Search results for "[genes] FOXL2"

31 hits were found for '[genes] FOXL2'

# Family MCID Name MIFTS Score
1
c PRM089 Premature Ovarian Failure 3 26 21.037
2
BLP004 Blepharophimosis 35 19.678
3
P PRM019 Premature Ovarian Failure 65 18.219
4
P BLP032 Blepharophimosis, Epicanthus Inversus, and Ptosis, Type 1 43 18.219
5
P PTS002 Ptosis 54 16.631
6
P OVR049 Ovarian Disease 57 14.875
7
P GND004 Gonadal Dysgenesis 49 12.882
8
P OVR046 Ovarian Cyst 46 12.882
9
SXC001 Sex Cord-Gonadal Stromal Tumor 44 12.882
10
P MXD016 Mixed Gonadal Dysgenesis 42 12.882
11
P PRR025 Perrault Syndrome 40 12.882
12
GND001 Gonadoblastoma 33 12.882
13
MBS002 Moebius Syndrome 54 10.518
14
FML039 Female Reproductive System Disease 51 10.518
15
RPR002 Reproductive System Disease 44 10.518
16
EYL005 Eyelid Disease 44 10.518
17
c PRM196 Premature Ovarian Failure 1 43 10.518
18
TRN060 Truncus Arteriosus 41 10.518
19
DVL002 Developmental Disabilities 36 10.518
20
STT003 Steatitis 35 10.518
21
HYP047 Hypertropia 35 10.518
22
BRC002 Brachial Plexus Neuritis 34 10.518
23
BLP034 Blepharophimosis-Intellectual Disability Syndrome, Sbbys Type 31 10.518
24
OHD004 Ohdo Syndrome 29 10.518
25
GYN003 Gynandroblastoma 28 10.518
26
c PTS008 Ptosis, Congenital 27 10.518
27
CRP004 Corpus Luteum Cyst 27 10.518
28
LRY002 Laryngostenosis 19 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