Search results for Phosphocreatine

125 hits were found for Phosphocreatine

# Family MCID Name MIFTS Score
1
CNG034 Congestive Heart Failure 70 0.165
2
ANX004 Anoxia 42 0.158
3
P HRT032 Heart Disease 75 0.132
4
ART140 Arteries, Anomalies of 53 0.132
5
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.122
6
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.122
7
P CRN018 Coronary Artery Anomaly 63 0.122
8
P CRN300 Coronary Heart Disease 1 63 0.122
9
ISC004 Ischemia 60 0.122
10
P MJR001 Major Depressive Disorder 68 0.112
11
P CRD119 Cardiac Arrest 67 0.112
12
P MSC005 Muscular Dystrophy 66 0.112
13
DPR016 Depression 63 0.112
14
MNT002 Mental Depression 57 0.112
15
c ATR087 Atrial Standstill 1 74 0.100
16
NRT001 Neurotic Disorder 52 0.100
17
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.086
18
PRP027 Peripheral Vascular Disease 71 0.086
19
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.086
20
TTN003 Tetanus 64 0.086
21
P SZR006 Seizure Disorder 58 0.086
22
VSL002 Visual Epilepsy 58 0.086
23
END040 Endogenous Depression 54 0.086
24
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.086
25
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.086
26
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.086
27
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.086
28
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.086
29
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
30
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.086
31
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
32
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.086
33
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.086
34
P ALZ034 Alzheimer Disease 88 0.071
35
c DLT002 Dilated Cardiomyopathy 79 0.071
36
P MLG056 Malignant Hyperthermia 67 0.071
37
P MYP004 Myopathy 64 0.071
38
P HYP750 Hypertriglyceridemia, Familial 61 0.071
39
HYP066 Hyperglycemia 61 0.071
40
P MYC008 Myocarditis 59 0.071
41
HYP266 Hypoxia 56 0.071
42
c ACT075 Acute Myocardial Infarction 56 0.071
43
P CRD246 Cardiovascular System Disease 56 0.071
44
HRT012 Heart Valve Disease 53 0.071
45
CRB150 Cerebral Creatine Deficiency Syndrome 2 52 0.071
46
P LCT001 Lactic Acidosis 51 0.071
47
CRB004 Cerebral Artery Occlusion 44 0.071
48
CRB148 Cerebral Creatine Deficiency Syndrome 3 43 0.071
49
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.071
50
ADG002 Audiogenic Seizures 26 0.071
51
SVR004 Severe Combined Immunodeficiency 73 0.050
52
P MLT020 Multiple Sclerosis 72 0.050
53
c HYP836 Hypercholesterolemia, Familial, 1 72 0.050
54
P LFR001 Li-Fraumeni Syndrome 72 0.050
55
P KDN018 Kidney Disease 70 0.050
56
CRB039 Cerebrovascular Disease 69 0.050
57
P HYP086 Hypothyroidism 68 0.050
58
OBS002 Obsessive-Compulsive Disorder 68 0.050
59
PSY004 Psychotic Disorder 67 0.050
60
c CHR684 Chronic Kidney Disease 66 0.050
61
P HYP061 Hypertrophic Cardiomyopathy 66 0.050
62
ANG054 Angina Pectoris 66 0.050
63
SRC014 Sarcoma 65 0.050
64
P HYD006 Hydrocephalus 65 0.050
65
c RHB024 Rhabdomyosarcoma 2 65 0.050
66
P ADN016 Adenocarcinoma 64 0.050
67
CLN015 Colon Adenocarcinoma 63 0.050
68
P VSC007 Vascular Disease 63 0.050
69
MSC007 Muscle Hypertrophy 63 0.050
70
LVR012 Liver Cirrhosis 63 0.050
71
NRM005 Neuromuscular Disease 63 0.050
72
KRN002 Kearns-Sayre Syndrome 63 0.050
73
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.050
74
c FNC043 Fanconi Anemia, Complementation Group E 62 0.050
75
MDD011 Mood Disorder 62 0.050
76
P DRM010 Dermatomyositis 61 0.050
77
NTR005 Nutritional Deficiency Disease 61 0.050
78
INT002 Intermittent Claudication 61 0.050
79
c GLY004 Glycogen Storage Disease V 61 0.050
80
SPN186 Spinal Cord Injury 60 0.050
81
DPH001 Diphtheria 60 0.050
82
P BRS044 Breast Adenocarcinoma 59 0.050
83
END030 End Stage Renal Failure 58 0.050
84
P PLY041 Polymyositis 57 0.050
85
DSS008 Disease of Mental Health 57 0.050
86
P PRP019 Peripheral Nervous System Disease 57 0.050
87
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.050
88
P NRP001 Neuropathy 56 0.050
89
P MTC069 Mitochondrial Disorders 56 0.050
90
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.050
91
P HYP076 Hyperthyroidism 55 0.050
92
c GLY011 Glycogen Storage Disease Vii 55 0.050
93
PRC013 Pericarditis 54 0.050
94
INT075 Intracranial Hypertension 53 0.050
95
P HYP083 Hypopituitarism 53 0.050
96
PRP080 Peripheral Artery Disease 53 0.050
97
c MCR113 Microvascular Complications of Diabetes 3 52 0.050
98
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.050
99
P MSC003 Muscular Atrophy 52 0.050
100
RYS001 Reye Syndrome 51 0.050
101
SPP010 Suppressor of Tumorigenicity 3 51 0.050
102
SPN035 Spindle Cell Sarcoma 51 0.050
103
P MYT002 Myotonic Dystrophy 49 0.050
104
c BPL002 Bipolar I Disorder 49 0.050
105
URM002 Uremia 49 0.050
106
P CMP008 Compartment Syndrome 48 0.050
107
MTC005 Mitochondrial Metabolism Disease 48 0.050
108
P ASP001 Asperger Syndrome 48 0.050
109
ATX019 Ataxia with Vitamin E Deficiency 48 0.050
110
TRC023 Trichinosis 47 0.050
111
HYP025 Hyperphosphatemia 47 0.050
112
c MCR120 Microvascular Complications of Diabetes 7 47 0.050
113
c MTR002 Mitral Valve Insufficiency 47 0.050
114
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.050
115
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.050
116
MYC005 Myocardial Stunning 46 0.050
117
c HYP272 Hypercholesterolemia, Familial, 3 43 0.050
118
P MTC004 Mitochondrial Encephalomyopathy 43 0.050
119
c LFR007 Li-Fraumeni Syndrome 2 42 0.050
120
c MCR130 Microvascular Complications of Diabetes 6 41 0.050
121
c MCR133 Microvascular Complications of Diabetes 4 41 0.050
122
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 40 0.050
123
PPL052 Papillomatosis, Confluent and Reticulated 34 0.050
124
c PRG106 Progressive Muscular Dystrophy 33 0.050
125
CHL079 Children's Interstitial Lung Disease 27 0.050
Content
Loading form....