Search results for dgtp

168 hits were found for dgtp

# Family MCID Name MIFTS Score
1
c OST125 Osteopetrosis, Autosomal Dominant 1 34 2.401
2
HMN044 Human Immunodeficiency Virus Type 1 76 2.200
3
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 1.722
4
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.616
5
P LKM071 Leukemia, Chronic Lymphocytic 74 1.460
6
P LKM002 Leukemia 66 1.410
7
SVR004 Severe Combined Immunodeficiency 71 1.251
8
OBN001 Ouabain Resistance 15 1.173
9
P MYC084 Mycobacterium Tuberculosis 1 68 1.143
10
HML018 Homologous Wasting Disease 21 1.143
11
P ACR001 Aicardi-Goutieres Syndrome 63 1.109
12
P HRP006 Herpes Simplex 65 1.080
13
GLB002 Glioblastoma 67 0.826
14
IMM167 Immune Deficiency Disease 77 0.665
15
CHC001 Chickenpox 56 0.618
16
P LKM062 Leukemia, Acute Lymphoblastic 69 0.585
17
LYM027 Lymphopenia 56 0.530
18
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.530
19
VCC001 Vaccinia 49 0.491
20
HLX001 Helix Syndrome 47 0.470
21
P PNC035 Pancreatic Cancer 86 0.425
22
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.425
23
c LKM005 Leukemia, T-Cell, Chronic 33 0.425
24
c RNG024 Ring Chromosome 8 28 0.401
25
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.375
26
MDD018 Middle East Respiratory Syndrome 44 0.375
27
P OVR042 Ovarian Cancer 88 0.375
28
ACQ007 Acquired Immunodeficiency Syndrome 58 0.375
29
c LKM061 Leukemia, Acute Myeloid 83 0.375
30
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.375
31
P MYL006 Myeloid Leukemia 60 0.347
32
ADN001 Adenosine Deaminase Deficiency 59 0.347
33
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.317
34
P FRG001 Fragile X Syndrome 70 0.317
35
P CCK001 Cockayne Syndrome 68 0.317
36
P SKN015 Skin Carcinoma 71 0.317
37
HRP004 Herpes Zoster 60 0.317
38
GNT003 Genital Herpes 54 0.317
39
MYL069 Myeloma, Multiple 77 0.284
40
CMB007 Combined Immunodeficiency 56 0.284
41
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.284
42
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.284
43
ALL029 Allergic Disease 61 0.284
44
HYP266 Hypoxia 56 0.284
45
P MYT002 Myotonic Dystrophy 51 0.284
46
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.284
47
c LKM063 Leukemia, Chronic Myeloid 71 0.246
48
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.246
49
ATS010 Autosomal Recessive Disease 42 0.246
50
PRM013 Premature Menopause 57 0.246
51
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.246
52
P CTN015 Cutaneous T Cell Lymphoma 48 0.246
53
ADR040 Adrenal Gland Pheochromocytoma 45 0.246
54
c HPT073 Hepatitis C Virus 71 0.246
55
P PHC003 Pheochromocytoma 70 0.246
56
GT001 Gout 63 0.246
57
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.246
58
TCL003 T Cell Deficiency 44 0.246
59
c HPT016 Hepatitis B 62 0.246
60
P HPT021 Hepatitis 68 0.246
61
NRF003 Neurofibrosarcoma 43 0.246
62
KRN002 Kearns-Sayre Syndrome 63 0.246
63
c MTC061 Mitochondrial Dna Depletion Syndrome 1 48 0.246
64
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.246
65
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.246
66
47X002 47,xyy 48 0.246
67
CHK001 Chikungunya 60 0.201
68
BRK010 Burkitt Lymphoma 66 0.201
69
P LNG032 Lung Cancer 98 0.201
70
P LYM118 Lymphoma 69 0.201
71
VTM002 Vitamin B12 Deficiency 48 0.201
72
P TRM004 Trimethylaminuria 45 0.201
73
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.201
74
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.201
75
P CLR023 Colorectal Cancer 100 0.201
76
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.201
77
ATM095 Autoimmune Disease 61 0.201
78
c SML038 Small Cell Cancer of the Lung 69 0.201
79
NRL016 Neural Tube Defects 81 0.201
80
SRC014 Sarcoma 64 0.201
81
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.201
82
c ACT073 Acute Leukemia 59 0.201
83
P HML002 Hemolytic Anemia 62 0.201
84
PPL022 Papilloma 53 0.201
85
SQM002 Squamous Cell Papilloma 45 0.201
86
NRN001 Neuroendocrine Carcinoma 47 0.201
87
CHL123 Chlamydia 58 0.201
88
SPN035 Spindle Cell Sarcoma 51 0.201
89
YLL002 Yellow Fever 61 0.201
90
SPL018 Splenomegaly 47 0.201
91
P BCL017 B-Cell Lymphoma 57 0.201
92
CHL061 Childhood Leukemia 47 0.201
93
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.201
94
GLM044 Glomerular Disease 34 0.201
95
P RTN024 Retinoblastoma 72 0.142
96
ESP021 Esophageal Cancer 84 0.142
97
c HMP029 Hemophilia a 69 0.142
98
AGN016 Aging 54 0.142
99
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.142
100
P RTN008 Retinitis Pigmentosa 79 0.142
101
MYC006 Mycosis Fungoides 65 0.142
102
c ANM038 Anemia, Autoimmune Hemolytic 63 0.142
103
P DNG005 Dengue Virus 55 0.142
104
DFF005 Diffuse Large B-Cell Lymphoma 55 0.142
106
P INF037 Inflammatory Bowel Disease 53 0.142
107
DSS032 Disease by Infectious Agent 55 0.142
108
NRR001 Neuroretinitis 42 0.142
109
BCT022 Bacterial Infectious Disease 56 0.142
110
P PRK039 Parkinsonism 55 0.142
111
MCS002 Mucositis 55 0.142
112
SLP001 Sleeping Sickness 56 0.142
113
P MDL005 Medulloblastoma 75 0.142
114
P PRK057 Parkinson Disease, Late-Onset 79 0.142
115
c TYP008 Type 1 Diabetes Mellitus 77 0.142
116
P EXN002 Exanthem 58 0.142
117
P APL001 Aplastic Anemia 73 0.142
118
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.142
119
CLF027 Cleft Palate, Isolated 64 0.142
120
FCT001 Factor Viii Deficiency 62 0.142
121
P LNG064 Lung Cancer Susceptibility 3 70 0.142
122
HNZ004 Heinz Body Anemias 40 0.142
123
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.142
124
LYM040 Lymphoblastic Lymphoma 53 0.142
125
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.142
126
SVR001 Severe Acute Respiratory Syndrome 68 0.142
127
P SBS003 Substance Abuse 54 0.142
128
HRY003 Hairy Cell Leukemia 61 0.142
129
P INF032 Infertility 60 0.142
130
PLM031 Poliomyelitis 62 0.142
131
DNT012 Dental Caries 53 0.142
132
c HPT001 Hepatitis C 61 0.142
133
P THR015 Thrombophilia 51 0.142
134
AZS001 Azoospermia 45 0.142
135
PRC013 Pericarditis 53 0.142
136
P NTR004 Neutropenia 62 0.142
137
TTN003 Tetanus 64 0.142
138
MTH009 Mouth Disease 57 0.142
139
P LVR013 Liver Disease 68 0.142
140
GLS001 Gliosarcoma 63 0.142
141
LNG031 Lung Benign Neoplasm 51 0.142
142
P DYS007 Dyskeratosis Congenita 66 0.142
143
PST011 Pustulosis of Palm and Sole 52 0.142
144
RTN023 Retinitis 45 0.142
145
NRL005 Neurilemmoma 60 0.142
146
ORT008 Orotic Aciduria 56 0.142
147
OST159 Osteogenic Sarcoma 66 0.142
148
SBC001 Subacute Sclerosing Panencephalitis 53 0.142
149
AML001 Amelanotic Melanoma 37 0.142
150
PRP030 Purpura 54 0.142
151
c HPT007 Hepatitis E 50 0.142
152
ANX004 Anoxia 40 0.142
153
P NRB001 Neuroblastoma 66 0.142
154
TTR011 Tetraploidy 43 0.142
155
P MYC033 Myoclonus 46 0.142
156
SPS057 Spasticity 43 0.142
157
P HMP007 Hemophilia 52 0.142
158
CRH001 Crohn's Disease 80 0.142
159
STM007 Stomatitis 52 0.142
160
48X005 48,xyyy 39 0.142
161
CHR178 Chromosomal Triplication 34 0.142
162
HPT022 Hepatoblastoma 54 0.142
163
c PRG011 Progressive Myoclonus Epilepsy 40 0.142
164
P PSR002 Psoriasis 63 0.142
166
P MYC026 Myoclonus Epilepsy 35 0.142
167
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.142
168
PRM329 Premature Aging 36 0.142
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