Search results for NADP

97 hits were found for NADP

# Family MCID Name MIFTS Score
1
HLX001 Helix Syndrome 47 0.170
2
P GLM045 Glioma 63 0.107
3
P CTR002 Cataract 60 0.107
4
HYP266 Hypoxia 57 0.107
5
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.107
6
LPT001 Leptospirosis 66 0.093
7
P HML002 Hemolytic Anemia 63 0.093
8
FTT001 Fatty Liver Disease 61 0.093
9
P TXP001 Toxoplasmosis 60 0.093
10
GLL048 Glial Tumor 45 0.093
11
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 0.093
12
MLR004 Malaria 81 0.076
13
GLB015 Glioblastoma Multiforme 75 0.076
14
P NRB001 Neuroblastoma 72 0.076
15
P MYC084 Mycobacterium Tuberculosis 1 68 0.076
16
HYP056 Hypoglycemia 66 0.076
17
PRT037 Pertussis 65 0.076
18
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.076
19
HYP066 Hyperglycemia 61 0.076
20
P MYC008 Myocarditis 59 0.076
21
CHL014 Cholera 59 0.076
22
ISC004 Ischemia 58 0.076
23
P AST007 Astrocytoma 51 0.076
24
P PLL002 Pellagra 46 0.076
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.076
26
ANX004 Anoxia 40 0.076
27
PPL052 Papillomatosis, Confluent and Reticulated 33 0.076
28
CND006 Candida Glabrata 32 0.076
29
PST092 Posttransplant Acute Limbic Encephalitis 29 0.076
30
P CLR023 Colorectal Cancer 99 0.054
31
P GLM040 Glioma Susceptibility 1 81 0.054
32
MSC157 Muscular Dystrophy, Duchenne Type 72 0.054
33
PLM001 Pulmonary Tuberculosis 69 0.054
34
P MLN008 Melanoma 69 0.054
35
c BSL007 Basal Cell Carcinoma 68 0.054
36
RCK004 Rickets 68 0.054
37
P MSC005 Muscular Dystrophy 66 0.054
38
CRN036 Craniopharyngioma 65 0.054
39
ATH013 Atherosclerosis Susceptibility 65 0.054
40
CLN015 Colon Adenocarcinoma 65 0.054
41
P VSC007 Vascular Disease 63 0.054
42
P PSR002 Psoriasis 62 0.054
43
TXC005 Toxic Shock Syndrome 62 0.054
44
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.054
45
DRM006 Dermatitis 61 0.054
46
P ENC018 Encephalopathy 61 0.054
47
LNG099 Lung Disease 60 0.054
48
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.054
49
INS001 Insulinoma 60 0.054
50
QFV001 Q Fever 60 0.054
51
GRD007 Grade Iii Astrocytoma 59 0.054
52
ADN018 Adenoma 59 0.054
53
ANT024 Anthrax Disease 58 0.054
54
P URT039 Urticaria 58 0.054
55
IRN002 Iron Metabolism Disease 57 0.054
56
AGN016 Aging 56 0.054
57
HYP005 Hypokalemia 55 0.054
58
DBT010 Diabetic Neuropathy 54 0.054
59
HMS001 Hemosiderosis 54 0.054
60
P RTN016 Retinal Degeneration 53 0.054
61
NNT012 Neonatal Jaundice 53 0.054
62
c MCR113 Microvascular Complications of Diabetes 3 52 0.054
63
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.054
64
PST011 Pustulosis of Palm and Sole 52 0.054
65
OCL069 Ocular Motor Apraxia 51 0.054
66
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.054
67
P LCT001 Lactic Acidosis 51 0.054
68
CCC002 Coccidiosis 51 0.054
69
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.054
70
VLV047 Volvulus of Midgut 49 0.054
71
47X002 47,xyy 49 0.054
72
P CTN015 Cutaneous T Cell Lymphoma 49 0.054
73
c MCR120 Microvascular Complications of Diabetes 7 47 0.054
74
P CRC039 Coarctation of Aorta 47 0.054
75
RTN023 Retinitis 46 0.054
76
P TRM004 Trimethylaminuria 46 0.054
77
c MLG068 Malignant Glioma 46 0.054
78
GRD001 Giardiasis 45 0.054
79
MYX004 Myxedema 43 0.054
80
DVR002 Diverticulitis 43 0.054
81
P HYP265 Hypotonia 43 0.054
82
HMP009 Haemophilus Influenzae 43 0.054
83
SNL007 Senile Cataract 42 0.054
84
NRR001 Neuroretinitis 42 0.054
85
P HYP769 Hyperlysinemia, Type I 41 0.054
86
c MCR130 Microvascular Complications of Diabetes 6 41 0.054
87
c MCR133 Microvascular Complications of Diabetes 4 41 0.054
88
P RRH023 Rare Hereditary Hemochromatosis 41 0.054
89
48X005 48,xyyy 39 0.054
90
HYP026 Hypoglycemic Coma 36 0.054
91
PYR009 Pyridoxine Deficiency Anemia 34 0.054
92
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.054
93
CYT014 Cytochrome P450 Oxidoreductase Deficiency 32 0.054
94
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 28 0.054
95
c RNG015 Ring Chromosome 2 26 0.054
96
CRT066 Cortisone Reductase Deficiency 2 24 0.054
97
c PRM209 Primary Trimethylaminuria 18 0.054
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