Search results for "[genes] FOXC1"

28 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 22.596
2
PTR006 Peters Anomaly 63 21.304
3
P HYD006 Hydrocephalus 54 16.842
4
ANR002 Aniridia 72 15.064
5
P IRD007 Iridogoniodysgenesis, Type 1 26 15.064
6
IRD005 Iridogoniodysgenesis Type1 11 15.064
7
PTN002 Patent Ductus Arteriosus 46 13.046
8
P PRS062 Persistent Hyperplastic Primary Vitreous 40 13.046
9
P JVN008 Juvenile Glaucoma 34 13.046
10
P ATR010 Atrial Heart Septal Defect 34 13.046
11
INT060 Intestinal Atresia 33 13.046
12
c CNG216 Congenital Hydrocephalus 33 13.046
13
c HRD007 Hereditary Lymphedema 31 13.046
14
c PRM032 Primary Congenital Glaucoma 26 13.046
15
IRS007 Iris Hypoplasia 24 13.046
16
P CRN249 Cornea Plana 24 13.046
17
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 44 10.652
18
P MGS004 Meige Syndrome 43 10.652
19
c IRD008 Iridogoniodysgenesis, Type 2 37 10.652
20
P ANT026 Anterior Segment Mesenchymal Dysgenesis 36 10.652
21
GRN003 Granulomatous Dermatitis 33 10.652
22
BPH001 Buphthalmos 27 10.652
23
IRS003 Iris Disease 25 10.652
24
c RNG022 Ring Chromosome 6 25 10.652
25
CRN225 Cranio-Facial Dystonia 22 10.652
26
HYD007 Hydrophthalmos 20 10.652
27
c HYD042 Hydrocephalus, Autosomal Dominant 14 10.652
28
RGR002 Rieger Syndrome, Type 2 25 7.532