Search results for "gliosis"

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

98 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 33 7.139
2
NRN002 Neuronitis 36 0.191
3
CRB009 Cerebritis 33 0.176
4
ISC004 Ischemia 53 0.159
5
RTN023 Retinitis 44 0.150
6
TRN015 Transient Cerebral Ischemia 44 0.140
7
P LGH007 Leigh Syndrome 65 0.092
8
P AST007 Astrocytoma 63 0.092
9
DMN002 Dementia 58 0.092
10
P MNN013 Meningitis 58 0.075
11
P HYD006 Hydrocephalus 56 0.075
12
STT001 Status Epilepticus 56 0.075
13
P SLP006 Sleep Apnea 50 0.075
14
P LTR001 Lateral Sclerosis 43 0.075
15
FCL014 Focal Epilepsy 37 0.075
16
c HNT010 Huntington Disease-Like 1 18 0.075
17
P ALZ034 Alzheimer Disease 100 0.053
18
HV1006 Hiv-1 83 0.053
19
P HNT016 Huntington Disease 80 0.053
20
P NRF002 Neurofibromatosis 69 0.053
21
P NRC002 Narcolepsy 67 0.053
22
P ALX003 Alexander Disease 66 0.053
23
c NRF018 Neurofibromatosis, Type 1 65 0.053
24
c PRK057 Parkinson Disease, Late-Onset 63 0.053
25
PCK002 Pick Disease 64 0.053
26
P AMY004 Amyloidosis 63 0.053
27
P SDD001 Sudden Infant Death Syndrome 62 0.053
28
P MCH002 Machado-Joseph Disease 61 0.053
29
P HYP086 Hypothyroidism 59 0.053
30
P CRB019 Cerebral Amyloid Angiopathy 59 0.053
31
SPN186 Spinal Cord Injury 54 0.053
32
c HRD010 Hereditary Spastic Paraplegia 62 0.053
33
TTN003 Tetanus 54 0.053
34
P SPN049 Spinocerebellar Ataxia 53 0.053
35
DBF001 D-Bifunctional Protein Deficiency 51 0.053
36
CTS003 Coats Disease 51 0.053
37
P ATX004 Ataxia 50 0.053
38
GLM004 Gliomatosis Cerebri 50 0.053
39
TMP001 Temporal Lobe Epilepsy 50 0.053
40
HYP266 Hypoxia 49 0.053
41
BRN029 Brain Disease 49 0.053
42
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 48 0.053
43
SBC001 Subacute Sclerosing Panencephalitis 47 0.053
44
MSC077 Muscle Eye Brain Disease 47 0.053
45
P EXP004 Exophthalmos 47 0.053
46
P SPR098 Supranuclear Palsy, Progressive 48 0.053
47
OCL006 Ocular Hypertension 47 0.053
48
P ZLL001 Zellweger Syndrome 46 0.053
49
P MCL001 Mucolipidosis 45 0.053
50
P GLT023 Glutaric Acidemia Iic 45 0.053
51
c L2H001 L-2-Hydroxyglutaric Aciduria 45 0.053
52
END072 Endotheliitis 44 0.053
53
MCL003 Macular Holes 43 0.053
54
c MCL013 Mucolipidosis Iv 41 0.053
55
NSH001 Nasu-Hakola Disease 41 0.053
56
CRN027 Corneal Neovascularization 40 0.053
57
RTN003 Retinal Ischemia 40 0.053
58
PRP016 Paraplegia 40 0.053
59
WLL004 Wallerian Degeneration 39 0.053
60
P RTN016 Retinal Degeneration 38 0.053
61
SCR011 Scrapie 37 0.053
62
PPL048 Papillorenal Syndrome 38 0.053
63
DBT087 Diabetes Insipidus, Neurohypophyseal 38 0.053
64
GLT021 Glutaricaciduria, Type I 37 0.053
65
c INF069 Infantile Neuroaxonal Dystrophy 1 36 0.053
66
MTC056 Mitochondrial Dna Depletion Syndrome 4a 37 0.053
67
VTR003 Vitreous Detachment 34 0.053
68
SPR066 Superficial Siderosis 33 0.053
69
c SPN296 Spinocerebellar Ataxia 17 34 0.053
70
SPS057 Spasticity 32 0.053
71
c PRK024 Parkinson Disease, Juvenile, Type 2 29 0.053
72
c PNT013 Pontocerebellar Hypoplasia Type 4 30 0.053
73
c PNT022 Pontocerebellar Hypoplasia Type 2a 27 0.053
74
P CMM008 Communicating Hydrocephalus 25 0.053
75
P CRB101 Cerebrooculofacioskeletal Syndrome 1 26 0.053
76
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 24 0.053
77
NNT021 Neonatal Meningitis 24 0.053
78
LGH016 Leigh Syndrome, French-Canadian Type 24 0.053
79
MLY006 Molybdenum Cofactor Deficiency a 21 0.053
80
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 22 0.053
81
c PRK059 Parkinson Disease 8 21 0.053
82
c LSS012 Lissencephaly, X-Linked 2 21 0.053
83
CMB044 Combined Oxidative Phosphorylation Deficiency 14 20 0.053
84
c PNT017 Pontocerebellar Hypoplasia Type 1a 20 0.053
85
ISC009 Ischemic Retinopathy 19 0.053
86
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 17 0.053
87
MLY005 Molybdenum Cofactor Deficiency B 17 0.053
88
HRD139 Hereditary Motor and Sensory Neuropathy, Proximal Type 17 0.053
89
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 16 0.053
90
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 15 0.053
91
P AMY093 Amyotrophic Lateral Sclerosis and/or Frontotemporal Dementia 15 0.053
92
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 13 0.053
93
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 12 0.053
94
SBP002 Subependymal Glioma 12 0.053
95
c SPR049 Supranuclear Palsy, Progressive, 2 13 0.053
96
PRN028 Prion Disease with Protracted Course 10 0.053
97
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 9 0.053
98
CLS006 Clasped Thumbs, Congenital 10 0.053