Search results for "[genes] LRP5"

41 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 55 24.698
2
P OST002 Osteoporosis 63 22.546
3
HYP299 Hyperostosis, Endosteal 45 20.166
4
c OST125 Osteopetrosis, Autosomal Dominant 1 26 18.863
5
c EXD008 Exudative Vitreoretinopathy 1 58 17.464
6
P EXD001 Exudative Vitreoretinopathy 48 17.464
7
VNB005 Van Buchem Disease 46 15.942
8
P OST001 Osteopetrosis 63 15.942
9
HYP068 Hyperostosis 39 15.942
10
HGH024 High Bone Mass Trait 24 15.942
11
VNB004 Van Buchem Disease, Type 2 20 14.259
12
RTN017 Retinal Detachment 58 14.259
13
IDP002 Idiopathic Juvenile Osteoporosis 48 14.259
14
P CMR001 Camurati-Engelmann Disease 63 12.349
15
PLY023 Polycystic Liver Disease 57 12.349
16
WRT001 Worth's Syndrome 37 12.349
17
P CRN013 Craniodiaphyseal Dysplasia 42 12.349
18
BSC001 Buschke-Ollendorff Syndrome 59 10.083
19
NRR002 Norrie Disease 60 10.083
20
MSS002 Mass Syndrome 49 10.083
21
FCL012 Facial Paralysis 50 10.083
22
P SCL048 Sclerosteosis 47 10.083
23
c EXD004 Exudative Vitreoretinopathy 4 25 10.083
24
GLN002 Glanders 36 10.083
25
LKC002 Leukocoria 37 10.083
26
SLL001 Sialolithiasis 39 10.083
27
HYP137 Hypotrichosis Simplex 34 10.083
28
SST001 Sost-Related Sclerosing Bone Dysplasia 34 10.083
29
PRM020 Premenstrual Tension 44 10.083
30
FCL011 Facial Nerve Disease 37 10.083
31
VRT003 Vertebrobasilar Insufficiency 38 10.083
32
RTN020 Retinal Vascular Disease 49 10.083
33
BNM008 Bone Mineral Density, Low 28 10.083
34
PRN008 Peroneal Nerve Paralysis 20 10.083
35
BNR001 Bone Remodeling Disease 40 10.083
36
BNR002 Bone Resorption Disease 21 10.083
37
BNF002 Bone Fracture 46 10.083
38
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 11 7.130
39
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 7.130
40
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 7.130
41
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 7.130