Search results for Phosphoric acid

203 hits were found for Phosphoric acid

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.364
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.359
3
P KDN018 Kidney Disease 72 0.285
4
P LVR013 Liver Disease 68 0.269
5
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.267
6
CHL068 Cholestasis 61 0.235
7
c CHR684 Chronic Kidney Disease 70 0.229
8
MTB004 Metabolic Acidosis 50 0.228
9
P CLR023 Colorectal Cancer 99 0.220
10
BNR002 Bone Resorption Disease 48 0.215
11
P SZR006 Seizure Disorder 56 0.206
12
48X005 48,xyyy 39 0.203
13
VSL002 Visual Epilepsy 59 0.200
14
LPD008 Lipid Metabolism Disorder 62 0.196
15
P OST002 Osteoporosis 74 0.192
16
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.187
17
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.187
18
HRW001 Hair Whorl 36 0.186
19
P BRS047 Breast Cancer 97 0.186
20
LNG099 Lung Disease 60 0.185
21
P INF037 Inflammatory Bowel Disease 54 0.180
22
P CRN300 Coronary Heart Disease 1 63 0.179
23
DFC004 Deficiency Anemia 70 0.179
24
HYP056 Hypoglycemia 66 0.179
25
END086 End Stage Renal Disease 51 0.176
26
ATH013 Atherosclerosis Susceptibility 65 0.173
27
P VSC007 Vascular Disease 63 0.168
28
IRN002 Iron Metabolism Disease 57 0.168
29
P ENC018 Encephalopathy 61 0.167
30
P LKM002 Leukemia 68 0.167
31
OST159 Osteogenic Sarcoma 66 0.167
32
P BPL003 Bipolar Disorder 56 0.166
33
PPT005 Peptic Ulcer Disease 59 0.166
34
c MJR024 Major Affective Disorder 9 41 0.166
35
c MJR022 Major Affective Disorder 8 38 0.166
36
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.166
37
P HYP069 Hyperparathyroidism 63 0.165
38
RCK004 Rickets 68 0.162
39
P OVR042 Ovarian Cancer 88 0.160
40
P PSR002 Psoriasis 62 0.160
41
DRM006 Dermatitis 61 0.159
42
PST011 Pustulosis of Palm and Sole 52 0.158
43
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.158
44
47X002 47,xyy 49 0.156
45
ALL026 Allergic Hypersensitivity Disease 62 0.155
46
SKN016 Skin Disease 63 0.153
47
P ADN016 Adenocarcinoma 64 0.153
48
CYS001 Cystic Fibrosis 81 0.150
49
DNT012 Dental Caries 53 0.147
50
P CRD246 Cardiovascular System Disease 57 0.145
51
NTR005 Nutritional Deficiency Disease 62 0.143
52
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.142
53
P GST053 Gastric Cancer 83 0.142
54
PPL052 Papillomatosis, Confluent and Reticulated 33 0.142
55
CYT002 Cytokine Deficiency 42 0.141
56
DPR016 Depression 63 0.140
57
P MYP004 Myopathy 70 0.139
58
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.139
59
c HYP595 Hypertension, Essential 84 0.139
60
OCL069 Ocular Motor Apraxia 51 0.139
61
P BLD134 Bladder Cancer 79 0.139
62
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.139
63
GST023 Gastric Ulcer 53 0.138
64
HYP781 Hypoascorbemia 51 0.134
65
CHL014 Cholera 59 0.132
66
MNT002 Mental Depression 58 0.131
67
OST003 Osteonecrosis 61 0.129
68
ALC007 Alcohol Dependence 66 0.126
69
P PRD008 Periodontitis 64 0.125
70
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.125
71
P HYP086 Hypothyroidism 69 0.123
72
c DBT099 Diabetes Mellitus, Type I 65 0.123
73
P MSC005 Muscular Dystrophy 66 0.122
74
URL001 Urolithiasis 45 0.122
75
MTH071 Methane Production 26 0.121
76
HYP025 Hyperphosphatemia 48 0.120
77
KRT009 Keratosis 51 0.118
78
CRB004 Cerebral Artery Occlusion 45 0.117
79
c ACT027 Acute Pancreatitis 60 0.117
80
c SCN007 Secondary Hyperparathyroidism 51 0.114
81
c THR092 Thrombophilia Due to Thrombin Defect 73 0.114
82
P SCH015 Schizophrenia 74 0.114
83
PLM010 Pulmonary Edema 54 0.114
84
P OVR082 Overgrowth Syndrome 50 0.112
85
P THR014 Thrombocytopenia 67 0.112
86
HYP017 Hypophosphatemia 50 0.112
87
P LNG064 Lung Cancer Susceptibility 3 78 0.112
88
P TMP001 Temporal Lobe Epilepsy 50 0.111
89
P PRP029 Porphyria 62 0.110
90
c ACT134 Acute Liver Failure 56 0.109
91
BRN024 Bronchitis 68 0.108
92
P ART023 Arthropathy 62 0.108
93
P MSC003 Muscular Atrophy 52 0.108
94
P AST007 Astrocytoma 51 0.108
95
EYD002 Eye Disease 58 0.108
96
PPL022 Papilloma 54 0.107
97
TXC005 Toxic Shock Syndrome 62 0.107
98
P GLM007 Glomerulonephritis 57 0.107
99
P MLT020 Multiple Sclerosis 72 0.107
100
P PNC044 Pancreatitis 61 0.107
101
INT066 Interstitial Lung Disease 60 0.106
102
SRC014 Sarcoma 65 0.105
103
SPN035 Spindle Cell Sarcoma 53 0.105
104
c ATR087 Atrial Standstill 1 75 0.105
105
P TRM003 Tremor 54 0.105
106
P LYM118 Lymphoma 68 0.104
107
SQM002 Squamous Cell Papilloma 46 0.104
108
P INF038 Influenza 68 0.104
109
P FBR017 Fibrosarcoma 56 0.104
110
c VRL010 Viral Hepatitis 52 0.103
111
TTN003 Tetanus 65 0.102
112
P INF032 Infertility 57 0.102
113
P PLM036 Pulmonary Fibrosis 65 0.099
114
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.098
115
SCH014 Schistosomiasis 57 0.098
116
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.098
117
c PRM005 Primary Hyperparathyroidism 58 0.098
118
NWC001 Newcastle Disease 45 0.095
119
BRN004 Brain Edema 56 0.094
120
PRP027 Peripheral Vascular Disease 71 0.094
121
SBC016 Subacute Delirium 44 0.094
122
PLG002 Plague 63 0.092
123
P THL005 Thalassemia 60 0.092
124
P PLM037 Pulmonary Hypertension 67 0.091
125
DNT001 Dental Fluorosis 43 0.089
126
OST017 Osteomyelitis 64 0.089
127
HMS001 Hemosiderosis 54 0.088
128
P URT039 Urticaria 58 0.088
129
IRN001 Iron Deficiency Anemia 59 0.087
130
P RRH023 Rare Hereditary Hemochromatosis 41 0.087
131
RTR008 Root Resorption 45 0.086
132
P SYS005 Systemic Scleroderma 68 0.086
133
ARG004 Argyria 27 0.086
134
PNM008 Pneumothorax 56 0.086
135
P ANP001 Anaplastic Large Cell Lymphoma 58 0.084
136
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.083
137
ANT018 Anthracosis 48 0.083
138
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.083
139
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.082
140
GNG013 Gingivitis 59 0.082
141
P PNM006 Pneumoconiosis 56 0.082
142
c PRD040 Periodontitis, Chronic 53 0.082
143
AMN006 Aminoaciduria 38 0.081
144
PST092 Posttransplant Acute Limbic Encephalitis 29 0.081
145
P SCL018 Scoliosis 60 0.081
146
MDD018 Middle East Respiratory Syndrome 43 0.080
147
MSC157 Muscular Dystrophy, Duchenne Type 72 0.079
148
TRN018 Transitional Cell Carcinoma 56 0.079
149
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.078
150
KWS001 Kwashiorkor 44 0.078
151
ADG002 Audiogenic Seizures 25 0.077
152
PRP083 Porphyria, Acute Intermittent 64 0.076
153
ANT024 Anthrax Disease 58 0.076
154
OVR094 Ovarian Epithelial Cancer 38 0.075
155
MYM001 Myoma 54 0.075
156
CLC006 Calcinosis 48 0.073
157
P BRB001 Beriberi 46 0.071
158
P PLY018 Polycythemia 56 0.069
159
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.069
160
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.069
161
INT002 Intermittent Claudication 61 0.069
162
P HYP024 Hypoparathyroidism 56 0.068
163
MLT157 Multiple System Atrophy 1 70 0.064
164
NRM005 Neuromuscular Disease 64 0.063
165
CCC002 Coccidiosis 51 0.062
166
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.062
167
BRS051 Breast Disease 58 0.061
168
c PRG106 Progressive Muscular Dystrophy 33 0.061
169
ENM001 Enamel Caries 28 0.060
170
BNG077 Benign Idiopathic Neonatal Seizures 26 0.060
171
PLY001 Polycythemia Vera 69 0.059
172
OST011 Osteomalacia 52 0.059
173
NPH003 Nephrocalcinosis 51 0.058
174
P FRN006 Frontotemporal Dementia 68 0.057
175
HMR002 Hemarthrosis 45 0.057
176
RNL011 Renal Osteodystrophy 50 0.056
177
SYN036 Syncope 45 0.054
178
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.054
179
MTB016 Metabolic Myopathy 32 0.054
180
P FML340 Familial Episodic Pain Syndrome 39 0.053
181
CRN036 Craniopharyngioma 65 0.053
182
TLR001 Tularemia 51 0.052
183
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.052
184
SML019 Smallpox 56 0.049
185
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.049
186
VRL003 Variola Major 42 0.048
187
ACT055 Actinomycosis 47 0.047
188
P PSD015 Pseudohypoparathyroidism 56 0.047
189
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.046
190
PLR022 Pleural Disease 45 0.046
191
SHR097 Short Tarsus with Absence of Lower Eyelashes 26 0.046
192
RNL024 Renal Glucosuria 58 0.045
193
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.045
194
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.043
195
HMP018 Hemophilic Arthropathy 34 0.043
196
MCR141 Mucormycosis 56 0.042
197
PRT030 Parathyroid Gland Disease 45 0.042
198
MYS004 Myiasis 38 0.042
199
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.040
200
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.040
201
GMS001 Gemistocytic Astrocytoma 36 0.039
202
c CRD163 Cardiofaciocutaneous Syndrome 2 39 0.037
203
PRR015 Preauricular Fistulae, Congenital 20 0.037
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