Search results for TNFRSF11B

106 hits were found for TNFRSF11B

# Family MCID Name MIFTS Score
1
c PGT008 Paget Disease of Bone 5, Juvenile-Onset 47 4.176
2
P BND020 Bone Disease 60 3.140
3
P OST002 Osteoporosis 74 3.098
4
P PRS040 Prostate Cancer 98 2.727
5
P BRS047 Breast Cancer 97 2.727
6
P KDN018 Kidney Disease 71 2.727
7
OST012 Osteoarthritis 78 2.422
8
P PGT001 Paget's Disease of Bone 60 2.422
9
P OTS001 Otosclerosis 50 2.394
10
P RHM011 Rheumatoid Arthritis 81 2.362
11
c BTT014 Beta-Thalassemia 73 2.362
12
MYL005 Myelofibrosis 68 2.362
13
OST159 Osteogenic Sarcoma 67 2.362
14
c CHR684 Chronic Kidney Disease 67 2.362
15
P VSC007 Vascular Disease 64 2.362
16
ANR007 Anorexia Nervosa 63 2.362
17
P HYP069 Hyperparathyroidism 63 2.362
18
P ART023 Arthropathy 63 2.362
19
PSR001 Psoriatic Arthritis 62 2.362
20
RHM027 Rheumatic Disease 56 2.362
21
SYN007 Synovitis 56 2.362
22
CHL122 Cholesteatoma of Middle Ear 52 2.362
23
c SCN007 Secondary Hyperparathyroidism 51 2.362
24
RNL011 Renal Osteodystrophy 50 2.362
25
URM002 Uremia 49 2.362
26
P GNT008 Giant Cell Tumor 45 2.362
27
P CHN059 Chondrocalcinosis 51 1.966
28
CRT013 Carotid Stenosis 50 1.966
29
c SPN225 Spondyloarthropathy 1 74 1.929
30
P CNR004 Cone-Rod Dystrophy 2 72 1.929
31
P OST001 Osteopetrosis 71 1.929
32
P MYC007 Myocardial Infarction 71 1.929
33
P HYP086 Hypothyroidism 69 1.929
34
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.929
35
P DBT009 Diabetes Mellitus 65 1.929
36
MGK001 Megakaryocytic Leukemia 64 1.929
37
c ART101 Aortic Valve Disease 2 64 1.929
38
P PRD008 Periodontitis 63 1.929
39
OST003 Osteonecrosis 61 1.929
40
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 61 1.929
41
P SCL018 Scoliosis 60 1.929
42
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.929
43
END081 Endosteal Hyperostosis, Autosomal Dominant 60 1.929
44
PMS001 Poems Syndrome 59 1.929
45
c PRM005 Primary Hyperparathyroidism 58 1.929
46
P BNC003 Bone Cancer 58 1.929
47
PGM001 Pigmented Villonodular Synovitis 57 1.929
48
P CRD246 Cardiovascular System Disease 56 1.929
49
PRP080 Peripheral Artery Disease 53 1.929
50
ANK001 Ankylosis 52 1.929
51
P AGG001 Aggressive Periodontitis 51 1.929
52
c SVR005 Severe Pre-Eclampsia 49 1.929
53
HYP068 Hyperostosis 48 1.929
54
c TRC091 Trichorhinophalangeal Syndrome, Type Ii 48 1.929
55
HYP025 Hyperphosphatemia 48 1.929
56
RTR008 Root Resorption 46 1.929
57
DBT008 Diabetic Angiopathy 45 1.929
58
GLC086 Glucocorticoid-Induced Osteoporosis 43 1.929
59
MLT016 Multicentric Reticulohistiocytosis 40 1.929
60
PRS037 Periostitis 38 1.929
61
c CHR013 Chronic Apical Periodontitis 32 1.929
62
MMM001 Mammary Paget's Disease 54 1.601
63
BNR002 Bone Resorption Disease 49 1.510
64
BRT054 Brittle Bone Disorder 70 1.413
65
MYL069 Myeloma, Multiple 85 1.364
66
c HMP004 Hemophilia B 68 1.364
67
CNN005 Connective Tissue Disease 67 1.364
68
BLD131 Bladder Urothelial Carcinoma 62 1.364
69
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 1.364
70
OST024 Osteoporosis-Pseudoglioma Syndrome 60 1.364
71
P VNB005 Van Buchem Disease 56 1.364
72
c PRD040 Periodontitis, Chronic 54 1.364
73
P SCL048 Sclerosteosis 54 1.364
74
c OST164 Osteoporosis, Juvenile 53 1.364
75
DFF036 Differentiated Thyroid Carcinoma 52 1.364
76
BNG036 Bone Giant Cell Tumor 48 1.364
77
BNN003 Bone Inflammation Disease 48 1.364
78
PRP017 Periapical Periodontitis 46 1.364
79
PRT030 Parathyroid Gland Disease 46 1.364
80
GNG011 Gingival Disease 44 1.364
81
FML345 Familial Expansile Osteolysis 43 1.364
82
PRS115 Prosthetic Joint Infection 42 1.364
83
OPT007 Optic Nerve Glioma 41 1.364
84
MNR003 Mineral Metabolism Disease 39 1.364
85
TTH008 Tooth Resorption 37 1.364
86
HMP018 Hemophilic Arthropathy 34 1.364
87
c PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 34 1.364
88
ISC005 Ischemic Bone Disease 30 1.364
89
BNR001 Bone Remodeling Disease 29 1.364
90
KMM001 Kummell's Disease 25 1.364
91
TTH005 Teeth Hard Tissue Disease 24 1.364
92
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.119
93
c BRN108 Branchiootic Syndrome 1 61 0.084
94
P GST053 Gastric Cancer 84 0.059
95
c HPT073 Hepatitis C Virus 71 0.059
96
P SLP006 Sleep Apnea 69 0.059
97
P CRN037 Craniosynostosis 68 0.059
98
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.059
99
c HPT001 Hepatitis C 63 0.059
100
P ENC004 Encephalitis 62 0.059
101
LMB062 Limb Ischemia 56 0.059
102
ATS010 Autosomal Recessive Disease 49 0.059
103
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.059
104
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.059
105
c PRG020 Paragangliomas 3 38 0.059
106
c CHR020 Chronic Interstitial Cystitis 37 0.059
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