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 48 7.720
2
NRN002 Neuronitis 42 0.209
3
CRB009 Cerebritis 38 0.189
4
ISC004 Ischemia 59 0.173
5
TRN015 Transient Cerebral Ischemia 56 0.157
6
RTN023 Retinitis 49 0.157
7
P LGH007 Leigh Syndrome 70 0.091
8
P EPL164 Epilepsy 66 0.091
9
P AST007 Astrocytoma 65 0.091
10
DMN002 Dementia 64 0.091
11
P SPR098 Supranuclear Palsy, Progressive 58 0.091
12
P GLM045 Glioma 58 0.091
13
PCK002 Pick Disease 67 0.074
14
P HYD006 Hydrocephalus 67 0.074
15
P MNN013 Meningitis 65 0.074
16
P SLP006 Sleep Apnea 61 0.074
17
STT001 Status Epilepticus 59 0.074
18
FCL014 Focal Epilepsy 56 0.074
19
P LTR001 Lateral Sclerosis 52 0.074
20
GLT021 Glutaricaciduria, Type I 48 0.074
21
OCL006 Ocular Hypertension 48 0.074
22
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 41 0.074
23
c PNT013 Pontocerebellar Hypoplasia Type 4 29 0.074
24
c PNT017 Pontocerebellar Hypoplasia Type 1a 23 0.074
25
c HNT010 Huntington Disease-Like 1 21 0.074
26
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 18 0.074
27
P ALZ034 Alzheimer Disease 93 0.052
28
HV1006 Hiv-1 82 0.052
29
P HNT016 Huntington Disease 80 0.052
30
P PRK057 Parkinson Disease, Late-Onset 72 0.052
31
c NRF018 Neurofibromatosis, Type 1 68 0.052
32
P HYP086 Hypothyroidism 65 0.052
33
c HRD010 Hereditary Spastic Paraplegia 65 0.052
34
P AMY004 Amyloidosis 64 0.052
35
P ALX003 Alexander Disease 64 0.052
36
P MCL013 Mucolipidosis Iv 63 0.052
37
P CRT072 Creutzfeldt-Jakob Disease 63 0.052
38
SPN186 Spinal Cord Injury 62 0.052
39
P NRC002 Narcolepsy 62 0.052
40
P MCH002 Machado-Joseph Disease 62 0.052
41
P SDD001 Sudden Infant Death Syndrome 61 0.052
42
TTN003 Tetanus 61 0.052
43
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 60 0.052
44
P ENC018 Encephalopathy 59 0.052
45
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.052
46
P CRB019 Cerebral Amyloid Angiopathy 58 0.052
47
CTS003 Coats Disease 57 0.052
48
RBS001 Rabies 56 0.052
49
MSC077 Muscle Eye Brain Disease 56 0.052
50
HYP266 Hypoxia 55 0.052
51
P EXP004 Exophthalmos 54 0.052
52
P RTN016 Retinal Degeneration 54 0.052
53
GLM004 Gliomatosis Cerebri 53 0.052
54
P ATX004 Ataxia 53 0.052
55
TRM010 Traumatic Brain Injury 52 0.052
56
c PRK059 Parkinson Disease 8 52 0.052
57
BRN071 Brain Injury 52 0.052
58
P GLT023 Glutaric Acidemia Iic 52 0.052
59
TMP001 Temporal Lobe Epilepsy 51 0.052
60
PRP016 Paraplegia 49 0.052
61
DBF001 D-Bifunctional Protein Deficiency 49 0.052
62
CRN027 Corneal Neovascularization 48 0.052
63
RTN003 Retinal Ischemia 48 0.052
64
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.052
65
c SPN296 Spinocerebellar Ataxia 17 48 0.052
66
NSH001 Nasu-Hakola Disease 45 0.052
67
MTC056 Mitochondrial Dna Depletion Syndrome 4a 43 0.052
68
c L2H001 L-2-Hydroxyglutaric Aciduria 43 0.052
69
END072 Endotheliitis 42 0.052
70
SPS057 Spasticity 42 0.052
71
c INF069 Infantile Neuroaxonal Dystrophy 1 42 0.052
72
MCL003 Macular Holes 41 0.052
73
SCR011 Scrapie 39 0.052
74
SBP002 Subependymal Glioma 39 0.052
75
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 37 0.052
76
P CMM008 Communicating Hydrocephalus 37 0.052
77
PPL048 Papillorenal Syndrome 35 0.052
78
c CRB101 Cerebrooculofacioskeletal Syndrome 1 35 0.052
79
WLL004 Wallerian Degeneration 35 0.052
80
VTR003 Vitreous Detachment 34 0.052
81
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.052
82
SPR066 Superficial Siderosis 33 0.052
83
MLY006 Molybdenum Cofactor Deficiency a 30 0.052
84
c PNT022 Pontocerebellar Hypoplasia Type 2a 30 0.052
85
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 28 0.052
86
DYS171 Dystonia-Parkinsonism, X-Linked 27 0.052
87
LGH016 Leigh Syndrome, French-Canadian Type 26 0.052
88
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 25 0.052
89
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 25 0.052
90
NNT021 Neonatal Meningitis 24 0.052
91
c LSS012 Lissencephaly, X-Linked 2 24 0.052
92
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 24 0.052
93
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 23 0.052
94
ISC009 Ischemic Retinopathy 22 0.052
95
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 22 0.052
96
MLY005 Molybdenum Cofactor Deficiency B 22 0.052
97
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 21 0.052
98
CMB044 Combined Oxidative Phosphorylation Deficiency 14 21 0.052
99
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 20 0.052
100
c SPR049 Supranuclear Palsy, Progressive, 2 20 0.052
101
c SPN364 Spinocerebellar Ataxia, X-Linked 3 20 0.052
102
ADD006 Adducted Thumbs Syndrome 19 0.052
103
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 19 0.052
104
PRN028 Prion Disease with Protracted Course 14 0.052