Search results for FURIN

182 hits were found for FURIN

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 99 3.790
2
DPH001 Diphtheria 60 3.429
3
P INF038 Influenza 68 3.390
4
CLN015 Colon Adenocarcinoma 65 2.901
5
P AMY004 Amyloidosis 70 2.861
6
c ART115 Aortic Valve Disease 1 75 2.813
7
ANT024 Anthrax Disease 58 2.663
8
AVN001 Avian Influenza 59 2.559
9
IMM167 Immune Deficiency Disease 78 2.509
10
c SVR001 Severe Acute Respiratory Syndrome 62 2.450
11
CVD001 Covid-19 44 2.397
12
SQM013 Squamous Cell Carcinoma, Head and Neck 80 2.353
13
CHK001 Chikungunya 57 2.353
14
CRM001 Crimean-Congo Hemorrhagic Fever 53 2.353
16
MDD018 Middle East Respiratory Syndrome 43 2.353
17
BRN018 Borna Disease 36 2.353
18
c HYP595 Hypertension, Essential 84 2.327
19
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 2.327
20
P ECT006 Ectodermal Dysplasia 62 2.327
21
P CNR004 Cone-Rod Dystrophy 2 73 2.296
23
P HYP818 Hypobetalipoproteinemia, Familial, 1 56 2.296
24
c HRD039 Hereditary Amyloidosis 45 1.695
25
EBL001 Ebola Hemorrhagic Fever 49 1.664
26
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 1.624
27
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 1.624
28
P WLL002 Weill-Marchesani Syndrome 56 1.624
29
P AMY084 Amyloidosis, Finnish Type 53 1.624
30
MSC164 Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency 48 1.624
31
INH001 Inhalation Anthrax 41 1.624
32
CRN322 Coronavirus Infectious Disease 40 1.624
33
MRB001 Marburg Hemorrhagic Fever 40 1.624
35
CTN013 Cutaneous Anthrax 37 1.624
36
TRC020 Tracheitis 36 1.624
37
c BRC062 Brachydactyly, Type D 34 1.624
38
RFR002 Refractory Hairy Cell Leukemia 33 1.624
39
RFR004 Refractory Hematologic Cancer 30 1.624
40
MRR003 Murray Valley Encephalitis 29 1.624
41
GST046 Gastrointestinal Anthrax 24 1.624
42
VCC001 Vaccinia 49 0.247
43
SQM006 Squamous Cell Carcinoma 60 0.137
44
PLG002 Plague 63 0.119
45
c HPT016 Hepatitis B 59 0.119
46
P DNG005 Dengue Virus 59 0.119
47
P ALZ034 Alzheimer Disease 88 0.108
48
INS001 Insulinoma 60 0.108
49
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.108
50
P BRS047 Breast Cancer 97 0.097
51
c HYP836 Hypercholesterolemia, Familial, 1 73 0.097
52
c HMP029 Hemophilia a 67 0.097
53
P RHB003 Rhabdomyosarcoma 63 0.097
54
BCT022 Bacterial Infectious Disease 56 0.097
55
WST005 West Nile Virus 54 0.097
56
P HMP007 Hemophilia 51 0.097
57
NWC001 Newcastle Disease 45 0.097
58
P HPT023 Hepatocellular Carcinoma 100 0.084
59
P PNC035 Pancreatic Cancer 84 0.084
60
GLB015 Glioblastoma Multiforme 75 0.084
61
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.084
62
HMN044 Human Immunodeficiency Virus Type 1 71 0.084
63
ATH013 Atherosclerosis Susceptibility 65 0.084
64
P ADN016 Adenocarcinoma 64 0.084
65
P GLM045 Glioma 63 0.084
66
LPP008 Lipoprotein Quantitative Trait Locus 62 0.084
67
MSL001 Measles 62 0.084
68
GNG013 Gingivitis 59 0.084
69
P FBR017 Fibrosarcoma 56 0.084
70
SFT003 Soft Tissue Sarcoma 56 0.084
71
HMS001 Hemosiderosis 54 0.084
72
ART140 Arteries, Anomalies of 52 0.084
73
c MLG068 Malignant Glioma 46 0.084
74
GLL048 Glial Tumor 45 0.084
75
P RRH023 Rare Hereditary Hemochromatosis 41 0.084
76
PLY150 Polykaryocytosis Inducer 31 0.084
77
P OVR042 Ovarian Cancer 88 0.068
79
OST012 Osteoarthritis 78 0.068
80
CRV035 Cervical Cancer 76 0.068
81
BRN024 Bronchitis 68 0.068
82
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.068
83
OST159 Osteogenic Sarcoma 66 0.068
84
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.068
85
c PRC016 Pre-Eclampsia 63 0.068
86
ATM095 Autoimmune Disease 62 0.068
87
P ENC004 Encephalitis 61 0.068
88
VRL011 Viral Infectious Disease 61 0.068
89
HYP266 Hypoxia 57 0.068
90
TCK001 Tick-Borne Encephalitis 56 0.068
91
c FRS014 Fraser Syndrome 1 56 0.068
92
P AST007 Astrocytoma 51 0.068
93
HLX001 Helix Syndrome 47 0.068
94
CHR074 Choriocarcinoma 47 0.068
95
TNG009 Tongue Squamous Cell Carcinoma 44 0.068
96
CYT002 Cytokine Deficiency 42 0.068
97
P LNG032 Lung Cancer 98 0.048
98
CYS001 Cystic Fibrosis 81 0.048
99
P RHM011 Rheumatoid Arthritis 80 0.048
100
INS024 Insulin-Like Growth Factor I 79 0.048
101
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.048
102
P LNG064 Lung Cancer Susceptibility 3 78 0.048
103
MRF001 Marfan Syndrome 77 0.048
104
c HMC039 Hemochromatosis, Type 1 74 0.048
105
SVR004 Severe Combined Immunodeficiency 73 0.048
106
c HPT073 Hepatitis C Virus 72 0.048
107
P GRF003 Graft-Versus-Host Disease 72 0.048
108
P PHC003 Pheochromocytoma 71 0.048
109
P ART022 Arthritis 69 0.048
110
P LYM118 Lymphoma 68 0.048
111
c RHB024 Rhabdomyosarcoma 2 67 0.048
112
P DMN002 Dementia 66 0.048
113
c FML021 Familial Hypercholesterolemia 66 0.048
114
P MSC005 Muscular Dystrophy 66 0.048
115
P SKN015 Skin Carcinoma 66 0.048
117
P VNW001 Von Willebrand's Disease 65 0.048
118
P PRD008 Periodontitis 64 0.048
119
P VSC007 Vascular Disease 63 0.048
120
TRN015 Transient Cerebral Ischemia 63 0.048
121
c HPT001 Hepatitis C 62 0.048
122
P HYP750 Hypertriglyceridemia, Familial 62 0.048
123
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.048
124
P ORT004 Orthostatic Intolerance 62 0.048
125
LVR012 Liver Cirrhosis 62 0.048
126
P KDN017 Kidney Cancer 60 0.048
127
P VNT002 Ventricular Septal Defect 60 0.048
128
c ACT027 Acute Pancreatitis 60 0.048
129
CHC001 Chickenpox 60 0.048
130
ORL011 Oral Cancer 60 0.048
131
P THL005 Thalassemia 60 0.048
132
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.048
133
c DNG003 Dengue Disease 59 0.048
134
P MMP001 Mumps 58 0.048
135
P INF032 Infertility 57 0.048
136
IRN002 Iron Metabolism Disease 57 0.048
137
c ACT075 Acute Myocardial Infarction 57 0.048
138
CHR177 Chromophobe Renal Cell Carcinoma 57 0.048
139
JPN002 Japanese Encephalitis 57 0.048
140
P ADL017 Adult T-Cell Leukemia 56 0.048
141
P CHN012 Chondrosarcoma 56 0.048
142
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 0.048
143
ZLL002 Zollinger-Ellison Syndrome 55 0.048
144
P DRR001 Diarrhea 55 0.048
145
P LRY044 Larynx Cancer 55 0.048
146
HRY003 Hairy Cell Leukemia 55 0.048
147
PPL022 Papilloma 54 0.048
148
P SML001 Small Cell Carcinoma 52 0.048
149
P SPP010 Suppressor of Tumorigenicity 3 51 0.048
150
LNG031 Lung Benign Neoplasm 51 0.048
151
P ECL001 Eclampsia 50 0.048
152
STM007 Stomatitis 50 0.048
153
MLL001 Molluscum Contagiosum 50 0.048
154
VPM001 Vipoma 50 0.048
155
HYP017 Hypophosphatemia 50 0.048
156
BNR002 Bone Resorption Disease 48 0.048
157
ATS010 Autosomal Recessive Disease 48 0.048
158
CLC006 Calcinosis 48 0.048
159
HYP025 Hyperphosphatemia 48 0.048
160
P HRD021 Hereditary Sensory Neuropathy 48 0.048
161
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.048
162
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.048
163
ANV001 Anovulation 47 0.048
164
ADR040 Adrenal Gland Pheochromocytoma 46 0.048
165
CWP001 Cowpox 46 0.048
166
SQM002 Squamous Cell Papilloma 46 0.048
167
GST030 Gastrinoma 45 0.048
168
SYN036 Syncope 45 0.048
169
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.048
170
ATN004 Autonomic Neuropathy 45 0.048
171
RNS001 Raine Syndrome 45 0.048
172
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.048
173
c PRS097 Prostate Cancer, Hereditary, 1 41 0.048
174
c NLD014 Nail Disorder, Nonsyndromic Congenital, 4 40 0.048
175
OVR094 Ovarian Epithelial Cancer 38 0.048
176
PRN029 Parainfluenza Virus Type 3 36 0.048
177
c LKM005 Leukemia, T-Cell, Chronic 34 0.048
178
MLG164 Malignant Epithelial Tumor of Ovary 26 0.048
179
CRY010 Cryptophthalmos 25 0.048
180
CHL131 Chlorpropamide-Alcohol Flushing 22 0.048
181
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.048
182
MLN071 Melanoma Tumor Antigen Gp90 17 0.048
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