Search results for vcan

78 hits were found for vcan

# Family MCID Name MIFTS Score
1
WGN003 Wagner Syndrome 36 14.819
2
WGN007 Wagner Vitreoretinopathy 38 14.138
4
P VTR007 Vitreoretinopathy 46 6.084
5
FND002 Fundus Dystrophy 55 3.157
6
P CTR002 Cataract 60 2.876
7
INT030 Intracranial Aneurysm 56 2.876
8
P MYP006 Myopia 55 2.876
9
c ART115 Aortic Valve Disease 1 75 2.834
10
CST001 Costello Syndrome 68 2.834
11
c INH030 Inherited Retinal Disorder 51 2.364
12
P STC001 Stickler Syndrome 56 2.100
13
P VTR008 Vitreoretinal Degeneration 29 2.100
14
PLG002 Plague 63 2.004
15
P ORT004 Orthostatic Intolerance 62 2.004
16
PNM005 Pneumonic Plague 51 2.004
17
TND004 Tendinopathy 43 2.004
18
BBN001 Bubonic Plague 41 2.004
19
SPT002 Septicemic Plague 33 2.004
20
ODN005 Odontogenic Myxoma 32 2.004
21
VTR002 Vitreous Syneresis 31 2.004
22
RTN017 Retinal Detachment 61 0.147
23
P PRS040 Prostate Cancer 97 0.131
24
P UVT001 Uveitis 57 0.114
25
P BRS047 Breast Cancer 97 0.093
26
P GST053 Gastric Cancer 83 0.093
27
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.093
28
P CLR023 Colorectal Cancer 99 0.066
29
c LKM061 Leukemia, Acute Myeloid 84 0.066
30
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.066
31
P RTN024 Retinoblastoma 73 0.066
32
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.066
33
AND002 Androgen Insensitivity Syndrome 66 0.066
34
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.066
35
P GLM045 Glioma 63 0.066
36
P ANR048 Aniridia 1 63 0.066
37
c MLG084 Malignant Fibrous Histiocytoma 63 0.066
38
ANR007 Anorexia Nervosa 63 0.066
39
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.066
40
P PLY014 Polycystic Kidney Disease 62 0.066
41
P TRC086 Trichohepatoenteric Syndrome 1 62 0.066
42
ALC006 Alcoholic Hepatitis 61 0.066
43
P VNT002 Ventricular Septal Defect 60 0.066
44
ACN002 Acanthosis Nigricans 60 0.066
45
P AXN002 Axenfeld-Rieger Syndrome 59 0.066
46
THY029 Thyroid Carcinoma 59 0.066
47
ANR040 Aneurysm 59 0.066
48
c GLC097 Glaucoma 3, Primary Congenital, a 58 0.066
49
ENH001 Enhanced S-Cone Syndrome 57 0.066
50
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.066
51
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.066
52
THR013 Thoracic Outlet Syndrome 54 0.066
53
P RTN016 Retinal Degeneration 53 0.066
54
c FML008 Familial Retinoblastoma 53 0.066
55
P RTN018 Retinal Disease 53 0.066
56
c CNT035 Central Nervous System Disease 52 0.066
57
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.066
58
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.066
59
VTR010 Vitreoretinochoroidopathy 51 0.066
60
PTT059 Pettigrew Syndrome 49 0.066
61
P NGH001 Night Blindness 48 0.066
62
P RTN014 Retinal Artery Occlusion 47 0.066
63
RTN023 Retinitis 46 0.066
64
c KNB006 Knobloch Syndrome 1 46 0.066
65
GLL048 Glial Tumor 45 0.066
66
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.066
67
c ATM099 Autoimmune Uveitis 45 0.066
68
RFR003 Refractive Error 43 0.066
69
c CNT028 Central Retinal Artery Occlusion 43 0.066
70
NRR001 Neuroretinitis 42 0.066
71
BRN026 Branch Retinal Artery Occlusion 40 0.066
72
c CHR020 Chronic Interstitial Cystitis 37 0.066
73
HRD016 Hereditary Retinal Dystrophy 35 0.066
74
ATX010 Ataxia Neuropathy Spectrum 34 0.066
75
ALR002 Al-Raqad Syndrome 33 0.066
76
ACT064 Acute Necrotizing Encephalitis 33 0.066
77
P KNB001 Knobloch Syndrome 32 0.066
78
BLD137 Blood Group--Ahonen 16 0.066
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