Search results for Uridine

123 hits were found for Uridine

# Family MCID Name MIFTS Score
1
ORT008 Orotic Aciduria 48 5.004
2
ANM012 Anemia, Hemolytic, Due to Umph1 Deficiency 20 4.849
3
GNR029 Generalized Galactose Epimerase Deficiency 15 3.412
4
ERY041 Erythrocyte Galactose Epimerase Deficiency 9 3.412
5
GLC011 Galactose Epimerase Deficiency 41 2.413
6
GLC006 Galactosemia 64 0.178
7
P BRS047 Breast Cancer 100 0.154
8
c CRG004 Crigler-Najjar Syndrome, Type Ii 48 0.126
9
P CLR023 Colorectal Cancer 97 0.115
10
P HPT021 Hepatitis 69 0.103
11
P LKM002 Leukemia 71 0.089
12
GLB001 Gilbert Syndrome 60 0.089
13
P CRG003 Crigler-Najjar Syndrome, Type I 59 0.089
14
PRS047 Prostatitis 56 0.089
15
c MTR002 Mitral Valve Insufficiency 44 0.089
16
P LNG032 Lung Cancer 95 0.073
17
P MYC007 Myocardial Infarction 79 0.073
18
P LVR013 Liver Disease 75 0.073
19
SCK003 Sickle Cell Anemia 71 0.073
20
P NRB001 Neuroblastoma 70 0.073
21
P ADN016 Adenocarcinoma 69 0.073
22
P LYM118 Lymphoma 69 0.073
23
P HRP006 Herpes Simplex 65 0.073
24
P BPL003 Bipolar Disorder 62 0.073
25
MDD011 Mood Disorder 61 0.073
26
P PNC044 Pancreatitis 61 0.073
27
PRM097 Primary Immunodeficiency Disease 60 0.073
28
CHL071 Child Syndrome 58 0.073
29
P FBR017 Fibrosarcoma 56 0.073
30
P LPD010 Lipodystrophy 55 0.073
31
LKC001 Leukocyte Adhesion Deficiency 55 0.073
32
KDS001 Kid Syndrome 53 0.073
33
END040 Endogenous Depression 53 0.073
34
MNT002 Mental Depression 53 0.073
35
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.073
36
c INH020 Inherited Metabolic Disorder 49 0.073
37
P RNL017 Renal Oncocytoma 47 0.073
38
END072 Endotheliitis 42 0.073
39
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.073
40
P RHM011 Rheumatoid Arthritis 89 0.051
41
P PNC035 Pancreatic Cancer 87 0.051
42
CYS001 Cystic Fibrosis 83 0.051
43
P MLT019 Multiple Myeloma 83 0.051
44
P RNL014 Renal Cell Carcinoma 82 0.051
45
HV1006 Hiv-1 80 0.051
46
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.051
47
GST053 Gastric Cancer 78 0.051
48
HDG012 Hodgkin Lymphoma 77 0.051
49
c CHR090 Chronic Lymphocytic Leukemia 76 0.051
50
NRL016 Neural Tube Defects 76 0.051
51
P ART022 Arthritis 75 0.051
52
P HRT032 Heart Disease 75 0.051
53
P CRN211 Coronary Artery Disease 74 0.051
54
P PLM036 Pulmonary Fibrosis 71 0.051
55
KRT004 Keratitis 71 0.051
56
SQM006 Squamous Cell Carcinoma 70 0.051
57
TBR010 Tuberculosis 70 0.051
58
P EPL164 Epilepsy 66 0.051
59
P BCL006 B-Cell Lymphomas 65 0.051
60
P THL005 Thalassemia 64 0.051
61
RNL101 Renal Cell Carcinoma, Papillary 63 0.051
62
MTH009 Mouth Disease 61 0.051
63
ACQ007 Acquired Immunodeficiency Syndrome 60 0.051
64
c ACT073 Acute Leukemia 60 0.051
65
P ENC018 Encephalopathy 59 0.051
66
P NTR004 Neutropenia 59 0.051
67
P GLM007 Glomerulonephritis 59 0.051
68
LPD008 Lipid Metabolism Disorder 58 0.051
69
P HYP060 Hyperinsulinism 58 0.051
70
RSP006 Respiratory System Disease 58 0.051
71
PNC034 Pancreas Disease 58 0.051
72
ORL015 Oral Squamous Cell Carcinoma 57 0.051
73
WST001 West Syndrome 57 0.051
74
HTC002 Hutchinson-Gilford Progeria 57 0.051
75
CHR177 Chromophobe Renal Cell Carcinoma 56 0.051
76
RBS001 Rabies 56 0.051
77
ART111 Artery Disease 55 0.051
78
P THY032 Thyroiditis 54 0.051
79
P MTC069 Mitochondrial Disorders 53 0.051
80
P LTR001 Lateral Sclerosis 53 0.051
81
P PLY014 Polycystic Kidney Disease 53 0.051
82
DSS008 Disease of Mental Health 52 0.051
83
ADL002 Adult Syndrome 52 0.051
84
c HPT015 Hepatitis D 52 0.051
85
ALL026 Allergic Hypersensitivity Disease 52 0.051
86
ART002 Arts Syndrome 51 0.051
87
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.051
88
EPD001 Epidermodysplasia Verruciformis 50 0.051
89
MGL001 Megaloblastic Anemia 50 0.051
90
MLL012 Miller Syndrome 49 0.051
91
CHL004 Cholelithiasis 48 0.051
92
SLP001 Sleeping Sickness 48 0.051
93
c BPL002 Bipolar I Disorder 47 0.051
94
CRB025 Carbohydrate Metabolic Disorder 46 0.051
95
ADR038 Adermatoglyphia 46 0.051
96
SCR002 Scurvy 46 0.051
97
P CRV039 Cervicitis 45 0.051
98
ALN001 Aland Island Eye Disease 45 0.051
99
MYC005 Myocardial Stunning 44 0.051
100
PRG004 Progeria 44 0.051
101
GRN017 Granulocytopenia 44 0.051
102
LKC003 Leukocyte Disease 43 0.051
103
GLC008 Glucose Metabolism Disease 42 0.051
104
SXL003 Sexual Disorder 42 0.051
105
FSC002 Fascioliasis 42 0.051
106
PHC013 Phaeochromocytoma 41 0.051
107
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.051
108
DRG001 Drug Psychosis 38 0.051
109
c PNC106 Pancreatic Agenesis 1 37 0.051
110
NTR005 Nutritional Deficiency Disease 36 0.051
111
MTC005 Mitochondrial Metabolism Disease 36 0.051
112
IMM078 Immunodeficiency 21 35 0.051
113
CHL039 Choledocholithiasis 34 0.051
114
PRN024 Purine-Pyrimidine Metabolic Disorder 31 0.051
115
PSD100 Pseudo-Hurler Polydystrophy 31 0.051
116
IRN007 Irinotecan Toxicity 30 0.051
117
PYR035 Pyrimidine Metabolic Disorder 29 0.051
118
IMM076 Immunodeficiency 24 27 0.051
119
CRT055 Creatine Deficiency Syndromes 27 0.051
120
IMM088 Immunodeficiency 36 22 0.051
121
c CNG435 Congenital Disorder of Glycosylation, Type Iz 19 0.051
122
CD4004 Cd4 Deficiency 14 0.051
123
5NC001 5-Nucleotidase Syndrome 6 0.051
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