Search results for "[genes] FOXC1"

26 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
PTR006 Peters Anomaly 65 21.518
2
P AXN010 Axenfeld-Rieger Syndrome, Type 3 56 21.518
3
P HYD006 Hydrocephalus 66 17.011
4
ANR002 Aniridia 60 15.215
5
P IRD007 Iridogoniodysgenesis, Type 1 22 15.215
6
c HRD007 Hereditary Lymphedema 47 13.177
7
P ATR010 Atrial Heart Septal Defect 44 13.177
8
P JVN008 Juvenile Glaucoma 42 13.177
9
c IRD008 Iridogoniodysgenesis, Type 2 42 13.177
10
P PRS062 Persistent Hyperplastic Primary Vitreous 41 13.177
11
INT060 Intestinal Atresia 39 13.177
12
c CNG216 Congenital Hydrocephalus 38 13.177
13
P CRN249 Cornea Plana 36 13.177
14
c PRM032 Primary Congenital Glaucoma 34 13.177
15
IRS007 Iris Hypoplasia 26 13.177
16
P MGS004 Meige Syndrome 50 10.759
17
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 44 10.759
18
EXC003 Excessive Tearing 42 10.759
19
GRN003 Granulomatous Dermatitis 36 10.759
20
P ANT026 Anterior Segment Mesenchymal Dysgenesis 36 10.759
21
IRS003 Iris Disease 33 10.759
22
BPH001 Buphthalmos 31 10.759
23
CRN225 Cranio-Facial Dystonia 28 10.759
24
HYD007 Hydrophthalmos 26 10.759
25
c RNG022 Ring Chromosome 6 26 10.759
26
CHR386 Chromosome 6pter-P24 Deletion Syndrome 24 10.759