Search results for CD36

333 hits were found for CD36

# Family MCID Name MIFTS Score
1
PLT004 Platelet Glycoprotein Iv Deficiency 51 17.576
2
MLR004 Malaria 80 5.155
3
c CRN177 Coronary Heart Disease 7 19 3.472
4
P HRT032 Heart Disease 75 3.029
5
P PRS040 Prostate Cancer 97 2.971
6
P OST002 Osteoporosis 73 2.935
7
PLS007 Plasmodium Falciparum Malaria 52 2.726
8
P KDN018 Kidney Disease 70 2.645
9
RCK004 Rickets 69 2.541
10
P BND020 Bone Disease 59 2.541
11
GNG012 Gingival Overgrowth 51 2.541
12
MGK001 Megakaryocytic Leukemia 64 2.159
13
BLD053 Blood Platelet Disease 51 2.142
14
GRY002 Gray Platelet Syndrome 58 2.101
15
RNL077 Renal Fibrosis 47 2.101
16
HYP457 Hypertrophic Scars 43 2.101
17
MRF001 Marfan Syndrome 75 2.075
18
CNN005 Connective Tissue Disease 66 2.075
19
P OST122 Osteogenesis Imperfecta, Type Iii 57 2.075
20
P EHL001 Ehlers-Danlos Syndrome 57 2.075
21
c OST135 Osteogenesis Imperfecta, Type I 55 2.075
22
c OST080 Osteogenesis Imperfecta, Type Ii 55 2.075
23
OST032 Osteofibrous Dysplasia 51 2.075
24
P OTS001 Otosclerosis 50 2.075
25
HYP006 Hypertensive Heart Disease 49 2.075
26
c OST121 Osteogenesis Imperfecta, Type Iv 49 2.075
27
NWC001 Newcastle Disease 44 2.075
28
THR035 Thrombasthenia 41 1.527
29
FST010 Fasting Hypoglycemia 35 1.527
30
c CHR417 Chronic Graft Versus Host Disease 56 1.501
31
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.467
32
BRT054 Brittle Bone Disorder 70 1.467
33
GLC006 Galactosemia 65 1.467
34
c SCL052 Scleroderma, Familial Progressive 62 1.467
35
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 1.467
36
ING001 Inguinal Hernia 60 1.467
37
P OST009 Osteochondritis Dissecans 60 1.467
38
P PLV020 Pelvic Organ Prolapse 59 1.467
39
PLM026 Pilomatrixoma 59 1.467
40
CFF003 Caffey Disease 54 1.467
41
OCL020 Ocular Cicatricial Pemphigoid 54 1.467
42
RFL001 Reflex Sympathetic Dystrophy 53 1.467
43
c OST164 Osteoporosis, Juvenile 53 1.467
44
OST016 Osteochondrosis 53 1.467
45
c ACH041 Achondrogenesis, Type Ii 52 1.467
46
PRS045 Prostatic Hypertrophy 52 1.467
47
DFF036 Differentiated Thyroid Carcinoma 51 1.467
48
c FBR084 Fibromatosis, Gingival, 1 51 1.467
49
P GNG025 Gingival Fibromatosis 51 1.467
50
IRK001 Irak4 Deficiency 50 1.467
51
MYD002 Myd88 Deficiency 50 1.467
52
ALV002 Alveolar Echinococcosis 50 1.467
53
c OST119 Osteogenesis Imperfecta, Type Vii 48 1.467
54
BBS001 Babesiosis 48 1.467
55
P BRC015 Bruck Syndrome 46 1.467
56
MLR003 Melorheostosis 45 1.467
57
c OST124 Osteogenesis Imperfecta, Type V 42 1.467
58
SPN050 Spinocerebellar Degeneration 41 1.467
59
FRM003 Farmer's Lung 40 1.467
60
CHN002 Chancroid 40 1.467
61
c EHL074 Ehlers-Danlos Syndrome, Classic Type, 2 40 1.467
62
KLD004 Keloid Disorder 40 1.467
63
MYX013 Myxofibrosarcoma 38 1.467
64
c GRS012 Griscelli Syndrome, Type 3 37 1.467
65
c INH004 Inherited Blood Coagulation Disease 34 1.467
66
ODN005 Odontogenic Myxoma 32 1.467
67
INT065 Interstitial Keratitis 30 1.467
68
P PRM016 Primary Optic Atrophy 22 1.467
69
ATH013 Atherosclerosis Susceptibility 66 0.313
70
LPD008 Lipid Metabolism Disorder 62 0.216
71
FTT001 Fatty Liver Disease 61 0.182
72
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.163
73
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.158
74
P HYP750 Hypertriglyceridemia, Familial 61 0.153
75
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.135
76
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.135
77
MLN008 Melanoma 69 0.135
78
P CRN018 Coronary Artery Anomaly 63 0.135
79
ART140 Arteries, Anomalies of 53 0.135
80
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.135
81
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.135
82
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.135
83
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.135
84
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.135
85
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.135
86
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.135
87
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.135
88
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.135
89
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.135
90
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.129
91
c ATR087 Atrial Standstill 1 74 0.129
92
c HYP836 Hypercholesterolemia, Familial, 1 72 0.129
93
P LVR013 Liver Disease 68 0.122
94
P THR014 Thrombocytopenia 68 0.122
95
c CHR684 Chronic Kidney Disease 66 0.122
96
PRP030 Purpura 55 0.122
97
c MCR113 Microvascular Complications of Diabetes 3 52 0.122
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.122
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.122
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.122
101
P ALZ034 Alzheimer Disease 88 0.115
102
P HYP061 Hypertrophic Cardiomyopathy 66 0.115
103
HYP066 Hyperglycemia 61 0.115
105
P CRN300 Coronary Heart Disease 1 63 0.108
106
P SCK005 Sickle Cell Disease 50 0.108
107
AML001 Amelanotic Melanoma 39 0.108
108
P LKM002 Leukemia 66 0.100
109
GLC003 Glucose Intolerance 54 0.100
110
NNL006 Non-Alcoholic Steatohepatitis 51 0.100
111
CRB004 Cerebral Artery Occlusion 44 0.100
112
CYT002 Cytokine Deficiency 44 0.100
113
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.100
114
c HYP595 Hypertension, Essential 84 0.091
115
STR067 Stroke, Ischemic 80 0.091
116
CRB039 Cerebrovascular Disease 69 0.091
117
P VSC007 Vascular Disease 63 0.091
118
P PLY011 Polycystic Ovary Syndrome 56 0.091
119
HYP060 Hyperinsulinism 54 0.091
120
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.091
121
c LKM061 Leukemia, Acute Myeloid 83 0.082
122
c DLT002 Dilated Cardiomyopathy 79 0.082
123
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.082
124
ISC004 Ischemia 60 0.082
125
THR024 Thrombosis 56 0.082
126
HYP266 Hypoxia 56 0.082
127
P INF037 Inflammatory Bowel Disease 56 0.082
128
P ART021 Arteriosclerosis 54 0.082
129
P CTN015 Cutaneous T Cell Lymphoma 49 0.082
130
CRN027 Corneal Neovascularization 47 0.082
131
P CLR023 Colorectal Cancer 98 0.071
132
P LNG032 Lung Cancer 97 0.071
133
HYP056 Hypoglycemia 66 0.071
134
MYC006 Mycosis Fungoides 66 0.071
135
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.071
136
P DBT009 Diabetes Mellitus 64 0.071
137
P ADN016 Adenocarcinoma 64 0.071
138
P PSR002 Psoriasis 62 0.071
139
ATM095 Autoimmune Disease 61 0.071
140
P MYL006 Myeloid Leukemia 60 0.071
141
ORL011 Oral Cancer 60 0.071
142
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.071
143
ERY051 Erythroleukemia, Familial 56 0.071
144
SLC006 Silicosis 56 0.071
145
P LYM031 Lymphocytic Leukemia 55 0.071
146
P MNC007 Monocytic Leukemia 54 0.071
147
THR004 Thrombocytosis 51 0.071
148
BRN071 Brain Injury 49 0.071
149
P HPT023 Hepatocellular Carcinoma 100 0.058
150
P BRS047 Breast Cancer 96 0.058
151
c SYS001 Systemic Lupus Erythematosus 86 0.058
152
P GST053 Gastric Cancer 83 0.058
153
NRL016 Neural Tube Defects 82 0.058
154
c LKM071 Leukemia, Chronic Lymphocytic 79 0.058
155
CRV035 Cervical Cancer 76 0.058
156
GLB015 Glioblastoma Multiforme 75 0.058
157
SVR004 Severe Combined Immunodeficiency 73 0.058
158
SCK003 Sickle Cell Anemia 72 0.058
159
P GRF003 Graft-Versus-Host Disease 71 0.058
160
c HPT073 Hepatitis C Virus 70 0.058
161
CNG034 Congestive Heart Failure 70 0.058
162
P ESS003 Essential Thrombocythemia 67 0.058
163
MNT001 Mantle Cell Lymphoma 66 0.058
164
P DRM053 Dermatitis, Atopic 66 0.058
165
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.058
166
P MSC005 Muscular Dystrophy 66 0.058
167
ANG054 Angina Pectoris 66 0.058
168
P HYD006 Hydrocephalus 65 0.058
169
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.058
170
LVR012 Liver Cirrhosis 63 0.058
171
c HPT001 Hepatitis C 63 0.058
172
SKN016 Skin Disease 63 0.058
173
P NPH012 Nephrotic Syndrome 63 0.058
174
P END044 Endometriosis 62 0.058
175
P PRD008 Periodontitis 62 0.058
176
SQM006 Squamous Cell Carcinoma 60 0.058
177
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.058
178
ADN018 Adenoma 58 0.058
179
P BCL017 B-Cell Lymphoma 58 0.058
180
P PRN023 Prion Disease 57 0.058
181
BCT022 Bacterial Infectious Disease 56 0.058
182
HPT022 Hepatoblastoma 56 0.058
183
DFF005 Diffuse Large B-Cell Lymphoma 56 0.058
184
ACT200 Acute Monoblastic Leukemia 55 0.058
185
PLM010 Pulmonary Edema 55 0.058
186
P LCH002 Lichen Planus 54 0.058
187
c LKM070 Leukemia, Acute Monocytic 53 0.058
188
P RTN016 Retinal Degeneration 53 0.058
189
MST005 Mastitis 53 0.058
190
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.058
191
BNR002 Bone Resorption Disease 48 0.058
192
KHN001 Kuhnt-Junius Degeneration 48 0.058
193
URT010 Ureteral Obstruction 46 0.058
194
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 44 0.058
195
ORL015 Oral Squamous Cell Carcinoma 43 0.058
196
GLC008 Glucose Metabolism Disease 40 0.058
197
NNT024 Neonatal Stroke 34 0.058
198
MYC019 Mycobacterium Marinum 29 0.058
199
P OVR042 Ovarian Cancer 89 0.041
200
MYL069 Myeloma, Multiple 85 0.041
201
P PNC035 Pancreatic Cancer 84 0.041
202
OST012 Osteoarthritis 78 0.041
203
IMM167 Immune Deficiency Disease 78 0.041
204
P PRK057 Parkinson Disease, Late-Onset 76 0.041
205
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.041
206
CRH001 Crohn's Disease 74 0.041
207
BRN028 Brain Cancer 73 0.041
208
ULC004 Ulcerative Colitis 73 0.041
209
ANX010 Anxiety 72 0.041
210
P FML011 Familial Adenomatous Polyposis 72 0.041
211
MSC157 Muscular Dystrophy, Duchenne Type 71 0.041
212
P MYC007 Myocardial Infarction 70 0.041
213
DWN001 Down Syndrome 70 0.041
214
PLM001 Pulmonary Tuberculosis 70 0.041
215
CRT072 Creutzfeldt-Jakob Disease 69 0.041
216
P SLP006 Sleep Apnea 69 0.041
217
P HYP086 Hypothyroidism 68 0.041
218
c BSL007 Basal Cell Carcinoma 68 0.041
219
P LYM118 Lymphoma 68 0.041
220
CRB037 Cerebral Palsy 68 0.041
221
P PNM007 Pneumonia 68 0.041
222
KRT019 Keratitis, Hereditary 67 0.041
223
PNC129 Pancreatic Adenocarcinoma 67 0.041
224
BRK010 Burkitt Lymphoma 67 0.041
225
P FLL037 Follicular Lymphoma 66 0.041
226
P MTR004 Maturity-Onset Diabetes of the Young 66 0.041
227
OST159 Osteogenic Sarcoma 66 0.041
228
GLN010 Glanzmann Thrombasthenia 66 0.041
229
P ATR011 Atrial Fibrillation 66 0.041
230
PRT037 Pertussis 65 0.041
231
PRT036 Peritonitis 65 0.041
232
INC002 Inclusion Body Myositis 64 0.041
233
KWS002 Kawasaki Disease 64 0.041
234
P MYP004 Myopathy 64 0.041
235
P SPN046 Spinal Muscular Atrophy 64 0.041
236
c ART101 Aortic Valve Disease 2 63 0.041
237
IDP011 Idiopathic Interstitial Pneumonia 63 0.041
238
MSC007 Muscle Hypertrophy 63 0.041
239
LSH001 Leishmaniasis 63 0.041
240
BRS099 Breast Ductal Carcinoma 62 0.041
241
CLT003 Colitis 62 0.041
243
ALC006 Alcoholic Hepatitis 61 0.041
244
P PLM036 Pulmonary Fibrosis 61 0.041
245
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.041
246
TKY002 Takayasu Arteritis 61 0.041
247
DRM006 Dermatitis 61 0.041
248
P TST021 Testicular Germ Cell Tumor 61 0.041
249
OST003 Osteonecrosis 61 0.041
250
LNG099 Lung Disease 61 0.041
251
PRT013 Portal Hypertension 60 0.041
252
SZR001 Sezary's Disease 60 0.041
253
SPN186 Spinal Cord Injury 60 0.041
254
P CYS018 Cystitis 59 0.041
255
c HPT016 Hepatitis B 59 0.041
256
P PRD006 Prader-Willi Syndrome 59 0.041
257
P SZR006 Seizure Disorder 58 0.041
258
P FCL005 Focal Segmental Glomerulosclerosis 58 0.041
259
EYD002 Eye Disease 58 0.041
260
c ACT073 Acute Leukemia 58 0.041
261
ANG020 Angiosarcoma 58 0.041
262
P URT039 Urticaria 58 0.041
263
VSL002 Visual Epilepsy 58 0.041
264
END030 End Stage Renal Failure 58 0.041
265
P PYL005 Pyelonephritis 56 0.041
266
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.041
267
P CRD246 Cardiovascular System Disease 56 0.041
268
P MYS005 Myositis 56 0.041
269
P PNM006 Pneumoconiosis 55 0.041
270
ICH001 Ichthyosis Vulgaris 55 0.041
271
INT007 Intermediate Coronary Syndrome 55 0.041
272
P DBT005 Diabetes Insipidus 55 0.041
273
P ANT006 Antiphospholipid Syndrome 54 0.041
274
P ICH004 Ichthyosis 54 0.041
275
CLR030 Clear Cell Renal Cell Carcinoma 53 0.041
276
HMC014 Homocysteinemia 53 0.041
277
P ART018 Aortic Valve Insufficiency 53 0.041
278
TRM010 Traumatic Brain Injury 53 0.041
279
P OVR049 Ovarian Disease 53 0.041
280
P CTN003 Cutaneous Lupus Erythematosus 52 0.041
281
PST011 Pustulosis of Palm and Sole 52 0.041
282
GTR002 Goiter 52 0.041
283
P HML001 Hemolytic-Uremic Syndrome 52 0.041
284
c GLL024 Gallbladder Disease 1 52 0.041
285
P MSC003 Muscular Atrophy 52 0.041
286
P TRT010 Teratoma 51 0.041
287
P LCT001 Lactic Acidosis 51 0.041
288
FML063 Familial Glucocorticoid Deficiency 51 0.041
289
RTN003 Retinal Ischemia 50 0.041
290
P MMB011 Membranous Nephropathy 50 0.041
291
SYS003 Systolic Heart Failure 50 0.041
292
NTR046 Neutrophil Migration 50 0.041
293
VCC001 Vaccinia 49 0.041
294
RFR010 Refractory Anemia 48 0.041
295
P ATT003 Attenuated Familial Adenomatous Polyposis 48 0.041
296
PLC007 Placental Abruption 48 0.041
297
ATX019 Ataxia with Vitamin E Deficiency 48 0.041
298
ANT018 Anthracosis 48 0.041
299
PRP007 Priapism 48 0.041
300
HPR003 Heparin-Induced Thrombocytopenia 47 0.041
301
LPD004 Lipoid Nephrosis 47 0.041
302
PPL002 Papillary Carcinoma 47 0.041
303
HRD005 Hard Palate Cancer 46 0.041
304
CRN019 Coronary Artery Vasospasm 46 0.041
305
P PRX014 Proximal Spinal Muscular Atrophy 45 0.041
306
SMN007 Seminoma 44 0.041
307
PTY001 Pityriasis Rosea 44 0.041
308
MTR010 Mature Teratoma 43 0.041
309
P KLZ004 Kala-Azar 1 41 0.041
310
RST023 Resting Heart Rate, Variation in 41 0.041
311
MMM006 Mammographic Density 41 0.041
312
GLM044 Glomerular Disease 39 0.041
313
FLL031 Follicular Adenoma 39 0.041
314
LKP003 Leukoplakia 39 0.041
315
SCR011 Scrapie 38 0.041
316
NCR002 Necrobiosis Lipoidica 38 0.041
317
CRT004 Carotid Artery Thrombosis 38 0.041
318
CRD016 Cardiac Rupture 38 0.041
319
PLT015 Platelet Aggregation, Spontaneous 37 0.041
320
P FML187 Familial Hypertension 37 0.041
321
LYM052 Lymphomatoid Papulosis 36 0.041
322
c ELL005 Elliptocytosis 2 36 0.041
323
BRK012 Broken Heart Syndrome 35 0.041
324
PPL052 Papillomatosis, Confluent and Reticulated 34 0.041
325
TST010 Testicular Spermatocytic Seminoma 33 0.041
326
c ELL006 Elliptocytosis 3 33 0.041
327
MYC015 Mycobacterium Fortuitum 31 0.041
328
LCH014 Lichen Amyloidosis 31 0.041
329
SPR018 Spermatocytoma 30 0.041
330
MTR087 Maternal Uniparental Disomy 30 0.041
331
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.041
332
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 16 0.041
333
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 0.041
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