Search results for "gliosis"

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

108 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 49 7.729
2
NRN002 Neuronitis 41 0.207
3
CRB009 Cerebritis 39 0.187
4
ISC004 Ischemia 61 0.172
5
TRN015 Transient Cerebral Ischemia 56 0.156
6
RTN023 Retinitis 50 0.156
7
P SPR098 Supranuclear Palsy, Progressive 56 0.104
8
P LGH007 Leigh Syndrome 70 0.090
9
P EPL164 Epilepsy 66 0.090
10
DMN002 Dementia 65 0.090
11
P AST007 Astrocytoma 65 0.090
12
P GLM045 Glioma 60 0.090
13
PCK002 Pick Disease 68 0.073
14
P MNN013 Meningitis 67 0.073
15
P HYD006 Hydrocephalus 66 0.073
16
P SLP006 Sleep Apnea 61 0.073
17
STT001 Status Epilepticus 59 0.073
18
FCL014 Focal Epilepsy 55 0.073
19
P LTR001 Lateral Sclerosis 53 0.073
20
OCL006 Ocular Hypertension 48 0.073
21
GLT021 Glutaricaciduria, Type I 46 0.073
22
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.073
23
c PNT013 Pontocerebellar Hypoplasia Type 4 29 0.073
24
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 23 0.073
25
c PNT017 Pontocerebellar Hypoplasia Type 1a 23 0.073
26
c HNT010 Huntington Disease-Like 1 21 0.073
27
P ALZ034 Alzheimer Disease 92 0.052
28
HV1006 Hiv-1 80 0.052
29
P HNT016 Huntington Disease 80 0.052
30
P NRF002 Neurofibromatosis 71 0.052
31
P PRK057 Parkinson Disease, Late-Onset 70 0.052
32
c NRF018 Neurofibromatosis, Type 1 67 0.052
33
c HRD010 Hereditary Spastic Paraplegia 67 0.052
34
P AMY004 Amyloidosis 65 0.052
35
P HYP086 Hypothyroidism 64 0.052
36
P ALX003 Alexander Disease 63 0.052
37
P MCH002 Machado-Joseph Disease 63 0.052
38
SPN186 Spinal Cord Injury 63 0.052
39
P MCL013 Mucolipidosis Iv 62 0.052
40
P NRC002 Narcolepsy 62 0.052
41
P CRT072 Creutzfeldt-Jakob Disease 61 0.052
42
P SDD001 Sudden Infant Death Syndrome 61 0.052
43
TTN003 Tetanus 61 0.052
44
P ENC018 Encephalopathy 59 0.052
45
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 59 0.052
46
P CRB019 Cerebral Amyloid Angiopathy 58 0.052
47
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.052
48
CTS003 Coats Disease 57 0.052
49
MSC077 Muscle Eye Brain Disease 57 0.052
50
ZLL001 Zellweger Syndrome 56 0.052
51
HYP266 Hypoxia 56 0.052
52
RBS001 Rabies 56 0.052
53
P RTN016 Retinal Degeneration 54 0.052
54
P EXP004 Exophthalmos 53 0.052
55
P ATX004 Ataxia 53 0.052
56
TRM010 Traumatic Brain Injury 52 0.052
57
BRN071 Brain Injury 52 0.052
58
P GLT023 Glutaric Acidemia Iic 52 0.052
59
DBF001 D-Bifunctional Protein Deficiency 50 0.052
60
TMP001 Temporal Lobe Epilepsy 50 0.052
61
PRP016 Paraplegia 49 0.052
62
GLM004 Gliomatosis Cerebri 49 0.052
63
c PRK059 Parkinson Disease 8 48 0.052
64
RTN003 Retinal Ischemia 48 0.052
65
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.052
66
MTC056 Mitochondrial Dna Depletion Syndrome 4a 48 0.052
67
c SPN296 Spinocerebellar Ataxia 17 48 0.052
68
CRN027 Corneal Neovascularization 47 0.052
69
NSH001 Nasu-Hakola Disease 44 0.052
70
c INF069 Infantile Neuroaxonal Dystrophy 1 43 0.052
71
END072 Endotheliitis 42 0.052
72
SPS057 Spasticity 42 0.052
73
c L2H001 L-2-Hydroxyglutaric Aciduria 42 0.052
74
MCL003 Macular Holes 41 0.052
75
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 38 0.052
76
SCR011 Scrapie 38 0.052
77
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 38 0.052
78
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.052
79
P CMM008 Communicating Hydrocephalus 36 0.052
80
SBP002 Subependymal Glioma 36 0.052
81
c CRB101 Cerebrooculofacioskeletal Syndrome 1 36 0.052
82
WLL004 Wallerian Degeneration 36 0.052
83
PPL048 Papillorenal Syndrome 35 0.052
84
SPR066 Superficial Siderosis 34 0.052
85
VTR003 Vitreous Detachment 34 0.052
86
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.052
87
c PNT022 Pontocerebellar Hypoplasia Type 2a 30 0.052
88
MLY006 Molybdenum Cofactor Deficiency a 30 0.052
89
NNT021 Neonatal Meningitis 28 0.052
90
DYS171 Dystonia-Parkinsonism, X-Linked 28 0.052
91
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 27 0.052
92
LGH016 Leigh Syndrome, French-Canadian Type 26 0.052
93
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 24 0.052
94
c LSS012 Lissencephaly, X-Linked 2 24 0.052
95
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 23 0.052
96
MLY005 Molybdenum Cofactor Deficiency B 22 0.052
97
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 22 0.052
98
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 22 0.052
99
ISC009 Ischemic Retinopathy 21 0.052
100
CMB044 Combined Oxidative Phosphorylation Deficiency 14 21 0.052
101
CMB064 Combined Oxidative Phosphorylation Deficiency 24 21 0.052
102
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 21 0.052
103
c MNT249 Mental Retardation, X-Linked 12/35 20 0.052
104
c SPN364 Spinocerebellar Ataxia, X-Linked 3 20 0.052
105
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 19 0.052
106
ADD006 Adducted Thumbs Syndrome 19 0.052
107
c SPR049 Supranuclear Palsy, Progressive, 2 18 0.052
108
PRN028 Prion Disease with Protracted Course 14 0.052