Search results for "[genes] FOXL2"

31 hits were found for '[genes] FOXL2'

# Family MCID Name MIFTS Score
1
c PRM089 Premature Ovarian Failure 3 22 20.973
2
P BLP032 Blepharophimosis, Epicanthus Inversus, and Ptosis, Type 1 42 19.618
3
BLP004 Blepharophimosis 38 19.618
4
P PRM019 Premature Ovarian Failure 64 18.163
5
P OVR049 Ovarian Disease 56 16.580
6
P PTS002 Ptosis 51 16.580
7
P OVR046 Ovarian Cyst 51 14.830
8
P GND004 Gonadal Dysgenesis 51 14.830
9
GND001 Gonadoblastoma 41 14.830
10
SXC001 Sex Cord-Gonadal Stromal Tumor 41 14.830
11
P PRR025 Perrault Syndrome 37 14.830
12
P MXD016 Mixed Gonadal Dysgenesis 34 14.830
13
FML039 Female Reproductive System Disease 48 12.843
14
MBS002 Moebius Syndrome 47 12.843
15
c PRM196 Premature Ovarian Failure 1 42 12.843
16
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 12.843
17
EYL005 Eyelid Disease 39 12.843
18
OHD004 Ohdo Syndrome 32 12.843
19
c PTS008 Ptosis, Congenital 31 12.843
20
HYP047 Hypertropia 28 12.843
21
BRC002 Brachial Plexus Neuritis 26 12.843
22
GYN003 Gynandroblastoma 26 12.843
23
CRP004 Corpus Luteum Cyst 24 12.843
24
SBB001 Sbbyss Syndrome 21 12.843
25
STT003 Steatitis 20 12.843
26
LRY002 Laryngostenosis 17 12.843
27
c BLP037 Blepharophimosis-Epicanthus Inversus-Ptosis Due to Copy Number Variations 8 12.843
28
c BLP039 Blepharophimosis-Epicanthus Inversus-Ptosis Due to a Point Mutation Syndrome 8 12.843
29
c BLP038 Blepharophimosis-Epicanthus Inversus-Ptosis Due to 3q23 Rearrangement Syndrome 7 12.843
30
c AXN009 Axenfeld-Rieger Syndrome, Type 1 47 10.486
31
RPR002 Reproductive System Disease 41 10.486