Search results for "gliosis"

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

105 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 37 5.493
2
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 21 3.867
3
NRN002 Neuronitis 40 0.199
4
CRB009 Cerebritis 37 0.184
5
ISC004 Ischemia 47 0.168
6
TRN015 Transient Cerebral Ischemia 43 0.150
7
RTN023 Retinitis 43 0.150
8
P LGH007 Leigh Syndrome 67 0.092
9
P AST007 Astrocytoma 55 0.092
10
DMN002 Dementia 53 0.092
11
PCK002 Pick Disease 61 0.075
12
P HYD006 Hydrocephalus 54 0.075
13
P SPR098 Supranuclear Palsy, Progressive 52 0.075
14
STT001 Status Epilepticus 51 0.075
15
P MNN013 Meningitis 51 0.075
16
FCL014 Focal Epilepsy 47 0.075
17
P SLP006 Sleep Apnea 46 0.075
18
P LTR001 Lateral Sclerosis 46 0.075
19
GLT021 Glutaricaciduria, Type I 42 0.075
20
c PNT013 Pontocerebellar Hypoplasia Type 4 32 0.075
21
c PNT017 Pontocerebellar Hypoplasia Type 1a 27 0.075
22
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 26 0.075
23
c HNT010 Huntington Disease-Like 1 20 0.075
24
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 19 0.075
25
P ALZ034 Alzheimer Disease 98 0.053
26
P HNT016 Huntington Disease 78 0.053
27
HV1006 Hiv-1 77 0.053
28
c PRK057 Parkinson Disease, Late-Onset 73 0.053
29
P NRC002 Narcolepsy 66 0.053
30
P NRF002 Neurofibromatosis 66 0.053
31
c HRD010 Hereditary Spastic Paraplegia 64 0.053
32
c NRF018 Neurofibromatosis, Type 1 63 0.053
33
P ALX003 Alexander Disease 61 0.053
34
P CRT072 Creutzfeldt-Jakob Disease 60 0.053
35
P AMY004 Amyloidosis 60 0.053
36
P MCH002 Machado-Joseph Disease 59 0.053
37
P SDD001 Sudden Infant Death Syndrome 59 0.053
38
P CRB019 Cerebral Amyloid Angiopathy 56 0.053
39
SPN186 Spinal Cord Injury 55 0.053
40
TTN003 Tetanus 55 0.053
41
P SPN049 Spinocerebellar Ataxia 54 0.053
42
P HYP086 Hypothyroidism 52 0.053
43
DBT087 Diabetes Insipidus, Neurohypophyseal 51 0.053
44
MSC077 Muscle Eye Brain Disease 49 0.053
45
c SPN296 Spinocerebellar Ataxia 17 49 0.053
46
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.053
47
P GLT023 Glutaric Acidemia Iic 49 0.053
48
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 48 0.053
49
TMP001 Temporal Lobe Epilepsy 48 0.053
50
DBF001 D-Bifunctional Protein Deficiency 47 0.053
51
c MCL013 Mucolipidosis Iv 46 0.053
52
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.053
53
P MCL001 Mucolipidosis 46 0.053
54
c L2H001 L-2-Hydroxyglutaric Aciduria 46 0.053
55
NSH001 Nasu-Hakola Disease 45 0.053
56
P ZLL001 Zellweger Syndrome 45 0.053
57
CTS003 Coats Disease 44 0.053
58
P EXP004 Exophthalmos 44 0.053
59
SBC001 Subacute Sclerosing Panencephalitis 43 0.053
60
PPL048 Papillorenal Syndrome 43 0.053
61
P ATX004 Ataxia 43 0.053
62
HYP266 Hypoxia 42 0.053
63
P RTN016 Retinal Degeneration 42 0.053
64
PRV004 Periventricular Leukomalacia 42 0.053
65
CRN027 Corneal Neovascularization 42 0.053
66
P ENC018 Encephalopathy 42 0.053
67
PRP016 Paraplegia 41 0.053
68
OCL006 Ocular Hypertension 41 0.053
69
RTN003 Retinal Ischemia 40 0.053
70
GLM004 Gliomatosis Cerebri 40 0.053
71
END072 Endotheliitis 39 0.053
72
MCL003 Macular Holes 37 0.053
73
P CMM008 Communicating Hydrocephalus 36 0.053
74
P CRB101 Cerebrooculofacioskeletal Syndrome 1 35 0.053
75
SCR011 Scrapie 35 0.053
76
WLL004 Wallerian Degeneration 34 0.053
77
c PNT022 Pontocerebellar Hypoplasia Type 2a 33 0.053
78
MLY006 Molybdenum Cofactor Deficiency a 33 0.053
79
c PRK024 Parkinson Disease, Juvenile, Type 2 33 0.053
80
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 33 0.053
81
SPR066 Superficial Siderosis 31 0.053
82
SPS057 Spasticity 30 0.053
83
c PRK059 Parkinson Disease 8 29 0.053
84
VTR003 Vitreous Detachment 28 0.053
85
P FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 28 0.053
86
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.053
87
LGH016 Leigh Syndrome, French-Canadian Type 27 0.053
88
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 27 0.053
89
DYS171 Dystonia-Parkinsonism, X-Linked 27 0.053
90
c LSS012 Lissencephaly, X-Linked 2 26 0.053
91
SBP002 Subependymal Glioma 25 0.053
92
CMB044 Combined Oxidative Phosphorylation Deficiency 14 24 0.053
93
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 24 0.053
94
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 23 0.053
95
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 23 0.053
96
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 21 0.053
97
MLY005 Molybdenum Cofactor Deficiency B 21 0.053
98
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 21 0.053
99
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 19 0.053
100
ISC009 Ischemic Retinopathy 19 0.053
101
NNT021 Neonatal Meningitis 18 0.053
102
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 17 0.053
103
PRN028 Prion Disease with Protracted Course 15 0.053
104
c SPR049 Supranuclear Palsy, Progressive, 2 14 0.053
105
CLS006 Clasped Thumbs, Congenital 10 0.053