Search results for EMP2

90 hits were found for EMP2

# Family MCID Name MIFTS Score
1
c NPH076 Nephrotic Syndrome, Type 10 37 38.226
2
P NPH012 Nephrotic Syndrome 62 19.490
3
END041 Endometrial Adenocarcinoma 63 13.004
4
P CHR071 Charcot-Marie-Tooth Disease 64 11.322
5
P FCL005 Focal Segmental Glomerulosclerosis 57 11.156
6
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 40 9.003
7
c FCL085 Focal Segmental Glomerulosclerosis 7 32 7.888
8
c FCL055 Focal Segmental Glomerulosclerosis 9 29 7.888
9
c DMN017 Diamond-Blackfan Anemia 10 36 7.888
10
c FCL053 Focal Segmental Glomerulosclerosis 8 29 7.888
11
c FCL025 Focal Segmental Glomerulosclerosis 1 49 7.888
12
ADN013 Adenoid Squamous Cell Carcinoma 37 7.888
13
PYS001 Pyosalpinx 23 7.888
14
VTR005 Vitreous Disease 40 7.888
15
END057 Endometrial Cancer 71 3.186
16
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 3.048
17
P VTR007 Vitreoretinopathy 45 3.048
18
P BRS047 Breast Cancer 97 2.981
19
GLB002 Glioblastoma 67 2.455
20
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.779
21
P NSP012 Nasopharyngeal Carcinoma 60 1.431
22
CHL123 Chlamydia 58 1.389
23
RTN017 Retinal Detachment 60 1.368
24
PLC005 Placental Insufficiency 56 1.368
25
c EXD008 Exudative Vitreoretinopathy 1 71 1.297
26
RTN020 Retinal Vascular Disease 45 1.297
27
INT395 Intracranial Meningioma 48 1.244
28
MNN043 Meningioma, Familial 79 1.244
29
SCR001 Secretory Meningioma 40 1.244
30
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.244
31
CRN027 Corneal Neovascularization 47 1.216
32
GLM045 Glioma 62 1.216
33
GLL048 Glial Tumor 52 1.216
34
P KDN018 Kidney Disease 72 1.216
35
HMP001 Hemopericardium 47 1.153
36
P PRC012 Pericardial Effusion 50 1.153
37
EST002 Estrogen-Receptor Negative Breast Cancer 45 1.078
38
P MLN008 Melanoma 75 1.078
39
SKN019 Skin Melanoma 70 1.078
40
P RTN018 Retinal Disease 53 0.831
41
P ALZ034 Alzheimer Disease 87 0.638
42
BRN032 Brain Glioma 45 0.600
43
P OVR042 Ovarian Cancer 88 0.576
44
END002 Endometrioid Ovary Carcinoma 52 0.576
45
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.573
46
P PNC035 Pancreatic Cancer 86 0.573
47
IRN008 Iron Overload in Africa 51 0.567
48
RJS001 Ruijs-Aalfs Syndrome 47 0.567
49
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.567
50
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.567
51
HPT079 Hepatoid Adenocarcinoma 39 0.567
52
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.567
53
c HPT073 Hepatitis C Virus 71 0.567
54
P HPT023 Hepatocellular Carcinoma 95 0.567
55
ADL096 Adult Hepatocellular Carcinoma 60 0.567
56
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.567
57
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.567
58
PDT042 Pediatric Hepatocellular Carcinoma 50 0.567
59
PTY007 Pityriasis Rotunda 26 0.567
60
P LNG021 Lung Occult Small Cell Carcinoma 20 0.567
61
FBR086 Fibrolamellar Carcinoma 59 0.567
62
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.567
63
P BCL017 B-Cell Lymphoma 57 0.526
64
END062 Endometrial Hyperplasia 48 0.499
65
BLD131 Bladder Urothelial Carcinoma 59 0.499
66
P LNG032 Lung Cancer 98 0.470
67
c SML038 Small Cell Cancer of the Lung 69 0.470
68
c BCT013 Bacterial Pneumonia 47 0.470
69
PRT251 Proteinuria, Chronic Benign 58 0.407
70
CMB007 Combined Immunodeficiency 56 0.372
71
SVR004 Severe Combined Immunodeficiency 71 0.372
72
P LKM062 Leukemia, Acute Lymphoblastic 69 0.333
73
P FML011 Familial Adenomatous Polyposis 71 0.288
74
ALV002 Alveolar Echinococcosis 56 0.288
75
ECH003 Echinococcosis 52 0.288
76
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.235
77
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 33 0.235
78
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 31 0.235
79
BRC012 Brucellosis 66 0.235
80
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 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
c DRM040 Dermatitis Herpetiformis, Familial 35 0.235
83
P DRM007 Dermatitis Herpetiformis 54 0.235
84
CHR621 Chromosome 16p11.2 Deletion Syndrome, 593-Kb 24 0.166
85
CHR498 Chromosome 16p11.2 Duplication Syndrome 26 0.166
86
P ATS364 Autism 72 0.166
87
THR024 Thrombosis 56 0.166
88
PLM001 Pulmonary Tuberculosis 69 0.166
89
TTH006 Tooth Disease 51 0.166
90
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.166
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