Search results for "[genes] LRP5"

41 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
P OST002 Osteoporosis 75 24.808
2
OST024 Osteoporosis-Pseudoglioma Syndrome 55 24.808
3
HYP299 Hyperostosis, Endosteal 46 21.485
4
P OST001 Osteopetrosis 63 18.948
5
P EXD001 Exudative Vitreoretinopathy 47 18.948
6
c OST125 Osteopetrosis, Autosomal Dominant 1 26 18.948
7
IDP002 Idiopathic Juvenile Osteoporosis 43 17.542
8
HYP068 Hyperostosis 45 16.014
9
VNB005 Van Buchem Disease 44 16.014
10
BNR001 Bone Remodeling Disease 28 16.014
11
HGH024 High Bone Mass Trait 20 16.014
12
c EXD008 Exudative Vitreoretinopathy 1 50 14.323
13
CNN005 Connective Tissue Disease 49 14.323
14
BNR002 Bone Resorption Disease 28 14.323
15
VNB004 Van Buchem Disease, Type 2 21 14.323
16
NRR002 Norrie Disease 63 12.404
17
P CMR001 Camurati-Engelmann Disease 54 12.404
18
RTN017 Retinal Detachment 44 12.404
19
P SCL048 Sclerosteosis 43 12.404
20
P CRN013 Craniodiaphyseal Dysplasia 41 12.404
21
RTN020 Retinal Vascular Disease 38 12.404
22
WRT001 Worth's Syndrome 25 12.404
23
BSC001 Buschke-Ollendorff Syndrome 57 10.128
24
PLY023 Polycystic Liver Disease 50 10.128
25
GLN002 Glanders 44 10.128
26
FCL012 Facial Paralysis 43 10.128
27
BNF002 Bone Fracture 39 10.128
28
HYP137 Hypotrichosis Simplex 37 10.128
29
MSS002 Mass Syndrome 36 10.128
30
VRT003 Vertebrobasilar Insufficiency 35 10.128
31
OST097 Osteoporotic Fracture 35 10.128
32
PRM020 Premenstrual Tension 34 10.128
33
LKC002 Leukocoria 31 10.128
34
SST001 Sost-Related Sclerosing Bone Dysplasia 31 10.128
35
c EXD004 Exudative Vitreoretinopathy 4 28 10.128
36
PRN008 Peroneal Nerve Paralysis 26 10.128
37
FCL011 Facial Nerve Disease 25 10.128
38
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 12 7.162
39
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 9 7.162
40
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 8 7.162
41
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 8 7.162