Search results for pyrophosphate

142 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 32 9.238
2
FML307 Familial Calcium Pyrophosphate Deposition 27 6.626
3
P CHN059 Chondrocalcinosis 47 3.968
4
P KDN018 Kidney Disease 69 0.217
5
URN009 Urinary System Disease 58 0.211
6
c CHR089 Chronic Kidney Failure 72 0.200
7
END030 End Stage Renal Failure 59 0.194
8
P HYP035 Hypophosphatasia 58 0.175
9
P ART023 Arthropathy 68 0.168
10
IRN001 Iron Deficiency Anemia 55 0.137
11
IRN002 Iron Metabolism Disease 45 0.137
12
P ART022 Arthritis 77 0.128
13
BRS064 Bursitis 42 0.119
14
P MYC007 Myocardial Infarction 81 0.108
15
P AMY004 Amyloidosis 69 0.108
16
OLC001 Olecranon Bursitis 35 0.108
17
CRY024 Crystal Arthropathies 26 0.108
18
P BRS047 Breast Cancer 100 0.097
19
P LNG032 Lung Cancer 99 0.097
20
OST012 Osteoarthritis 88 0.097
21
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.097
22
c BLD140 Blood Group, I System 37 0.097
23
SBN001 Subendocardial Myocardial Infarction 31 0.097
24
P PRS040 Prostate Cancer 88 0.084
25
MYL069 Myeloma, Multiple 86 0.084
26
GNG013 Gingivitis 64 0.084
27
BRR014 Barrett Esophagus 64 0.084
28
DFC004 Deficiency Anemia 62 0.084
29
GTL001 Gitelman Syndrome 62 0.084
30
SYN007 Synovitis 61 0.084
31
GT001 Gout 60 0.084
32
PLR008 Pleurisy 52 0.084
33
c HYP292 Hypophosphatasia, Infantile 48 0.084
34
HYD003 Hydrarthrosis 43 0.084
35
BRB001 Beriberi 40 0.084
36
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.084
37
HYP596 Hypophosphatasia, Childhood 31 0.084
38
DSC004 Discitis 28 0.084
39
INT182 Intermittent Hydrarthrosis 19 0.084
40
c CHN021 Chondrocalcinosis 1 15 0.084
41
P MYC084 Mycobacterium Tuberculosis 1 69 0.068
42
P PSD087 Pseudoxanthoma Elasticum 67 0.068
43
c SML038 Small Cell Cancer of the Lung 67 0.068
44
OST017 Osteomyelitis 64 0.068
45
HLC007 Helicobacter Pylori Infection 64 0.068
46
P PNC044 Pancreatitis 64 0.068
47
P NRP001 Neuropathy 63 0.068
48
P MYS005 Myositis 63 0.068
49
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.068
50
P INF032 Infertility 59 0.068
51
BNC003 Bone Cancer 59 0.068
52
CFF002 Coffin-Lowry Syndrome 58 0.068
53
CLC006 Calcinosis 51 0.068
54
P CRV039 Cervicitis 49 0.068
55
c HYP293 Hypophosphatasia, Adult 48 0.068
56
HYP025 Hyperphosphatemia 48 0.068
57
SYN031 Synovial Chondromatosis 47 0.068
58
GNG003 Gingival Recession 45 0.068
59
TTH032 Tooth Size 44 0.068
60
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.068
61
GRW036 Growth Control, Y-Chromosome Influenced 33 0.068
62
MYS001 Myositis Ossificans 33 0.068
63
CRN264 Craniosynostosis with Fibular Aplasia 29 0.068
64
c THM013 Thiamine Metabolism Dysfunction Syndrome 5 22 0.068
65
c SYS001 Systemic Lupus Erythematosus 86 0.048
66
CYS001 Cystic Fibrosis 85 0.048
67
P OST002 Osteoporosis 75 0.048
68
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.048
69
P LKM002 Leukemia 75 0.048
70
P HPT021 Hepatitis 75 0.048
71
SQM006 Squamous Cell Carcinoma 74 0.048
72
P HRP006 Herpes Simplex 70 0.048
73
CHL065 Cholangiocarcinoma 70 0.048
74
ACR007 Acromegaly 70 0.048
75
P LPS004 Lupus Erythematosus 69 0.048
76
P MYP004 Myopathy 69 0.048
77
P CRN037 Craniosynostosis 68 0.048
78
P ANR048 Aniridia 1 68 0.048
79
P NMN002 Niemann-Pick Disease 68 0.048
80
P MCL013 Mucolipidosis Iv 67 0.048
81
P PRD008 Periodontitis 67 0.048
82
BRT054 Brittle Bone Disorder 67 0.048
83
P TMP003 Temporal Arteritis 67 0.048
84
PRT036 Peritonitis 67 0.048
85
P MPL001 Maple Syrup Urine Disease 66 0.048
86
ISC004 Ischemia 66 0.048
87
TTN003 Tetanus 65 0.048
88
CRP001 Carpal Tunnel Syndrome 64 0.048
89
c ACT075 Acute Myocardial Infarction 64 0.048
90
HYP266 Hypoxia 61 0.048
91
P GLM045 Glioma 61 0.048
92
JNT002 Joint Disorders 60 0.048
93
SPN027 Spinal Stenosis 60 0.048
94
PRS047 Prostatitis 59 0.048
95
GNT003 Genital Herpes 58 0.048
96
CYT008 Cytomegalovirus Infection 57 0.048
97
P ZLL001 Zellweger Syndrome 56 0.048
98
ISL001 Islet Cell Tumor 54 0.048
99
CLC001 Calciphylaxis 53 0.048
100
URM002 Uremia 52 0.048
101
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.048
102
P SHR001 Short Bowel Syndrome 52 0.048
103
MMM001 Mammary Paget's Disease 51 0.048
104
HMR002 Hemarthrosis 51 0.048
105
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 51 0.048
106
HMS001 Hemosiderosis 50 0.048
107
P TCL004 T-Cell Leukemia 50 0.048
108
IDP024 Idiopathic Inflammatory Myopathy 49 0.048
109
ADN024 Adenine Phosphoribosyltransferase Deficiency 49 0.048
110
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.048
111
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.048
112
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.048
113
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.048
114
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.048
115
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.048
116
CHN010 Chondroma 44 0.048
117
PYM001 Pyomyositis 42 0.048
118
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.048
119
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.048
120
TND005 Tendinitis 42 0.048
121
OST097 Osteoporotic Fracture 41 0.048
122
c HYP794 Hyperoxaluria, Primary, Type I 41 0.048
123
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.048
124
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 40 0.048
125
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.048
126
ART035 Arterial Calcification of Infancy 38 0.048
127
CLC004 Calcific Tendinitis 38 0.048
128
TTH007 Tooth Erosion 36 0.048
129
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.048
130
CYT004 Cytomegalic Inclusion Disease 35 0.048
131
CRD016 Cardiac Rupture 34 0.048
132
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.048
133
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.048
134
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.048
135
EPD005 Epidural Abscess 31 0.048
136
c GLY017 Glycogen Storage Disease Ic 28 0.048
137
P XLN007 X-Linked Disease 28 0.048
138
CLC064 Calcifying Aponeurotic Fibroma 26 0.048
139
ANR038 Anorexia Nervosa 1 21 0.048
140
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.048
141
BLD137 Blood Group--Ahonen 17 0.048
142
WLF014 Wolfram Syndrome, Mitochondrial Form 15 0.048
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