719
322
BCT004 Bacteriuria 48 0.710
323
P MTH007 Methemoglobinemia 46 0.709
324
PLV003 Pelvic Inflammatory Disease 54 0.705
325
GTR002 Goiter 52 0.704
326
THY029 Thyroid Carcinoma 55 0.702
327
PRT038 Protein-Energy Malnutrition 53 0.701
328
GST092 Gastroesophageal Reflux 59 0.687
329
ATH013 Atherosclerosis Susceptibility 63 0.663
330
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.658
331
MLD018 Mild Cognitive Impairment 48 0.650
332
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.650
333
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.650
334
MYL009 Myelodysplastic Syndrome 67 0.644
335
c TYP008 Type 1 Diabetes Mellitus 77 0.644
336
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.638
337
ANG054 Angina Pectoris 65 0.625
338
LPT014 Leptin Deficiency or Dysfunction 77 0.625
339
IRR002 Irritable Bowel Syndrome 64 0.616
340
47X002 47,xyy 47 0.615
341
P MYC033 Myoclonus 46 0.601
342
P HNT016 Huntington Disease 73 0.588
343
P VSC007 Vascular Disease 62 0.583
344
PPL022 Papilloma 53 0.582
345
SQM002 Squamous Cell Papilloma 45 0.582
346
NNT012 Neonatal Jaundice 53 0.579
347
DBT010 Diabetic Neuropathy 54 0.574
348
VTM002 Vitamin B12 Deficiency 48 0.566
349
P PRK057 Parkinson Disease, Late-Onset 79 0.566
350
c DWL002 Dowling-Degos Disease 1 58 0.541
351
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.541
352
P LTR001 Lateral Sclerosis 57 0.541
353
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.539
354
HRN029 Hearing Loss, Noise-Induced 37 0.535
355
P CTR002 Cataract 59 0.529
356
P NSP012 Nasopharyngeal Carcinoma 60 0.523
357
LNG099 Lung Disease 62 0.513
358
NNL006 Non-Alcoholic Steatohepatitis 54 0.480
359
SQM006 Squamous Cell Carcinoma 59 0.480
360
CRC021 Carcinosarcoma 62 0.480
361
INS001 Insulinoma 59 0.476
362
P BNG032 Benign Mesothelioma 53 0.466
363
PLG002 Plague 58 0.460
364
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.455
365
P LCT001 Lactic Acidosis 50 0.454
366
ATS010 Autosomal Recessive Disease 42 0.440
367
FBR054 Fibroma 44 0.436
368
HMC014 Homocysteinemia 52 0.436
369
ART002 Arts Syndrome 66 0.436
370
URT001 Urethritis 52 0.436
371
P SBS003 Substance Abuse 54 0.436
372
RSC001 Rosacea 55 0.436
373
CYT018 Cytochrome P450 2d6 Variant 26 0.436
374
INT007 Intermediate Coronary Syndrome 53 0.436
375
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.436
377
BNG077 Benign Idiopathic Neonatal Seizures 23 0.436
378
GLM045 Glioma 62 0.435
379
GLL048 Glial Tumor 51 0.435
380
c GRV008 Graves Disease 1 54 0.430
381
P DDN001 Duodenal Ulcer 52 0.420
382
P AMY004 Amyloidosis 69 0.402
383
c MST023 Mesothelioma, Malignant 56 0.399
384
SPL018 Splenomegaly 47 0.388
385
HDN002 Head Injury 44 0.388
386
P ART023 Arthropathy 59 0.380
387
PNC001 Pancytopenia 52 0.378
388
NRL016 Neural Tube Defects 80 0.360
389
P LPR021 Leprosy 3 71 0.360
390
HNS001 Hansen's Disease 32 0.360
391
CLR109 Colorectal Adenocarcinoma 50 0.359
392
ACT098 Acute Erythroid Leukemia 55 0.359
393
P THY032 Thyroiditis 56 0.357
394
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.354
395
P SYS005 Systemic Scleroderma 73 0.354
396
DYS015 Dysentery 49 0.337
397
BRC012 Brucellosis 66 0.327
398
PNC129 Pancreatic Adenocarcinoma 64 0.326
399
P HYP265 Hypotonia 42 0.326
400
P BLD134 Bladder Cancer 79 0.312
401
DSS009 Disseminated Intravascular Coagulation 56 0.312
402
MGL001 Megaloblastic Anemia 59 0.312
403
ANT024 Anthrax Disease 57 0.311
404
c VSC019 Vesicoureteral Reflux 1 56 0.294
405
OST159 Osteogenic Sarcoma 66 0.294
406
CHR100 Chronic Ulcer of Skin 57 0.294
407
CHL065 Cholangiocarcinoma 57 0.294
408
HPT019 Hepatic Encephalopathy 59 0.294
409
P GLM007 Glomerulonephritis 59 0.294
410
INT079 Intrahepatic Cholangiocarcinoma 51 0.294
411
PRT013 Portal Hypertension 59 0.294
412
HPT004 Hepatic Coma 43 0.294
413
SPS057 Spasticity 43 0.294
415
THR004 Thrombocytosis 52 0.284
416
PCD001 Pica Disease 38 0.284
417
RHM001 Rheumatic Fever 59 0.284
418
PRM020 Premenstrual Tension 39 0.284
419
CLF027 Cleft Palate, Isolated 64 0.283
420
P PLY014 Polycystic Kidney Disease 71 0.283
421
LPD008 Lipid Metabolism Disorder 61 0.283
422
THY030 Thyroid Gland Disease 50 0.283
423
ORL015 Oral Squamous Cell Carcinoma 43 0.251
424
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.251
425
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.251
426
P ART005 Arteriovenous Malformation 64 0.251
427
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.250
428
MLD001 Melioidosis 67 0.250
429
IGR001 Ige Responsiveness, Atopic 58 0.250
430
PRP030 Purpura 54 0.250
431
BCT002 Bacterial Vaginosis 52 0.250
432
STT001 Status Epilepticus 58 0.250
433
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.250
434
P MYL006 Myeloid Leukemia 60 0.250
435
DDN006 Duodenitis 49 0.250
436
ORL011 Oral Cancer 60 0.250
437
INF034 Infective Endocarditis 53 0.208
438
CLL021 Collagenous Colitis 41 0.208
439
c WLM013 Wilms Tumor 1 65 0.208
440
PLY150 Polykaryocytosis Inducer 29 0.208
441
SPP011 Suppression of Tumorigenicity 12 61 0.208
442
c DRM040 Dermatitis Herpetiformis, Familial 35 0.208
443
BRT054 Brittle Bone Disorder 74 0.208
444
HSH003 Hashimoto Thyroiditis 60 0.208
445
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.208
446
MYL005 Myelofibrosis 70 0.208
447
PHN003 Phenylketonuria 76 0.208
448
c LKM063 Leukemia, Chronic Myeloid 70 0.208
449
BRK010 Burkitt Lymphoma 65 0.208
450
PPL002 Papillary Carcinoma 46 0.208
451
HYP014 Hyperuricemia 51 0.208
452
TRC003 Trichomoniasis 53 0.208
453
FBR047 Fibromyalgia 57 0.208
454
P EPL164 Epilepsy 70 0.208
455
P CRN026 Corneal Edema 42 0.208
456
P END033 Endocarditis 58 0.208
457
BRN002 Bronchiolitis 57 0.208
458
THR016 Thrombophlebitis 50 0.208
459
P ANG015 Angioedema 56 0.208
460
P BRS044 Breast Adenocarcinoma 58 0.208
461
MRS001 Marasmus 41 0.208
462
P FNC004 Fanconi Syndrome 60 0.208
463
P UVT001 Uveitis 57 0.208
464
ACT003 Acute Kidney Tubular Necrosis 46 0.208
465
P DRM007 Dermatitis Herpetiformis 54 0.208
466
P RBL001 Rubella 58 0.208
467
P HYP083 Hypopituitarism 51 0.208
468
P MNC007 Monocytic Leukemia 48 0.208
469
MYC019 Mycobacterium Marinum 29 0.208
470
MSL001 Measles 61 0.208
471
ETN001 Eating Disorder 59 0.208
472
HML018 Homologous Wasting Disease 21 0.208
473
GRW007 Growth Hormone Deficiency 47 0.208
474
RFR010 Refractory Anemia 49 0.208
475
SRT004 Serotonin Syndrome 54 0.208
476
c ACT134 Acute Liver Failure 57 0.208
477
CRD137 Cardiogenic Shock 56 0.208
478
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.208
Content
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