Search results for "Sodium bicarbonate"

297 hits were found for 'Sodium bicarbonate'

# Family MCID Name MIFTS Score
1
P KDN018 Kidney Disease 66 0.243
2
P URF003 Urofacial Syndrome 1 50 0.233
3
URN009 Urinary System Disease 50 0.232
4
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.225
5
IMP003 Impaired Renal Function Disease 34 0.216
6
MTB004 Metabolic Acidosis 48 0.210
7
c CHR089 Chronic Kidney Failure 66 0.165
8
P PNC044 Pancreatitis 61 0.164
9
c ACT071 Acute Kidney Failure 49 0.161
10
CYS001 Cystic Fibrosis 83 0.149
11
PRT036 Peritonitis 63 0.145
12
END030 End Stage Renal Failure 55 0.144
13
c CRN214 Coronary Heart Disease 5 22 0.138
14
P CRN178 Coronary Heart Disease 6 21 0.135
15
P HRT032 Heart Disease 75 0.127
16
NRN002 Neuronitis 41 0.125
17
DDN006 Duodenitis 42 0.125
18
P RSP003 Respiratory Failure 71 0.118
19
c CRN175 Coronary Heart Disease 4 19 0.118
20
RNL007 Renal Tubular Acidosis 50 0.117
21
c CRN172 Coronary Heart Disease 3 19 0.113
22
MTH009 Mouth Disease 61 0.110
23
c HYP595 Hypertension, Essential 69 0.108
24
P MYP004 Myopathy 67 0.108
25
P RNL015 Renal Hypertension 48 0.106
26
NTR005 Nutritional Deficiency Disease 36 0.101
27
MSC004 Muscle Tissue Disease 34 0.101
28
CRD119 Cardiac Arrest 61 0.101
29
P MSC033 Muscle Disorders 52 0.100
30
RNL097 Renal Artery Disease 43 0.099
31
P EPL164 Epilepsy 66 0.099
32
ISC004 Ischemia 61 0.098
33
c PND001 Pain Disorder 54 0.097
34
c AST037 Asthma 1 29 0.095
35
P OST002 Osteoporosis 64 0.094
36
GST092 Gastroesophageal Reflux 62 0.093
37
GNG013 Gingivitis 61 0.093
38
P INF032 Infertility 59 0.093
39
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.093
40
P CNJ013 Conjunctivitis 64 0.093
41
c AST039 Asthma 2 28 0.092
42
CNG034 Congestive Heart Failure 72 0.092
43
GST050 Gastrointestinal System Disease 56 0.088
44
ALL026 Allergic Hypersensitivity Disease 52 0.088
45
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.088
46
c RNL016 Renal Infectious Disease 20 0.087
47
MCS002 Mucositis 55 0.087
48
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.087
49
P AST005 Asthma 82 0.087
50
HYP266 Hypoxia 56 0.087
51
BNS002 Bone Structure Disease 37 0.087
52
MNR003 Mineral Metabolism Disease 38 0.086
53
c CRN174 Coronary Heart Disease 2 20 0.085
54
PLP001 Pulpitis 47 0.084
55
END072 Endotheliitis 42 0.084
56
TTH006 Tooth Disease 52 0.084
57
P ART022 Arthritis 75 0.083
58
P LKM002 Leukemia 71 0.083
59
P PLM037 Pulmonary Hypertension 79 0.082
60
P MYC007 Myocardial Infarction 79 0.080
61
NRM005 Neuromuscular Disease 56 0.080
62
P MSC003 Muscular Atrophy 50 0.078
63
VND001 Vein Disease 47 0.078
64
RHM027 Rheumatic Disease 58 0.077
65
SKN016 Skin Disease 66 0.076
66
c CRN173 Coronary Heart Disease 8 18 0.076
67
P LCT001 Lactic Acidosis 51 0.076
68
P DRR001 Diarrhea 60 0.075
69
STM006 Stomach Disease 50 0.075
70
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.075
71
P GST049 Gastrointestinal System Cancer 60 0.074
72
APH001 Aphthous Stomatitis 62 0.074
73
HYP005 Hypokalemia 51 0.073
74
P LYM118 Lymphoma 69 0.073
75
RSP006 Respiratory System Disease 58 0.072
76
P ATR011 Atrial Fibrillation 66 0.072
77
ESP023 Esophageal Disease 54 0.072
78
SKN027 Skin Conditions 43 0.072
79
PRS047 Prostatitis 56 0.071
80
ORL011 Oral Cancer 56 0.071
81
P CRN211 Coronary Artery Disease 74 0.071
82
BLD054 Blood Protein Disease 37 0.071
83
P PNC035 Pancreatic Cancer 87 0.070
84
P ORL007 Oral Cavity Cancer 59 0.070
85
EYD002 Eye Disease 61 0.070
86
ACD009 Acid-Labile Subunit, Deficiency of 45 0.070
87
GLC008 Glucose Metabolism Disease 42 0.070
88
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.070
89
c CRN177 Coronary Heart Disease 7 20 0.070
90
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.069
91
LPD008 Lipid Metabolism Disorder 58 0.069
92
ART111 Artery Disease 55 0.069
93
SWL001 Swallowing Disorders 33 0.069
94
ATR076 Atrophic Muscular Disease 15 0.069
95
ADL002 Adult Syndrome 52 0.068
96
DYS073 Dysphagia 48 0.068
97
GLT021 Glutaricaciduria, Type I 46 0.068
98
CTS003 Coats Disease 57 0.068
99
SLP005 Sleep Disorder 53 0.068
100
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.067
101
ART017 Aortic Disease 57 0.067
102
STT002 Status Asthmaticus 42 0.067
103
STR067 Stroke, Ischemic 75 0.066
104
ISC006 Ischemic Heart Disease 68 0.066
105
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.066
106
c ACT075 Acute Myocardial Infarction 60 0.065
107
DYS011 Dyskinesia of Esophagus 28 0.065
108
ETH011 Ethylmalonic Encephalopathy 56 0.065
109
CLC006 Calcinosis 50 0.065
110
BRT030 Birth Defects 43 0.065
111
P CHR345 Chronic Pain 50 0.064
112
ATN002 Autonomic Nervous System Disease 48 0.064
113
c TRC078 Trichohepatoenteric Syndrome 2 29 0.064
114
ADN018 Adenoma 58 0.063
115
HDC001 Headache 54 0.063
116
ACR041 Acromelic Frontonasal Dysostosis 45 0.063
117
BNR001 Bone Remodeling Disease 37 0.063
118
P PLM036 Pulmonary Fibrosis 71 0.063
119
PLM010 Pulmonary Edema 54 0.063
120
PHY002 Physical Disorder 43 0.063
121
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.063
122
CRB009 Cerebritis 39 0.063
123
P PRX033 Proximal Renal Tubular Acidosis 35 0.062
124
c FML001 Familial Atrial Fibrillation 58 0.062
125
PNC034 Pancreas Disease 58 0.062
126
GNG011 Gingival Disease 46 0.062
127
ACT058 Active Peptic Ulcer Disease 43 0.062
128
c PNC106 Pancreatic Agenesis 1 37 0.062
129
P KDN017 Kidney Cancer 65 0.062
130
GST045 Gastroenteritis 59 0.062
131
P OBS005 Obesity 92 0.061
132
PCK002 Pick Disease 68 0.061
133
P PNM007 Pneumonia 68 0.061
134
P HYP086 Hypothyroidism 64 0.061
135
P FML187 Familial Hypertension 38 0.061
136
ADJ001 Adjustment Disorder 38 0.061
137
P RTN016 Retinal Degeneration 54 0.060
138
BLD053 Blood Platelet Disease 46 0.060
139
KND001 Kindler Syndrome 57 0.059
140
P MMB011 Membranous Nephropathy 54 0.059
141
STM007 Stomatitis 50 0.059
142
P FNC004 Fanconi Syndrome 49 0.059
143
c MCR113 Microvascular Complications of Diabetes 3 45 0.059
144
P INT068 Intestinal Disease 60 0.059
145
OCL009 Ocular Cancer 59 0.059
146
BNF002 Bone Fracture 50 0.059
147
ALN001 Aland Island Eye Disease 45 0.059
148
VSC008 Vascular Hemostatic Disease 30 0.059
149
VSC006 Vascular Cancer 51 0.058
150
CRN024 Corneal Disease 44 0.058
151
CRB031 Cerebral Arterial Disease 27 0.058
152
P DDN001 Duodenal Ulcer 50 0.058
153
P RNL017 Renal Oncocytoma 47 0.058
154
P HYP120 Hypoaldosteronism 36 0.058
155
P ACT080 Acute Pulmonary Heart Disease 31 0.058
156
P NPH009 Nephrolithiasis 60 0.057
157
CHL071 Child Syndrome 58 0.057
158
GST023 Gastric Ulcer 56 0.057
159
KDS001 Kid Syndrome 53 0.057
160
P PLY014 Polycystic Kidney Disease 53 0.057
161
RTN023 Retinitis 50 0.057
162
CSY001 C Syndrome 50 0.057
163
AYM001 Ayme-Gripp Syndrome 41 0.057
164
TXC005 Toxic Shock Syndrome 60 0.057
165
PRT030 Parathyroid Gland Disease 47 0.057
166
HMT002 Hematologic Cancer 64 0.056
167
P TRC086 Trichohepatoenteric Syndrome 1 48 0.056
168
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.056
169
PRD011 Proud Syndrome 42 0.056
170
P RNL014 Renal Cell Carcinoma 82 0.055
171
LRN003 Learning Disability 49 0.055
172
CNT025 Central Pontine Myelinolysis 41 0.055
173
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.055
174
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.055
175
ACT084 Acute Stress Disorder 40 0.055
176
ESP021 Esophageal Cancer 76 0.054
177
RNL101 Renal Cell Carcinoma, Papillary 63 0.054
178
P ESP024 Esophagitis 61 0.054
179
BRN071 Brain Injury 52 0.054
180
LPD004 Lipoid Nephrosis 48 0.054
181
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.054
182
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.054
183
P END033 Endocarditis 54 0.053
184
P HYP024 Hypoparathyroidism 53 0.053
185
C3D001 C3 Deficiency 53 0.053
186
IMM136 Immune System Disease 51 0.053
187
NPH003 Nephrocalcinosis 48 0.053
188
HDN002 Head Injury 45 0.053
189
SPC003 Specific Developmental Disorder 38 0.053
190
ALR002 Al-Raqad Syndrome 36 0.053
191
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.053
192
ENM002 Enamel Erosion 26 0.053
193
c ACT210 Acute Respiratory Distress Syndrome 57 0.052
194
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.052
195
LYM019 Lymphosarcoma 53 0.052
196
THY030 Thyroid Gland Disease 48 0.052
197
CRD118 Cardiovascular Cancer 44 0.052
198
P BLD051 Blood Coagulation Disease 42 0.052
199
c CRN176 Coronary Heart Disease 9 18 0.052
200
LGD001 Leg Dermatosis 16 0.052
201
P VNS003 Venous Insufficiency 54 0.052
202
CRB090 Cerebral Hypoxia 45 0.052
203
P ART084 Arteriovenous Fistula 44 0.052
204
EXR007 Exercise-Induced Anaphylaxis 24 0.052
205
P CLR108 Colorectal Adenoma 60 0.051
206
FDL002 Food Allergy 53 0.051
207
GST078 Gastrointestinal Allergy 40 0.051
208
BND014 Bone Development Disease 40 0.051
209
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.051
210
ACR002 Acrocapitofemoral Dysplasia 33 0.051
211
P CTR002 Cataract 58 0.050
212
TRM010 Traumatic Brain Injury 52 0.050
213
UPP004 Upper Respiratory Tract Disease 46 0.050
214
RDN001 Reading Disorder 34 0.050
215
HYP114 Hypertensive Nephropathy 33 0.050
216
INF034 Infective Endocarditis 51 0.050
217
c CHR431 Chronic Venous Insufficiency 44 0.050
218
PLS009 Plasma Cell Neoplasm 48 0.049
219
SDD007 Sudden Cardiac Death 47 0.049
220
CRB025 Carbohydrate Metabolic Disorder 46 0.049
221
INS024 Insulin-Like Growth Factor I 75 0.047
222
MTR014 Motor Neuron Disease 58 0.047
223
P HMR003 Hemorrhagic Disease 57 0.047
224
PTH002 Pathological Gambling 51 0.047
225
P FML035 Familial Hyperlipidemia 48 0.047
226
BNM008 Bone Mineral Density, Low 16 0.047
227
AQG001 Aquagenic Pruritus 15 0.047
228
P HYP117 Hypertriglyceridemia 61 0.046
229
DNT012 Dental Caries 46 0.046
230
P CRD132 Cardiac Conduction Defect 43 0.046
231
CPL005 Capillary Disease 36 0.046
232
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.046
233
DDN007 Duodenal Disease 33 0.046
234
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.046
235
P MLT019 Multiple Myeloma 83 0.044
236
MLT021 Multiple System Atrophy 70 0.044
237
ANR040 Aneurysm 57 0.044
238
MYC002 Mycobacterium Avium Complex Disease 52 0.044
239
GNR004 Generalized Anxiety Disorder 51 0.044
240
DYS014 Dyspepsia 50 0.044
241
CHL061 Childhood Leukemia 49 0.044
242
LKC003 Leukocyte Disease 43 0.044
243
CHR413 Chronic Myocardial Ischemia 41 0.044
244
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 38 0.044
245
LNS003 Lens Disease 33 0.044
246
DNT014 Dental Pulp Disease 31 0.044
247
BNR002 Bone Resorption Disease 21 0.044
248
ART016 Aortic Aneurysm 69 0.043
249
PPT005 Peptic Ulcer Disease 58 0.043
250
ASP007 Aspiration Pneumonia 47 0.043
251
CML001 Cumulative Trauma Disorders 18 0.043
252
CYS013 Cystinuria 63 0.041
253
P CND004 Candidiasis 57 0.041
254
ORL005 Oral Candidiasis 48 0.041
255
c HMG001 Hemoglobin C Disease 47 0.041
256
VST004 Vestibular Disease 44 0.041
257
BLR008 Bilirubin Metabolic Disorder 42 0.041
258
c CNG031 Congenital Nervous System Abnormality 37 0.041
259
SCR003 Secretory Diarrhea 36 0.041
260
CMP006 Complex Partial Epilepsy 30 0.041
261
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.039
262
OST016 Osteochondrosis 50 0.039
263
ANX004 Anoxia 43 0.039
264
BLP005 Blepharitis 40 0.039
265
c PRG001 Progressive Muscular Atrophy 39 0.039
266
PPT001 Peptic Esophagitis 35 0.039
267
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.039
268
RNL026 Renal Tubular Acidosis with Deafness 26 0.039
269
HYP226 Hyporeninemic Hypoaldosteronism 23 0.039
270
P LGH007 Leigh Syndrome 70 0.037
271
CHL068 Cholestasis 59 0.037
272
NNT012 Neonatal Jaundice 50 0.037
273
NRL004 Neuroleptic Malignant Syndrome 41 0.037
274
SKN005 Skin Atrophy 40 0.037
275
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.037
276
c ACT004 Acute Diarrhea 39 0.037
277
P ACQ009 Acquired Metabolic Disease 38 0.037
278
CRN197 Coronary Arterial Fistulas 23 0.037
279
MCC011 Mucociliary Clearance Disorder 16 0.037
280
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.033
281
LWS003 Lowe Syndrome 61 0.033
282
P CMR001 Camurati-Engelmann Disease 58 0.033
283
P HRD011 Hereditary Spherocytosis 54 0.033
284
P ACT105 Acute Mountain Sickness 52 0.033
285
PSD007 Pseudomyxoma Peritonei 48 0.033
286
PYL006 Pyloric Stenosis 46 0.033
287
UNV001 Unverricht-Lundborg Syndrome 41 0.033
288
STT004 Steatorrhea 40 0.033
289
c EPL121 Epilepsy, Progressive Myoclonic 1a 39 0.033
290
GST007 Gastric Dilatation 38 0.033
291
HYP231 Hypothalamic Hamartomas 34 0.033
292
CHR028 Chronic Wasting Disease 34 0.033
293
SCC010 Succinyl Coa:3-Oxoacid Coa Transferase Deficiency 25 0.033
294
GST013 Gastrojejunal Ulcer 25 0.033
295
c ATR075 Atrial Fibrillation 15 24 0.033
296
CCN009 Cocaine Intoxication 20 0.033
297
CRT057 Critical Congenital Heart Disease 20 0.033