Search results for dolichol phosphate

84 hits were found for dolichol phosphate

# Family MCID Name MIFTS Score
1
c CNG199 Congenital Disorder of Glycosylation, Type Im 35 6.298
2
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 31 0.228
3
P LKM002 Leukemia 66 0.194
4
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.175
5
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.173
6
PRT037 Pertussis 65 0.153
7
P ALC033 Alcohol Use Disorder 58 0.132
8
ALC007 Alcohol Dependence 66 0.128
9
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.127
10
CHL014 Cholera 55 0.118
11
ALL026 Allergic Hypersensitivity Disease 64 0.117
12
c INH020 Inherited Metabolic Disorder 46 0.114
13
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.114
14
HLX001 Helix Syndrome 47 0.111
15
AGN016 Aging 56 0.109
16
DWN001 Down Syndrome 70 0.108
17
c ACT073 Acute Leukemia 58 0.108
18
c DLT002 Dilated Cardiomyopathy 79 0.107
19
HYP066 Hyperglycemia 61 0.106
20
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.104
21
P MSC005 Muscular Dystrophy 66 0.103
22
LVR012 Liver Cirrhosis 63 0.102
23
P TCL004 T-Cell Leukemia 47 0.101
24
P ALZ034 Alzheimer Disease 88 0.099
25
BCT022 Bacterial Infectious Disease 56 0.097
26
LYS002 Lysosomal Storage Disease 52 0.093
27
P LVR013 Liver Disease 68 0.092
28
ADN018 Adenoma 58 0.091
29
P HYP265 Hypotonia 42 0.091
30
P CTR002 Cataract 60 0.090
31
STM007 Stomatitis 49 0.089
32
LNG099 Lung Disease 61 0.083
33
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.083
34
CYS001 Cystic Fibrosis 80 0.077
35
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.077
36
c ATR087 Atrial Standstill 1 74 0.076
37
DPR016 Depression 63 0.076
38
KRT002 Keratomalacia 48 0.074
39
RTN023 Retinitis 46 0.073
40
CRD043 Ceroid Storage Disease 43 0.073
41
NRR001 Neuroretinitis 43 0.073
42
CHG001 Chagas Disease 66 0.071
43
P RTN008 Retinitis Pigmentosa 77 0.070
44
CHR074 Choriocarcinoma 46 0.070
45
c CNG206 Congenital Disorder of Glycosylation, Type Ie 47 0.067
46
c MSC182 Muscular Dystrophy-Dystroglycanopathy , Type C, 15 30 0.067
47
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.067
48
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.064
49
WST001 West Syndrome 60 0.064
50
P THY023 Thymoma 65 0.063
51
c THY107 Thymoma, Familial 54 0.063
52
ARG004 Argyria 28 0.063
53
P HYP061 Hypertrophic Cardiomyopathy 66 0.061
54
HYD038 Hydrops Fetalis, Nonimmune 61 0.061
55
CHL068 Cholestasis 60 0.061
56
ACR006 Aceruloplasminemia 73 0.059
57
c DNG003 Dengue Disease 59 0.059
58
c CNG205 Congenital Disorder of Glycosylation, Type Ij 35 0.059
59
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 31 0.059
60
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 21 0.059
61
P MCR010 Microcephaly 58 0.057
62
P DNG005 Dengue Virus 57 0.057
63
P GNG009 Gangliosidosis 44 0.057
64
CHR178 Chromosomal Triplication 35 0.057
65
P TYS001 Tay-Sachs Disease 68 0.054
66
P PRM006 Primary Biliary Cirrhosis 61 0.054
67
VLV047 Volvulus of Midgut 50 0.054
68
c ATS007 Autism Spectrum Disorder 67 0.051
70
c GM1007 Gm1 Gangliosidosis 61 0.051
71
c CHL119 Cholangitis, Primary Sclerosing 57 0.051
72
ALC009 Alcoholic Liver Cirrhosis 53 0.051
73
P CHL066 Cholangitis 50 0.051
74
P SCL009 Sclerosing Cholangitis 47 0.051
75
EXT022 Exotropia 42 0.051
76
c HNT011 Huntington Disease-Like 3 38 0.051
77
P MSC002 Muscular Dystrophy-Dystroglycanopathy 35 0.051
78
ALT003 Alternating Exotropia 34 0.051
79
SMT004 Smith-Lemli-Opitz Syndrome 69 0.048
80
PCK003 Pick Disease of Brain 68 0.048
81
P ICH004 Ichthyosis 54 0.048
82
P CRB045 Cerebellar Hypoplasia 37 0.048
83
c CNG386 Congenital Disorder of Glycosylation, Type Iu 35 0.048
84
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.048
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