Search results for Phosphoric acid

201 hits were found for Phosphoric acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.379
2
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.365
3
P KDN018 Kidney Disease 73 0.297
4
P LVR013 Liver Disease 71 0.274
5
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.267
6
CHL068 Cholestasis 61 0.241
7
c CHR684 Chronic Kidney Disease 68 0.236
8
MTB004 Metabolic Acidosis 48 0.234
9
P CLR023 Colorectal Cancer 100 0.230
10
BNR002 Bone Resorption Disease 51 0.219
11
P SZR006 Seizure Disorder 59 0.213
12
PLM017 Pulmonary Alveolar Microlithiasis 54 0.208
13
VSL002 Visual Epilepsy 58 0.207
14
P OST002 Osteoporosis 79 0.199
15
LPD008 Lipid Metabolism Disorder 64 0.199
16
48X005 48,xyyy 37 0.197
17
P BRS047 Breast Cancer 99 0.193
18
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.191
19
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.191
20
P INF037 Inflammatory Bowel Disease 57 0.190
21
HRW001 Hair Whorl 36 0.190
22
LNG099 Lung Disease 62 0.190
23
ISC004 Ischemia 62 0.188
24
END030 End Stage Renal Failure 60 0.188
25
P CRN300 Coronary Heart Disease 1 59 0.185
26
HYP056 Hypoglycemia 68 0.184
27
P ENC018 Encephalopathy 64 0.176
28
DFC004 Deficiency Anemia 77 0.175
29
P VSC007 Vascular Disease 65 0.173
30
P LKM002 Leukemia 69 0.172
31
IRN002 Iron Metabolism Disease 58 0.172
32
PPT005 Peptic Ulcer Disease 60 0.172
33
ALL026 Allergic Hypersensitivity Disease 65 0.170
34
OST159 Osteogenic Sarcoma 67 0.169
35
P BPL003 Bipolar Disorder 59 0.169
36
c MJR024 Major Affective Disorder 9 42 0.168
37
c MJR022 Major Affective Disorder 8 39 0.168
38
DRM006 Dermatitis 63 0.166
39
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.166
40
P PSR002 Psoriasis 63 0.166
41
PST011 Pustulosis of Palm and Sole 51 0.164
42
P HYP069 Hyperparathyroidism 64 0.163
43
P LYM031 Lymphocytic Leukemia 56 0.159
44
P ADN016 Adenocarcinoma 65 0.159
45
RCK004 Rickets 70 0.158
46
CYS001 Cystic Fibrosis 84 0.156
47
SKN016 Skin Disease 64 0.154
48
P OVR042 Ovarian Cancer 89 0.152
49
DNT012 Dental Caries 52 0.148
50
c HYP595 Hypertension, Essential 87 0.147
51
OCL069 Ocular Motor Apraxia 53 0.146
52
P GST053 Gastric Cancer 85 0.146
53
P BLD134 Bladder Cancer 79 0.146
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.145
55
P MYP004 Myopathy 63 0.144
56
DPR016 Depression 64 0.143
57
PPL052 Papillomatosis, Confluent and Reticulated 34 0.143
58
GST023 Gastric Ulcer 53 0.141
59
47X002 47,xyy 49 0.141
60
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.137
61
CHL014 Cholera 58 0.136
62
HYP781 Hypoascorbemia 48 0.135
63
MNT002 Mental Depression 60 0.134
64
NTR005 Nutritional Deficiency Disease 61 0.131
65
OST003 Osteonecrosis 62 0.131
66
ALC007 Alcohol Dependence 68 0.130
67
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.130
68
P HYP086 Hypothyroidism 70 0.127
69
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.126
70
P MSC005 Muscular Dystrophy 68 0.125
71
P INF038 Influenza 69 0.125
72
P PRD008 Periodontitis 66 0.123
73
HYP025 Hyperphosphatemia 47 0.121
74
P SCH015 Schizophrenia 76 0.121
75
MTH071 Methane Production 26 0.121
76
CRB004 Cerebral Artery Occlusion 38 0.118
77
c ACT027 Acute Pancreatitis 60 0.118
78
c SCN007 Secondary Hyperparathyroidism 52 0.117
79
P THR014 Thrombocytopenia 67 0.116
80
PLM010 Pulmonary Edema 56 0.116
81
c THR092 Thrombophilia Due to Thrombin Defect 74 0.116
82
P MLT020 Multiple Sclerosis 73 0.115
83
OVR082 Overgrowth Syndrome 51 0.114
84
HYP017 Hypophosphatemia 48 0.114
85
P PRP029 Porphyria 58 0.113
86
P LNG064 Lung Cancer Susceptibility 3 79 0.112
87
P TMP001 Temporal Lobe Epilepsy 53 0.112
88
c ATR087 Atrial Standstill 1 76 0.112
89
P PNC044 Pancreatitis 61 0.111
90
SRC014 Sarcoma 67 0.111
91
SPN035 Spindle Cell Sarcoma 57 0.111
92
BRN024 Bronchitis 70 0.111
93
P AST007 Astrocytoma 52 0.111
94
P MSC003 Muscular Atrophy 52 0.110
95
P GLM007 Glomerulonephritis 58 0.110
96
P ART023 Arthropathy 61 0.110
97
P LYM118 Lymphoma 70 0.109
98
TXC005 Toxic Shock Syndrome 63 0.108
99
INT066 Interstitial Lung Disease 61 0.107
100
EYD002 Eye Disease 59 0.107
101
P TRM003 Tremor 55 0.107
102
P FBR017 Fibrosarcoma 57 0.107
103
c VRL010 Viral Hepatitis 56 0.106
104
P INF032 Infertility 60 0.105
105
c LRG017 Large Intestine Cancer 53 0.105
106
TTN003 Tetanus 62 0.105
107
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.105
108
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.100
109
SCH014 Schistosomiasis 57 0.099
110
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.099
111
P MYC084 Mycobacterium Tuberculosis 1 69 0.099
112
P PLM036 Pulmonary Fibrosis 66 0.097
113
IDP011 Idiopathic Interstitial Pneumonia 65 0.097
114
NWC001 Newcastle Disease 45 0.097
115
c ACT134 Acute Liver Failure 53 0.097
116
PRP027 Peripheral Vascular Disease 72 0.097
117
BRN004 Brain Edema 57 0.096
118
P PLM037 Pulmonary Hypertension 69 0.096
119
SBC016 Subacute Delirium 43 0.096
120
PLG002 Plague 54 0.094
121
P THL005 Thalassemia 62 0.092
122
DNT001 Dental Fluorosis 44 0.091
123
OST017 Osteomyelitis 65 0.091
124
c PRM005 Primary Hyperparathyroidism 60 0.090
125
HMS001 Hemosiderosis 54 0.090
126
P URT039 Urticaria 61 0.090
127
IRN001 Iron Deficiency Anemia 59 0.089
128
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.088
129
ARG004 Argyria 28 0.088
130
PNM008 Pneumothorax 56 0.088
131
P RRH023 Rare Hereditary Hemochromatosis 41 0.088
132
P SYS005 Systemic Scleroderma 68 0.088
133
RTR008 Root Resorption 44 0.087
134
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.086
135
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.085
136
ANT018 Anthracosis 46 0.085
137
GNG013 Gingivitis 60 0.084
138
P PNM006 Pneumoconiosis 55 0.084
139
AMN006 Aminoaciduria 39 0.083
140
TRN018 Transitional Cell Carcinoma 57 0.083
141
PST092 Posttransplant Acute Limbic Encephalitis 29 0.082
142
P SCL018 Scoliosis 61 0.082
143
c PRD040 Periodontitis, Chronic 56 0.082
144
MSC157 Muscular Dystrophy, Duchenne Type 70 0.081
145
KWS001 Kwashiorkor 46 0.080
146
ADG002 Audiogenic Seizures 25 0.080
147
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.079
148
PRP083 Porphyria, Acute Intermittent 62 0.078
149
OVR094 Ovarian Epithelial Cancer 39 0.078
150
CLC006 Calcinosis 48 0.077
151
ANT024 Anthrax Disease 56 0.077
152
MYM001 Myoma 52 0.074
153
P BRB001 Beriberi 41 0.074
154
P PLY018 Polycythemia 56 0.072
155
INT002 Intermittent Claudication 60 0.071
156
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.071
157
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.070
158
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.070
159
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.068
160
MLT157 Multiple System Atrophy 1 71 0.067
161
NRM005 Neuromuscular Disease 62 0.066
162
BRS051 Breast Disease 59 0.063
163
MLC004 Mulchandani-Bhoj-Conlin Syndrome 31 0.063
164
PLY001 Polycythemia Vera 70 0.062
165
CCC002 Coccidiosis 46 0.062
166
c PRG106 Progressive Muscular Dystrophy 34 0.062
167
ENM001 Enamel Caries 29 0.062
168
BNG077 Benign Idiopathic Neonatal Seizures 27 0.062
169
OST011 Osteomalacia 51 0.060
170
NPH003 Nephrocalcinosis 52 0.059
171
FRN006 Frontotemporal Dementia 70 0.057
172
RNL011 Renal Osteodystrophy 49 0.057
173
P HYP024 Hypoparathyroidism 56 0.056
174
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.056
175
HMR002 Hemarthrosis 46 0.055
176
MTB016 Metabolic Myopathy 34 0.055
177
CRN036 Craniopharyngioma 65 0.055
178
SYN036 Syncope 46 0.055
179
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.054
180
TLR001 Tularemia 44 0.054
181
SML019 Smallpox 55 0.050
182
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.050
183
VRL003 Variola Major 48 0.049
184
ACT055 Actinomycosis 43 0.049
185
P PSD015 Pseudohypoparathyroidism 54 0.048
186
PLR022 Pleural Disease 50 0.048
187
SHR097 Short Tarsus with Absence of Lower Eyelashes 24 0.047
188
RNL024 Renal Glucosuria 59 0.046
189
SCN001 Secondary Hyperparathyroidism of Renal Origin 23 0.046
190
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.045
191
HMP018 Hemophilic Arthropathy 35 0.044
192
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.044
193
PRT030 Parathyroid Gland Disease 45 0.042
194
MYS004 Myiasis 39 0.042
195
GMS001 Gemistocytic Astrocytoma 35 0.042
196
c PSD108 Pseudohypoparathyroidism, Type Ia 61 0.041
197
MCR141 Mucormycosis 48 0.041
198
P FML340 Familial Episodic Pain Syndrome 28 0.041
199
PSD119 Pseudohypoparathyroidism with Albright Hereditary Osteodystrophy 31 0.039
200
c CRD163 Cardiofaciocutaneous Syndrome 2 26 0.037
201
PRR015 Preauricular Fistulae, Congenital 20 0.037
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