Search results for foxe3

89 hits were found for foxe3

# Family MCID Name MIFTS Score
1
P ANT088 Anterior Segment Dysgenesis 53 45.861
2
c ANT086 Anterior Segment Dysgenesis 2 47 39.939
3
c ART133 Aortic Aneurysm, Familial Thoracic 11 20 30.541
4
c CTR097 Cataract 34, Multiple Types 29 29.228
5
c ANT077 Anterior Segment Dysgenesis 1 46 25.442
6
c AXN010 Axenfeld-Rieger Syndrome, Type 3 47 24.795
7
PTR032 Peters-Plus Syndrome 63 19.822
8
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 19.238
9
P CTR002 Cataract 59 16.795
10
MCR013 Microphthalmia 60 13.924
11
ERL027 Early-Onset Non-Syndromic Cataract 31 13.191
12
ART016 Aortic Aneurysm 69 12.746
13
P SCL047 Sclerocornea 32 12.080
14
ART017 Aortic Disease 49 10.630
15
ANR040 Aneurysm 60 10.630
16
CNG005 Congenital Aphakia 23 10.492
17
ART074 Aortic Dissection 53 9.413
18
KRT019 Keratitis, Hereditary 66 9.413
19
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 9.413
20
HRT036 Heritable Thoracic Aortic Disease 36 9.348
21
P ANR048 Aniridia 1 66 7.954
22
CLB010 Coloboma of Macula 53 7.929
23
c PRM032 Primary Congenital Glaucoma 40 6.945
24
P AXN002 Axenfeld-Rieger Syndrome 62 6.892
25
c MCR241 Microphthalmia, Syndromic 3 55 6.823
26
P CRN024 Corneal Disease 43 6.823
27
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 6.656
28
FCT003 Factor X Deficiency 54 6.656
29
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 6.656
30
AMB002 Amblyopia 49 6.656
31
P JVN008 Juvenile Glaucoma 50 6.656
32
P ISL020 Isolated Microphthalmia 23 6.656
33
P NNP021 Nanophthalmos 40 6.656
34
EYC003 Eye Accommodation Disease 18 6.656
35
DSS006 Disuse Amblyopia 23 6.656
36
c GLC097 Glaucoma 3, Primary Congenital, a 57 6.656
37
c AXN009 Axenfeld-Rieger Syndrome, Type 1 48 6.656
38
ANS002 Aniseikonia 32 6.656
39
P PRS062 Persistent Hyperplastic Primary Vitreous 47 6.656
40
c EHL073 Ehlers-Danlos Syndrome, Classic Type, 1 55 6.656
41
LYM029 Lymphedema-Distichiasis Syndrome 52 6.656
42
PHC001 Phacolytic Glaucoma 22 6.656
43
P LNS003 Lens Disease 33 6.656
44
IRS003 Iris Disease 31 6.656
45
ORB007 Orbital Cyst 22 6.656
46
c CHR054 Chronic Closed-Angle Glaucoma 33 6.656
47
SPH003 Sphenoorbital Meningioma 20 6.656
48
EST005 Esotropia 42 6.656
49
FRY006 Fryns Microphthalmia Syndrome 52 2.448
50
P BRS047 Breast Cancer 97 1.788
51
P LYS001 Loeys-Dietz Syndrome 65 1.217
52
AYM001 Ayme-Gripp Syndrome 57 1.154
53
P EYD002 Eye Disease 57 1.118
54
P RTN008 Retinitis Pigmentosa 79 1.034
55
LBR036 Leber Plus Disease 67 1.034
56
NRR001 Neuroretinitis 42 1.034
57
RTN023 Retinitis 45 1.034
58
c SCL052 Scleroderma, Familial Progressive 60 0.912
59
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.766
60
P PNC035 Pancreatic Cancer 86 0.602
61
SX2004 Sox2 Disorder 13 0.408
62
c ERL012 Early-Onset Glaucoma 23 0.333
63
c BSL007 Basal Cell Carcinoma 68 0.289
64
P RHB003 Rhabdomyosarcoma 66 0.289
65
HMT002 Hematologic Cancer 61 0.289
66
P LKM062 Leukemia, Acute Lymphoblastic 69 0.236
67
NRL016 Neural Tube Defects 81 0.236
68
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.236
70
c LKM005 Leukemia, T-Cell, Chronic 33 0.236
71
CLB026 Colobomatous Microphthalmia 46 0.236
72
c GLC111 Galactosemia Ii 54 0.167
73
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.167
74
c MCR252 Microphthalmia, Syndromic 5 38 0.167
75
INT395 Intracranial Meningioma 48 0.167
76
P GLC113 Galactosemia I 65 0.167
77
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.167
78
c CTR111 Cataract 36 35 0.167
79
P CRN249 Cornea Plana 30 0.167
80
KRT002 Keratomalacia 54 0.167
81
c MCR263 Microphthalmia, Syndromic 1 47 0.167
82
MNN043 Meningioma, Familial 79 0.167
83
CLR030 Clear Cell Renal Cell Carcinoma 54 0.167
84
SCR001 Secretory Meningioma 40 0.167
85
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.167
86
P NRF002 Neurofibromatosis 60 0.167
87
CNG067 Congenital Cystic Eye 14 0.167
88
CRY010 Cryptophthalmos 25 0.167
Content
Loading form....