Search results for "[genes] FOXC1"

31 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 22.245
2
P HYD006 Hydrocephalus 66 18.163
3
PTR006 Peters Anomaly 65 18.163
4
P IRD007 Iridogoniodysgenesis, Type 1 23 18.163
5
P ANR002 Aniridia 64 16.580
6
ADM013 Adamantinoma of Long Bones 57 14.830
7
P ATR010 Atrial Heart Septal Defect 45 14.830
8
INT060 Intestinal Atresia 42 14.830
9
P PRS062 Persistent Hyperplastic Primary Vitreous 38 14.830
10
c CNG216 Congenital Hydrocephalus 37 14.830
11
P CRN249 Cornea Plana 32 14.830
12
c PRM032 Primary Congenital Glaucoma 30 14.830
13
c IRD008 Iridogoniodysgenesis, Type 2 29 14.830
14
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 43 12.843
15
P MGS004 Meige Syndrome 43 12.843
16
c HRD007 Hereditary Lymphedema 42 12.843
17
P JVN008 Juvenile Glaucoma 36 12.843
18
CHR386 Chromosome 6pter-P24 Deletion Syndrome 35 12.843
19
GRN003 Granulomatous Dermatitis 31 12.843
20
IRS003 Iris Disease 31 12.843
21
BPH001 Buphthalmos 30 12.843
22
CRN225 Cranio-Facial Dystonia 28 12.843
23
DST033 Distichiasis 27 12.843
24
HYD007 Hydrophthalmos 26 12.843
25
ISL011 Isolated Aniridia 25 12.843
26
IRS007 Iris Hypoplasia 25 12.843
27
c RNG022 Ring Chromosome 6 23 12.843
28
P RTS001 Ritscher-Schinzel Syndrome 42 10.486
29
P ANT026 Anterior Segment Mesenchymal Dysgenesis 42 10.486
30
c BRC082 Brachydactyly, Type E 42 10.486
31
RGR002 Rieger Syndrome, Type 2 32 10.486