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Search results for
cap2
51 hits were found for cap2
#
Family
MCID
Name
MIFTS
Score
1
FML304
Familial Isolated Dilated Cardiomyopathy
49
9.407
2
c
DLT002
Dilated Cardiomyopathy
78
5.265
3
CRD132
Cardiac Conduction Defect
60
4.759
4
P
GST053
Gastric Cancer
83
4.707
5
c
ATR087
Atrial Standstill 1
74
4.516
6
P
MLN008
Melanoma
76
4.447
7
P
HPT023
Hepatocellular Carcinoma
96
3.862
8
P
OVR042
Ovarian Cancer
88
3.187
9
GLL048
Glial Tumor
52
3.027
10
GLM045
Glioma
63
3.027
11
MCR013
Microphthalmia
60
2.913
12
OVR094
Ovarian Epithelial Cancer
39
2.614
13
NDL001
Nodular Malignant Melanoma
45
2.420
14
P
MYP004
Myopathy
67
2.380
15
c
FBR046
Fibrosis of Extraocular Muscles, Congenital, 1
59
2.317
16
TRD008
Triiodothyronine Receptor Auxiliary Protein
33
2.317
17
c
MJR022
Major Affective Disorder 8
38
2.215
18
c
MJR024
Major Affective Disorder 9
41
2.215
19
P
BPL003
Bipolar Disorder
56
2.215
20
TRN015
Transient Cerebral Ischemia
63
2.095
21
P
VSC007
Vascular Disease
63
2.095
22
P
PNM007
Pneumonia
67
1.562
23
LNG111
Lung Non-Squamous Non-Small Cell Carcinoma
56
1.442
24
P
LNG021
Lung Occult Small Cell Carcinoma
20
1.442
25
LNG019
Lung Combined Type Small Cell Carcinoma
32
1.442
26
P
PNC035
Pancreatic Cancer
86
1.272
27
ALL029
Allergic Disease
59
1.210
28
P
BND020
Bone Disease
59
1.210
29
P
HRP006
Herpes Simplex
65
0.988
30
P
RNV001
Renovascular Hypertension
49
0.988
31
P
ATR011
Atrial Fibrillation
66
0.857
32
c
FML001
Familial Atrial Fibrillation
65
0.857
33
P
BRS047
Breast Cancer
98
0.811
34
ACR009
Acromesomelic Dysplasia, Hunter-Thompson Type
41
0.698
35
c
DFN137
Deafness, Autosomal Dominant 13
32
0.698
36
c
DFN154
Deafness, Autosomal Dominant 31
22
0.698
37
PRP027
Peripheral Vascular Disease
71
0.698
38
ALV005
Alveolar Soft Part Sarcoma
61
0.698
39
ALC028
Alacrima, Achalasia, and Mental Retardation Syndrome
68
0.698
40
MYL005
Myelofibrosis
71
0.698
41
PLY001
Polycythemia Vera
69
0.698
42
P
PRS040
Prostate Cancer
95
0.698
43
c
DFN150
Deafness, Autosomal Dominant 21
24
0.698
44
TRM010
Traumatic Brain Injury
51
0.698
45
P
PLY018
Polycythemia
56
0.698
46
CMB007
Combined Immunodeficiency
57
0.698
47
P
ESS003
Essential Thrombocythemia
69
0.698
48
CNG034
Congestive Heart Failure
69
0.698
49
SVR004
Severe Combined Immunodeficiency
72
0.698
50
CHL068
Cholestasis
61
0.698
51
BRN071
Brain Injury
50
0.698
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