Search results for Retinyl ester

86 hits were found for Retinyl ester

# Family MCID Name MIFTS Score
1
KRT002 Keratomalacia 48 0.277
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.262
3
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.259
4
48X005 48,xyyy 39 0.236
5
ATH013 Atherosclerosis Susceptibility 66 0.235
6
P CRN300 Coronary Heart Disease 1 63 0.228
7
P HYP750 Hypertriglyceridemia, Familial 61 0.203
8
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.177
9
P CRN018 Coronary Artery Anomaly 63 0.176
10
P LVR013 Liver Disease 68 0.176
11
ART140 Arteries, Anomalies of 53 0.166
12
DRM006 Dermatitis 61 0.164
13
P HYP058 Hypervitaminosis a 49 0.164
14
P VSC007 Vascular Disease 63 0.145
15
P BRS047 Breast Cancer 96 0.141
16
P MYL006 Myeloid Leukemia 60 0.141
17
P DRR001 Diarrhea 57 0.139
18
FTT001 Fatty Liver Disease 61 0.138
19
P CRD246 Cardiovascular System Disease 56 0.138
20
CNT047 Contact Dermatitis 57 0.134
21
P HPT023 Hepatocellular Carcinoma 100 0.128
22
P ADN016 Adenocarcinoma 64 0.128
23
HMN044 Human Immunodeficiency Virus Type 1 71 0.125
24
INS024 Insulin-Like Growth Factor I 79 0.124
25
ISC004 Ischemia 60 0.122
26
PPL022 Papilloma 54 0.119
27
SQM002 Squamous Cell Papilloma 42 0.119
28
47X002 47,xyy 49 0.112
29
c LKM061 Leukemia, Acute Myeloid 83 0.112
30
P NRF023 Neurofibromatosis, Type Ii 76 0.111
31
P KDN018 Kidney Disease 70 0.108
32
P FBR017 Fibrosarcoma 56 0.108
33
ORL011 Oral Cancer 60 0.108
34
ALL010 Allergic Contact Dermatitis 55 0.106
35
c DWL002 Dowling-Degos Disease 1 58 0.106
37
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.105
38
MSL001 Measles 61 0.096
39
PRT013 Portal Hypertension 60 0.094
40
MLN008 Melanoma 69 0.092
41
ATM095 Autoimmune Disease 61 0.090
42
P RTN016 Retinal Degeneration 53 0.088
43
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.088
44
P MLT020 Multiple Sclerosis 72 0.085
45
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.085
46
SQM006 Squamous Cell Carcinoma 60 0.083
47
ADN018 Adenoma 58 0.083
48
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.082
49
P ART022 Arthritis 70 0.080
50
MLR004 Malaria 80 0.080
51
PTT037 Pituitary Tumors 44 0.078
52
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.078
53
IRN002 Iron Metabolism Disease 57 0.075
54
KRT013 Keratolytic Winter Erythema 46 0.075
55
LNG099 Lung Disease 61 0.075
56
ATX019 Ataxia with Vitamin E Deficiency 48 0.075
57
P OST002 Osteoporosis 73 0.072
58
P NPH012 Nephrotic Syndrome 63 0.072
59
P LBR001 Leber Congenital Amaurosis 67 0.069
60
HYP068 Hyperostosis 48 0.069
61
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.068
62
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.068
63
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.068
64
P GLM007 Glomerulonephritis 57 0.064
65
MST005 Mastitis 53 0.064
66
IRR003 Irritant Dermatitis 47 0.064
67
DRY001 Dry Eye Syndrome 47 0.064
68
EXC002 Exocrine Pancreatic Insufficiency 41 0.064
69
GST019 Gastrointestinal Stromal Tumor 76 0.059
70
SKN019 Skin Melanoma 67 0.059
71
ANR007 Anorexia Nervosa 63 0.059
72
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.059
73
AGN016 Aging 56 0.059
74
P LRY044 Larynx Cancer 54 0.059
75
DFC004 Deficiency Anemia 75 0.053
76
FND001 Fundus Albipunctatus 61 0.053
77
BRN056 Bronchopulmonary Dysplasia 57 0.053
78
P SHR001 Short Bowel Syndrome 52 0.053
79
CRT016 Carotid Artery Disease 52 0.053
80
FND002 Fundus Dystrophy 51 0.053
81
KRT001 Keratoconjunctivitis Sicca 50 0.053
82
BLR001 Biliary Atresia 50 0.053
83
c INH030 Inherited Retinal Disorder 47 0.053
84
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.053
85
CHL079 Children's Interstitial Lung Disease 27 0.053
86
EPT001 Epithelioid Cell Melanoma 23 0.053
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