Search results for lrp5

72 hits were found for lrp5

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 55 6.500
2
P OST002 Osteoporosis 76 5.765
3
END081 Endosteal Hyperostosis, Autosomal Dominant 47 5.095
4
P EXD001 Exudative Vitreoretinopathy 50 4.965
5
c OST125 Osteopetrosis, Autosomal Dominant 1 23 4.829
6
BNM016 Bone Mineral Density Quantitative Trait Locus 1 19 4.464
7
c EXD008 Exudative Vitreoretinopathy 1 69 4.434
8
VNB004 Van Buchem Disease, Type 2 17 4.095
9
P OST001 Osteopetrosis 61 3.978
10
VNB005 Van Buchem Disease 50 3.978
11
c EXD004 Exudative Vitreoretinopathy 4 23 3.745
12
HYP068 Hyperostosis 53 3.587
13
PLY175 Polycystic Liver Disease 4 with or Without Kidney Cysts 12 3.496
14
P DBT009 Diabetes Mellitus 64 3.315
15
NRR002 Norrie Disease 61 3.239
16
c OST164 Osteoporosis, Juvenile 53 3.239
17
PLY023 Polycystic Liver Disease 53 3.239
18
RTN017 Retinal Detachment 58 3.209
19
P CMR001 Camurati-Engelmann Disease 61 2.779
20
P CRN013 Craniodiaphyseal Dysplasia 47 2.779
21
P SCL048 Sclerosteosis 46 2.779
22
c LRP007 Lrp5-Related Primary Osteoporosis 6 2.344
23
BND020 Bone Disease 62 2.310
24
BNF002 Bone Fracture 55 2.310
25
MSS002 Mass Syndrome 37 2.310
26
CTS003 Coats Disease 53 2.269
27
FCL012 Facial Paralysis 51 2.269
28
PRM020 Premenstrual Tension 50 2.269
29
CNN011 Cenani-Lenz Syndactyly Syndrome 48 2.269
30
OST022 Osteopathia Striata with Cranial Sclerosis 47 2.269
31
RTN020 Retinal Vascular Disease 46 2.269
32
c SCL042 Sclerosteosis 2 41 2.269
33
GLN002 Glanders 41 2.269
34
SLL001 Sialolithiasis 40 2.269
35
FCL011 Facial Nerve Disease 36 2.269
36
HYP137 Hypotrichosis Simplex 34 2.269
37
BNR002 Bone Resorption Disease 32 2.269
38
LKC002 Leukocoria 31 2.269
39
BNR001 Bone Remodeling Disease 30 2.269
40
PRN008 Peroneal Nerve Paralysis 23 2.269
41
c TYP030 Type 1 Diabetes Mellitus 4 14 2.269
42
PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 45 2.020
43
P LBR001 Leber Congenital Amaurosis 64 1.763
44
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 14 1.657
45
PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 62 0.256
46
FND002 Fundus Dystrophy 49 0.181
47
TYP041 Type I 56 0.111
48
P PRS040 Prostate Cancer 90 0.091
49
OST012 Osteoarthritis 82 0.091
50
PRS047 Prostatitis 60 0.091
51
P CHR342 Chiari Malformation 45 0.091
52
P BRS047 Breast Cancer 100 0.064
53
c LKM061 Leukemia, Acute Myeloid 80 0.064
54
P HYP607 Hypercholesterolemia, Familial 79 0.064
55
P HPT021 Hepatitis 76 0.064
56
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.064
57
P LKM002 Leukemia 72 0.064
58
c SPN225 Spondyloarthropathy 1 71 0.064
59
P PLM036 Pulmonary Fibrosis 69 0.064
60
P MYL006 Myeloid Leukemia 68 0.064
61
P CRN037 Craniosynostosis 67 0.064
62
c MCP004 Mucopolysaccharidosis Iv 59 0.064
63
P HYP069 Hyperparathyroidism 58 0.064
64
SPN051 Spondylitis 55 0.064
65
OST015 Osteochondrodysplasia 53 0.064
66
RTN023 Retinitis 50 0.064
67
P CRV039 Cervicitis 49 0.064
68
SKL017 Skeletal Dysplasias 48 0.064
69
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.064
70
BNM029 Bone Mineral Density Quantitative Trait Locus 15 38 0.064
71
P MRQ003 Morquio Syndrome 31 0.064
72
c JVN025 Juvenile Primary Osteoporosis 19 0.064
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