Search results for "[genes] LRP5"

37 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 54 23.971
2
P OST002 Osteoporosis 64 22.855
3
HYP299 Hyperostosis, Endosteal 49 21.682
4
P EXD001 Exudative Vitreoretinopathy 46 19.122
5
c OST125 Osteopetrosis, Autosomal Dominant 1 28 19.122
6
P OST001 Osteopetrosis 62 17.704
7
c EXD008 Exudative Vitreoretinopathy 1 60 17.704
8
VNB005 Van Buchem Disease 50 17.704
9
IDP002 Idiopathic Juvenile Osteoporosis 49 17.704
10
HYP068 Hyperostosis 40 16.161
11
HGH024 High Bone Mass Trait 23 16.161
12
RTN017 Retinal Detachment 57 14.455
13
VNB004 Van Buchem Disease, Type 2 19 14.455
14
NRR002 Norrie Disease 61 12.518
15
P CMR001 Camurati-Engelmann Disease 59 12.518
16
PLY023 Polycystic Liver Disease 57 12.518
17
P SCL048 Sclerosteosis 45 12.518
18
P CRN013 Craniodiaphyseal Dysplasia 40 12.518
19
MSS002 Mass Syndrome 59 10.221
20
FCL012 Facial Paralysis 50 10.221
21
RTN020 Retinal Vascular Disease 50 10.221
22
BNF002 Bone Fracture 47 10.221
23
PRM020 Premenstrual Tension 46 10.221
24
NRT001 Neurotic Disorder 42 10.221
25
BNR001 Bone Remodeling Disease 40 10.221
26
VRT003 Vertebrobasilar Insufficiency 39 10.221
27
FCL011 Facial Nerve Disease 38 10.221
28
LKC002 Leukocoria 37 10.221
29
GLN002 Glanders 36 10.221
30
HYP137 Hypotrichosis Simplex 32 10.221
31
c EXD004 Exudative Vitreoretinopathy 4 24 10.221
32
PRN008 Peroneal Nerve Paralysis 22 10.221
33
BNR002 Bone Resorption Disease 22 10.221
34
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 10 7.227
35
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 7.227
36
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 7.227
37
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 7.227