Search results for "[genes] UGT1A1"

36 hits were found for '[genes] UGT1A1'

# Family MCID Name MIFTS Score
1
GLB001 Gilbert Syndrome 61 22.940
2
P CRG003 Crigler-Najjar Syndrome, Type I 58 22.940
3
c CRG004 Crigler-Najjar Syndrome, Type Ii 48 20.518
4
HYP618 Hyperbilirubinemia, Familial Transient Neonatal 19 17.769
5
P CLR023 Colorectal Cancer 97 16.221
6
P NTR004 Neutropenia 59 16.221
7
BLR008 Bilirubin Metabolic Disorder 47 16.221
8
P KRN004 Kernicterus 46 16.221
9
P THL005 Thalassemia 61 14.508
10
P HRD011 Hereditary Spherocytosis 53 14.508
11
NNT012 Neonatal Jaundice 51 14.508
12
CHL004 Cholelithiasis 48 14.508
13
SCK003 Sickle Cell Anemia 68 12.565
14
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 12.565
15
P GLL020 Gallbladder Disease 59 12.565
16
THL016 Thalassemias, Alpha- 54 12.565
17
HMG005 Hemoglobinopathy 50 12.565
18
SCK005 Sickle Cell Disease 49 12.565
19
GLC009 Glucosephosphate Dehydrogenase Deficiency 40 12.565
20
CHL039 Choledocholithiasis 34 12.565
21
IRN007 Irinotecan Toxicity 32 12.565
22
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 10.259
23
P DRR001 Diarrhea 51 10.259
24
c INH020 Inherited Metabolic Disorder 49 10.259
25
P ADM011 Adams-Oliver Syndrome 48 10.259
26
OLV002 Oliver Syndrome 44 10.259
27
PGM003 Pigmentation Disease 42 10.259
28
MLF002 Malouf Syndrome 41 10.259
29
P BRN035 Brain Stem Glioma 39 10.259
30
THL010 Thalassemia Minor 38 10.259
31
DSC005 Descending Colon Cancer 32 10.259
32
LCY001 Lucey-Driscoll Syndrome 11 10.259
33
LKC003 Leukocyte Disease 47 7.254
34
RLT001 Raltegravir Toxicity 11 7.254
35
CNG117 Congenital Nonhemolytic Jaundice 7 7.254
36
c UGT001 Ugt1a1-Related Altered Drug Metabolism 3 7.254