Search results for Calcium levulinate

62 hits were found for Calcium levulinate

# Family MCID Name MIFTS Score
1
P OST002 Osteoporosis 74 0.307
2
LPP008 Lipoprotein Quantitative Trait Locus 62 0.188
3
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.187
4
CNG034 Congestive Heart Failure 69 0.181
5
ART140 Arteries, Anomalies of 52 0.177
6
P CRN300 Coronary Heart Disease 1 63 0.171
7
P HRT032 Heart Disease 75 0.167
8
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.154
9
c MGR028 Migraine with or Without Aura 1 67 0.141
10
47X002 47,xyy 49 0.136
11
GLB015 Glioblastoma Multiforme 75 0.128
12
P NRP001 Neuropathy 56 0.124
13
P DRR001 Diarrhea 55 0.123
14
P TRM003 Tremor 54 0.118
15
ATX019 Ataxia with Vitamin E Deficiency 42 0.117
16
P DBT009 Diabetes Mellitus 64 0.116
17
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.111
18
SQM006 Squamous Cell Carcinoma 60 0.110
19
PNG002 Pain Agnosia 51 0.109
20
P PRP029 Porphyria 62 0.108
21
P PRP019 Peripheral Nervous System Disease 58 0.107
22
P BLD134 Bladder Cancer 79 0.105
23
NTR005 Nutritional Deficiency Disease 62 0.103
24
P LCT001 Lactic Acidosis 51 0.103
25
P INS002 in Situ Carcinoma 53 0.101
26
P SKN015 Skin Carcinoma 66 0.100
27
49X006 49, Xxxxy Syndrome 41 0.100
28
c CHR682 Chronic Bilirubin Encephalopathy 39 0.098
29
AST005 Asthma 76 0.096
30
P GLM040 Glioma Susceptibility 1 81 0.094
31
P PLY019 Polyneuropathy 56 0.093
32
P MLN008 Melanoma 69 0.090
33
c ESS001 Essential Tremor 56 0.087
34
TRN018 Transitional Cell Carcinoma 56 0.085
35
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.082
36
c DRR009 Diarrhea 6 46 0.081
38
c BSL007 Basal Cell Carcinoma 68 0.081
39
GLS001 Gliosarcoma 54 0.081
40
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.080
41
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.080
42
GNT002 Giant Cell Glioblastoma 50 0.079
43
SKN013 Skin Benign Neoplasm 51 0.077
44
P ANP001 Anaplastic Large Cell Lymphoma 58 0.076
45
SKN022 Skin Squamous Cell Carcinoma 57 0.075
46
c BSL024 Basal Cell Carcinoma 1 56 0.073
47
MTH071 Methane Production 26 0.070
48
PRS063 Paresthesia 41 0.069
49
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.069
50
SKN019 Skin Melanoma 68 0.067
51
AMN006 Aminoaciduria 38 0.067
52
c HPT003 Hepatitis a 62 0.064
53
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.064
54
AVN001 Avian Influenza 59 0.062
55
PGM030 Pigmentation Anomaly of the Skin 26 0.062
56
KRT009 Keratosis 51 0.061
57
P PRP056 Porphyria, Acute Hepatic 48 0.059
58
PSD088 Pseudobulbar Affect 36 0.057
59
PRP083 Porphyria, Acute Intermittent 64 0.055
60
P ACT008 Actinic Keratosis 53 0.055
61
ALP077 Alpha-Methylacetoacetic Aciduria 55 0.051
62
c ACT078 Acute Porphyria 51 0.051
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