Search results for lrp5

64 hits were found for lrp5

# Family MCID Name MIFTS Score
1
OST024 Osteoporosis-Pseudoglioma Syndrome 54 6.368
2
P OST002 Osteoporosis 64 5.618
3
HYP299 Hyperostosis, Endosteal 43 5.128
4
P EXD001 Exudative Vitreoretinopathy 47 4.925
5
c OST125 Osteopetrosis, Autosomal Dominant 1 29 4.562
6
c EXD008 Exudative Vitreoretinopathy 1 59 4.439
7
IDP002 Idiopathic Juvenile Osteoporosis 50 4.397
8
VNB004 Van Buchem Disease, Type 2 19 4.162
9
P OST001 Osteopetrosis 63 4.078
10
VNB005 Van Buchem Disease 49 4.054
11
NRR002 Norrie Disease 60 3.705
12
HGH024 High Bone Mass Trait 23 3.705
13
HYP068 Hyperostosis 40 3.677
14
PLY023 Polycystic Liver Disease 56 3.348
15
c EXD004 Exudative Vitreoretinopathy 4 24 3.348
16
P CMR001 Camurati-Engelmann Disease 58 3.289
17
RTN017 Retinal Detachment 56 3.289
18
P SCL048 Sclerosteosis 45 3.289
19
P CRN013 Craniodiaphyseal Dysplasia 42 3.289
20
BNF002 Bone Fracture 50 2.883
21
MSS002 Mass Syndrome 48 2.883
22
BNR001 Bone Remodeling Disease 37 2.883
23
OST114 Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome 10 2.883
24
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 2.883
25
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 2.883
26
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.883
27
FCL012 Facial Paralysis 50 2.848
28
RTN020 Retinal Vascular Disease 48 2.848
29
PRM020 Premenstrual Tension 44 2.848
30
NRT001 Neurotic Disorder 40 2.848
31
VRT003 Vertebrobasilar Insufficiency 38 2.848
32
FCL011 Facial Nerve Disease 36 2.848
33
GLN002 Glanders 35 2.848
34
LKC002 Leukocoria 33 2.848
35
HYP137 Hypotrichosis Simplex 33 2.848
36
PRN008 Peroneal Nerve Paralysis 22 2.848
37
BNR002 Bone Resorption Disease 21 2.848
38
WRT001 Worth's Syndrome 34 2.535
39
P ISL020 Isolated Microphthalmia 25 2.325
40
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 2.325
41
P OBS005 Obesity 92 0.094
42
P PRS040 Prostate Cancer 90 0.094
43
P OST012 Osteoarthritis 83 0.094
44
PRS047 Prostatitis 56 0.094
45
P BRS047 Breast Cancer 100 0.066
46
P PLM036 Pulmonary Fibrosis 71 0.066
47
P LKM002 Leukemia 71 0.066
48
P HPT021 Hepatitis 69 0.066
49
P MYL006 Myeloid Leukemia 66 0.066
50
P CRN037 Craniosynostosis 66 0.066
51
c MCP004 Mucopolysaccharidosis Iv 60 0.066
52
P HYP069 Hyperparathyroidism 58 0.066
53
OST015 Osteochondrodysplasia 52 0.066
54
SPN051 Spondylitis 51 0.066
55
SKL014 Skeletal Dysplasia 46 0.066
56
P CRV039 Cervicitis 45 0.066
57
SKL017 Skeletal Dysplasias 45 0.066
58
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.066
59
BND014 Bone Development Disease 40 0.066
60
ATS008 Autosomal Dominant Disease 39 0.066
61
MNR003 Mineral Metabolism Disease 38 0.066
62
SXD001 Sex Differentiation Disease 38 0.066
63
ACR002 Acrocapitofemoral Dysplasia 33 0.066
64
BNM008 Bone Mineral Density, Low 16 0.066
Content
Loading form....