Search results for pyrophosphate

127 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 25 7.836
2
FML307 Familial Calcium Pyrophosphate Deposition 17 6.387
3
P CHN059 Chondrocalcinosis 41 3.925
4
P HYP035 Hypophosphatasia 57 0.181
5
P ART023 Arthropathy 64 0.174
6
c CHR089 Chronic Kidney Failure 66 0.142
7
URN009 Urinary System Disease 50 0.142
8
P URF003 Urofacial Syndrome 1 50 0.142
9
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.142
10
IMP003 Impaired Renal Function Disease 34 0.142
11
P KDN018 Kidney Disease 66 0.133
12
END030 End Stage Renal Failure 55 0.133
13
P ART022 Arthritis 75 0.123
14
P MYC007 Myocardial Infarction 79 0.112
15
DFC004 Deficiency Anemia 64 0.112
16
IRN001 Iron Deficiency Anemia 52 0.112
17
LPD004 Lipoid Nephrosis 48 0.112
18
BRS064 Bursitis 39 0.112
19
NTR005 Nutritional Deficiency Disease 36 0.112
20
P BRS047 Breast Cancer 100 0.100
21
P LNG032 Lung Cancer 95 0.100
22
P OST012 Osteoarthritis 83 0.100
23
P AMY004 Amyloidosis 65 0.100
24
OLC001 Olecranon Bursitis 35 0.100
25
SBN001 Subendocardial Myocardial Infarction 32 0.100
26
CRY024 Crystal Arthropathies 21 0.100
27
P PRS040 Prostate Cancer 90 0.087
28
P MLT019 Multiple Myeloma 83 0.087
29
GNG013 Gingivitis 61 0.087
30
GTL001 Gitelman Syndrome 61 0.087
31
SYN007 Synovitis 58 0.087
32
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.087
33
PLR008 Pleurisy 50 0.087
34
IRN002 Iron Metabolism Disease 41 0.087
35
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.087
36
TBR010 Tuberculosis 70 0.071
37
P PSD087 Pseudoxanthoma Elasticum 66 0.071
38
P NRP001 Neuropathy 59 0.071
39
P INF032 Infertility 59 0.071
40
P GT001 Gout 58 0.071
41
BNC003 Bone Cancer 58 0.071
42
P MYS005 Myositis 57 0.071
43
HTC002 Hutchinson-Gilford Progeria 57 0.071
44
CFF002 Coffin-Lowry Syndrome 55 0.071
45
SML033 Small Cell Cancer of the Lung, Somatic 54 0.071
46
c HMG001 Hemoglobin C Disease 47 0.071
47
HYP025 Hyperphosphatemia 47 0.071
48
P CRV039 Cervicitis 45 0.071
49
PRG004 Progeria 44 0.071
50
HYP596 Hypophosphatasia, Childhood 44 0.071
51
c HYP292 Hypophosphatasia, Infantile 42 0.071
52
GNG003 Gingival Recession 38 0.071
53
MYS001 Myositis Ossificans 37 0.071
54
HYD003 Hydrarthrosis 37 0.071
55
DSC004 Discitis 26 0.071
56
INT182 Intermittent Hydrarthrosis 18 0.071
57
P OBS005 Obesity 92 0.050
58
c SYS001 Systemic Lupus Erythematosus 86 0.050
59
CYS001 Cystic Fibrosis 83 0.050
60
HV1006 Hiv-1 80 0.050
61
P LKM002 Leukemia 71 0.050
62
SQM006 Squamous Cell Carcinoma 70 0.050
63
P HPT021 Hepatitis 69 0.050
64
P OST005 Osteogenesis Imperfecta 69 0.050
65
PRP027 Peripheral Vascular Disease 68 0.050
66
PCK002 Pick Disease 68 0.050
67
ACR007 Acromegaly 66 0.050
68
P CRN037 Craniosynostosis 66 0.050
69
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.050
70
P NMN002 Niemann-Pick Disease 65 0.050
71
P HRP006 Herpes Simplex 65 0.050
72
P LPS004 Lupus Erythematosus 64 0.050
73
P OST002 Osteoporosis 64 0.050
74
P PRD008 Periodontitis 63 0.050
75
PRT036 Peritonitis 63 0.050
76
P MCL013 Mucolipidosis Iv 62 0.050
77
ISC004 Ischemia 61 0.050
78
OST017 Osteomyelitis 61 0.050
79
TTN003 Tetanus 61 0.050
80
P PNC044 Pancreatitis 61 0.050
81
HPY002 H. Pylori Infection 61 0.050
82
c ACT075 Acute Myocardial Infarction 60 0.050
83
P GLM045 Glioma 60 0.050
84
ZLL001 Zellweger Syndrome 56 0.050
85
HYP266 Hypoxia 56 0.050
86
PRS047 Prostatitis 56 0.050
87
JNT002 Joint Disorders 55 0.050
88
SPN027 Spinal Stenosis 55 0.050
89
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.050
90
GNT003 Genital Herpes 53 0.050
91
CYT008 Cytomegalovirus Infection 52 0.050
92
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.050
93
PRT011 Protein C Deficiency 52 0.050
94
ADN024 Adenine Phosphoribosyltransferase Deficiency 51 0.050
95
STM006 Stomach Disease 50 0.050
96
ISL001 Islet Cell Tumor 50 0.050
97
CLC006 Calcinosis 50 0.050
98
P SHR001 Short Bowel Syndrome 49 0.050
99
URM002 Uremia 48 0.050
100
HMR002 Hemarthrosis 48 0.050
101
P TCL004 T-Cell Leukemia 47 0.050
102
HMS001 Hemosiderosis 46 0.050
103
CLC001 Calciphylaxis 46 0.050
104
MMM001 Mammary Paget's Disease 45 0.050
105
ACD009 Acid-Labile Subunit, Deficiency of 45 0.050
106
SYN031 Synovial Chondromatosis 42 0.050
107
CHN010 Chondroma 42 0.050
108
PRM025 Primary Bacterial Infectious Disease 41 0.050
109
BRB001 Beriberi 41 0.050
110
PYM001 Pyomyositis 40 0.050
111
TND005 Tendinitis 39 0.050
112
c HYP617 Hyperoxaluria, Primary, Type 1 39 0.050
113
MYH012 Myhre Syndrome 38 0.050
114
ADJ001 Adjustment Disorder 38 0.050
115
ART035 Arterial Calcification of Infancy 37 0.050
116
BNS002 Bone Structure Disease 37 0.050
117
PLS010 Plasma Protein Metabolism Disease 34 0.050
118
CRD016 Cardiac Rupture 34 0.050
119
P XLN007 X-Linked Disease 34 0.050
120
EPD005 Epidural Abscess 33 0.050
121
TTH007 Tooth Erosion 33 0.050
122
c HMG004 Hemoglobin D Disease 31 0.050
123
CYT004 Cytomegalic Inclusion Disease 31 0.050
124
OST097 Osteoporotic Fracture 28 0.050
125
CLC004 Calcific Tendinitis 27 0.050
126
c RNL016 Renal Infectious Disease 20 0.050
127
HMG009 Hemoglobin Zurich 16 0.050
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