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Search results for TGFB2

113 hits were found for TGFB2

# Family MCID Name MIFTS Score
1
c LYS017 Loeys-Dietz Syndrome 4 51 5.179
2
P CLR023 Colorectal Cancer 99 4.033
3
P LYS001 Loeys-Dietz Syndrome 65 3.928
4
HLT001 Holt-Oram Syndrome 63 3.636
5
P PNC035 Pancreatic Cancer 84 3.557
6
P HPT023 Hepatocellular Carcinoma 100 3.006
7
P BRS047 Breast Cancer 97 3.006
8
P OVR042 Ovarian Cancer 88 3.006
9
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 2.887
10
ART016 Aortic Aneurysm 69 2.841
11
P GST053 Gastric Cancer 83 2.716
12
P PRS040 Prostate Cancer 97 2.689
13
MLR004 Malaria 81 2.689
14
ART017 Aortic Disease 49 2.434
15
ANR040 Aneurysm 59 2.387
16
P OST002 Osteoporosis 74 2.360
17
P OPN001 Open-Angle Glaucoma 49 2.360
18
P RHM011 Rheumatoid Arthritis 80 2.329
19
c DLT002 Dilated Cardiomyopathy 79 2.329
20
P GLM045 Glioma 63 2.329
21
P CTR002 Cataract 60 2.329
22
P UVT001 Uveitis 57 2.329
23
NVS001 Neovascular Glaucoma 53 2.329
24
BLL004 Bullous Keratopathy 49 2.329
25
MLK006 Milk Allergy 48 2.329
26
BRS050 Breast Cyst 40 2.329
27
CNN005 Connective Tissue Disease 68 2.065
28
MRF001 Marfan Syndrome 77 1.996
29
P SCL018 Scoliosis 60 1.996
30
P MTR012 Mitral Valve Disease 58 1.969
31
CLF027 Cleft Palate, Isolated 64 1.938
32
c GLC092 Glaucoma, Primary Open Angle 62 1.938
33
INT323 Intraocular Pressure Quantitative Trait Locus 62 1.938
34
P MYP006 Myopia 55 1.938
36
c ART115 Aortic Valve Disease 1 75 1.901
37
P APL001 Aplastic Anemia 74 1.901
38
P HYP061 Hypertrophic Cardiomyopathy 70 1.901
39
PNC129 Pancreatic Adenocarcinoma 68 1.901
40
P MSC005 Muscular Dystrophy 66 1.901
41
P MCR115 Microvascular Complications of Diabetes 5 66 1.901
42
c MCR129 Microvascular Complications of Diabetes 1 66 1.901
43
P HYD006 Hydrocephalus 66 1.901
44
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 1.901
45
TRN015 Transient Cerebral Ischemia 63 1.901
46
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.901
47
RTN017 Retinal Detachment 61 1.901
48
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 1.901
49
P MLN069 Melanoma, Uveal 59 1.901
50
KRT071 Keratosis, Seborrheic 58 1.901
51
INT030 Intracranial Aneurysm 56 1.901
52
P INF037 Inflammatory Bowel Disease 54 1.901
53
STF002 Stiff Skin Syndrome 54 1.901
54
OCL006 Ocular Hypertension 53 1.901
55
ART074 Aortic Dissection 52 1.901
56
P INT099 Intrahepatic Cholestasis of Pregnancy 51 1.901
57
GNG012 Gingival Overgrowth 51 1.901
58
c PYR010 Peyronie's Disease 50 1.901
59
P KRT007 Keratoconus 50 1.901
60
KRT008 Keratopathy 47 1.901
61
c ATM099 Autoimmune Uveitis 45 1.901
62
P CRN024 Corneal Disease 44 1.901
63
MCL003 Macular Holes 40 1.901
64
PRR004 Preretinal Fibrosis 37 1.901
65
FCH002 Fuchs' Heterochromic Uveitis 35 1.901
66
c CHR054 Chronic Closed-Angle Glaucoma 32 1.901
67
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.487
68
ART001 Arterial Tortuosity Syndrome 66 1.429
69
P HRS035 Hirschsprung Disease 1 65 1.429
70
HRT036 Heritable Thoracic Aortic Disease 35 1.429
71
P ORT004 Orthostatic Intolerance 62 1.392
72
c LYS021 Loeys-Dietz Syndrome 3 58 1.392
73
c LYS019 Loeys-Dietz Syndrome 1 57 1.392
74
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.344
75
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 61 1.344
76
EYD002 Eye Disease 58 1.344
77
c LYS020 Loeys-Dietz Syndrome 5 50 1.344
78
P ALP061 Alopecia, Androgenetic, 1 49 1.344
79
AND014 Androgenic Alopecia 46 1.344
80
P OST028 Osteochondroma 45 1.344
81
P PRS062 Persistent Hyperplastic Primary Vitreous 44 1.344
82
TBR006 Tuberculoid Leprosy 44 1.344
83
P ORF002 Orofacial Cleft 44 1.344
84
TND006 Tendinosis 42 1.344
85
VTR005 Vitreous Disease 39 1.344
86
TRC007 Tricuspid Valve Prolapse 36 1.344
87
WRT003 Warthin Tumor 34 1.344
88
STR019 Steroid-Induced Glaucoma 32 1.344
89
HGH041 High-Grade Astrocytoma 32 1.344
90
THL004 Theileriasis 30 1.344
91
PHC002 Phacogenic Glaucoma 25 1.344
92
HYD004 Hydrops of Gallbladder 24 1.344
93
UPP002 Upper Lip Cancer 18 1.344
94
CLF004 Cleft Lip/palate 54 0.082
95
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.082
96
CLF001 Cleft Lip 53 0.082
97
RFR003 Refractive Error 43 0.082
98
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.058
99
P MLT020 Multiple Sclerosis 72 0.058
100
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.058
101
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.058
102
P CRN300 Coronary Heart Disease 1 63 0.058
103
c SCL052 Scleroderma, Familial Progressive 61 0.058
104
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.058
105
P BCL017 B-Cell Lymphoma 58 0.058
106
P VND007 Van Der Woude Syndrome 1 58 0.058
107
P RTN016 Retinal Degeneration 53 0.058
108
BLD053 Blood Platelet Disease 49 0.058
109
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.058
110
AST006 Astigmatism 47 0.058
111
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.058
112
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.058
113
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.058
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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