Search results for map2

60 hits were found for map2

# Family MCID Name MIFTS Score
1
CNT019 Central Neurocytoma 42 3.870
2
MRK001 Merkel Cell Carcinoma 59 3.462
3
GNG004 Ganglioglioma 51 3.462
4
P SCH015 Schizophrenia 71 3.168
5
ISC004 Ischemia 66 3.121
6
P ALZ034 Alzheimer Disease 95 3.066
7
P MDL005 Medulloblastoma 76 3.034
8
PRN023 Prion Disease 51 3.034
9
BRN080 Brain Ischemia 45 3.034
10
SCR011 Scrapie 40 3.034
11
TRN015 Transient Cerebral Ischemia 58 2.998
12
P OLV001 Olivopontocerebellar Atrophy 51 2.998
13
P STR001 Striatonigral Degeneration 34 2.998
14
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.491
15
CRT015 Carotid Artery Occlusion 42 2.491
16
DYS006 Dysembryoplastic Neuroepithelial Tumor 37 2.491
17
STR067 Stroke, Ischemic 84 2.448
18
P PRK057 Parkinson Disease, Late-Onset 78 2.448
19
c MCP043 Mucopolysaccharidosis, Type Iiia 52 2.448
20
HMM003 Hemimegalencephaly 47 2.448
21
OPT007 Optic Nerve Glioma 45 2.448
22
P CHR342 Chiari Malformation 45 2.448
23
NRN016 Neuronal Migration Disorders 42 2.448
24
OPT008 Optic Nerve Neoplasm 38 2.448
25
CRB022 Cerebellar Liponeurocytoma 36 2.448
26
PPL050 Papillary Tumor of the Pineal Region 36 2.448
27
CLR011 Clear Cell Ependymoma 34 2.448
28
CHN009 Chondroid Chordoma 31 2.448
29
PTC005 Pituicytoma 28 2.448
30
HMN001 Human Monocytic Ehrlichiosis 27 2.448
31
OCC005 Occlusion Precerebral Artery 27 2.448
32
MXD025 Mixed Germ Cell Cancer 24 2.448
33
NRN002 Neuronitis 43 0.293
34
MLN008 Melanoma 72 0.116
35
c BLD140 Blood Group, I System 37 0.116
36
ORL011 Oral Cancer 60 0.095
37
P RTN024 Retinoblastoma 76 0.067
38
P NRB001 Neuroblastoma 73 0.067
39
P ADN016 Adenocarcinoma 71 0.067
40
P ATS364 Autism 70 0.067
41
DMN002 Dementia 68 0.067
42
P ENC004 Encephalitis 66 0.067
43
P ESP024 Esophagitis 64 0.067
44
P HYP086 Hypothyroidism 62 0.067
45
HYP266 Hypoxia 61 0.067
46
STT001 Status Epilepticus 60 0.067
47
GST040 Gastric Adenocarcinoma 60 0.067
48
P LTR001 Lateral Sclerosis 58 0.067
49
P LRY019 Laryngitis 57 0.067
50
BRN071 Brain Injury 54 0.067
51
ESP020 Esophageal Atresia 54 0.067
52
P TRT010 Teratoma 53 0.067
53
P MYT002 Myotonic Dystrophy 50 0.067
54
CRB009 Cerebritis 41 0.067
55
CHR073 Choreatic Disease 40 0.067
56
c CTR122 Cataract 5, Multiple Types 38 0.067
57
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.067
58
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 35 0.067
59
OVR109 Ovarian Germ Cell Teratoma 35 0.067
60
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 33 0.067
Content
Loading form....