Search results for ZNF469

51 hits were found for ZNF469

# Family MCID Name MIFTS Score
1
P BRT047 Brittle Cornea Syndrome 42 65.951
2
c BRT028 Brittle Cornea Syndrome 1 39 61.623
3
c KRT029 Keratoconus 1 31 30.854
4
P KRT007 Keratoconus 50 25.621
5
P MYP006 Myopia 56 19.067
6
P EHL001 Ehlers-Danlos Syndrome 58 13.559
7
RFR003 Refractive Error 41 12.360
8
P SCL018 Scoliosis 57 11.994
9
P CRN276 Corneal Endothelial Dystrophy 53 10.574
10
BRT054 Brittle Bone Disorder 74 9.679
11
c GLC092 Glaucoma, Primary Open Angle 62 9.607
12
FCH001 Fuchs' Endothelial Dystrophy 50 8.187
13
MRT007 Martsolf Syndrome 48 7.477
14
P ANT088 Anterior Segment Dysgenesis 55 7.477
15
P CRN024 Corneal Disease 44 7.477
16
RGL001 Regular Astigmatism 19 7.477
17
CRN009 Corneal Ectasia 29 7.477
18
IRR001 Irregular Astigmatism 32 7.477
19
P AXN002 Axenfeld-Rieger Syndrome 63 7.477
20
P CLL015 Collagen Disease 48 7.477
21
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 7.227
22
ATS010 Autosomal Recessive Disease 42 3.857
23
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.343
24
P OPN001 Open-Angle Glaucoma 55 3.138
25
GST092 Gastroesophageal Reflux 61 2.727
26
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.694
27
BNN005 Bunion 31 2.336
28
P STC001 Stickler Syndrome 60 2.203
29
PHN003 Phenylketonuria 76 1.787
30
CNN005 Connective Tissue Disease 67 1.787
31
P SNS001 Sensorineural Hearing Loss 59 1.787
32
P HYP265 Hypotonia 42 1.492
33
c BRN108 Branchiootic Syndrome 1 62 1.421
34
RTN017 Retinal Detachment 60 1.230
35
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.230
36
HRW001 Hair Whorl 35 1.230
37
c BRT029 Brittle Cornea Syndrome 2 33 1.004
38
P DVL012 Developmental Dysplasia of the Hip 1 46 1.004
39
P EYD002 Eye Disease 57 1.004
40
P CRN025 Corneal Dystrophy 49 1.004
42
MRF001 Marfan Syndrome 76 0.710
43
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.710
44
ESP021 Esophageal Cancer 83 0.710
45
c EHL085 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2 46 0.710
46
c CTS044 Cutis Laxa, Autosomal Recessive, Type Iic 24 0.710
47
c EHL089 Ehlers-Danlos Syndrome, Classic-Like, 2 26 0.710
48
P ADN016 Adenocarcinoma 63 0.710
49
P CTS001 Cutis Laxa 65 0.710
50
MYL005 Myelofibrosis 71 0.602
51
P MLN008 Melanoma 76 0.602
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