Search results for dATP

209 hits were found for dATP

# Family MCID Name MIFTS Score
1
ADN001 Adenosine Deaminase Deficiency 59 4.466
2
CMB007 Combined Immunodeficiency 56 2.091
3
SVR004 Severe Combined Immunodeficiency 71 1.651
4
LYM027 Lymphopenia 56 1.435
5
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 1.405
6
P GLM040 Glioma Susceptibility 1 70 1.405
7
MLG169 Malignant Astrocytoma 57 1.405
8
P LKM002 Leukemia 66 1.196
9
P MNC007 Monocytic Leukemia 48 1.145
10
P GRF003 Graft-Versus-Host Disease 71 1.116
11
c LKM070 Leukemia, Acute Monocytic 56 1.084
12
ACT200 Acute Monoblastic Leukemia 40 1.084
13
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.047
14
P LYM118 Lymphoma 69 1.047
15
HMN044 Human Immunodeficiency Virus Type 1 76 0.806
16
IMM167 Immune Deficiency Disease 77 0.758
17
VCC001 Vaccinia 49 0.708
18
P HRP006 Herpes Simplex 65 0.708
19
P LKM071 Leukemia, Chronic Lymphocytic 74 0.624
20
P LKM062 Leukemia, Acute Lymphoblastic 69 0.594
21
PRT037 Pertussis 49 0.578
22
CYS001 Cystic Fibrosis 77 0.510
23
CHL014 Cholera 62 0.510
24
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.491
25
c ATR087 Atrial Standstill 1 74 0.452
26
c DLT002 Dilated Cardiomyopathy 79 0.452
27
MLN071 Melanoma Tumor Antigen Gp90 17 0.431
28
ANT024 Anthrax Disease 58 0.409
29
MDD018 Middle East Respiratory Syndrome 44 0.385
30
TTN003 Tetanus 64 0.385
31
P SKN015 Skin Carcinoma 71 0.385
32
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.385
33
c LKM005 Leukemia, T-Cell, Chronic 33 0.385
34
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.360
35
HLX001 Helix Syndrome 47 0.360
36
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.360
37
c HPT016 Hepatitis B 62 0.360
38
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.360
39
c HPT073 Hepatitis C Virus 71 0.334
40
SLP001 Sleeping Sickness 56 0.305
41
HRY003 Hairy Cell Leukemia 61 0.305
42
c CHR418 Chronic Leukemia 48 0.305
43
KRN002 Kearns-Sayre Syndrome 63 0.305
44
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.305
45
HYP266 Hypoxia 56 0.305
46
LNG099 Lung Disease 62 0.305
47
SYS003 Systolic Heart Failure 49 0.305
48
47X002 47,xyy 48 0.305
49
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.305
50
WRN001 Werner Syndrome 69 0.272
51
MCS002 Mucositis 55 0.272
52
P OVR042 Ovarian Cancer 88 0.272
53
P PNC035 Pancreatic Cancer 86 0.272
54
48X005 48,xyyy 39 0.272
55
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.272
56
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.236
57
ATS010 Autosomal Recessive Disease 42 0.236
58
CRB004 Cerebral Artery Occlusion 46 0.236
59
SRC014 Sarcoma 64 0.236
60
HRW001 Hair Whorl 35 0.236
61
c ACT073 Acute Leukemia 59 0.236
62
P CCK001 Cockayne Syndrome 68 0.236
63
SVR001 Severe Acute Respiratory Syndrome 68 0.236
64
P HML002 Hemolytic Anemia 62 0.236
65
P INF032 Infertility 60 0.236
66
c HPT001 Hepatitis C 61 0.236
67
CHL123 Chlamydia 58 0.236
68
DPH001 Diphtheria 59 0.236
69
LNG031 Lung Benign Neoplasm 51 0.236
70
c LKM061 Leukemia, Acute Myeloid 83 0.236
71
c MTC061 Mitochondrial Dna Depletion Syndrome 1 48 0.236
72
SPN035 Spindle Cell Sarcoma 51 0.236
73
P NRB001 Neuroblastoma 66 0.236
74
P BCL017 B-Cell Lymphoma 57 0.236
75
c ACT134 Acute Liver Failure 57 0.236
76
MTH078 Methylmalonic Aciduria, Cblb Type 47 0.193
77
MYL069 Myeloma, Multiple 77 0.193
79
P TMR010 Tumor Predisposition Syndrome 69 0.193
80
DSS032 Disease by Infectious Agent 55 0.193
81
PRL017 Prolymphocytic Leukemia 47 0.193
82
P OPN001 Open-Angle Glaucoma 55 0.193
83
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.193
84
P FML011 Familial Adenomatous Polyposis 71 0.193
85
c OST125 Osteopetrosis, Autosomal Dominant 1 34 0.193
86
NRL016 Neural Tube Defects 81 0.193
87
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.193
88
c GLC092 Glaucoma, Primary Open Angle 61 0.193
89
HND015 Hand Skill, Relative 29 0.193
90
ACQ007 Acquired Immunodeficiency Syndrome 58 0.193
91
P HPT021 Hepatitis 68 0.193
92
P MTH008 Methylmalonic Acidemia 52 0.193
93
NRN001 Neuroendocrine Carcinoma 47 0.193
94
ALL029 Allergic Disease 61 0.193
95
BCL002 B Cell Deficiency 40 0.193
96
GST045 Gastroenteritis 58 0.193
97
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.193
98
STR046 Stargardt Macular Degeneration 27 0.193
99
BRN071 Brain Injury 50 0.193
100
DYS073 Dysphagia 53 0.193
101
PTT037 Pituitary Tumors 44 0.193
102
P SZR006 Seizure Disorder 69 0.193
103
ISL099 Isolated Methylmalonic Acidemia 35 0.193
104
TRM010 Traumatic Brain Injury 50 0.193
105
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.193
106
ADN090 Adenosylcobalamin Deficiency 35 0.193
107
INH023 Inherited Cancer-Predisposing Syndrome 53 0.193
108
ARG004 Argyria 26 0.193
109
PRM329 Premature Aging 36 0.193
110
HLC007 Helicobacter Pylori Infection 67 0.136
111
P SPP010 Suppressor of Tumorigenicity 3 51 0.136
112
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.136
113
P RTN008 Retinitis Pigmentosa 79 0.136
114
c BRN108 Branchiootic Syndrome 1 63 0.136
115
NCL008 Nuclear Ribonucleic Acid 15 0.136
116
OBN001 Ouabain Resistance 15 0.136
117
TTR014 Tetrasomy 18p 30 0.136
118
CHK001 Chikungunya 60 0.136
119
ACT119 Acute Promyelocytic Leukemia 62 0.136
120
P DNG005 Dengue Virus 55 0.136
121
P STR022 Stargardt Disease 61 0.136
122
EPD015 Epidemic Typhus 44 0.136
123
MNT001 Mantle Cell Lymphoma 65 0.136
124
c PCH010 Pachyonychia Congenita 3 43 0.136
125
NRR001 Neuroretinitis 42 0.136
126
BCT022 Bacterial Infectious Disease 56 0.136
127
ADN011 Adenoid Cystic Carcinoma 68 0.136
128
LYM157 Lymph Node Carcinoma 33 0.136
129
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.136
130
PRM013 Premature Menopause 57 0.136
131
P MDL005 Medulloblastoma 75 0.136
132
PRX015 Paroxysmal Extreme Pain Disorder 56 0.136
133
BRK010 Burkitt Lymphoma 66 0.136
134
c TYP008 Type 1 Diabetes Mellitus 77 0.136
135
c STR084 Stargardt Disease 1 53 0.136
136
WTH001 Withdrawal Disorder 47 0.136
137
MTB004 Metabolic Acidosis 48 0.136
138
LRY004 Laryngotracheitis 33 0.136
139
P MYC084 Mycobacterium Tuberculosis 1 68 0.136
140
MTG002 Mutagen Sensitivity 35 0.136
142
P CLR023 Colorectal Cancer 100 0.136
143
CLF027 Cleft Palate, Isolated 64 0.136
144
c BTT014 Beta-Thalassemia 72 0.136
145
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 38 0.136
146
SHR107 Short Stature-Obesity Syndrome 25 0.136
147
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.136
148
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 42 0.136
149
KRT019 Keratitis, Hereditary 66 0.136
150
BTT017 Beta-Thalassemia Major 53 0.136
151
ALT002 Aleutian Mink Disease 27 0.136
152
ADN018 Adenoma 58 0.136
153
BRN004 Brain Edema 54 0.136
154
BRN024 Bronchitis 67 0.136
155
IMM001 Immune-Complex Glomerulonephritis 36 0.136
156
P CNJ013 Conjunctivitis 66 0.136
157
P RTN018 Retinal Disease 53 0.136
158
DNT012 Dental Caries 53 0.136
159
ACR007 Acromegaly 70 0.136
160
MRP001 Morphine Dependence 41 0.136
161
P AGM001 Agammaglobulinemia 67 0.136
162
PPL022 Papilloma 53 0.136
163
SQM002 Squamous Cell Papilloma 45 0.136
164
AZS001 Azoospermia 45 0.136
165
P CYS018 Cystitis 59 0.136
166
P HYD006 Hydrocephalus 63 0.136
167
P MLN007 Male Infertility 56 0.136
168
PNC129 Pancreatic Adenocarcinoma 65 0.136
169
P GLM007 Glomerulonephritis 59 0.136
170
NWC001 Newcastle Disease 48 0.136
171
GLS001 Gliosarcoma 63 0.136
172
ERL001 Early Myoclonic Encephalopathy 63 0.136
173
P PTT006 Pituitary Adenoma 55 0.136
174
TRC012 Trichuriasis 43 0.136
175
CLN015 Colon Adenocarcinoma 64 0.136
176
RTN023 Retinitis 45 0.136
177
CCC002 Coccidiosis 50 0.136
178
HMT002 Hematologic Cancer 61 0.136
179
TRT001 Teratocarcinoma 41 0.136
180
P TMP001 Temporal Lobe Epilepsy 49 0.136
181
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.136
182
ORT008 Orotic Aciduria 56 0.136
183
OST159 Osteogenic Sarcoma 66 0.136
184
SBC001 Subacute Sclerosing Panencephalitis 53 0.136
185
P CRN300 Coronary Heart Disease 1 73 0.136
186
P NSP012 Nasopharyngeal Carcinoma 60 0.136
187
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.136
188
OST016 Osteochondrosis 52 0.136
189
AML001 Amelanotic Melanoma 37 0.136
190
c HPT007 Hepatitis E 50 0.136
191
CYT002 Cytokine Deficiency 43 0.136
192
GLM045 Glioma 62 0.136
193
HML018 Homologous Wasting Disease 21 0.136
194
P THL005 Thalassemia 56 0.136
195
ANX004 Anoxia 40 0.136
196
P MYL006 Myeloid Leukemia 60 0.136
197
GLL048 Glial Tumor 52 0.136
198
DYS032 Dystrophinopathies 47 0.136
199
STM007 Stomatitis 52 0.136
200
SRC011 Sarcocystosis 30 0.136
201
P RTN016 Retinal Degeneration 52 0.136
202
SKN019 Skin Melanoma 70 0.136
203
CHC001 Chickenpox 56 0.136
204
P OST009 Osteochondritis Dissecans 61 0.136
205
HYP056 Hypoglycemia 65 0.136
206
EXN003 Exencephaly 30 0.136
207
MLL001 Molluscum Contagiosum 48 0.136
208
P VTR007 Vitreoretinopathy 45 0.136
209
DSR074 Disorder of Purine Metabolism 23 0.136
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