Search results for Insulin glargine

207 hits were found for Insulin glargine

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 66 1.862
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.663
3
P DBT009 Diabetes Mellitus 64 1.606
4
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.186
5
c DBT099 Diabetes Mellitus, Type I 65 1.045
6
HYP066 Hyperglycemia 61 0.947
7
INS024 Insulin-Like Growth Factor I 79 0.857
8
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.831
9
HYP060 Hyperinsulinism 54 0.722
10
GLC003 Glucose Intolerance 54 0.525
11
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.439
12
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.408
13
FTT001 Fatty Liver Disease 61 0.400
14
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.399
15
LPD008 Lipid Metabolism Disorder 62 0.396
16
P KDN018 Kidney Disease 72 0.386
17
GST033 Gestational Diabetes 61 0.375
18
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.354
19
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.340
20
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.340
21
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.340
22
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.340
23
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.340
24
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.340
25
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.340
26
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.340
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.339
28
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.339
29
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.335
30
P LVR013 Liver Disease 68 0.335
31
OCL069 Ocular Motor Apraxia 51 0.302
32
48X005 48,xyyy 39 0.299
33
INS001 Insulinoma 60 0.298
34
P CRD246 Cardiovascular System Disease 57 0.287
35
c HYP595 Hypertension, Essential 84 0.285
36
P MCR115 Microvascular Complications of Diabetes 5 66 0.284
37
c MCR113 Microvascular Complications of Diabetes 3 52 0.280
38
ATH013 Atherosclerosis Susceptibility 65 0.276
39
P VSC007 Vascular Disease 63 0.275
40
c MCR120 Microvascular Complications of Diabetes 7 47 0.271
41
c MCR130 Microvascular Complications of Diabetes 6 41 0.270
42
c MCR133 Microvascular Complications of Diabetes 4 41 0.270
43
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.261
44
P CRN300 Coronary Heart Disease 1 63 0.261
45
c CHR684 Chronic Kidney Disease 70 0.258
46
c RHB024 Rhabdomyosarcoma 2 67 0.256
47
P TRN020 Turner Syndrome 67 0.236
48
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.233
49
ADL002 Adult Syndrome 70 0.228
50
ISC004 Ischemia 58 0.228
51
NTR005 Nutritional Deficiency Disease 62 0.225
52
P NRP001 Neuropathy 56 0.224
53
c ACT075 Acute Myocardial Infarction 57 0.223
54
ATM095 Autoimmune Disease 62 0.221
55
NNL006 Non-Alcoholic Steatohepatitis 54 0.221
56
LPP008 Lipoprotein Quantitative Trait Locus 62 0.220
57
P BRS047 Breast Cancer 97 0.220
58
P MYC007 Myocardial Infarction 70 0.220
59
ALL026 Allergic Hypersensitivity Disease 62 0.220
60
CNG034 Congestive Heart Failure 69 0.218
61
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.214
62
PRD004 Prediabetes Syndrome 47 0.212
63
LVR012 Liver Cirrhosis 62 0.211
64
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.211
65
P HRT032 Heart Disease 75 0.210
66
c PRC016 Pre-Eclampsia 63 0.210
67
c PRM038 Primary Agammaglobulinemia 44 0.208
68
END086 End Stage Renal Disease 51 0.208
69
CYS001 Cystic Fibrosis 81 0.208
70
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.206
71
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.206
72
c MCR129 Microvascular Complications of Diabetes 1 66 0.206
73
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.202
74
HYP005 Hypokalemia 55 0.201
75
CRB039 Cerebrovascular Disease 67 0.198
76
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.198
77
DWN001 Down Syndrome 70 0.197
78
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.195
79
LPT014 Leptin Deficiency or Dysfunction 74 0.192
80
ART140 Arteries, Anomalies of 52 0.192
81
STR067 Stroke, Ischemic 81 0.188
82
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.182
83
c HYP836 Hypercholesterolemia, Familial, 1 73 0.179
84
P CLR023 Colorectal Cancer 99 0.178
85
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.176
86
P HYP086 Hypothyroidism 69 0.174
87
DBT010 Diabetic Neuropathy 54 0.174
88
c HPT001 Hepatitis C 62 0.172
89
OST159 Osteogenic Sarcoma 66 0.171
90
ATX019 Ataxia with Vitamin E Deficiency 42 0.168
91
P PNC035 Pancreatic Cancer 84 0.167
92
ATN004 Autonomic Neuropathy 45 0.164
93
c HPT073 Hepatitis C Virus 72 0.157
95
HYP266 Hypoxia 57 0.151
96
47X002 47,xyy 49 0.150
97
P MTR004 Maturity-Onset Diabetes of the Young 65 0.149
98
P PRP019 Peripheral Nervous System Disease 58 0.149
99
PRP027 Peripheral Vascular Disease 71 0.149
100
P DRR001 Diarrhea 55 0.148
101
P LNG032 Lung Cancer 98 0.146
102
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.141
103
c MCR112 Microvascular Complications of Diabetes 2 41 0.140
104
GLC008 Glucose Metabolism Disease 40 0.139
105
END057 Endometrial Cancer 74 0.136
106
CHL079 Children's Interstitial Lung Disease 26 0.132
107
MTB004 Metabolic Acidosis 50 0.132
108
c ACT071 Acute Kidney Failure 60 0.132
109
P HPT021 Hepatitis 67 0.131
110
DPR016 Depression 63 0.129
111
ANX010 Anxiety 73 0.129
112
P ALC033 Alcohol Use Disorder 58 0.128
113
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.125
114
ANG054 Angina Pectoris 66 0.124
115
MNT002 Mental Depression 58 0.120
116
49X006 49, Xxxxy Syndrome 41 0.119
117
P ADN016 Adenocarcinoma 64 0.118
118
LNG099 Lung Disease 60 0.117
119
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.116
120
PRP080 Peripheral Artery Disease 53 0.116
121
P NNT009 Neonatal Diabetes Mellitus 50 0.115
122
P END084 Endocrine System Disease 45 0.115
123
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.113
124
P LCT001 Lactic Acidosis 51 0.113
125
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.113
126
BLR008 Bilirubin Metabolic Disorder 57 0.107
127
P ECL001 Eclampsia 50 0.107
128
PLC008 Placenta Disease 50 0.106
129
c FNC043 Fanconi Anemia, Complementation Group E 62 0.104
130
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.104
131
P DMN002 Dementia 66 0.104
132
DBT002 Diabetic Autonomic Neuropathy 41 0.104
133
HYP081 Hypolipoproteinemia 51 0.103
134
THY029 Thyroid Carcinoma 59 0.101
135
P URT039 Urticaria 58 0.100
136
EYD002 Eye Disease 58 0.099
137
P BLD134 Bladder Cancer 79 0.098
138
FTL021 Fetal Macrosomia 42 0.094
139
c DBT103 Diabetes Mellitus, Permanent Neonatal 4 46 0.092
140
TRP009 Triple X Syndrome 42 0.091
141
MCL006 Macular Retinal Edema 55 0.090
142
P LKM002 Leukemia 68 0.090
143
DFC004 Deficiency Anemia 70 0.089
144
HYP017 Hypophosphatemia 50 0.089
145
P LYM118 Lymphoma 68 0.088
146
ATM052 Autoimmune Disease 1 37 0.087
147
AST005 Asthma 76 0.086
148
P LKM062 Leukemia, Acute Lymphoblastic 69 0.086
149
PSY004 Psychotic Disorder 67 0.086
150
P RTN018 Retinal Disease 53 0.086
151
NSP002 Nasopharyngitis 43 0.086
152
c HYP272 Hypercholesterolemia, Familial, 3 44 0.085
153
ALC007 Alcohol Dependence 66 0.085
154
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 0.085
155
CRD223 Cardiac Arrhythmia 60 0.085
156
c TYP032 Type 1 Diabetes Mellitus 6 20 0.085
157
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.084
158
CRD137 Cardiogenic Shock 47 0.084
159
SNS003 Sensory Peripheral Neuropathy 54 0.084
160
HYP781 Hypoascorbemia 51 0.083
161
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.083
162
BRK010 Burkitt Lymphoma 67 0.082
163
GLS018 Glass Syndrome 57 0.082
164
GST071 Gastrointestinal Carcinoma 47 0.081
165
P BRS044 Breast Adenocarcinoma 59 0.081
166
GST020 Gastric Antral Vascular Ectasia 41 0.081
167
LMB062 Limb Ischemia 55 0.080
168
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.080
169
MNG006 Monogenic Diabetes 46 0.079
170
c TRN032 Transient Neonatal Diabetes Mellitus 41 0.079
171
c TYP030 Type 1 Diabetes Mellitus 4 20 0.079
172
GST049 Gastrointestinal System Cancer 49 0.078
173
TRN015 Transient Cerebral Ischemia 63 0.078
174
KHL003 Kohlschutter-Tonz Syndrome 65 0.077
175
JVN026 Jeavons Syndrome 24 0.076
176
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.075
177
RNL024 Renal Glucosuria 58 0.075
178
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.074
179
P CNR004 Cone-Rod Dystrophy 2 73 0.073
180
OST017 Osteomyelitis 64 0.072
181
HMR039 Hemorrhage, Intracerebral 57 0.072
182
LYM019 Lymphosarcoma 46 0.072
183
IDP033 Idiopathic Edema 44 0.072
184
P KDN017 Kidney Cancer 60 0.071
185
P NRV007 Nervous System Disease 66 0.070
186
P EXN002 Exanthem 57 0.068
187
DSS008 Disease of Mental Health 58 0.067
188
CNS004 Constipation 58 0.067
189
PST021 Postpartum Depression 50 0.067
190
DBT006 Diabetic Macular Edema 48 0.067
191
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.066
192
LYM040 Lymphoblastic Lymphoma 54 0.066
193
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.066
194
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.059
195
IMM064 Immunodeficiency, Common Variable, 10 44 0.058
196
OBS002 Obsessive-Compulsive Disorder 68 0.057
197
P ENC004 Encephalitis 61 0.057
198
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.056
199
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.054
200
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.053
201
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.053
202
ERY029 Erythermalgia, Primary 58 0.051
204
AND020 Androgen Insensitivity, Partial 56 0.049
205
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.048
206
LYM053 Lymphomatous Thyroiditis 22 0.048
207
PLM013 Pulmonary Immaturity 30 0.039
Content
Loading form....