Search results for "[genes] LRP5"

41 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 52 23.766
2
P OST002 Osteoporosis 76 22.660
3
HYP299 Hyperostosis, Endosteal 45 20.268
4
c OST125 Osteopetrosis, Autosomal Dominant 1 24 18.959
5
P OST001 Osteopetrosis 61 17.552
6
P EXD001 Exudative Vitreoretinopathy 49 17.552
7
IDP002 Idiopathic Juvenile Osteoporosis 49 17.552
8
c EXD008 Exudative Vitreoretinopathy 1 51 16.023
9
VNB005 Van Buchem Disease 47 16.023
10
HYP068 Hyperostosis 44 16.023
11
HGH024 High Bone Mass Trait 19 16.023
12
RTN017 Retinal Detachment 46 14.332
13
VNB004 Van Buchem Disease, Type 2 20 14.332
14
NRR002 Norrie Disease 59 12.411
15
P CMR001 Camurati-Engelmann Disease 58 12.411
16
PLY023 Polycystic Liver Disease 49 12.411
17
P SCL048 Sclerosteosis 49 12.411
18
WRT001 Worth's Syndrome 28 12.411
19
BSC001 Buschke-Ollendorff Syndrome 59 10.134
20
GLN002 Glanders 50 10.134
21
MLR003 Melorheostosis 47 10.134
22
FCL012 Facial Paralysis 43 10.134
23
P CRN013 Craniodiaphyseal Dysplasia 42 10.134
24
RTN020 Retinal Vascular Disease 41 10.134
25
PRM020 Premenstrual Tension 40 10.134
26
MSS002 Mass Syndrome 40 10.134
27
NRT001 Neurotic Disorder 39 10.134
28
BNF002 Bone Fracture 37 10.134
29
VRT003 Vertebrobasilar Insufficiency 37 10.134
30
SST001 Sost-Related Sclerosing Bone Dysplasia 33 10.134
31
BNR001 Bone Remodeling Disease 33 10.134
32
BNR002 Bone Resorption Disease 32 10.134
33
LKC002 Leukocoria 31 10.134
34
FCL011 Facial Nerve Disease 29 10.134
35
c EXD004 Exudative Vitreoretinopathy 4 25 10.134
36
BNM008 Bone Mineral Density, Low 21 10.134
37
PRN008 Peroneal Nerve Paralysis 19 10.134
38
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 11 7.166
39
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 7.166
40
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 7.166
41
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 7.166