Search results for "[genes] LRP5"

41 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 56 23.766
2
P OST002 Osteoporosis 80 22.660
3
HYP299 Hyperostosis, Endosteal 49 20.268
4
c OST125 Osteopetrosis, Autosomal Dominant 1 25 18.959
5
P OST001 Osteopetrosis 69 17.552
6
IDP002 Idiopathic Juvenile Osteoporosis 54 17.552
7
P EXD001 Exudative Vitreoretinopathy 50 17.552
8
c EXD008 Exudative Vitreoretinopathy 1 59 16.023
9
HYP068 Hyperostosis 49 16.023
10
VNB005 Van Buchem Disease 47 16.023
11
HGH024 High Bone Mass Trait 22 16.023
12
RTN017 Retinal Detachment 54 14.332
13
VNB004 Van Buchem Disease, Type 2 18 14.332
14
P CMR001 Camurati-Engelmann Disease 66 12.411
15
NRR002 Norrie Disease 60 12.411
16
PLY023 Polycystic Liver Disease 57 12.411
17
P SCL048 Sclerosteosis 48 12.411
18
WRT001 Worth's Syndrome 34 12.411
19
BSC001 Buschke-Ollendorff Syndrome 59 10.134
20
GLN002 Glanders 56 10.134
21
FCL012 Facial Paralysis 53 10.134
22
PRM020 Premenstrual Tension 51 10.134
23
RTN020 Retinal Vascular Disease 51 10.134
24
MSS002 Mass Syndrome 47 10.134
25
BNF002 Bone Fracture 47 10.134
26
P CRN013 Craniodiaphyseal Dysplasia 46 10.134
27
NRT001 Neurotic Disorder 46 10.134
28
MLR003 Melorheostosis 43 10.134
29
BNR001 Bone Remodeling Disease 43 10.134
30
FCL011 Facial Nerve Disease 42 10.134
31
BNR002 Bone Resorption Disease 42 10.134
32
VRT003 Vertebrobasilar Insufficiency 40 10.134
33
SST001 Sost-Related Sclerosing Bone Dysplasia 38 10.134
34
LKC002 Leukocoria 36 10.134
35
BNM008 Bone Mineral Density, Low 31 10.134
36
c EXD004 Exudative Vitreoretinopathy 4 22 10.134
37
PRN008 Peroneal Nerve Paralysis 22 10.134
38
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 12 7.166
39
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 10 7.166
40
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 9 7.166
41
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 8 7.166