Search results for "[genes] LRP5"

40 hits were found for '[genes] LRP5'

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 54 24.828
2
P OST002 Osteoporosis 64 22.665
3
HYP299 Hyperostosis, Endosteal 43 21.501
4
P EXD001 Exudative Vitreoretinopathy 47 20.272
5
c EXD008 Exudative Vitreoretinopathy 1 59 18.963
6
IDP002 Idiopathic Juvenile Osteoporosis 50 18.963
7
c OST125 Osteopetrosis, Autosomal Dominant 1 29 18.963
8
P OST001 Osteopetrosis 63 17.556
9
VNB005 Van Buchem Disease 49 17.556
10
VNB004 Van Buchem Disease, Type 2 19 17.556
11
NRR002 Norrie Disease 60 16.026
12
HYP068 Hyperostosis 40 16.026
13
HGH024 High Bone Mass Trait 23 16.026
14
P CMR001 Camurati-Engelmann Disease 58 14.334
15
PLY023 Polycystic Liver Disease 56 14.334
16
RTN017 Retinal Detachment 56 14.334
17
P SCL048 Sclerosteosis 45 14.334
18
P CRN013 Craniodiaphyseal Dysplasia 42 14.334
19
c EXD004 Exudative Vitreoretinopathy 4 24 14.334
20
FCL012 Facial Paralysis 50 12.414
21
BNF002 Bone Fracture 50 12.414
22
MSS002 Mass Syndrome 48 12.414
23
RTN020 Retinal Vascular Disease 48 12.414
24
PRM020 Premenstrual Tension 44 12.414
25
NRT001 Neurotic Disorder 40 12.414
26
VRT003 Vertebrobasilar Insufficiency 38 12.414
27
BNR001 Bone Remodeling Disease 37 12.414
28
FCL011 Facial Nerve Disease 36 12.414
29
GLN002 Glanders 35 12.414
30
LKC002 Leukocoria 33 12.414
31
HYP137 Hypotrichosis Simplex 33 12.414
32
PRN008 Peroneal Nerve Paralysis 22 12.414
33
BNR002 Bone Resorption Disease 21 12.414
34
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 11 12.414
35
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 12.414
36
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 12.414
37
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 12.414
38
WRT001 Worth's Syndrome 34 10.136
39
P ISL020 Isolated Microphthalmia 25 10.136
40
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 10.136