Search results for Pentetic acid

253 hits were found for Pentetic acid

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 68 0.279
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.266
3
LVR012 Liver Cirrhosis 62 0.221
4
P CLR023 Colorectal Cancer 99 0.218
5
P KDN018 Kidney Disease 72 0.209
6
c NRF023 Neurofibromatosis, Type Ii 80 0.198
7
P DRR001 Diarrhea 55 0.194
8
48X005 48,xyyy 39 0.187
9
P BRS047 Breast Cancer 97 0.183
10
ISC004 Ischemia 58 0.177
11
P CRN300 Coronary Heart Disease 1 63 0.177
12
P GLM045 Glioma 63 0.175
13
GLL048 Glial Tumor 45 0.173
14
P PRS040 Prostate Cancer 97 0.168
15
P HPT023 Hepatocellular Carcinoma 100 0.168
16
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.167
17
P LKM002 Leukemia 68 0.165
18
HYP056 Hypoglycemia 66 0.163
19
HMN044 Human Immunodeficiency Virus Type 1 71 0.163
20
PRT037 Pertussis 65 0.160
21
GLB015 Glioblastoma Multiforme 75 0.157
22
LPP008 Lipoprotein Quantitative Trait Locus 62 0.157
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.155
24
c CHR684 Chronic Kidney Disease 70 0.154
25
P DBT009 Diabetes Mellitus 64 0.154
26
DFC004 Deficiency Anemia 70 0.153
27
P VSC007 Vascular Disease 63 0.153
28
ATM095 Autoimmune Disease 62 0.152
29
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.151
30
CYT002 Cytokine Deficiency 42 0.150
31
P ADN016 Adenocarcinoma 64 0.150
32
CYS001 Cystic Fibrosis 81 0.148
33
P LNG032 Lung Cancer 98 0.146
34
ART140 Arteries, Anomalies of 52 0.145
35
HRW001 Hair Whorl 36 0.145
36
P OVR042 Ovarian Cancer 88 0.144
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.144
38
P PNC035 Pancreatic Cancer 84 0.143
39
P HRT032 Heart Disease 75 0.143
40
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.140
41
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.140
42
P ALZ034 Alzheimer Disease 88 0.139
43
P NRP001 Neuropathy 56 0.137
44
IRN002 Iron Metabolism Disease 57 0.134
45
RCK004 Rickets 68 0.133
46
P MYC007 Myocardial Infarction 70 0.132
47
LNG099 Lung Disease 60 0.132
48
HYP781 Hypoascorbemia 51 0.131
49
SQM006 Squamous Cell Carcinoma 60 0.130
50
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.129
51
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.129
52
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.129
53
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.129
54
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.129
55
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.129
56
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.129
57
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.129
58
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.129
59
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.129
60
END086 End Stage Renal Disease 51 0.128
61
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.127
62
NTR005 Nutritional Deficiency Disease 62 0.127
63
CNG034 Congestive Heart Failure 69 0.127
64
c ACT071 Acute Kidney Failure 60 0.127
65
P GST053 Gastric Cancer 83 0.126
66
P NTR004 Neutropenia 63 0.126
67
CRB039 Cerebrovascular Disease 67 0.123
68
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.123
69
c ACT075 Acute Myocardial Infarction 57 0.123
70
CRV035 Cervical Cancer 76 0.123
71
P PRD008 Periodontitis 64 0.122
72
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.122
73
STR067 Stroke, Ischemic 81 0.122
74
AGN016 Aging 56 0.122
75
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.121
76
BCT022 Bacterial Infectious Disease 56 0.121
77
c RHB024 Rhabdomyosarcoma 2 67 0.121
78
P HYP086 Hypothyroidism 69 0.120
79
c DBT099 Diabetes Mellitus, Type I 65 0.120
80
HYP005 Hypokalemia 55 0.120
81
DWN001 Down Syndrome 70 0.119
82
P ART022 Arthritis 69 0.119
83
THR024 Thrombosis 57 0.117
84
P TRN020 Turner Syndrome 67 0.117
85
HMP009 Haemophilus Influenzae 43 0.116
86
P RHM011 Rheumatoid Arthritis 80 0.116
87
ADL002 Adult Syndrome 70 0.114
88
c ACT068 Acute Cystitis 63 0.113
89
c DWL002 Dowling-Degos Disease 1 58 0.112
90
P SKN015 Skin Carcinoma 66 0.112
91
P PRP019 Peripheral Nervous System Disease 58 0.111
92
P MLN008 Melanoma 69 0.111
93
ACQ007 Acquired Immunodeficiency Syndrome 60 0.110
94
AST005 Asthma 76 0.109
95
THY029 Thyroid Carcinoma 59 0.108
96
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.108
97
P CNR004 Cone-Rod Dystrophy 2 73 0.107
98
P HPT021 Hepatitis 67 0.106
99
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.106
100
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.106
101
c SML038 Small Cell Cancer of the Lung 65 0.105
102
P AST007 Astrocytoma 51 0.105
103
c MLG068 Malignant Glioma 46 0.105
104
TXC005 Toxic Shock Syndrome 62 0.105
105
P MLT020 Multiple Sclerosis 72 0.104
106
KRT002 Keratomalacia 47 0.104
107
SPN035 Spindle Cell Sarcoma 53 0.103
108
P LYM118 Lymphoma 68 0.102
109
ATX019 Ataxia with Vitamin E Deficiency 42 0.102
110
ESP021 Esophageal Cancer 90 0.102
111
ANG054 Angina Pectoris 66 0.102
112
c VRL010 Viral Hepatitis 52 0.101
113
CNS004 Constipation 58 0.100
114
TTN003 Tetanus 65 0.100
115
P INF032 Infertility 57 0.100
116
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.100
117
ANX010 Anxiety 73 0.099
118
P RHN004 Rhinitis 57 0.099
119
BRN028 Brain Cancer 74 0.099
120
CHL079 Children's Interstitial Lung Disease 26 0.098
121
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.097
122
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.097
123
c PRS136 Prostate Cancer, Hereditary, 6 33 0.096
124
c PRS130 Prostate Cancer, Hereditary, 8 32 0.096
125
c HPT016 Hepatitis B 59 0.095
126
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.095
127
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.094
128
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.093
129
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.093
130
c ACT134 Acute Liver Failure 56 0.093
131
PRP027 Peripheral Vascular Disease 71 0.092
132
DPH001 Diphtheria 60 0.092
133
c PRM038 Primary Agammaglobulinemia 44 0.091
134
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.091
135
INT007 Intermediate Coronary Syndrome 55 0.091
136
P HDC001 Headache 57 0.090
137
P PYL005 Pyelonephritis 56 0.090
138
P GLM040 Glioma Susceptibility 1 81 0.089
139
P THL005 Thalassemia 60 0.089
140
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.089
141
ALL003 Allergic Rhinitis 67 0.088
142
LYM019 Lymphosarcoma 46 0.088
143
MLR004 Malaria 81 0.086
144
P END044 Endometriosis 63 0.085
145
P INT068 Intestinal Disease 53 0.084
146
c LKM005 Leukemia, T-Cell, Chronic 34 0.083
147
P MDL005 Medulloblastoma 77 0.083
148
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.083
149
P KDN017 Kidney Cancer 60 0.083
150
HYP017 Hypophosphatemia 50 0.082
151
OTT002 Otitis Media 72 0.081
152
P CNJ013 Conjunctivitis 65 0.081
153
P INT143 Interstitial Cystitis 61 0.081
154
PLM031 Poliomyelitis 64 0.079
155
c PRD040 Periodontitis, Chronic 53 0.079
156
c PNS012 Paine Syndrome 61 0.079
157
c FML035 Familial Hyperlipidemia 55 0.079
158
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.079
159
PST092 Posttransplant Acute Limbic Encephalitis 29 0.079
160
MNN042 Meningioma, Radiation-Induced 62 0.078
161
c MNN043 Meningioma, Familial 74 0.078
162
c CHR064 Chronic Monocytic Leukemia 33 0.078
163
SPN021 Spinal Meningioma 50 0.078
164
SCR001 Secretory Meningioma 41 0.078
165
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.078
166
P HMP007 Hemophilia 51 0.076
167
P SRC025 Sarcoidosis 1 70 0.076
168
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.075
169
MXD026 Mixed Glioma 45 0.075
170
SFT003 Soft Tissue Sarcoma 56 0.075
171
PRP080 Peripheral Artery Disease 53 0.075
172
P NRV007 Nervous System Disease 66 0.072
173
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.072
174
GLS001 Gliosarcoma 54 0.072
175
c BTT014 Beta-Thalassemia 74 0.071
176
SKN019 Skin Melanoma 68 0.070
177
THY030 Thyroid Gland Disease 52 0.069
178
49X006 49, Xxxxy Syndrome 41 0.069
179
P OLG002 Oligodendroglioma 67 0.068
180
CNT033 Central Nervous System Cancer 47 0.068
181
P ADL017 Adult T-Cell Leukemia 56 0.067
182
HMT002 Hematologic Cancer 62 0.067
183
P MLG074 Malignant Mesenchymoma 40 0.066
184
FCT007 Factor Vii Deficiency 67 0.066
185
c ACT042 Acute Pyelonephritis 46 0.066
186
c INF145 Infantile Liver Failure Syndrome 1 50 0.065
187
SPP011 Suppression of Tumorigenicity 12 59 0.065
188
THY122 Thyroid Gland Cancer 57 0.062
189
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.062
190
P BNG030 Benign Ependymoma 60 0.061
191
P SYP003 Syphilis 58 0.061
192
CLL010 Cellular Ependymoma 54 0.060
193
c OVR114 Ovarian Cancer 1 38 0.060
194
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.060
195
TXC002 Toxic Encephalopathy 53 0.060
196
P OCL013 Oculodentodigital Dysplasia 69 0.060
197
CLL003 Cellulitis 54 0.059
198
URN010 Urinary Tract Obstruction 55 0.059
199
P EPD016 Epidermolysis Bullosa 53 0.059
200
LMB062 Limb Ischemia 55 0.058
201
c ALP101 Alpha-Thalassemia 62 0.058
202
ATM052 Autoimmune Disease 1 37 0.057
203
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.056
204
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.054
205
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.054
206
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.054
207
ACR041 Acromelic Frontonasal Dysostosis 52 0.053
208
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.052
209
P SML001 Small Cell Carcinoma 52 0.052
210
P KRT007 Keratoconus 50 0.052
211
P PRP056 Porphyria, Acute Hepatic 48 0.051
212
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.051
213
AMB002 Amblyopia 49 0.050
214
P BLD036 Bile Duct Disease 43 0.050
215
SPP007 Suppression Amblyopia 39 0.050
216
HDG004 Hodgkin's Granuloma 23 0.050
217
HDG006 Hodgkin's Paragranuloma 22 0.050
218
c BCT006 Bacterial Conjunctivitis 37 0.050
219
MNN020 Meningococcal Infection 46 0.049
220
SRC027 Sarcoma, Synovial 58 0.047
221
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.047
222
P URF003 Urofacial Syndrome 1 57 0.047
223
ANS011 Anus Cancer 56 0.047
224
URN009 Urinary System Disease 48 0.047
225
NSS002 Neisseria Meningitidis Infection 47 0.047
226
PRP017 Periapical Periodontitis 46 0.047
227
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.047
228
P OCY003 Oocyte Maturation Defect 1 45 0.046
229
ACT011 Acute Contagious Conjunctivitis 40 0.046
230
CLP006 Clopidogrel Resistance 40 0.046
231
P EPN001 Ependymoblastoma 44 0.045
232
KLB004 Klebsiella Infection 27 0.045
233
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.044
234
P PNB001 Pineoblastoma 50 0.044
235
c ADL096 Adult Hepatocellular Carcinoma 40 0.044
236
HPT085 Hepatitis, Fulminant Viral 32 0.044
237
ADR005 Adrenal Carcinoma 58 0.043
238
NCR004 Nocardiosis 54 0.042
239
AST006 Astigmatism 47 0.042
240
FNT004 Fainting 30 0.042
241
MDD010 Middle Ear Disease 48 0.041
242
P CHR573 Choroid Plexus Cancer 46 0.041
243
PNC056 Pineocytoma 45 0.041
244
DNT014 Dental Pulp Disease 42 0.040
245
P HMN036 Hemangiopericytoma, Malignant 59 0.039
246
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.039
247
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.039
248
P HRD018 Hair Disease 43 0.039
249
PNL014 Pineal Gland Cancer 41 0.039
250
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.038
251
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.038
252
PSD078 Pseudofolliculitis Barbae 25 0.038
253
c END071 Endometriosis 1 23 0.038
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