|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
C1861859
|
Other
|
Known
|
Explain
|
76.17869
|
|
2
|
Avitaminosis
|
Disease
|
Known
|
Explain
|
33.63358
|
|
3
|
LRAT gene
|
Gene
|
Known
|
Explain
|
18.32236
|
|
4
|
Quantitative Trait Loci
|
Gene
|
Inferred
|
Explain
|
14.98756
|
|
5
|
TGM1 gene
|
Gene
|
Known
|
Explain
|
12.29129
|
|
6
|
RBP4 gene
|
Gene
|
Known
|
Explain
|
12.12226
|
|
7
|
Vitamin A
|
Compound
|
Known
|
Explain
|
8.02822
|
|
8
|
BMP4 gene
|
Gene
|
Known
|
Explain
|
3.59922
|
|
9
|
Ascorbic Acid Deficiency
|
Disease
|
Inferred
|
Explain
|
0.62796
|
|
10
|
Vitamin E Deficiency
|
Disease
|
Inferred
|
Explain
|
0.61229
|
|
11
|
Vitamin D Deficiency
|
Disease
|
Inferred
|
Explain
|
0.53584
|
|
12
|
Vitamin B Deficiency
|
Disease
|
Inferred
|
Explain
|
0.44907
|
|
13
|
Deficiency Diseases
|
Disease
|
Inferred
|
Explain
|
0.43503
|
|
14
|
Vitamin K Deficiency
|
Disease
|
Inferred
|
Explain
|
0.39959
|
|
15
|
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1
|
Disease
|
Inferred
|
Explain
|
0.31731
|
|
16
|
MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1
|
Disease
|
Inferred
|
Explain
|
0.30571
|
|
17
|
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3
|
Disease
|
Inferred
|
Explain
|
0.26059
|
|
18
|
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2
|
Disease
|
Inferred
|
Explain
|
0.26059
|
|
19
|
BILIRUBIN, ELEVATED CONCENTRATIONS OF, IN SERUM
|
Disease
|
Inferred
|
Explain
|
0.25982
|
|
20
|
LEPTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
|
Disease
|
Inferred
|
Explain
|
0.25846
|
|
21
|
Scurvy
|
Disease
|
Inferred
|
Explain
|
0.24726
|
|
22
|
MENARCHE, AGE AT, QUANTITATIVE TRAIT LOCUS 1
|
Disease
|
Inferred
|
Explain
|
0.23594
|
|
23
|
Steatitis
|
Disease
|
Inferred
|
Explain
|
0.23378
|
|
24
|
Genetic Loci
|
Gene
|
Inferred
|
Explain
|
0.18145
|
|
25
|
Specimen Type - Serum
|
Other
|
Inferred
|
Explain
|
0.11725
|
|
26
|
Menopause
|
Function
|
Inferred
|
Explain
|
0.11291
|
|
27
|
Serum
|
Other
|
Inferred
|
Explain
|
0.09387
|
|
28
|
Osteomalacia
|
Disease
|
Inferred
|
Explain
|
0.07530
|
|
29
|
Rickets
|
Disease
|
Inferred
|
Explain
|
0.05962
|
|
30
|
IMMUNOGLOBULIN E CONCENTRATION, SERUM
|
Disease
|
Inferred
|
Explain
|
0.05490
|
|
31
|
Folic Acid Deficiency
|
Disease
|
Inferred
|
Explain
|
0.05145
|
|
32
|
Thiamine Deficiency
|
Disease
|
Inferred
|
Explain
|
0.04687
|
|
33
|
ADIPOQ gene
|
Gene
|
Inferred
|
Explain
|
0.04301
|
|
34
|
Magnesium Deficiency
|
Disease
|
Inferred
|
Explain
|
0.04269
|
|
35
|
Vitamin B 12 Deficiency
|
Disease
|
Inferred
|
Explain
|
0.04216
|
|
36
|
Swayback
|
Disease
|
Inferred
|
Explain
|
0.03988
|
|
37
|
11-cis-Retinol
|
Compound
|
Inferred
|
Explain
|
0.02977
|
|
38
|
Retinyl ester
|
Compound
|
Inferred
|
Explain
|
0.02977
|
|
39
|
11-cis-Retinyl palmitate
|
Compound
|
Inferred
|
Explain
|
0.02977
|
|
40
|
phosphatidylcholine-retinol O-acyltransferase activity
|
Function
|
Inferred
|
Explain
|
0.02538
|
|
41
|
Menarche
|
Function
|
Inferred
|
Explain
|
0.02344
|
|
42
|
2-Acyl-sn-glycero-3-phosphocholine
|
Compound
|
Inferred
|
Explain
|
0.02184
|
|
43
|
Dry Eye Syndromes
|
Disease
|
Inferred
|
Explain
|
0.02138
|
|
44
|
Hyperhomocysteinemia
|
Disease
|
Inferred
|
Explain
|
0.01931
|
|
45
|
RPE65 gene
|
Gene
|
Inferred
|
Explain
|
0.01922
|
|
46
|
Retinol
|
Compound
|
Inferred
|
Explain
|
0.01877
|
|
47
|
Optic Atrophy, Hereditary, Leber
|
Disease
|
Inferred
|
Explain
|
0.01802
|
|
48
|
RBP2 gene
|
Gene
|
Inferred
|
Explain
|
0.01749
|
|
49
|
Leber Congenital Amaurosis
|
Disease
|
Inferred
|
Explain
|
0.01642
|
|
50
|
Retinol Metabolism Pathway
|
Function
|
Inferred
|
Explain
|
0.01556
|
|
51
|
retinoid metabolic process
|
Function
|
Inferred
|
Explain
|
0.01520
|
|
52
|
RBP1 gene
|
Gene
|
Inferred
|
Explain
|
0.01483
|
|
53
|
Alcoholic Liver Diseases
|
Disease
|
Inferred
|
Explain
|
0.01453
|
|
54
|
Minor Histocompatibility Loci
|
Gene
|
Inferred
|
Explain
|
0.01409
|
|
55
|
Minor Lymphocyte Stimulatory Loci
|
Gene
|
Inferred
|
Explain
|
0.01409
|
|
56
|
retinol transporter activity
|
Function
|
Inferred
|
Explain
|
0.01387
|
|
57
|
Immunogenetic Phenomena
|
Function
|
Inferred
|
Explain
|
0.01382
|
|
58
|
Lipocalins
|
Compound
|
Inferred
|
Explain
|
0.01376
|
|
59
|
C1539288
|
Other
|
Inferred
|
Explain
|
0.01316
|
|
60
|
development of secondary female sexual characteristics
|
Function
|
Inferred
|
Explain
|
0.01311
|
|
61
|
LEP gene
|
Gene
|
Inferred
|
Explain
|
0.01285
|
|
62
|
Locus Control Region
|
Compound
|
Inferred
|
Explain
|
0.01232
|
|
63
|
Major Histocompatibility Complex
|
Gene
|
Inferred
|
Explain
|
0.01165
|
|
64
|
Multivesicular body
|
Component
|
Inferred
|
Explain
|
0.01162
|
|
65
|
spermatogonial cell division
|
Function
|
Inferred
|
Explain
|
0.01151
|
|
66
|
Menopause, Premature
|
Disease
|
Inferred
|
Explain
|
0.01147
|
|
67
|
Retinol Binding Proteins
|
Compound
|
Inferred
|
Explain
|
0.01134
|
|
68
|
Vitamin K Deficiency Bleeding
|
Disease
|
Inferred
|
Explain
|
0.01126
|
|
69
|
Eye Diseases, Hereditary
|
Disease
|
Inferred
|
Explain
|
0.01126
|
|
70
|
Congenital ichthyosis
|
Disease
|
Inferred
|
Explain
|
0.01107
|
|
71
|
Phosphatidylcholine
|
Compound
|
Inferred
|
Explain
|
0.01091
|
|
72
|
vagina development
|
Function
|
Inferred
|
Explain
|
0.01085
|
|
73
|
embryonic retina morphogenesis in camera-type eye
|
Function
|
Inferred
|
Explain
|
0.01079
|
|
74
|
urinary bladder development
|
Function
|
Inferred
|
Explain
|
0.01037
|
|
75
|
RARRES3 gene
|
Gene
|
Inferred
|
Explain
|
0.01019
|
|
76
|
retinal binding
|
Function
|
Inferred
|
Explain
|
0.01004
|
|
77
|
Malnutrition
|
Disease
|
Inferred
|
Explain
|
0.00989
|
|
78
|
AWAT2 gene
|
Gene
|
Inferred
|
Explain
|
0.00988
|
|
79
|
Transglutaminase, C-terminal
|
Domain
|
Inferred
|
Explain
|
0.00977
|
|
80
|
retinal metabolism
|
Function
|
Inferred
|
Explain
|
0.00976
|
|
81
|
retinol binding
|
Function
|
Inferred
|
Explain
|
0.00973
|
|
82
|
Climacteric
|
Function
|
Inferred
|
Explain
|
0.00963
|
|
83
|
uterus development
|
Function
|
Inferred
|
Explain
|
0.00960
|
|
84
|
menstrual cycle phase
|
Function
|
Inferred
|
Explain
|
0.00960
|
|
85
|
ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1
|
Disease
|
Inferred
|
Explain
|
0.00957
|
|
86
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.00949
|
|
87
|
Congenital Nonbullous Ichthyosiform Erythroderma
|
Other
|
Inferred
|
Explain
|
0.00946
|
|
88
|
Nucleolus Organizer Region
|
Component
|
Inferred
|
Explain
|
0.00914
|
|
89
|
Transglutaminase, conserved site
|
Domain
|
Inferred
|
Explain
|
0.00906
|
|
90
|
KEGG:hsa04977
|
Pathway
|
Inferred
|
Explain
|
0.00894
|
|
91
|
Alkylamine
|
Compound
|
Inferred
|
Explain
|
0.00890
|
|
92
|
Protein glutamine
|
Compound
|
Inferred
|
Explain
|
0.00890
|
|
93
|
Protein N5-alkylglutamine
|
Compound
|
Inferred
|
Explain
|
0.00890
|
|
94
|
female genitalia morphogenesis
|
Function
|
Inferred
|
Explain
|
0.00877
|
|
95
|
Transglutaminase-like
|
Domain
|
Inferred
|
Explain
|
0.00851
|
|
96
|
positive regulation of immunoglobulin secretion
|
Function
|
Inferred
|
Explain
|
0.00849
|
|
97
|
cell envelope organization
|
Function
|
Inferred
|
Explain
|
0.00830
|
|
98
|
Rough endoplasmic reticulum
|
Component
|
Inferred
|
Explain
|
0.00827
|
|
99
|
protein-glutamine gamma-glutamyltransferase activity
|
Function
|
Inferred
|
Explain
|
0.00820
|
|
100
|
Transglutaminase, N-terminal
|
Domain
|
Inferred
|
Explain
|
0.00802
|