Search results for CCL19

74 hits were found for CCL19

# Family MCID Name MIFTS Score
1
c SYS001 Systemic Lupus Erythematosus 86 4.058
2
c LKM071 Leukemia, Chronic Lymphocytic 79 3.386
3
CMM004 Common Variable Immunodeficiency 67 3.353
4
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 3.313
5
P CNT005 Central Nervous System Lymphoma 53 3.313
6
P PLY020 Polyradiculoneuropathy 46 3.313
7
c LKM060 Leukemia, Acute Lymphoblastic 3 56 2.395
8
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.139
9
ATM095 Autoimmune Disease 61 0.108
10
P LYM031 Lymphocytic Leukemia 55 0.108
11
ALL014 Allergic Encephalomyelitis 39 0.108
12
P LNG032 Lung Cancer 97 0.088
13
P OVR042 Ovarian Cancer 89 0.088
14
IMM167 Immune Deficiency Disease 78 0.088
15
ALL003 Allergic Rhinitis 67 0.088
16
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.088
17
PRT037 Pertussis 65 0.088
18
P RHN004 Rhinitis 57 0.088
19
c CHR020 Chronic Interstitial Cystitis 37 0.088
20
P BRS047 Breast Cancer 96 0.062
21
P PNC035 Pancreatic Cancer 84 0.062
22
P RHM011 Rheumatoid Arthritis 80 0.062
23
P BLD134 Bladder Cancer 78 0.062
24
P LNG064 Lung Cancer Susceptibility 3 77 0.062
25
CRV035 Cervical Cancer 76 0.062
26
c SPN225 Spondyloarthropathy 1 73 0.062
27
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.062
28
P GRF003 Graft-Versus-Host Disease 71 0.062
29
c LKM063 Leukemia, Chronic Myeloid 71 0.062
30
P ART022 Arthritis 70 0.062
31
SMT004 Smith-Lemli-Opitz Syndrome 69 0.062
32
MLN008 Melanoma 69 0.062
33
P LVR013 Liver Disease 68 0.062
34
c JVN010 Juvenile Rheumatoid Arthritis 67 0.062
35
MNT001 Mantle Cell Lymphoma 66 0.062
36
ATH013 Atherosclerosis Susceptibility 66 0.062
37
c SML038 Small Cell Cancer of the Lung 65 0.062
38
P HRP006 Herpes Simplex 65 0.062
39
INC002 Inclusion Body Myositis 64 0.062
40
LYM017 Lyme Disease 63 0.062
41
P CRN018 Coronary Artery Anomaly 63 0.062
42
SKN016 Skin Disease 63 0.062
43
CNT061 Conotruncal Heart Malformations 63 0.062
44
LPD008 Lipid Metabolism Disorder 62 0.062
45
c SCL052 Scleroderma, Familial Progressive 62 0.062
46
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.062
47
PSR001 Psoriatic Arthritis 62 0.062
48
FTT001 Fatty Liver Disease 61 0.062
49
VRL011 Viral Infectious Disease 61 0.062
50
ACQ007 Acquired Immunodeficiency Syndrome 60 0.062
51
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.062
52
HLC007 Helicobacter Pylori Infection 59 0.062
53
P FBR017 Fibrosarcoma 56 0.062
54
BCT022 Bacterial Infectious Disease 56 0.062
55
AVN001 Avian Influenza 56 0.062
56
P MYS005 Myositis 56 0.062
57
RHM027 Rheumatic Disease 56 0.062
58
P GST044 Gastritis 55 0.062
59
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.062
60
ART140 Arteries, Anomalies of 53 0.062
61
SPN051 Spondylitis 52 0.062
62
P MTR003 Mitral Valve Stenosis 50 0.062
63
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.062
64
P CTN015 Cutaneous T Cell Lymphoma 49 0.062
65
VCC001 Vaccinia 49 0.062
66
BNR002 Bone Resorption Disease 48 0.062
67
ENT004 Enthesopathy 48 0.062
68
CRB004 Cerebral Artery Occlusion 44 0.062
69
c PRM038 Primary Agammaglobulinemia 43 0.062
70
ORL015 Oral Squamous Cell Carcinoma 43 0.062
71
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.062
72
c OVR114 Ovarian Cancer 1 38 0.062
73
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.062
74
INF009 Inflammatory Spondylopathy 32 0.062
Content
Loading form....