Search results for gliosis

120 hits were found for gliosis

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 36 7.251
2
SYM006 Symmetrical Thalamic Calcifications 14 2.727
3
NRN002 Neuronitis 39 0.203
4
CRB009 Cerebritis 39 0.197
5
ISC004 Ischemia 59 0.183
6
TRN015 Transient Cerebral Ischemia 53 0.169
7
P LGH007 Leigh Syndrome 69 0.153
8
RTN023 Retinitis 49 0.153
9
P SPR098 Supranuclear Palsy, Progressive 59 0.114
10
P PRK057 Parkinson Disease, Late-Onset 68 0.102
11
P EPL164 Epilepsy 65 0.102
12
P GLT023 Glutaric Acidemia Iic 49 0.102
13
c PNT017 Pontocerebellar Hypoplasia Type 1a 29 0.102
14
P AST007 Astrocytoma 63 0.088
15
P GLM045 Glioma 59 0.088
16
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 53 0.088
17
DMN002 Dementia 52 0.088
18
NSH001 Nasu-Hakola Disease 47 0.088
19
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 43 0.088
20
c CRB101 Cerebrooculofacioskeletal Syndrome 1 39 0.088
21
AMY068 Amyotrophic Lateral Sclerosis 15, with or Without Frontotemporal Dementia 28 0.088
22
c LSS012 Lissencephaly, X-Linked 2 27 0.088
23
c HNT010 Huntington Disease-Like 1 25 0.088
24
c SPN364 Spinocerebellar Ataxia, X-Linked 3 23 0.088
25
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 19 0.088
26
P HNT016 Huntington Disease 76 0.072
27
PCK002 Pick Disease 68 0.072
28
P HYD006 Hydrocephalus 66 0.072
29
P MNN013 Meningitis 65 0.072
30
P MCH002 Machado-Joseph Disease 62 0.072
31
P SLP006 Sleep Apnea 60 0.072
32
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.072
33
STT001 Status Epilepticus 58 0.072
34
DBF001 D-Bifunctional Protein Deficiency 57 0.072
35
LKN001 Leukoencephalopathy with Vanishing White Matter 57 0.072
36
FCL014 Focal Epilepsy 55 0.072
37
P LTR001 Lateral Sclerosis 53 0.072
38
PPL048 Papillorenal Syndrome 51 0.072
39
TMP001 Temporal Lobe Epilepsy 50 0.072
40
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.072
41
c SPN296 Spinocerebellar Ataxia 17 47 0.072
42
OCL006 Ocular Hypertension 46 0.072
43
c INF069 Infantile Neuroaxonal Dystrophy 1 45 0.072
44
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 0.072
45
c L2H001 L-2-Hydroxyglutaric Aciduria 44 0.072
46
c PRK059 Parkinson Disease 8 42 0.072
47
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 40 0.072
48
GLT021 Glutaricaciduria, Type I 39 0.072
49
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 39 0.072
50
MLY006 Molybdenum Cofactor Deficiency a 33 0.072
51
c PNT022 Pontocerebellar Hypoplasia Type 2a 30 0.072
52
c PNT013 Pontocerebellar Hypoplasia Type 4 30 0.072
53
LGH016 Leigh Syndrome, French-Canadian Type 29 0.072
54
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 28 0.072
55
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 27 0.072
56
MLY005 Molybdenum Cofactor Deficiency B 24 0.072
57
c SPR049 Supranuclear Palsy, Progressive, 2 24 0.072
58
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 24 0.072
59
CMB064 Combined Oxidative Phosphorylation Deficiency 24 23 0.072
60
CMB044 Combined Oxidative Phosphorylation Deficiency 14 23 0.072
61
ADD006 Adducted Thumbs Syndrome 22 0.072
62
c MNT249 Mental Retardation, X-Linked 12/35 22 0.072
63
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 20 0.072
64
PRN028 Prion Disease with Protracted Course 17 0.072
65
HV1006 Hiv-1 80 0.051
66
P NRF018 Neurofibromatosis, Type 1 78 0.051
67
P ALZ034 Alzheimer Disease 76 0.051
68
c HRD010 Hereditary Spastic Paraplegia 66 0.051
69
ALX003 Alexander Disease 65 0.051
70
P MCL013 Mucolipidosis Iv 64 0.051
71
P AMY004 Amyloidosis 64 0.051
72
P NRC002 Narcolepsy 62 0.051
73
SPN186 Spinal Cord Injury 62 0.051
74
CRT072 Creutzfeldt-Jakob Disease 62 0.051
75
P HYP086 Hypothyroidism 60 0.051
76
P SDD001 Sudden Infant Death Syndrome 60 0.051
77
TTN003 Tetanus 60 0.051
78
P RHN004 Rhinitis 59 0.051
79
MSC077 Muscle Eye Brain Disease 58 0.051
80
CTS003 Coats Disease 58 0.051
81
ZLL001 Zellweger Syndrome 58 0.051
82
HYP266 Hypoxia 55 0.051
83
RBS001 Rabies 54 0.051
84
c MNN025 Mannosidosis, Alpha-, Types I and Ii 54 0.051
85
P RTN016 Retinal Degeneration 53 0.051
86
P ATX004 Ataxia 52 0.051
87
P ENC018 Encephalopathy 52 0.051
88
c PRK031 Parkinson Disease 1 51 0.051
89
TRM010 Traumatic Brain Injury 51 0.051
90
BRN071 Brain Injury 50 0.051
91
EXP004 Exophthalmos 50 0.051
92
GLM004 Gliomatosis Cerebri 49 0.051
93
PRP016 Paraplegia 48 0.051
94
RTN003 Retinal Ischemia 47 0.051
95
P CRB019 Cerebral Amyloid Angiopathy 46 0.051
96
CRN027 Corneal Neovascularization 46 0.051
97
SPS057 Spasticity 42 0.051
98
END072 Endotheliitis 41 0.051
99
MCL003 Macular Holes 41 0.051
100
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 39 0.051
101
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 39 0.051
102
CNG436 Congenital Disorder of Deglycosylation 38 0.051
103
SBP002 Subependymal Glioma 38 0.051
104
SCR011 Scrapie 36 0.051
105
WLL004 Wallerian Degeneration 36 0.051
106
DYS171 Dystonia-Parkinsonism, X-Linked 34 0.051
107
SPR066 Superficial Siderosis 33 0.051
108
P CMM008 Communicating Hydrocephalus 32 0.051
109
c SPN200 Spinocerebellar Ataxia, Autosomal Recessive 2 32 0.051
110
VTR003 Vitreous Detachment 32 0.051
111
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 28 0.051
112
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 28 0.051
113
NNT021 Neonatal Meningitis 27 0.051
114
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 26 0.051
115
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 25 0.051
116
c OTF003 Otofaciocervical Syndrome 2 22 0.051
117
ISC009 Ischemic Retinopathy 21 0.051
118
c CTS043 Cutis Laxa, Autosomal Recessive, Type Iid 18 0.051
119
ENC047 Encephalopathy, Progressive, Early-Onset, with Brain Atrophy and Thin Corpus Callosum 17 0.051
120
c VTR009 Vitreoretinochoroidopathy Dominant 10 0.051
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