Search results for dctp

242 hits were found for dctp

# Family MCID Name MIFTS Score
1
HMN044 Human Immunodeficiency Virus Type 1 76 1.830
2
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.588
3
OBN001 Ouabain Resistance 15 1.537
4
PRT037 Pertussis 49 1.466
5
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 1.199
6
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.104
7
P FLL037 Follicular Lymphoma 73 1.104
8
IMM167 Immune Deficiency Disease 77 0.869
9
P HRP006 Herpes Simplex 65 0.795
10
P LKM062 Leukemia, Acute Lymphoblastic 69 0.530
11
c ACT073 Acute Leukemia 59 0.478
12
MLN071 Melanoma Tumor Antigen Gp90 17 0.459
13
VCC001 Vaccinia 49 0.459
14
c LKM061 Leukemia, Acute Myeloid 83 0.419
15
P MYL006 Myeloid Leukemia 60 0.398
16
c HPT016 Hepatitis B 62 0.351
17
P LKM002 Leukemia 66 0.351
18
47X002 47,xyy 48 0.351
19
P SPP010 Suppressor of Tumorigenicity 3 51 0.325
20
DWN001 Down Syndrome 70 0.325
21
HLX001 Helix Syndrome 47 0.325
22
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.325
23
BLM001 Bloom Syndrome 65 0.325
24
SRC014 Sarcoma 64 0.325
25
EXT007 Extracutaneous Mastocytoma 38 0.325
26
MST004 Mast Cell Neoplasm 41 0.325
27
P PNC035 Pancreatic Cancer 86 0.325
28
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.325
29
c LKM005 Leukemia, T-Cell, Chronic 33 0.325
30
LYM019 Lymphosarcoma 46 0.325
31
c HPT073 Hepatitis C Virus 71 0.296
32
c BTT014 Beta-Thalassemia 72 0.296
33
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.296
34
c LKM070 Leukemia, Acute Monocytic 56 0.296
35
P LKM071 Leukemia, Chronic Lymphocytic 74 0.296
36
ACQ007 Acquired Immunodeficiency Syndrome 58 0.296
37
PNC129 Pancreatic Adenocarcinoma 65 0.296
38
P THL005 Thalassemia 56 0.296
39
P MNC007 Monocytic Leukemia 48 0.296
40
48X005 48,xyyy 39 0.296
41
ACT200 Acute Monoblastic Leukemia 40 0.296
42
CHR178 Chromosomal Triplication 34 0.296
43
HMP009 Haemophilus Influenzae 41 0.296
44
ATS010 Autosomal Recessive Disease 42 0.265
45
P LNG032 Lung Cancer 98 0.265
46
KRN002 Kearns-Sayre Syndrome 63 0.265
47
ADN001 Adenosine Deaminase Deficiency 59 0.265
48
P GST053 Gastric Cancer 82 0.230
49
MYL009 Myelodysplastic Syndrome 67 0.230
50
NRR001 Neuroretinitis 42 0.230
51
MDD018 Middle East Respiratory Syndrome 44 0.230
52
VTM002 Vitamin B12 Deficiency 48 0.230
53
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.230
54
P CCK001 Cockayne Syndrome 68 0.230
55
LVR012 Liver Cirrhosis 62 0.230
56
P PRP019 Peripheral Nervous System Disease 57 0.230
57
P HPT021 Hepatitis 68 0.230
58
PPL022 Papilloma 53 0.230
59
P LRY044 Larynx Cancer 53 0.230
60
SQM002 Squamous Cell Papilloma 45 0.230
61
MGL001 Megaloblastic Anemia 59 0.230
62
CHL123 Chlamydia 58 0.230
63
RTN023 Retinitis 45 0.230
64
P ART021 Arteriosclerosis 53 0.230
65
TRT001 Teratocarcinoma 41 0.230
66
SPN035 Spindle Cell Sarcoma 51 0.230
67
GST045 Gastroenteritis 58 0.230
68
ANX004 Anoxia 40 0.230
70
P MTC133 Mitochondrial Myopathy 51 0.230
71
P MYP004 Myopathy 67 0.230
72
DHY008 Dihydroxyadeninuria 24 0.230
73
MLL001 Molluscum Contagiosum 48 0.230
74
ARG004 Argyria 26 0.230
75
P RTN024 Retinoblastoma 72 0.187
76
P BRS047 Breast Cancer 97 0.187
77
ESP021 Esophageal Cancer 84 0.187
78
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.187
79
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.187
80
WRN001 Werner Syndrome 69 0.187
81
P ATX030 Ataxia-Telangiectasia 80 0.187
82
c BRN108 Branchiootic Syndrome 1 63 0.187
83
CRV035 Cervical Cancer 72 0.187
84
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.187
85
ADR016 Adrenal Cortical Carcinoma 61 0.187
86
PRT013 Portal Hypertension 59 0.187
87
URL001 Urolithiasis 45 0.187
88
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.187
89
P MDL005 Medulloblastoma 75 0.187
90
PRX015 Paroxysmal Extreme Pain Disorder 56 0.187
91
P MLN069 Melanoma, Uveal 59 0.187
92
P OVR042 Ovarian Cancer 88 0.187
93
c TYP008 Type 1 Diabetes Mellitus 77 0.187
94
c OST125 Osteopetrosis, Autosomal Dominant 1 34 0.187
95
PPL052 Papillomatosis, Confluent and Reticulated 34 0.187
96
c SYS001 Systemic Lupus Erythematosus 86 0.187
97
P HMG032 Hemoglobin H Disease 51 0.187
98
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.187
99
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.187
100
KRT019 Keratitis, Hereditary 66 0.187
101
CYT005 Cytomegalovirus Retinitis 50 0.187
102
DFC004 Deficiency Anemia 74 0.187
103
GLB002 Glioblastoma 67 0.187
104
SVR001 Severe Acute Respiratory Syndrome 68 0.187
105
HRY003 Hairy Cell Leukemia 61 0.187
106
CRV040 Cervix Carcinoma 50 0.187
107
ALT002 Aleutian Mink Disease 27 0.187
108
LYM027 Lymphopenia 56 0.187
109
HYP063 Hypersplenism 52 0.187
110
DNT012 Dental Caries 53 0.187
111
c HPT001 Hepatitis C 61 0.187
112
MYL031 Myeloproliferative Neoplasm 66 0.187
113
TLN003 Telangiectasis 51 0.187
114
ALL029 Allergic Disease 61 0.187
115
GLS001 Gliosarcoma 63 0.187
116
ADR004 Adrenal Cortical Adenocarcinoma 38 0.187
117
EMB004 Embryonal Carcinoma 55 0.187
118
c MTC061 Mitochondrial Dna Depletion Syndrome 1 48 0.187
119
STN013 Stenotrophomonas Maltophilia Infection 26 0.187
120
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.187
121
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.187
122
SMN007 Seminoma 42 0.187
123
P INS002 in Situ Carcinoma 53 0.187
124
P NRB001 Neuroblastoma 66 0.187
125
HYP266 Hypoxia 56 0.187
126
P LPS004 Lupus Erythematosus 61 0.187
127
ULC004 Ulcerative Colitis 74 0.187
128
P MSC005 Muscular Dystrophy 66 0.187
129
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.187
130
PRM329 Premature Aging 36 0.187
131
P PRS040 Prostate Cancer 95 0.133
132
c TYP009 Type 2 Diabetes Mellitus 92 0.133
133
CYS001 Cystic Fibrosis 77 0.133
134
P RTN008 Retinitis Pigmentosa 79 0.133
135
INS024 Insulin-Like Growth Factor I 77 0.133
136
c THY102 Thyroid Cancer, Nonmedullary, 2 54 0.133
137
c DFN360 Deafness, Autosomal Dominant 69 34 0.133
138
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.133
139
CHR005 Chorioamnionitis 50 0.133
140
P INF037 Inflammatory Bowel Disease 53 0.133
141
DSS032 Disease by Infectious Agent 55 0.133
142
CMB007 Combined Immunodeficiency 56 0.133
143
BCT022 Bacterial Infectious Disease 56 0.133
144
c PRC016 Pre-Eclampsia 64 0.133
145
SLP001 Sleeping Sickness 56 0.133
146
TRY001 Trypanosomiasis 50 0.133
147
PLY150 Polykaryocytosis Inducer 29 0.133
148
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.133
149
BRK010 Burkitt Lymphoma 66 0.133
150
c FBR084 Fibromatosis, Gingival, 1 49 0.133
151
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.133
152
ORL015 Oral Squamous Cell Carcinoma 43 0.133
153
P EXN002 Exanthem 58 0.133
154
P GNG025 Gingival Fibromatosis 46 0.133
155
SPN446 Spondylometaphyseal Dysplasia with Corneal Dystrophy 21 0.133
156
P MYC084 Mycobacterium Tuberculosis 1 68 0.133
157
c HYP595 Hypertension, Essential 84 0.133
158
c HYP836 Hypercholesterolemia, Familial, 1 73 0.133
159
c SML038 Small Cell Cancer of the Lung 69 0.133
160
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.133
161
CLF027 Cleft Palate, Isolated 64 0.133
162
P MMB011 Membranous Nephropathy 50 0.133
163
RBS001 Rabies 58 0.133
164
LCH016 Lichen Sclerosus Et Atrophicus 41 0.133
165
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.133
166
CLT003 Colitis 63 0.133
167
ACT098 Acute Erythroid Leukemia 55 0.133
168
CHL014 Cholera 62 0.133
169
c FML021 Familial Hypercholesterolemia 71 0.133
170
CHL068 Cholestasis 61 0.133
171
ISC004 Ischemia 61 0.133
172
HMG005 Hemoglobinopathy 55 0.133
173
P ANT006 Antiphospholipid Syndrome 55 0.133
174
P ADN016 Adenocarcinoma 63 0.133
175
GRM005 Germ Cell Cancer 46 0.133
176
ADN018 Adenoma 58 0.133
177
P INF032 Infertility 60 0.133
178
SVR004 Severe Combined Immunodeficiency 71 0.133
179
THY030 Thyroid Gland Disease 50 0.133
180
P TST026 Testicular Germ Cell Cancer 42 0.133
181
URM002 Uremia 47 0.133
182
LPT001 Leptospirosis 66 0.133
183
P LTR001 Lateral Sclerosis 58 0.133
184
CRY003 Cryptosporidiosis 55 0.133
185
P VSC007 Vascular Disease 62 0.133
186
P HYP086 Hypothyroidism 69 0.133
187
P INT143 Interstitial Cystitis 59 0.133
188
AZS001 Azoospermia 45 0.133
189
P CYS018 Cystitis 59 0.133
190
GTR002 Goiter 52 0.133
191
PLM010 Pulmonary Edema 54 0.133
192
P NPH012 Nephrotic Syndrome 62 0.133
193
GST033 Gestational Diabetes 61 0.133
194
P ADL010 Adult Respiratory Distress Syndrome 71 0.133
195
P GLM007 Glomerulonephritis 59 0.133
196
TST014 Testicular Cancer 51 0.133
197
HGH043 High Grade Glioma 46 0.133
198
GNG012 Gingival Overgrowth 49 0.133
199
P EPD016 Epidermolysis Bullosa 53 0.133
200
CLN015 Colon Adenocarcinoma 64 0.133
201
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.133
202
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.133
203
ORT008 Orotic Aciduria 56 0.133
204
c ALP101 Alpha-Thalassemia 62 0.133
205
OST159 Osteogenic Sarcoma 66 0.133
206
SBC001 Subacute Sclerosing Panencephalitis 53 0.133
207
PHN003 Phenylketonuria 76 0.133
208
ANR007 Anorexia Nervosa 59 0.133
209
c ART068 Aortic Aneurysm, Familial Thoracic 2 33 0.133
210
P NSP012 Nasopharyngeal Carcinoma 60 0.133
211
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.133
212
MSC152 Muscular Dystrophy, Becker Type 69 0.133
213
c HPT007 Hepatitis E 50 0.133
214
CYT002 Cytokine Deficiency 43 0.133
215
GLM045 Glioma 62 0.133
216
HML018 Homologous Wasting Disease 21 0.133
217
PST046 Post-Transplant Lymphoproliferative Disease 53 0.133
218
P MSC003 Muscular Atrophy 52 0.133
219
GLL048 Glial Tumor 52 0.133
220
PTT037 Pituitary Tumors 44 0.133
221
CRV002 Cervix Uteri Carcinoma in Situ 48 0.133
222
P LCH002 Lichen Planus 55 0.133
223
P MTR014 Motor Neuron Disease 65 0.133
224
BLD052 Blood Group Incompatibility 31 0.133
225
STM007 Stomatitis 52 0.133
226
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.133
227
MTC005 Mitochondrial Metabolism Disease 45 0.133
228
CRV045 Cervical Intraepithelial Neoplasia 38 0.133
229
MTC004 Mitochondrial Encephalomyopathy 43 0.133
230
PRT036 Peritonitis 65 0.133
231
SKN019 Skin Melanoma 70 0.133
232
P VND001 Vein Disease 42 0.133
233
P BCL017 B-Cell Lymphoma 57 0.133
234
PRT029 Parathyroid Adenoma 51 0.133
235
P MTC069 Mitochondrial Disorders 57 0.133
236
P ENC004 Encephalitis 61 0.133
237
P NRP001 Neuropathy 59 0.133
238
GRM010 Germ Cells Tumors 33 0.133
239
FBR019 Fibromatosis 44 0.133
240
ORL011 Oral Cancer 60 0.133
241
PRT058 Pure Autonomic Failure 58 0.133
242
INH031 Inherited Epidermolysis Bullosa 35 0.133
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