Search results for "gliosis"

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

102 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 50 5.865
2
NRN002 Neuronitis 43 0.191
3
CRB009 Cerebritis 38 0.176
4
ISC004 Ischemia 62 0.159
5
RTN023 Retinitis 53 0.150
6
TRN015 Transient Cerebral Ischemia 52 0.140
7
P ALZ001 Alzheimer's Disease 98 0.106
8
P AST007 Astrocytoma 72 0.092
9
PCK001 Pick's Disease 71 0.092
10
P LGH001 Leigh Disease 69 0.092
11
DMN002 Dementia 66 0.092
12
P HYD006 Hydrocephalus 69 0.075
13
c MNN013 Meningitis 67 0.075
14
c AMY001 Amyotrophic Lateral Sclerosis 66 0.075
15
STT001 Status Epilepticus 65 0.075
16
c SLP006 Sleep Apnea 59 0.075
17
c LTR001 Lateral Sclerosis 55 0.075
18
FCL014 Focal Epilepsy 46 0.075
19
c HNT010 Huntington Disease-Like 1 19 0.075
20
P NRF002 Neurofibromatosis 94 0.053
21
P PRK002 Parkinson's Disease 92 0.053
22
P HNT001 Huntington's Disease 87 0.053
23
P HYP075 Hypertension 85 0.053
24
VNH001 Von Hippel-Lindau Disease 81 0.053
25
P NRC002 Narcolepsy 74 0.053
26
P AMY004 Amyloidosis 73 0.053
27
P SDD001 Sudden Infant Death Syndrome 71 0.053
28
P MCH002 Machado-Joseph Disease 70 0.053
29
P CCK003 Cockayne Syndrome Type Ii 69 0.053
30
c HYP086 Hypothyroidism 68 0.053
31
P PRG006 Progressive Supranuclear Palsy 68 0.053
32
P CRB019 Cerebral Amyloid Angiopathy 64 0.053
33
TTN003 Tetanus 64 0.053
34
CTS003 Coats Disease 63 0.053
35
c HRD010 Hereditary Spastic Paraplegia 63 0.053
36
HV1006 Hiv-1 63 0.053
37
ALP003 Alpers Syndrome 62 0.053
38
SPN186 Spinal Cord Injury 61 0.053
39
DBF001 D-Bifunctional Protein Deficiency 61 0.053
40
GLM004 Gliomatosis Cerebri 58 0.053
41
TMP001 Temporal Lobe Epilepsy 58 0.053
42
BRN029 Brain Disease 57 0.053
43
HYP266 Hypoxia 57 0.053
44
OCL006 Ocular Hypertension 54 0.053
45
c SPN077 Spinocerebellar Ataxia Type 17 54 0.053
46
P EXP004 Exophthalmos 54 0.053
47
P ZLL001 Zellweger Syndrome 54 0.053
48
c MCL001 Mucolipidosis 53 0.053
49
P L2H001 L-2-Hydroxyglutaric Aciduria 51 0.053
50
SBC001 Subacute Sclerosing Panencephalitis 51 0.053
51
MCL003 Macular Holes 51 0.053
52
END072 Endotheliitis 50 0.053
53
P GLT012 Glutaric Acidemia Type I 49 0.053
54
RTN003 Retinal Ischemia 48 0.053
55
CRN027 Corneal Neovascularization 47 0.053
56
PRP016 Paraplegia 47 0.053
57
c MCL013 Mucolipidosis Iv 47 0.053
58
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 46 0.053
59
WLL004 Wallerian Degeneration 45 0.053
60
RNL029 Renal Coloboma Syndrome 45 0.053
61
c RTN016 Retinal Degeneration 44 0.053
62
SCR011 Scrapie 44 0.053
63
NRG004 Neurogenic Diabetes Insipidus 42 0.053
64
P PLY082 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 41 0.053
65
VTR003 Vitreous Detachment 41 0.053
66
ADS004 Aids Dementia Complex 40 0.053
67
MLY006 Molybdenum Cofactor Deficiency a 38 0.053
68
SPR066 Superficial Siderosis 38 0.053
69
SPS057 Spasticity 37 0.053
70
FML059 Familial Encephalopathy with Neuroserpin Inclusion Bodies 35 0.053
71
c GLT023 Glutaric Acidemia Iic 35 0.053
72
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 34 0.053
73
c PNT017 Pontocerebellar Hypoplasia Type 1a 34 0.053
74
P INF069 Infantile Neuroaxonal Dystrophy 1 33 0.053
75
XLN107 X-Linked Lissencephaly with Abnormal Genitalia 33 0.053
76
c PNT013 Pontocerebellar Hypoplasia Type 4 31 0.053
77
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 30 0.053
78
P CMM008 Communicating Hydrocephalus 30 0.053
79
c PRK057 Parkinson Disease, Late-Onset 29 0.053
80
MSC077 Muscle Eye Brain Disease 28 0.053
81
NNT021 Neonatal Meningitis 28 0.053
82
MLG120 Malignant Migrating Partial Seizures of Infancy 27 0.053
83
LGH003 Leigh Syndrome, French Canadian Type 27 0.053
84
P LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 27 0.053
85
FTD003 Ftdals1 25 0.053
86
ISC009 Ischemic Retinopathy 23 0.053
87
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 20 0.053
88
NRP009 Neuropathy, Hereditary Motor and Sensory, Okinawa Type 20 0.053
89
c PNT022 Pontocerebellar Hypoplasia Type 2a 19 0.053
90
CMB044 Combined Oxidative Phosphorylation Deficiency 14 19 0.053
91
P SPN115 Spinocerebellar Ataxia X-Linked Type 3 19 0.053
92
MLY005 Molybdenum Cofactor Deficiency B 18 0.053
93
FML258 Familial Acute Necrotizing Encephalopathy 17 0.053
94
SBP002 Subependymal Glioma 16 0.053
95
c PRK059 Parkinson Disease 8 16 0.053
96
XLN036 X-Linked Leigh Syndrome 15 0.053
97
c PRK024 Parkinson Disease, Juvenile, Type 2 15 0.053
98
ADD004 Adducted Thumbs - Arthrogryposis, Christian Type 14 0.053
99
c SPR049 Supranuclear Palsy, Progressive, 2 12 0.053
100
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 9 0.053
101
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 8 0.053
102
PRN028 Prion Disease with Protracted Course 7 0.053