Search results for lathosterol

169 hits were found for lathosterol

# Family MCID Name MIFTS Score
1
LTH002 Lathosterolosis 38 4.709
2
c HYP836 Hypercholesterolemia, Familial, 1 73 3.822
3
c FML021 Familial Hypercholesterolemia 71 2.018
4
CRB011 Cerebrotendinous Xanthomatosis 64 1.926
5
XNT003 Xanthomatosis 48 1.926
6
c OPT051 Opitz Gbbb Syndrome, Type I 45 1.674
7
SMT004 Smith-Lemli-Opitz Syndrome 69 1.674
8
P CRN300 Coronary Heart Disease 1 73 1.472
9
LPD008 Lipid Metabolism Disorder 61 1.442
10
P NPH012 Nephrotic Syndrome 61 1.226
11
PRT251 Proteinuria, Chronic Benign 58 1.178
12
47X002 47,xyy 47 1.153
13
DSM002 Desmosterolosis 39 1.125
14
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 1.095
15
P CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 48 1.095
16
CLF027 Cleft Palate, Isolated 64 1.095
17
P MCL001 Mucolipidosis 49 1.095
18
P KLZ004 Kala-Azar 1 41 1.023
19
LSH001 Leishmaniasis 63 1.023
20
CTN007 Cutaneous Leishmaniasis 61 1.023
21
MND023 Mend Syndrome 49 0.941
22
c GLL024 Gallbladder Disease 1 53 0.826
23
LPP008 Lipoprotein Quantitative Trait Locus 65 0.708
24
ART140 Arteries, Anomalies of 52 0.679
25
P STS003 Sitosterolemia 53 0.665
26
PRM236 Primary Biliary Cholangitis 62 0.618
27
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.601
28
CHL068 Cholestasis 61 0.567
29
LVR012 Liver Cirrhosis 62 0.567
30
P ALZ034 Alzheimer Disease 87 0.549
31
c TYP009 Type 2 Diabetes Mellitus 91 0.511
32
P HRT032 Heart Disease 84 0.511
33
P HNT016 Huntington Disease 73 0.491
34
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.470
35
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.470
36
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.425
37
P DBT009 Diabetes Mellitus 67 0.425
38
CRH001 Crohn's Disease 80 0.425
39
CYS001 Cystic Fibrosis 77 0.401
40
ATS010 Autosomal Recessive Disease 42 0.401
41
c ATR087 Atrial Standstill 1 74 0.401
42
c DLT002 Dilated Cardiomyopathy 79 0.401
43
P CTR002 Cataract 59 0.401
44
FTT001 Fatty Liver Disease 61 0.401
45
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.375
46
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.375
47
AGN016 Aging 53 0.375
48
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.375
49
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.375
50
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.375
51
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.375
52
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.375
53
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.375
54
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.375
55
P VSC007 Vascular Disease 62 0.375
56
c CHL119 Cholangitis, Primary Sclerosing 57 0.347
57
ANR007 Anorexia Nervosa 59 0.347
58
P HYP750 Hypertriglyceridemia, Familial 61 0.347
59
P SCL009 Sclerosing Cholangitis 46 0.347
60
P LVR013 Liver Disease 68 0.347
61
P CHL066 Cholangitis 51 0.347
62
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.317
63
VSC002 Vascular Dementia 59 0.317
65
ANG054 Angina Pectoris 65 0.283
66
ALC006 Alcoholic Hepatitis 61 0.283
67
48X005 48,xyyy 39 0.283
68
c ACT134 Acute Liver Failure 57 0.283
69
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.245
70
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.245
71
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.245
72
MLD018 Mild Cognitive Impairment 48 0.245
73
HYP081 Hypolipoproteinemia 49 0.245
74
P PLY019 Polyneuropathy 52 0.245
75
P MCR010 Microcephaly 59 0.245
76
c ACT075 Acute Myocardial Infarction 55 0.245
77
SNG003 Single Ventricular Heart 30 0.245
78
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.200
79
P INF037 Inflammatory Bowel Disease 53 0.200
80
c ART115 Aortic Valve Disease 1 72 0.200
81
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.200
82
P MLT020 Multiple Sclerosis 79 0.200
83
WLS001 Wilson Disease 70 0.200
84
PRP027 Peripheral Vascular Disease 71 0.200
85
ADR016 Adrenal Cortical Carcinoma 61 0.200
86
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.200
87
c TYP008 Type 1 Diabetes Mellitus 77 0.200
88
c ART101 Aortic Valve Disease 2 65 0.200
89
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.200
90
P ACT244 Acth-Independent Cushing Syndrome 38 0.200
91
P SHR001 Short Bowel Syndrome 53 0.200
92
ADN018 Adenoma 58 0.200
93
P EPL164 Epilepsy 70 0.200
94
c HPT001 Hepatitis C 61 0.200
95
BLR001 Biliary Atresia 55 0.200
96
P MYP004 Myopathy 67 0.200
97
PLC005 Placental Insufficiency 55 0.200
98
ADR004 Adrenal Cortical Adenocarcinoma 38 0.200
99
CNN003 Conn's Syndrome 77 0.200
100
CRT013 Carotid Stenosis 51 0.200
101
CHL122 Cholesteatoma of Middle Ear 51 0.200
102
CHG001 Chagas Disease 65 0.200
103
P DMN002 Dementia 65 0.200
104
HPT022 Hepatoblastoma 54 0.200
105
CND006 Candida Glabrata 29 0.200
106
IRR002 Irritable Bowel Syndrome 64 0.200
107
GRW007 Growth Hormone Deficiency 47 0.200
108
c MJR022 Major Affective Disorder 8 37 0.142
109
c NMN014 Niemann-Pick Disease, Type C2 49 0.142
110
CRH005 Crohn's Colitis 53 0.142
111
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.142
112
TRN021 Transaldolase Deficiency 43 0.142
113
ATH013 Atherosclerosis Susceptibility 63 0.142
114
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.142
115
CTR172 Citrullinemia, Classic 64 0.142
116
P SRC025 Sarcoidosis 1 70 0.142
117
HYD038 Hydrops Fetalis, Nonimmune 57 0.142
118
OCL069 Ocular Motor Apraxia 57 0.142
119
c MCP049 Mucopolysaccharidosis, Type Vii 62 0.142
120
P RTT002 Rett Syndrome 79 0.142
121
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.142
122
c LYM150 Lymphatic Malformation 7 43 0.142
123
c HPT073 Hepatitis C Virus 70 0.142
124
c MJR024 Major Affective Disorder 9 40 0.142
125
c LWD007 Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 7 12 0.142
126
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.142
127
ANT003 Antley-Bixler Syndrome 50 0.142
128
P EXN002 Exanthem 58 0.142
129
c STS010 Sitosterolemia 1 46 0.142
130
P MTC003 Metachromatic Leukodystrophy 71 0.142
131
P AST005 Asthma 75 0.142
132
c MCR115 Microvascular Complications of Diabetes 5 65 0.142
133
P MJR001 Major Depressive Disorder 68 0.142
134
LPT014 Leptin Deficiency or Dysfunction 77 0.142
135
HYP732 Hyperalphalipoproteinemia 1 53 0.142
136
NNL006 Non-Alcoholic Steatohepatitis 54 0.142
137
PRP080 Peripheral Artery Disease 54 0.142
138
HYP060 Hyperinsulinism 53 0.142
139
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.142
140
HYP080 Hypogonadism 49 0.142
141
P TMP001 Temporal Lobe Epilepsy 49 0.142
142
c BSL007 Basal Cell Carcinoma 67 0.142
143
RTN020 Retinal Vascular Disease 45 0.142
144
CRD003 Cardiac Sarcoidosis 44 0.142
145
P PRP019 Peripheral Nervous System Disease 57 0.142
146
P BPL003 Bipolar Disorder 56 0.142
147
CNG034 Congestive Heart Failure 69 0.142
148
P HPT021 Hepatitis 68 0.142
149
STT001 Status Epilepticus 58 0.142
150
MDD011 Mood Disorder 61 0.142
151
GST033 Gestational Diabetes 60 0.142
152
P LKD001 Leukodystrophy 58 0.142
153
RCK004 Rickets 64 0.142
154
TXC005 Toxic Shock Syndrome 61 0.142
155
MNT002 Mental Depression 56 0.142
156
P RTN018 Retinal Disease 53 0.142
157
c INH020 Inherited Metabolic Disorder 47 0.142
158
P HYP121 Hypoalphalipoproteinemia 42 0.142
159
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.142
160
AMN012 Aminoacidopathies 19 0.142
161
PRX001 Peroxisomal Disease 46 0.142
162
P MSC003 Muscular Atrophy 52 0.142
163
P NRB001 Neuroblastoma 66 0.142
164
P MYC008 Myocarditis 59 0.142
165
P NRP001 Neuropathy 59 0.142
166
CYT014 Cytochrome P450 Oxidoreductase Deficiency 35 0.142
167
GLM044 Glomerular Disease 34 0.142
168
P HYP265 Hypotonia 42 0.142
169
HDN002 Head Injury 44 0.142
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