Search results for IFIH1

112 hits were found for IFIH1

# Family MCID Name MIFTS Score
1
MD5001 Mda5 Deficiency 6 7.237
2
c ACR084 Aicardi-Goutieres Syndrome 7 29 5.944
3
c SNG011 Singleton-Merten Syndrome 1 30 5.756
4
P SNG014 Singleton-Merten Syndrome 30 3.359
5
P ACR001 Aicardi-Goutieres Syndrome 62 3.342
6
P DRM010 Dermatomyositis 61 3.240
7
P MLN008 Melanoma 69 3.215
8
P INF038 Influenza 68 3.187
9
P HPT021 Hepatitis 67 3.187
10
P HRP006 Herpes Simplex 65 3.187
11
P DBT009 Diabetes Mellitus 64 3.187
12
c SYS001 Systemic Lupus Erythematosus 86 2.928
13
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 18 2.889
14
P PSR002 Psoriasis 62 2.845
15
INT066 Interstitial Lung Disease 60 2.820
16
LNG099 Lung Disease 60 2.792
17
MLR004 Malaria 81 2.760
18
MSL001 Measles 62 2.760
19
P MYS005 Myositis 56 2.760
20
BSL008 Basal Ganglia Disease 43 2.350
21
c HRD010 Hereditary Spastic Paraplegia 66 2.323
22
P MCR010 Microcephaly 59 2.323
23
RTR008 Root Resorption 45 2.323
24
P THR014 Thrombocytopenia 67 2.291
25
c SVR001 Severe Acute Respiratory Syndrome 62 2.254
26
VRL011 Viral Infectious Disease 61 2.254
27
P DNG005 Dengue Virus 59 2.254
28
SBC001 Subacute Sclerosing Panencephalitis 56 2.254
29
MTH009 Mouth Disease 56 2.254
30
WST005 West Nile Virus 54 2.254
31
MDD018 Middle East Respiratory Syndrome 43 2.254
32
c CHL140 Chilblain Lupus 1 58 1.642
33
CHL028 Childhood Type Dermatomyositis 58 1.642
34
c DBT099 Diabetes Mellitus, Type I 65 1.594
35
P EXN002 Exanthem 57 1.594
36
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 56 1.594
37
MCR165 Microphthalmia with Limb Anomalies 53 1.594
38
LSS003 Lassa Fever 50 1.594
39
ACT029 Acute Interstitial Pneumonia 49 1.594
40
c NNN013 Noonan Syndrome 6 45 1.594
41
NNS002 Nonspecific Interstitial Pneumonia 45 1.594
42
HRP001 Herpangina 45 1.594
43
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 1.594
44
CRP002 Croup 44 1.594
45
CRN322 Coronavirus Infectious Disease 40 1.594
46
c NNN009 Noonan Syndrome 2 39 1.594
47
P DBT034 Diabetes Mellitus, Insulin-Dependent, 20 38 1.594
48
MSC190 Muscular Disease 37 1.594
49
c ADL027 Adult Dermatomyositis 30 1.594
50
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 25 1.594
51
c TYP040 Type 1 Diabetes Mellitus 18 22 1.594
52
MSC004 Muscle Tissue Disease 21 1.594
53
ATM095 Autoimmune Disease 62 0.256
54
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.220
55
P LPS004 Lupus Erythematosus 61 0.144
56
P GRV001 Graves' Disease 55 0.131
57
PRP016 Paraplegia 52 0.117
58
P THY032 Thyroiditis 52 0.117
59
P HYP086 Hypothyroidism 69 0.102
60
P PRD008 Periodontitis 64 0.102
61
PST011 Pustulosis of Palm and Sole 52 0.102
62
P PRS040 Prostate Cancer 97 0.083
63
P MLT020 Multiple Sclerosis 72 0.083
64
P ENC018 Encephalopathy 61 0.083
65
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.083
66
P PLY041 Polymyositis 57 0.083
67
THY030 Thyroid Gland Disease 52 0.083
68
IMM003 Immunoglobulin Alpha Deficiency 45 0.083
69
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.083
70
SPS019 Spastic Paraparesis 38 0.083
71
c ACR092 Aicardi-Goutieres Syndrome 5 38 0.083
72
c ACR090 Aicardi-Goutieres Syndrome 2 36 0.083
73
c ACR081 Aicardi-Goutieres Syndrome 6 32 0.083
74
PRN035 Perniosis 28 0.083
75
TYP044 Type 1 Interferonopathy 17 0.083
76
c DLT002 Dilated Cardiomyopathy 79 0.059
77
c ATR087 Atrial Standstill 1 75 0.059
78
c HPT073 Hepatitis C Virus 72 0.059
79
P MYP004 Myopathy 70 0.059
80
P PLM037 Pulmonary Hypertension 67 0.059
81
P CLC063 Celiac Disease 1 66 0.059
82
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.059
83
CHR063 Chronic Mucocutaneous Candidiasis 63 0.059
84
c HPT001 Hepatitis C 62 0.059
85
P VSC011 Vasculitis 62 0.059
86
PSR001 Psoriatic Arthritis 61 0.059
87
c ACT027 Acute Pancreatitis 60 0.059
88
P CTR002 Cataract 60 0.059
89
P MYC008 Myocarditis 59 0.059
90
P LKD001 Leukodystrophy 59 0.059
91
P CND004 Candidiasis 58 0.059
92
P PRP019 Peripheral Nervous System Disease 58 0.059
93
P GLM007 Glomerulonephritis 57 0.059
94
P NRP001 Neuropathy 56 0.059
95
c GRV008 Graves Disease 1 56 0.059
96
c PRD040 Periodontitis, Chronic 53 0.059
97
P PRC012 Pericardial Effusion 51 0.059
98
SPL018 Splenomegaly 48 0.059
99
HMP001 Hemopericardium 48 0.059
100
DYS022 Dyschromatosis Symmetrica Hereditaria 48 0.059
101
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.059
102
PNC085 Penicillin Allergy 45 0.059
103
SPS057 Spasticity 45 0.059
104
ENC005 Encephalomalacia 43 0.059
105
IMM154 Immunoglobulin a Deficiency 1 42 0.059
106
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.059
107
P CRB088 Cerebral Atrophy 37 0.059
108
SYS071 Systemic Autoimmune Disease 37 0.059
109
c ACR091 Aicardi-Goutieres Syndrome 4 36 0.059
110
ACR062 Acroosteolysis 35 0.059
111
c CHL114 Chilblain Lupus 2 26 0.059
112
P FML337 Familial Chilblain Lupus 25 0.059
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