Search results for "[genes] ABCC8"

41 hits were found for '[genes] ABCC8'

# Family MCID Name MIFTS Score
1
P DBT083 Diabetes Mellitus, Permanent Neonatal 55 20.204
2
HYP056 Hypoglycemia 61 18.899
3
P HYP050 Hyperinsulinemic Hypoglycemia 56 18.899
4
P NNT009 Neonatal Diabetes Mellitus 52 18.899
5
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 17.497
6
P HYP060 Hyperinsulinism 58 17.497
7
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 39 17.497
8
P OBS005 Obesity 92 15.972
9
HYP066 Hyperglycemia 61 15.972
10
INS001 Insulinoma 61 15.972
11
c DBT065 Diabetes Mellitus, Transient Neonatal 2 23 15.972
12
HYP619 Hypoglycemia of Infancy, Leucine-Sensitive 19 15.972
13
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 45 14.286
14
P PNC045 Pancreatic Agenesis 42 14.286
15
c ABC010 Abcc8-Related Hyperinsulinism 6 14.286
16
P MTR004 Maturity-Onset Diabetes of the Young 58 12.372
17
PNC034 Pancreas Disease 58 12.372
18
P BCK002 Beckwith-Wiedemann Syndrome 56 12.372
19
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 12.372
20
FNC009 Fanconi-Bickel Syndrome 52 12.372
21
CRB025 Carbohydrate Metabolic Disorder 46 12.372
22
FCT008 Factitious Disorder 41 12.372
23
HMH002 Hemihypertrophy 41 12.372
24
END038 Endocrine Pancreas Disease 41 12.372
25
ATS008 Autosomal Dominant Disease 39 12.372
26
ACT088 Acute Insulin Response 39 12.372
27
INT011 Interstitial Emphysema 38 12.372
28
MNG006 Monogenic Diabetes 35 12.372
29
ASP004 Asphyxia Neonatorum 35 12.372
30
CRB132 Cerebral Sinovenous Thrombosis 31 12.372
31
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 30 12.372
32
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 29 12.372
33
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 27 12.372
34
MNC002 Munchausen by Proxy 27 12.372
35
c ABC012 Abcc8-Related Transient Neonatal Diabetes Mellitus 2 9 12.372
36
c ABC011 Abcc8-Related Permanent Neonatal Diabetes Mellitus 5 12.372
37
GLC008 Glucose Metabolism Disease 42 10.102
38
c USH007 Usher Syndrome, Type 1c 42 10.102
39
P ACQ009 Acquired Metabolic Disease 38 10.102
40
c CRD105 Cardiomyopathy, Dilated, 1o 37 10.102
41
HYP695 Hypertrichotic Osteochondrodysplasia Cantu Type 24 10.102