Search results for "[genes] FOXL2"

31 hits were found for '[genes] FOXL2'

# Family MCID Name MIFTS Score
1
c PRM089 Premature Ovarian Failure 3 18 21.037
2
BLP004 Blepharophimosis 30 19.678
3
P PRM019 Premature Ovarian Failure 62 18.219
4
P BLP032 Blepharophimosis, Epicanthus Inversus, and Ptosis, Type 1 42 18.219
5
P PTS002 Ptosis 40 16.631
6
P OVR049 Ovarian Disease 45 14.875
7
P PRR025 Perrault Syndrome 43 12.882
8
P GND004 Gonadal Dysgenesis 40 12.882
9
SXC001 Sex Cord-Gonadal Stromal Tumor 38 12.882
10
GND001 Gonadoblastoma 35 12.882
11
P OVR046 Ovarian Cyst 35 12.882
12
P MXD016 Mixed Gonadal Dysgenesis 35 12.882
13
MBS002 Moebius Syndrome 53 10.518
14
c PRM196 Premature Ovarian Failure 1 43 10.518
15
TRN060 Truncus Arteriosus 40 10.518
16
FML039 Female Reproductive System Disease 35 10.518
17
DVL002 Developmental Disabilities 34 10.518
18
HYP047 Hypertropia 30 10.518
19
EYL005 Eyelid Disease 29 10.518
20
STT003 Steatitis 29 10.518
21
RPR002 Reproductive System Disease 29 10.518
22
BLP034 Blepharophimosis-Intellectual Disability Syndrome, Sbbys Type 28 10.518
23
BRC002 Brachial Plexus Neuritis 27 10.518
24
c PTS008 Ptosis, Congenital 27 10.518
25
OHD004 Ohdo Syndrome 25 10.518
26
CRP004 Corpus Luteum Cyst 23 10.518
27
GYN003 Gynandroblastoma 22 10.518
28
LRY002 Laryngostenosis 14 10.518
29
c BLP037 Blepharophimosis-Epicanthus Inversus-Ptosis Due to Copy Number Variations 9 7.438
30
c BLP039 Blepharophimosis-Epicanthus Inversus-Ptosis Due to a Point Mutation Syndrome 8 7.438
31
c BLP038 Blepharophimosis-Epicanthus Inversus-Ptosis Due to 3q23 Rearrangement Syndrome 7 7.438