Search results for "[genes] LRP5"

25 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 51 30.348
2
HYP299 Hyperostosis, Endosteal 30 27.355
3
P OST002 Osteoporosis 71 26.282
4
P EXD001 Exudative Vitreoretinopathy 48 26.282
5
c OST125 Osteopetrosis, Autosomal Dominant 1 23 18.584
6
VNB005 Van Buchem Disease 47 15.174
7
HYP068 Hyperostosis 43 15.174
8
c EXD004 Exudative Vitreoretinopathy 4 20 15.174
9
IDP002 Idiopathic Juvenile Osteoporosis 48 13.141
10
c EXD008 Exudative Vitreoretinopathy 1 39 13.141
11
VNB004 Van Buchem Disease, Type 2 17 13.141
12
NRR002 Norrie Disease 65 10.730
13
P CMR001 Camurati-Engelmann Disease 60 10.730
14
P SCL048 Sclerosteosis 48 10.730
15
HYP137 Hypotrichosis Simplex 38 10.730
16
GLN002 Glanders 36 10.730
17
P CRN013 Craniodiaphyseal Dysplasia 35 10.730
18
HGH024 High Bone Mass Trait 10 10.730
19
PLY023 Polycystic Liver Disease 54 7.587
20
SST001 Sost-Related Sclerosing Bone Dysplasia 29 7.587
21
WRT001 Worth's Syndrome 15 7.587
22
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 12 7.587
23
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 8 7.587
24
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 7.587
25
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 6 7.587