Search results for "[genes] FOXC1"

26 hits were found for '[genes] FOXC1'

# Family MCID Name MIFTS Score
1
PTR006 Peters Anomaly 58 21.518
2
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 21.518
3
P HYD006 Hydrocephalus 58 17.011
4
ANR002 Aniridia 62 15.215
5
P IRD007 Iridogoniodysgenesis, Type 1 29 15.215
6
c HRD007 Hereditary Lymphedema 45 13.177
7
P PRS062 Persistent Hyperplastic Primary Vitreous 39 13.177
8
c IRD008 Iridogoniodysgenesis, Type 2 38 13.177
9
P ATR010 Atrial Heart Septal Defect 37 13.177
10
P JVN008 Juvenile Glaucoma 36 13.177
11
c CNG216 Congenital Hydrocephalus 34 13.177
12
INT060 Intestinal Atresia 34 13.177
13
P CRN249 Cornea Plana 29 13.177
14
c PRM032 Primary Congenital Glaucoma 27 13.177
15
IRS007 Iris Hypoplasia 24 13.177
16
P MGS004 Meige Syndrome 44 10.759
17
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 39 10.759
18
P ANT026 Anterior Segment Mesenchymal Dysgenesis 37 10.759
19
GRN003 Granulomatous Dermatitis 34 10.759
20
EXC003 Excessive Tearing 28 10.759
21
BPH001 Buphthalmos 28 10.759
22
c RNG022 Ring Chromosome 6 27 10.759
23
CHR386 Chromosome 6pter-P24 Deletion Syndrome 24 10.759
24
IRS003 Iris Disease 23 10.759
25
CRN225 Cranio-Facial Dystonia 23 10.759
26
HYD007 Hydrophthalmos 22 10.759