Search results for "[genes] FOXC1"

27 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
PTR006 Peters Anomaly 64 21.312
2
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 21.312
3
P HYD006 Hydrocephalus 68 15.070
4
ANR002 Aniridia 62 15.070
5
P IRD007 Iridogoniodysgenesis, Type 1 21 15.070
6
c HRD007 Hereditary Lymphedema 48 13.051
7
P PRS062 Persistent Hyperplastic Primary Vitreous 38 13.051
8
INT060 Intestinal Atresia 37 13.051
9
c CNG216 Congenital Hydrocephalus 35 13.051
10
P JVN008 Juvenile Glaucoma 33 13.051
11
P CRN249 Cornea Plana 32 13.051
12
IRS007 Iris Hypoplasia 24 13.051
13
c PRM032 Primary Congenital Glaucoma 27 13.051
14
P ANT026 Anterior Segment Mesenchymal Dysgenesis 36 10.656
15
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 43 10.656
16
P MGS004 Meige Syndrome 46 10.656
17
c IRD008 Iridogoniodysgenesis, Type 2 31 10.656
18
PTN002 Patent Ductus Arteriosus 50 10.656
19
CHR386 Chromosome 6pter-P24 Deletion Syndrome 23 10.656
20
EXC003 Excessive Tearing 39 10.656
21
c RNG022 Ring Chromosome 6 23 10.656
22
CRN225 Cranio-Facial Dystonia 26 10.656
23
BPH001 Buphthalmos 28 10.656
24
DST033 Distichiasis 28 10.656
25
HYD007 Hydrophthalmos 24 10.656
26
IRS003 Iris Disease 32 10.656
27
GRN003 Granulomatous Dermatitis 32 10.656