Search results for t2

312 hits were found for t2

# Family MCID Name MIFTS Score
1
ALP077 Alpha-Methylacetoacetic Aciduria 41 5.011
2
P THL005 Thalassemia 64 0.178
3
CRB009 Cerebritis 41 0.147
4
PRS047 Prostatitis 60 0.138
5
HMS001 Hemosiderosis 51 0.129
6
P HPT021 Hepatitis 76 0.124
7
P SDR002 Siderosis 47 0.118
8
P BRS047 Breast Cancer 100 0.107
9
P PRS040 Prostate Cancer 90 0.107
10
P LRY019 Laryngitis 56 0.101
11
P ADN016 Adenocarcinoma 70 0.094
12
ISC004 Ischemia 65 0.094
13
SQM006 Squamous Cell Carcinoma 59 0.094
14
P MLT020 Multiple Sclerosis 78 0.087
15
c BTT014 Beta-Thalassemia 69 0.087
16
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.080
17
CRH001 Crohn's Disease 78 0.080
18
P INT068 Intestinal Disease 64 0.080
19
P LRY044 Larynx Cancer 60 0.080
20
HMG005 Hemoglobinopathy 53 0.080
21
GLL018 Gallbladder Cancer 51 0.080
22
P CLR023 Colorectal Cancer 97 0.071
23
OST012 Osteoarthritis 82 0.071
24
AST005 Asthma 82 0.071
25
P DBT009 Diabetes Mellitus 64 0.071
26
P PNC044 Pancreatitis 64 0.071
27
P MYC008 Myocarditis 58 0.071
28
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.071
29
GLC008 Glucose Metabolism Disease 52 0.071
30
P CRV039 Cervicitis 49 0.071
31
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.071
32
GST053 Gastric Cancer 77 0.062
33
MLT157 Multiple System Atrophy 1 73 0.062
34
CNG034 Congestive Heart Failure 72 0.062
35
P LYM118 Lymphoma 70 0.062
36
P MYP004 Myopathy 68 0.062
37
LNG099 Lung Disease 67 0.062
38
GST050 Gastrointestinal System Disease 64 0.062
39
P ENC018 Encephalopathy 62 0.062
40
ANR040 Aneurysm 60 0.062
41
TNG003 Tongue Cancer 58 0.062
42
P OST009 Osteochondritis Dissecans 57 0.062
43
RCT018 Rectal Neoplasm 54 0.062
44
P GLM045 Glioma 54 0.062
45
ORL015 Oral Squamous Cell Carcinoma 45 0.062
46
NRN002 Neuronitis 41 0.062
47
CRD003 Cardiac Sarcoidosis 41 0.062
48
RCT017 Rectal Disease 39 0.062
49
CHN011 Chondromalacia 35 0.062
50
c TRC078 Trichohepatoenteric Syndrome 2 34 0.062
51
c CRB051 Cerebral Cavernous Malformation, Familial 29 0.062
52
P LNG032 Lung Cancer 98 0.050
53
P HPT023 Hepatocellular Carcinoma 94 0.050
54
P OVR042 Ovarian Cancer 81 0.050
55
P ART022 Arthritis 76 0.050
56
P HRT032 Heart Disease 74 0.050
57
MYL009 Myelodysplastic Syndrome 70 0.050
58
P BLD134 Bladder Cancer 69 0.050
59
P SCH015 Schizophrenia 69 0.050
60
P EPL164 Epilepsy 69 0.050
61
P KDN018 Kidney Disease 68 0.050
62
CRT072 Creutzfeldt-Jakob Disease 65 0.050
63
GST045 Gastroenteritis 64 0.050
64
c CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 63 0.050
65
P ESP024 Esophagitis 63 0.050
66
GST040 Gastric Adenocarcinoma 63 0.050
67
MLN008 Melanoma 62 0.050
68
HYP266 Hypoxia 61 0.050
69
SPP011 Suppression of Tumorigenicity 12 61 0.050
70
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.050
71
JNT002 Joint Disorders 59 0.050
72
HPT019 Hepatic Encephalopathy 58 0.050
73
c GNG001 Gangliosidosis Gm1 57 0.050
74
ILT001 Ileitis 56 0.050
75
ADN027 Adenomyosis 56 0.050
76
SCK005 Sickle Cell Disease 54 0.050
77
OST016 Osteochondrosis 54 0.050
78
RDC002 Radiculopathy 53 0.050
79
c INF071 Inflammatory Bowel Disease 1 53 0.050
80
P INF037 Inflammatory Bowel Disease 53 0.050
81
P MYM013 Moyamoya Disease 1 51 0.050
82
P CMP008 Compartment Syndrome 47 0.050
83
MCR011 Microinvasive Gastric Cancer 46 0.050
84
CRB090 Cerebral Hypoxia 46 0.050
85
CRT015 Carotid Artery Occlusion 44 0.050
86
TND006 Tendinosis 43 0.050
87
SPR066 Superficial Siderosis 40 0.050
88
c GM2005 Gm2-Gangliosidosis, Ab Variant 38 0.050
89
LGH012 Leigh Syndrome with Leukodystrophy 35 0.050
90
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 35 0.050
91
c MTC074 Metachromatic Leukodystrophy, Adult Form 28 0.050
92
c MTC076 Metachromatic Leukodystrophy, Juvenile Form 28 0.050
93
c MTC075 Metachromatic Leukodystrophy, Late Infantile Form 28 0.050
94
c STR092 Striatal Degeneration, Autosomal Dominant 2 25 0.050
95
CNZ005 Coenzyme Q10 Deficiency, Primary, 4 25 0.050
96
c SCN048 Secondary Syringomyelia 21 0.050
97
c SYS001 Systemic Lupus Erythematosus 86 0.036
98
c MCL042 Macular Degeneration, Age-Related, 1 84 0.036
99
P RHM011 Rheumatoid Arthritis 80 0.036
100
P MYC007 Myocardial Infarction 79 0.036
101
ESP021 Esophageal Cancer 77 0.036
102
P DLT002 Dilated Cardiomyopathy 76 0.036
103
P PRK057 Parkinson Disease, Late-Onset 76 0.036
104
P INF038 Influenza 76 0.036
105
P PLM037 Pulmonary Hypertension 75 0.036
106
P LVR013 Liver Disease 75 0.036
107
NRF026 Neurofibromatosis, Type Iv, of Riccardi 73 0.036
108
P NRV007 Nervous System Disease 73 0.036
109
BRN028 Brain Cancer 72 0.036
110
c CHR089 Chronic Kidney Failure 72 0.036
111
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.036
112
ISC006 Ischemic Heart Disease 72 0.036
113
P LKM002 Leukemia 72 0.036
114
GLB002 Glioblastoma 72 0.036
115
MYC006 Mycosis Fungoides 72 0.036
116
SCK003 Sickle Cell Anemia 72 0.036
117
ADR007 Adrenoleukodystrophy 71 0.036
118
WLS001 Wilson Disease 71 0.036
119
P TYS001 Tay-Sachs Disease 71 0.036
120
RNL065 Renal Cell Carcinoma, Papillary, 1 70 0.036
121
P PNM007 Pneumonia 69 0.036
122
P CRV035 Cervical Cancer 69 0.036
123
c LKM062 Leukemia, Acute Lymphoblastic 69 0.036
124
LVR012 Liver Cirrhosis 68 0.036
125
c SML038 Small Cell Cancer of the Lung 68 0.036
126
P LPS004 Lupus Erythematosus 68 0.036
127
SRC014 Sarcoma 68 0.036
128
P TBR001 Tuberous Sclerosis 68 0.036
129
VSC007 Vascular Disease 68 0.036
130
P CRN018 Coronary Artery Anomaly 68 0.036
131
MSC157 Muscular Dystrophy, Duchenne Type 68 0.036
132
P ART023 Arthropathy 67 0.036
133
P NSP012 Nasopharyngeal Carcinoma 67 0.036
134
CRB039 Cerebrovascular Disease 67 0.036
135
c HPT016 Hepatitis B 67 0.036
136
SKN016 Skin Disease 66 0.036
137
P MSC005 Muscular Dystrophy 66 0.036
138
BRS051 Breast Disease 66 0.036
139
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 66 0.036
140
c NRF024 Neurofibromatosis, Type I 66 0.036
141
ART140 Arteries, Anomalies of 65 0.036
142
P NRM001 Neuromyelitis Optica 65 0.036
143
P MPL001 Maple Syrup Urine Disease 65 0.036
144
c CRN300 Coronary Heart Disease 1 64 0.036
145
P LYM026 Lymphoblastic Leukemia 64 0.036
146
PNC033 Pancreas Adenocarcinoma 64 0.036
147
P DYS154 Dystonia 64 0.036
148
AGN016 Aging 64 0.036
149
P DRM010 Dermatomyositis 64 0.036
150
ART005 Arteriovenous Malformation 63 0.036
151
c CNT035 Central Nervous System Disease 63 0.036
152
OST017 Osteomyelitis 63 0.036
153
HYP066 Hyperglycemia 63 0.036
154
ADN018 Adenoma 63 0.036
155
RSP006 Respiratory System Disease 63 0.036
156
c OVR114 Ovarian Cancer 1 62 0.036
157
CLT003 Colitis 62 0.036
158
P MCH002 Machado-Joseph Disease 62 0.036
159
P INT143 Interstitial Cystitis 62 0.036
160
RHM027 Rheumatic Disease 62 0.036
161
c PNS012 Paine Syndrome 62 0.036
162
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.036
163
P ORL007 Oral Cavity Cancer 61 0.036
164
THR024 Thrombosis 61 0.036
165
INT002 Intermittent Claudication 61 0.036
166
PLS011 Plasmacytoma 60 0.036
167
c MNN043 Meningioma, Familial 60 0.036
168
CHL068 Cholestasis 60 0.036
169
P PLY014 Polycystic Kidney Disease 60 0.036
170
c ACT027 Acute Pancreatitis 60 0.036
171
BLD131 Bladder Urothelial Carcinoma 60 0.036
172
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 60 0.036
173
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.036
174
KRN002 Kearns-Sayre Syndrome 60 0.036
175
STT001 Status Epilepticus 60 0.036
176
P SPN052 Spondyloarthropathy 60 0.036
177
P ACT074 Acute Lymphocytic Leukemia 59 0.036
178
P OLG002 Oligodendroglioma 59 0.036
179
CHK001 Chikungunya 59 0.036
180
P BPL003 Bipolar Disorder 59 0.036
181
P VNT002 Ventricular Septal Defect 58 0.036
182
SFT003 Soft Tissue Sarcoma 58 0.036
183
P END033 Endocarditis 58 0.036
184
P MLN069 Melanoma, Uveal 58 0.036
185
UND005 Undifferentiated Pleomorphic Sarcoma 58 0.036
186
c ACT075 Acute Myocardial Infarction 58 0.036
187
NRT004 Neuritis 57 0.036
188
FCL081 Focal Cortical Dysplasia, Type Ii 57 0.036
189
MCR088 Microscopic Polyangiitis 57 0.036
190
CMP010 Complex Regional Pain Syndrome 57 0.036
191
P CRB048 Cerebral Cavernous Malformations 57 0.036
192
INT146 Intervertebral Disc Disease 57 0.036
193
TRG002 Trigeminal Neuralgia 57 0.036
194
PTT009 Pituitary Gland Disease 56 0.036
195
IMM136 Immune System Disease 56 0.036
196
ART141 Arteriovenous Malformations of the Brain 56 0.036
197
P CYS018 Cystitis 56 0.036
198
CHL028 Childhood Type Dermatomyositis 56 0.036
199
END030 End Stage Renal Failure 56 0.036
200
EWN002 Ewing's Family of Tumors 56 0.036
201
TRN015 Transient Cerebral Ischemia 56 0.036
202
LYS002 Lysosomal Storage Disease 56 0.036
203
P HYP076 Hyperthyroidism 56 0.036
204
LYM019 Lymphosarcoma 55 0.036
205
PRC013 Pericarditis 55 0.036
206
FCL014 Focal Epilepsy 55 0.036
207
CHL061 Childhood Leukemia 55 0.036
208
PLM014 Pleomorphic Adenoma 55 0.036
209
SPN019 Spondylolisthesis 55 0.036
210
TRM010 Traumatic Brain Injury 55 0.036
211
CYS010 Cystinosis 54 0.036
212
P TRC086 Trichohepatoenteric Syndrome 1 54 0.036
213
SPS003 Spastic Diplegia 54 0.036
214
INF034 Infective Endocarditis 54 0.036
215
LYM024 Lymphatic System Disease 54 0.036
216
P PNM006 Pneumoconiosis 54 0.036
217
P ATR010 Atrial Heart Septal Defect 54 0.036
218
P LPC002 Lip Cancer 53 0.036
219
OPT009 Optic Neuritis 53 0.036
220
BRN071 Brain Injury 53 0.036
221
P FBR031 Febrile Seizures 53 0.036
222
RST001 Restless Legs Syndrome 52 0.036
223
P CLL015 Collagen Disease 52 0.036
224
THR016 Thrombophlebitis 52 0.036
225
P TRT010 Teratoma 52 0.036
226
GLM004 Gliomatosis Cerebri 52 0.036
227
WLF002 Wolf-Hirschhorn Syndrome 52 0.036
228
SPN020 Spondylosis 51 0.036
229
MGL038 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome 51 0.036
230
P PLY017 Polyarteritis Nodosa 51 0.036
231
P AST007 Astrocytoma 51 0.036
232
PRT018 Portal Vein Thrombosis 50 0.036
233
THR013 Thoracic Outlet Syndrome 50 0.036
234
DNT005 Dentatorubral-Pallidoluysian Atrophy 50 0.036
235
PTT004 Pituitary Apoplexy 50 0.036
236
IDP024 Idiopathic Inflammatory Myopathy 49 0.036
237
CLR030 Clear Cell Renal Cell Carcinoma 49 0.036
238
PPL021 Papilledema 49 0.036
239
PRS129 Prostatic Hyperplasia, Benign 48 0.036
240
CRT017 Cartilage Disease 48 0.036
241
SKN027 Skin Conditions 48 0.036
242
c ACT076 Acute Myocarditis 47 0.036
243
SYN036 Syncope 47 0.036
244
CRB085 Cerebral Hemorrhage 47 0.036
245
CRB004 Cerebral Artery Occlusion 46 0.036
246
ENT004 Enthesopathy 46 0.036
247
ANR009 Aneurysmal Bone Cysts 46 0.036
248
ANS011 Anus Cancer 46 0.036
249
DYS073 Dysphagia 46 0.036
250
NSP002 Nasopharyngitis 46 0.036
251
P HRN001 Horner's Syndrome 46 0.036
252
NNS002 Nonspecific Interstitial Pneumonia 46 0.036
253
BNS003 Binswanger's Disease 45 0.036
254
CRN031 Cranial Nerve Disease 45 0.036
255
PDT001 Pediatric Lymphoma 45 0.036
256
ANT018 Anthracosis 45 0.036
257
ENC055 Encephalopathy, Ethylmalonic 45 0.036
258
END072 Endotheliitis 45 0.036
259
CNT025 Central Pontine Myelinolysis 45 0.036
260
AZS001 Azoospermia 45 0.036
261
ARC002 Arachnoiditis 45 0.036
262
BRN080 Brain Ischemia 44 0.036
263
LYM067 Lymphoid Leukemia 44 0.036
264
P MNN018 Mannosidosis 43 0.036
265
PHC013 Phaeochromocytoma 43 0.036
266
HRT011 Heart Septal Defect 43 0.036
267
BRN032 Brain Glioma 43 0.036
268
c GM1004 Gm1-Gangliosidosis, Type I 42 0.036
269
CRB008 Cerebral Atherosclerosis 41 0.036
270
P HMF004 Hemifacial Spasm 41 0.036
271
CRB086 Cerebral Aneurysms 41 0.036
272
OCL011 Ocular Motility Disease 41 0.036
273
c PRN053 Porencephaly 1 41 0.036
274
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 40 0.036
275
P SPS133 Spastic Paraplegia 2, X-Linked 40 0.036
276
TRN012 Transient Global Amnesia 40 0.036
277
c ADL001 Adult Lymphoma 39 0.036
278
WHP002 Whiplash 39 0.036
279
c MLG068 Malignant Glioma 38 0.036
280
OVR094 Ovarian Epithelial Cancer 38 0.036
281
MLN013 Melanoma Metastasis 38 0.036
282
PST048 Postural Orthostatic Tachycardia Syndrome 38 0.036
283
PLM021 Pilomyxoid Astrocytoma 37 0.036
284
CVR010 Cavernous Malformation 37 0.036
285
PRN022 Perineurioma 37 0.036
286
SML031 Small Cell Carcinoma of the Bladder 37 0.036
287
LYM043 Lymphocytic Hypophysitis 37 0.036
288
ANS012 Anus Disease 36 0.036
289
MNN042 Meningioma, Radiation-Induced 36 0.036
290
c FML084 Familial Porencephaly 36 0.036
291
ALL014 Allergic Encephalomyelitis 36 0.036
292
FNT004 Fainting 36 0.036
293
PLY112 Polyarteritis Nodosa, Childhood-Onset 36 0.036
294
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 35 0.036
295
INT003 Intracranial Hypotension 34 0.036
296
FRG010 Fragile X Tremor/ataxia Syndrome 32 0.036
297
SCR024 Sacrococcygeal Teratoma 31 0.036
298
P HYP700 Hypomyelinating Leukodystrophy 31 0.036
299
CMB026 Combined Oxidative Phosphorylation Deficiency 12 28 0.036
300
SPN340 Spontaneous Intracranial Hypotension 28 0.036
301
NNT003 Neonatal Thyrotoxicosis 28 0.036
302
c GLY017 Glycogen Storage Disease Ic 28 0.036
303
SPR032 Superficial Siderosis of the Central Nervous System 25 0.036
304
c ANT010 Anterior Compartment Syndrome 24 0.036
305
P STR101 Striatal Degeneration, Autosomal Dominant 1 22 0.036
306
LDD006 Ledderhose Disease 22 0.036
307
MTR031 Motor Neuro-Ophthalmic Disorders 20 0.036
308
NTL003 Notalgia Paresthetica 19 0.036
309
LWS001 Lewis-Sumner Syndrome 19 0.036
310
CNT067 Central Cord Syndrome 19 0.036
311
SCL041 Sclerosing Perineurioma 14 0.036
312
PRR034 Pruritus, Hereditary Localized 8 0.036
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