Search results for "gliosis"

The MalaCard for "gliosis" has been retired.
Searching MalaCards for entries containing "gliosis"

104 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 38 7.151
2
NRN002 Neuronitis 40 0.203
3
CRB009 Cerebritis 36 0.189
4
ISC004 Ischemia 56 0.174
5
TRN015 Transient Cerebral Ischemia 57 0.157
6
RTN023 Retinitis 49 0.148
7
P LGH007 Leigh Syndrome 70 0.091
8
DMN002 Dementia 62 0.091
9
P AST007 Astrocytoma 66 0.091
10
P EPL164 Epilepsy 60 0.091
11
P GLM045 Glioma 53 0.091
12
P SPR098 Supranuclear Palsy, Progressive 57 0.074
13
GLT021 Glutaricaciduria, Type I 47 0.074
14
P HYD006 Hydrocephalus 68 0.074
15
PCK002 Pick Disease 66 0.074
16
STT001 Status Epilepticus 59 0.074
17
c PNT013 Pontocerebellar Hypoplasia Type 4 30 0.074
18
FCL014 Focal Epilepsy 55 0.074
19
c HNT010 Huntington Disease-Like 1 21 0.074
20
P MNN013 Meningitis 66 0.074
21
P SLP006 Sleep Apnea 60 0.074
22
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 28 0.074
23
c PNT017 Pontocerebellar Hypoplasia Type 1a 25 0.074
24
P LTR001 Lateral Sclerosis 50 0.074
25
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 16 0.074
26
P ALZ034 Alzheimer Disease 92 0.052
27
P PRK057 Parkinson Disease, Late-Onset 72 0.052
28
P HNT016 Huntington Disease 80 0.052
29
P CRT072 Creutzfeldt-Jakob Disease 62 0.052
30
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 0.052
31
HV1006 Hiv-1 80 0.052
32
P GLT023 Glutaric Acidemia Iic 51 0.052
33
P MCH002 Machado-Joseph Disease 63 0.052
34
P NRC002 Narcolepsy 62 0.052
35
c INF069 Infantile Neuroaxonal Dystrophy 1 44 0.052
36
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.052
37
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.052
38
c HRD010 Hereditary Spastic Paraplegia 66 0.052
39
P ALX003 Alexander Disease 64 0.052
40
NSH001 Nasu-Hakola Disease 46 0.052
41
P NRF002 Neurofibromatosis 66 0.052
42
PPL048 Papillorenal Syndrome 36 0.052
43
P ZLL001 Zellweger Syndrome 49 0.052
44
LGH016 Leigh Syndrome, French-Canadian Type 27 0.052
45
c SPN296 Spinocerebellar Ataxia 17 46 0.052
46
P SDD001 Sudden Infant Death Syndrome 60 0.052
47
P CRB019 Cerebral Amyloid Angiopathy 56 0.052
48
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.052
49
c NRF018 Neurofibromatosis, Type 1 69 0.052
50
c L2H001 L-2-Hydroxyglutaric Aciduria 42 0.052
51
DYS171 Dystonia-Parkinsonism, X-Linked 26 0.052
52
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.052
53
c PNT022 Pontocerebellar Hypoplasia Type 2a 31 0.052
54
TTN003 Tetanus 62 0.052
55
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.052
56
P HYP086 Hypothyroidism 63 0.052
57
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 23 0.052
58
c PRK059 Parkinson Disease 8 51 0.052
59
DBF001 D-Bifunctional Protein Deficiency 47 0.052
60
MLY006 Molybdenum Cofactor Deficiency a 28 0.052
61
MLY005 Molybdenum Cofactor Deficiency B 22 0.052
62
CMB044 Combined Oxidative Phosphorylation Deficiency 14 22 0.052
63
RBS001 Rabies 55 0.052
64
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.052
65
P EXP004 Exophthalmos 56 0.052
66
CTS003 Coats Disease 57 0.052
67
MSC077 Muscle Eye Brain Disease 54 0.052
68
P ENC018 Encephalopathy 59 0.052
69
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 25 0.052
70
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 26 0.052
71
c LSS012 Lissencephaly, X-Linked 2 23 0.052
72
PRP016 Paraplegia 49 0.052
73
c SPN364 Spinocerebellar Ataxia, X-Linked 3 18 0.052
74
c MCL013 Mucolipidosis Iv 44 0.052
75
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 17 0.052
76
c CRB101 Cerebrooculofacioskeletal Syndrome 1 35 0.052
77
P FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 22 0.052
78
PRN028 Prion Disease with Protracted Course 14 0.052
79
ADD006 Adducted Thumbs Syndrome 19 0.052
80
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 20 0.052
81
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 21 0.052
82
GLM004 Gliomatosis Cerebri 48 0.052
83
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 25 0.052
84
TMP001 Temporal Lobe Epilepsy 47 0.052
85
P AMY004 Amyloidosis 63 0.052
86
P RTN016 Retinal Degeneration 50 0.052
87
OCL006 Ocular Hypertension 47 0.052
88
P CMM008 Communicating Hydrocephalus 31 0.052
89
SBP002 Subependymal Glioma 38 0.052
90
P ATX004 Ataxia 53 0.052
91
SPS057 Spasticity 41 0.052
92
CRN027 Corneal Neovascularization 47 0.052
93
HYP266 Hypoxia 55 0.052
94
VTR003 Vitreous Detachment 29 0.052
95
SPN186 Spinal Cord Injury 62 0.052
96
MCL003 Macular Holes 43 0.052
97
c SPR049 Supranuclear Palsy, Progressive, 2 19 0.052
98
WLL004 Wallerian Degeneration 34 0.052
99
NNT021 Neonatal Meningitis 23 0.052
100
SCR011 Scrapie 34 0.052
101
RTN003 Retinal Ischemia 48 0.052
102
SPR066 Superficial Siderosis 33 0.052
103
END072 Endotheliitis 41 0.052
104
ISC009 Ischemic Retinopathy 22 0.052