Search results for EMP2

91 hits were found for EMP2

# Family MCID Name MIFTS Score
1
c NPH076 Nephrotic Syndrome, Type 10 37 38.242
2
P NPH012 Nephrotic Syndrome 61 19.495
3
END041 Endometrial Adenocarcinoma 63 13.006
4
P CHR071 Charcot-Marie-Tooth Disease 64 11.326
5
P FCL005 Focal Segmental Glomerulosclerosis 57 11.160
6
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 40 9.008
7
c FCL025 Focal Segmental Glomerulosclerosis 1 49 7.891
8
c FCL055 Focal Segmental Glomerulosclerosis 9 30 7.891
9
c DMN017 Diamond-Blackfan Anemia 10 36 7.891
10
c FCL085 Focal Segmental Glomerulosclerosis 7 32 7.891
11
c FCL053 Focal Segmental Glomerulosclerosis 8 29 7.891
12
PYS001 Pyosalpinx 22 7.891
13
ADN013 Adenoid Squamous Cell Carcinoma 38 7.891
14
VTR005 Vitreous Disease 41 7.891
15
END057 Endometrial Cancer 76 3.183
16
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 3.045
17
P VTR007 Vitreoretinopathy 45 3.045
18
GLB002 Glioblastoma 67 2.453
19
P BRS047 Breast Cancer 97 2.081
20
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.778
21
P NSP012 Nasopharyngeal Carcinoma 60 1.430
22
CHL123 Chlamydia 58 1.388
23
RTN017 Retinal Detachment 60 1.366
24
PLC005 Placental Insufficiency 55 1.366
25
c EXD008 Exudative Vitreoretinopathy 1 71 1.296
26
RTN020 Retinal Vascular Disease 45 1.296
27
MNN043 Meningioma, Familial 79 1.243
28
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.243
29
SCR001 Secretory Meningioma 40 1.243
30
INT395 Intracranial Meningioma 47 1.243
31
P KDN018 Kidney Disease 71 1.215
32
CRN027 Corneal Neovascularization 47 1.215
33
GLM045 Glioma 62 1.215
34
GLL048 Glial Tumor 51 1.215
35
HMP001 Hemopericardium 47 1.152
36
P PRC012 Pericardial Effusion 50 1.152
37
EST002 Estrogen-Receptor Negative Breast Cancer 45 1.077
38
P MLN008 Melanoma 75 1.077
39
SKN019 Skin Melanoma 70 1.077
40
P RTN018 Retinal Disease 53 0.830
41
P ALZ034 Alzheimer Disease 87 0.637
42
BRN032 Brain Glioma 45 0.598
43
P OVR042 Ovarian Cancer 88 0.575
44
END002 Endometrioid Ovary Carcinoma 53 0.575
45
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.573
46
P PNC035 Pancreatic Cancer 87 0.573
47
IRN008 Iron Overload in Africa 50 0.564
48
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.564
49
c HPT073 Hepatitis C Virus 70 0.564
50
RJS001 Ruijs-Aalfs Syndrome 47 0.564
51
P HPT023 Hepatocellular Carcinoma 95 0.564
52
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.564
53
ADL096 Adult Hepatocellular Carcinoma 60 0.564
54
HPT079 Hepatoid Adenocarcinoma 39 0.564
55
PDT042 Pediatric Hepatocellular Carcinoma 51 0.564
56
P LNG021 Lung Occult Small Cell Carcinoma 20 0.564
57
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.564
58
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.564
59
FBR086 Fibrolamellar Carcinoma 59 0.564
60
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.564
61
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.564
62
PTY007 Pityriasis Rotunda 27 0.564
63
P BCL017 B-Cell Lymphoma 57 0.525
64
BLD131 Bladder Urothelial Carcinoma 59 0.498
65
END062 Endometrial Hyperplasia 47 0.498
66
c SML038 Small Cell Cancer of the Lung 68 0.469
67
P LNG032 Lung Cancer 98 0.469
68
c BCT013 Bacterial Pneumonia 47 0.469
69
PRT251 Proteinuria, Chronic Benign 58 0.406
70
CMB007 Combined Immunodeficiency 56 0.371
71
SVR004 Severe Combined Immunodeficiency 70 0.371
72
P LKM062 Leukemia, Acute Lymphoblastic 69 0.332
73
P FML011 Familial Adenomatous Polyposis 70 0.287
74
ECH003 Echinococcosis 52 0.287
75
ALV002 Alveolar Echinococcosis 56 0.287
76
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.235
77
c DRM040 Dermatitis Herpetiformis, Familial 35 0.235
78
P MYC084 Mycobacterium Tuberculosis 1 68 0.235
79
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 33 0.235
80
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 30 0.235
81
P INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 26 0.235
82
BRC012 Brucellosis 66 0.235
83
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 0.235
84
P DRM007 Dermatitis Herpetiformis 54 0.235
85
P ATS364 Autism 72 0.166
86
CHR498 Chromosome 16p11.2 Duplication Syndrome 26 0.166
87
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.166
88
CHR621 Chromosome 16p11.2 Deletion Syndrome, 593-Kb 24 0.166
89
THR024 Thrombosis 56 0.166
90
TTH006 Tooth Disease 51 0.166
91
PLM001 Pulmonary Tuberculosis 69 0.166
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