Search results for PTH-(1-34) (human)

110 hits were found for PTH-(1-34) (human)

# Family MCID Name MIFTS Score
1
BNR002 Bone Resorption Disease 49 0.624
2
P OST002 Osteoporosis 74 0.623
3
P HYP069 Hyperparathyroidism 63 0.599
4
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.585
5
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.585
6
OST159 Osteogenic Sarcoma 67 0.457
7
P HYP024 Hypoparathyroidism 56 0.426
8
c PRM005 Primary Hyperparathyroidism 58 0.394
9
P KDN018 Kidney Disease 71 0.348
10
P BND020 Bone Disease 60 0.332
11
ADN018 Adenoma 59 0.332
12
c SCN007 Secondary Hyperparathyroidism 51 0.326
13
SVR004 Severe Combined Immunodeficiency 74 0.266
14
RCK004 Rickets 69 0.265
15
48X005 48,xyyy 39 0.261
16
END030 End Stage Renal Failure 58 0.251
17
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.246
18
P PSD015 Pseudohypoparathyroidism 56 0.243
19
c CHR684 Chronic Kidney Disease 67 0.242
20
INS024 Insulin-Like Growth Factor I 80 0.240
21
HLX001 Helix Syndrome 48 0.234
22
OST012 Osteoarthritis 78 0.221
23
HYP025 Hyperphosphatemia 48 0.220
24
P PRD008 Periodontitis 63 0.211
25
P HYP726 Hypercalcemia, Infantile, 1 57 0.205
26
URM002 Uremia 49 0.203
27
P SCL048 Sclerosteosis 54 0.199
28
47X002 47,xyy 49 0.181
29
AGN016 Aging 56 0.177
30
P PSR002 Psoriasis 63 0.177
31
P BDY004 Body Mass Index Quantitative Trait Locus 11 77 0.174
32
PST011 Pustulosis of Palm and Sole 53 0.173
33
P HYP802 Hypocalcemia, Autosomal Dominant 1 70 0.172
34
P HYP599 Hypoparathyroidism, Familial Isolated 45 0.171
35
NPH003 Nephrocalcinosis 52 0.171
36
c HYP595 Hypertension, Essential 85 0.170
37
ADL002 Adult Syndrome 70 0.170
38
OST011 Osteomalacia 53 0.156
39
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.154
40
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.154
41
SKN016 Skin Disease 63 0.152
42
HYP017 Hypophosphatemia 50 0.152
43
P TRN020 Turner Syndrome 65 0.151
44
c BDY021 Body Mass Index Quantitative Trait Locus 20 53 0.148
45
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.147
46
c BDY011 Body Mass Index Quantitative Trait Locus 10 46 0.147
47
c BDY010 Body Mass Index Quantitative Trait Locus 4 47 0.147
48
c BDY015 Body Mass Index Quantitative Trait Locus 12 47 0.147
49
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.147
50
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.147
51
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.147
52
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.147
53
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.147
54
P HYP733 Hypercalciuria, Absorptive, 2 46 0.146
55
P RHM011 Rheumatoid Arthritis 81 0.145
56
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 63 0.144
57
DWR001 Dwarfism 44 0.142
58
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.140
59
OST003 Osteonecrosis 61 0.140
60
P DBT009 Diabetes Mellitus 65 0.139
61
P CND004 Candidiasis 58 0.135
62
c RHB024 Rhabdomyosarcoma 2 66 0.133
63
PLY150 Polykaryocytosis Inducer 31 0.132
64
P HYP086 Hypothyroidism 69 0.125
65
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 67 0.121
66
P PRM006 Primary Biliary Cirrhosis 62 0.120
67
HYP005 Hypokalemia 56 0.115
68
P CHR345 Chronic Pain 50 0.113
69
SYN007 Synovitis 56 0.112
70
c ATM011 Autoimmune Hepatitis 62 0.111
71
LPD008 Lipid Metabolism Disorder 63 0.111
72
PRT058 Pure Autonomic Failure 60 0.111
73
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 50 0.109
74
P SZR006 Seizure Disorder 59 0.109
75
RTR008 Root Resorption 46 0.109
76
ATX019 Ataxia with Vitamin E Deficiency 48 0.106
77
VSL002 Visual Epilepsy 57 0.106
78
MMM001 Mammary Paget's Disease 54 0.102
79
ACH004 Achondroplasia 67 0.101
80
BNN003 Bone Inflammation Disease 48 0.101
81
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.099
82
c PSR023 Psoriasis 1 49 0.097
83
OST004 Osteitis Fibrosa 40 0.096
84
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.096
85
c PSR017 Psoriasis 2 50 0.095
86
c PSR028 Psoriasis 7 39 0.095
87
c PSR032 Psoriasis 11 39 0.095
88
c PSR018 Psoriasis 13 39 0.095
89
CNN005 Connective Tissue Disease 67 0.091
90
PSD014 Pseudopseudohypoparathyroidism 57 0.089
91
RHM027 Rheumatic Disease 56 0.089
92
DGR001 Digeorge Syndrome 64 0.089
93
RRD056 Rare Disease in Surgical Orthopedic 28 0.088
94
c CHR682 Chronic Bilirubin Encephalopathy 39 0.087
95
c PSD104 Pseudohypoparathyroidism, Type Ii 31 0.086
96
CLC001 Calciphylaxis 51 0.082
97
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.081
98
P PLY188 Polyendocrinopathy 33 0.080
99
EXS001 Exostosis 47 0.078
100
ENT004 Enthesopathy 49 0.077
101
c FNC043 Fanconi Anemia, Complementation Group E 63 0.074
102
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.069
103
FNT004 Fainting 31 0.069
104
VLC001 Velocardiofacial Syndrome 55 0.068
105
OST115 Osteonecrosis of the Jaw 39 0.068
106
BSL036 Basal Cell Nevus Syndrome 73 0.064
107
P THN009 Thanatophoric Dysplasia, Type I 62 0.062
108
IDP073 Idiopathic Hypercalciuria 43 0.062
109
c OST164 Osteoporosis, Juvenile 53 0.060
110
c ATM068 Autoimmune Hypoparathyroidism 32 0.051
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