Search results for slc25a13
46 hits were found for slc25a13
# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
P
|
CTR177 |
Citrullinemia, Type Ii, Adult-Onset |
57 |
6.607 |
|
2 |
|
P
|
CTR077 |
Citrullinemia, Type Ii, Neonatal-Onset |
42 |
5.589 |
|
3 |
|
|
CHL068 |
Cholestasis |
61 |
4.641 |
|
4 |
|
|
CTR172 |
Citrullinemia, Classic |
64 |
4.418 |
|
5 |
|
P
|
LVR013 |
Liver Disease |
68 |
3.702 |
|
6 |
|
|
BRN004 |
Brain Edema |
56 |
3.188 |
|
7 |
|
|
HPT019 |
Hepatic Encephalopathy |
60 |
3.149 |
|
8 |
|
|
ATS010 |
Autosomal Recessive Disease |
48 |
2.827 |
|
9 |
|
|
ARG002 |
Argininosuccinic Aciduria |
61 |
2.778 |
|
10 |
|
P
|
OBS001 |
Obstructive Jaundice |
50 |
2.617 |
|
11 |
|
P
|
ASP001 |
Asperger Syndrome |
48 |
2.571 |
|
12 |
|
|
CRB197 |
Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to |
57 |
2.086 |
|
13 |
|
c
|
CHL116 |
Cholestasis, Intrahepatic, of Pregnancy, 1 |
53 |
2.086 |
|
14 |
|
|
URC002 |
Urea Cycle Disorder |
51 |
1.925 |
|
15 |
|
|
ORN008 |
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to |
59 |
1.818 |
|
16 |
|
P
|
TYR004 |
Tyrosinemia |
58 |
1.818 |
|
17 |
|
|
ARG007 |
Argininemia |
57 |
1.818 |
|
18 |
|
c
|
GLC112 |
Galactosemia Iii |
56 |
1.818 |
|
19 |
|
|
HYP774 |
Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome |
55 |
1.818 |
|
20 |
|
c
|
MTC063 |
Mitochondrial Dna Depletion Syndrome 3 |
51 |
1.818 |
|
21 |
|
|
3MT001 |
3-Methylcrotonyl-Coa Carboxylase Deficiency |
49 |
1.818 |
|
22 |
|
P
|
BLR006 |
Biliary Tract Disease |
47 |
1.818 |
|
23 |
|
c
|
BLC007 |
Bile Acid Synthesis Defect, Congenital, 1 |
45 |
1.818 |
|
24 |
|
P
|
BLD036 |
Bile Duct Disease |
43 |
1.818 |
|
25 |
|
|
HYP003 |
Hypermethioninemia |
40 |
1.818 |
|
26 |
|
c
|
EPL185 |
Epileptic Encephalopathy, Early Infantile, 39 |
39 |
1.818 |
|
27 |
|
|
AMN002 |
Amino Acid Metabolic Disorder |
39 |
1.818 |
|
28 |
|
|
SPL068 |
Split-Hand/foot Malformation 1 with Sensorineural Hearing Loss, Autosomal Recessive |
34 |
1.818 |
|
29 |
|
|
BLR008 |
Bilirubin Metabolic Disorder |
57 |
0.127 |
|
30 |
|
P
|
HPT023 |
Hepatocellular Carcinoma |
100 |
0.104 |
|
31 |
|
|
HYP056 |
Hypoglycemia |
66 |
0.104 |
|
32 |
|
|
LPD008 |
Lipid Metabolism Disorder |
62 |
0.104 |
|
33 |
|
P
|
TRM003 |
Tremor |
54 |
0.104 |
|
34 |
|
|
NNT012 |
Neonatal Jaundice |
53 |
0.104 |
|
35 |
|
|
OCL069 |
Ocular Motor Apraxia |
51 |
0.104 |
|
36 |
|
|
PHN003 |
Phenylketonuria |
75 |
0.073 |
|
37 |
|
P
|
HPT021 |
Hepatitis |
67 |
0.073 |
|
38 |
|
P
|
ABD014 |
Abdominal Obesity-Metabolic Syndrome 1 |
64 |
0.073 |
|
39 |
|
P
|
HYP750 |
Hypertriglyceridemia, Familial |
62 |
0.073 |
|
40 |
|
|
LVR012 |
Liver Cirrhosis |
62 |
0.073 |
|
41 |
|
|
ESP020 |
Esophageal Atresia |
62 |
0.073 |
|
42 |
|
|
FTT001 |
Fatty Liver Disease |
61 |
0.073 |
|
43 |
|
|
DSS009 |
Disseminated Intravascular Coagulation |
57 |
0.073 |
|
44 |
|
c
|
VRL010 |
Viral Hepatitis |
52 |
0.073 |
|
45 |
|
|
BLR001 |
Biliary Atresia |
50 |
0.073 |
|
46 |
|
|
SBC016 |
Subacute Delirium |
44 |
0.073 |
|