Search results for ATF6

82 hits were found for ATF6

# Family MCID Name MIFTS Score
1
c ACH038 Achromatopsia 7 39 5.979
2
P ACH003 Achromatopsia 61 5.298
3
P HPT023 Hepatocellular Carcinoma 100 4.153
4
CYS001 Cystic Fibrosis 81 3.634
5
P CNR004 Cone-Rod Dystrophy 2 73 2.988
6
P LNG028 Long Qt Syndrome 66 2.917
7
c WLF013 Wolfram Syndrome 1 60 2.917
8
P WLF004 Wolfram Syndrome 60 2.917
9
P RTN008 Retinitis Pigmentosa 79 2.152
10
FND002 Fundus Dystrophy 55 2.113
11
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 2.062
12
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 56 2.062
13
c ACH023 Achromatopsia 4 38 2.062
14
WST010 West Nile Virus Infection 32 2.062
15
ATS010 Autosomal Recessive Disease 48 0.122
16
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.106
17
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.106
18
ISC004 Ischemia 58 0.106
19
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.106
20
P LTR001 Lateral Sclerosis 54 0.106
21
PTH003 Pathologic Nystagmus 52 0.106
22
P CLR019 Color Blindness 48 0.106
23
CLR033 Color Vision Deficiency 41 0.106
24
P CLR023 Colorectal Cancer 99 0.086
25
P ENC004 Encephalitis 61 0.086
26
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.086
27
P BCL017 B-Cell Lymphoma 58 0.086
28
P RTN016 Retinal Degeneration 53 0.086
29
P RTN018 Retinal Disease 53 0.086
30
RTN023 Retinitis 46 0.086
31
NRR001 Neuroretinitis 42 0.086
32
P ALZ034 Alzheimer Disease 88 0.061
33
P PNC035 Pancreatic Cancer 84 0.061
34
OST012 Osteoarthritis 78 0.061
35
GLB015 Glioblastoma Multiforme 75 0.061
36
c ATR087 Atrial Standstill 1 75 0.061
37
SVR004 Severe Combined Immunodeficiency 73 0.061
38
c HYP836 Hypercholesterolemia, Familial, 1 73 0.061
39
ULC004 Ulcerative Colitis 73 0.061
40
c HPT073 Hepatitis C Virus 72 0.061
41
P NRB001 Neuroblastoma 72 0.061
42
P ATS364 Autism 70 0.061
43
P AMY004 Amyloidosis 70 0.061
44
P LVR013 Liver Disease 68 0.061
45
c ATS007 Autism Spectrum Disorder 67 0.061
46
P LPS002 Liposarcoma 65 0.061
47
P MTR014 Motor Neuron Disease 65 0.061
48
LPD008 Lipid Metabolism Disorder 62 0.061
49
P SPN046 Spinal Muscular Atrophy 62 0.061
50
c SVR001 Severe Acute Respiratory Syndrome 62 0.061
51
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.061
52
FTT001 Fatty Liver Disease 61 0.061
53
P ENC018 Encephalopathy 61 0.061
54
P PNC044 Pancreatitis 61 0.061
55
LNG099 Lung Disease 60 0.061
56
P MCR010 Microcephaly 59 0.061
57
c HPT016 Hepatitis B 59 0.061
58
PST028 Post-Traumatic Stress Disorder 58 0.061
59
EYD002 Eye Disease 58 0.061
60
JPN002 Japanese Encephalitis 57 0.061
61
HYP266 Hypoxia 57 0.061
62
TCK001 Tick-Borne Encephalitis 56 0.061
63
BCT022 Bacterial Infectious Disease 56 0.061
64
GLC003 Glucose Intolerance 54 0.061
65
WST005 West Nile Virus 54 0.061
66
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.061
67
P MSC003 Muscular Atrophy 52 0.061
68
c INH030 Inherited Retinal Disorder 51 0.061
69
P AST007 Astrocytoma 51 0.061
70
URC002 Urea Cycle Disorder 51 0.061
71
c ACH020 Achromatopsia 2 50 0.061
72
TRT020 Tritanopia 49 0.061
73
RNL077 Renal Fibrosis 47 0.061
74
ACT084 Acute Stress Disorder 47 0.061
75
CRB004 Cerebral Artery Occlusion 45 0.061
76
MND023 Mend Syndrome 43 0.061
77
P CND005 Cone Dystrophy 43 0.061
78
c ADN012 Adenocarcinoma in Situ 42 0.061
79
c PRG020 Paragangliomas 3 39 0.061
80
PPL052 Papillomatosis, Confluent and Reticulated 33 0.061
81
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.061
82
c CNR023 Cone-Rod Dystrophy 8 31 0.061
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