Search results for "[genes] FOXC1"

27 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 22.599
2
PTR006 Peters Anomaly 64 21.306
3
P HYD006 Hydrocephalus 67 16.844
4
ANR002 Aniridia 60 15.066
5
P IRD007 Iridogoniodysgenesis, Type 1 22 15.066
6
ADM013 Adamantinoma of Long Bones 59 13.047
7
P ATR010 Atrial Heart Septal Defect 43 13.047
8
INT060 Intestinal Atresia 40 13.047
9
P PRS062 Persistent Hyperplastic Primary Vitreous 37 13.047
10
c CNG216 Congenital Hydrocephalus 36 13.047
11
c IRD008 Iridogoniodysgenesis, Type 2 36 13.047
12
P CRN249 Cornea Plana 32 13.047
13
P JVN008 Juvenile Glaucoma 32 13.047
14
c PRM032 Primary Congenital Glaucoma 29 13.047
15
IRS007 Iris Hypoplasia 23 13.047
16
P MGS004 Meige Syndrome 45 10.653
17
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 44 10.653
18
P ANT026 Anterior Segment Mesenchymal Dysgenesis 38 10.653
19
CHR386 Chromosome 6pter-P24 Deletion Syndrome 35 10.653
20
IRS003 Iris Disease 32 10.653
21
GRN003 Granulomatous Dermatitis 31 10.653
22
BPH001 Buphthalmos 30 10.653
23
CRN225 Cranio-Facial Dystonia 27 10.653
24
DST033 Distichiasis 27 10.653
25
HYD007 Hydrophthalmos 26 10.653
26
c RNG022 Ring Chromosome 6 24 10.653
27
ISL011 Isolated Aniridia 22 7.533