Search results for "[genes] ABCC8"

43 hits were found for '[genes] ABCC8'

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 51 20.136
2
P HYP050 Hyperinsulinemic Hypoglycemia 49 18.836
3
P DBT083 Diabetes Mellitus, Permanent Neonatal 48 18.836
4
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 17.439
5
P NNT009 Neonatal Diabetes Mellitus 47 17.439
6
HYP066 Hyperglycemia 53 15.919
7
P HYP060 Hyperinsulinism 49 15.919
8
P OBS005 Obesity 87 14.238
9
INS001 Insulinoma 49 14.238
10
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 29 14.238
11
c DBT065 Diabetes Mellitus, Transient Neonatal 2 19 14.238
12
P PSD087 Pseudoxanthoma Elasticum 63 12.331
13
P PNC045 Pancreatic Agenesis 41 12.331
14
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 37 12.331
15
HYP619 Hypoglycemia of Infancy, Leucine-Sensitive 20 12.331
16
c ABC010 Abcc8-Related Hyperinsulinism 7 12.331
17
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 10.068
18
P BCK002 Beckwith-Wiedemann Syndrome 54 10.068
19
P MTR004 Maturity-Onset Diabetes of the Young 53 10.068
20
PRL032 Perlman Syndrome 50 10.068
21
FNC009 Fanconi-Bickel Syndrome 49 10.068
22
PNC034 Pancreas Disease 39 10.068
23
GLC010 Galactokinase Deficiency with Cataracts 38 10.068
24
CRB025 Carbohydrate Metabolic Disorder 36 10.068
25
END038 Endocrine Pancreas Disease 33 10.068
26
FCT008 Factitious Disorder 33 10.068
27
MNG006 Monogenic Diabetes 32 10.068
28
ACT088 Acute Insulin Response 32 10.068
29
INT011 Interstitial Emphysema 31 10.068
30
CRB132 Cerebral Sinovenous Thrombosis 30 10.068
31
MNC002 Munchausen by Proxy 30 10.068
32
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 44 7.119
33
GLC008 Glucose Metabolism Disease 35 7.119
34
ATS008 Autosomal Dominant Disease 34 7.119
35
P ACQ009 Acquired Metabolic Disease 33 7.119
36
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 28 7.119
37
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 26 7.119
38
P DND019 Dend Syndrome 23 7.119
39
c ABC012 Abcc8-Related Transient Neonatal Diabetes Mellitus 2 9 7.119
40
DZX001 Diazoxide-Resistant Focal Hyperinsulinism Due to Sur1 Deficiency 5 7.119
41
ATS215 Autosomal Dominant Hyperinsulinism Due to Sur1 Deficiency 5 7.119
42
ATS255 Autosomal Recessive Hyperinsulinism Due to Sur1 Deficiency 5 7.119
43
c ABC011 Abcc8-Related Permanent Neonatal Diabetes Mellitus 5 7.119