Search results for gliosis

135 hits were found for gliosis

# Family MCID Name MIFTS Score
1
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 9.052
2
SYM006 Symmetrical Thalamic Calcifications 18 2.721
3
NRN002 Neuronitis 43 0.201
4
CRB009 Cerebritis 41 0.195
5
ISC004 Ischemia 66 0.176
6
TRN015 Transient Cerebral Ischemia 58 0.162
7
RTN023 Retinitis 52 0.147
8
P ALZ034 Alzheimer Disease 95 0.109
9
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.109
10
P EPL164 Epilepsy 70 0.098
11
LGH007 Leigh Syndrome 68 0.098
12
P AST007 Astrocytoma 66 0.098
13
PCK003 Pick Disease of Brain 66 0.098
14
c PNT045 Pontocerebellar Hypoplasia, Type 1a 31 0.098
15
DMN002 Dementia 68 0.085
16
AGN016 Aging 65 0.085
17
P GLM045 Glioma 61 0.085
18
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 42 0.085
19
P CRB101 Cerebrooculofacioskeletal Syndrome 1 42 0.085
20
PLY082 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 40 0.085
21
c HNT010 Huntington Disease-Like 1 24 0.085
22
c SPN364 Spinocerebellar Ataxia, X-Linked 3 23 0.085
23
AMY104 Amyotrophic Lateral Sclerosis 15 with or Without Frontotemporal Dementia 21 0.085
24
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 20 0.085
25
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.069
26
P PRK057 Parkinson Disease, Late-Onset 78 0.069
27
P HNT016 Huntington Disease 78 0.069
28
P MNN013 Meningitis 71 0.069
29
P HYD006 Hydrocephalus 68 0.069
30
P SLP006 Sleep Apnea 65 0.069
31
P MCH002 Machado-Joseph Disease 63 0.069
32
c MNN047 Mannosidosis, Alpha B, Lysosomal 63 0.069
33
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.069
34
STT001 Status Epilepticus 60 0.069
35
P LTR001 Lateral Sclerosis 58 0.069
36
DBF001 D-Bifunctional Protein Deficiency 57 0.069
37
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 57 0.069
38
FCL014 Focal Epilepsy 56 0.069
39
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 54 0.069
40
TMP001 Temporal Lobe Epilepsy 54 0.069
41
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.069
42
PPL048 Papillorenal Syndrome 53 0.069
43
OCL006 Ocular Hypertension 51 0.069
44
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.069
45
c SPN296 Spinocerebellar Ataxia 17 46 0.069
46
c L2H001 L-2-Hydroxyglutaric Aciduria 43 0.069
47
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 42 0.069
48
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 42 0.069
49
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 40 0.069
50
P GLT035 Glutaric Acidemia I 40 0.069
51
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 32 0.069
52
c LSS037 Lissencephaly, X-Linked, 2 31 0.069
53
c PRK093 Parkinson Disease 8, Autosomal Dominant 30 0.069
54
c PNT043 Pontocerebellar Hypoplasia, Type 4 29 0.069
55
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 29 0.069
56
LGH003 Leigh Syndrome, French Canadian Type 28 0.069
57
c PNT044 Pontocerebellar Hypoplasia, Type 2a 28 0.069
58
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 24 0.069
59
NRP009 Neuropathy, Hereditary Motor and Sensory, Okinawa Type 24 0.069
60
ADD006 Adducted Thumbs Syndrome 23 0.069
61
ENC047 Encephalopathy, Progressive, Early-Onset, with Brain Atrophy and Thin Corpus Callosum 23 0.069
62
MLY009 Molybdenum Cofactor Deficiency, Complementation Group B 22 0.069
63
CMB064 Combined Oxidative Phosphorylation Deficiency 24 21 0.069
64
CMB044 Combined Oxidative Phosphorylation Deficiency 14 21 0.069
65
c MNT305 Mental Retardation, X-Linked 12 20 0.069
66
c SPR049 Supranuclear Palsy, Progressive, 2 19 0.069
67
SKL027 Skeletal Dysplasia and Progressive Central Nervous System Degeneration, Lethal 17 0.069
68
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 16 0.069
69
SPN409 Spongiform Encephalopathy with Neuropsychiatric Features 16 0.069
70
CHR152 Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism 13 0.069
71
DMN041 Dementia/parkinsonism with Non-Alzheimer Amyloid Plaques 10 0.069
72
VNH007 Von Hippel-Lindau Syndrome 72 0.049
73
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.049
74
HMN044 Human Immunodeficiency Virus Type 1 71 0.049
75
P AMY004 Amyloidosis 69 0.049
76
c HRD010 Hereditary Spastic Paraplegia 68 0.049
77
P MCL013 Mucolipidosis Iv 67 0.049
78
SPN186 Spinal Cord Injury 67 0.049
79
SND001 Sandhoff Disease 65 0.049
80
TTN003 Tetanus 65 0.049
81
CRT072 Creutzfeldt-Jakob Disease 65 0.049
82
P NRC002 Narcolepsy 64 0.049
83
RBS001 Rabies 63 0.049
84
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.049
85
P PLC011 Pilocytic Astrocytoma 63 0.049
86
P HYP086 Hypothyroidism 62 0.049
87
P RHN004 Rhinitis 62 0.049
88
HYP266 Hypoxia 61 0.049
89
SDD001 Sudden Infant Death Syndrome 61 0.049
90
P ENC018 Encephalopathy 58 0.049
91
CRB172 Cerebral Amyloid Angiopathy, Cst3-Related 58 0.049
92
ALX003 Alexander Disease 58 0.049
93
P ZLL001 Zellweger Syndrome 56 0.049
94
P RTN016 Retinal Degeneration 56 0.049
95
LKN001 Leukoencephalopathy with Vanishing White Matter 56 0.049
96
BRN071 Brain Injury 54 0.049
97
TRM010 Traumatic Brain Injury 54 0.049
98
OVR063 Overnutrition 53 0.049
99
GLM004 Gliomatosis Cerebri 53 0.049
100
PRP016 Paraplegia 53 0.049
101
MSC077 Muscle Eye Brain Disease 51 0.049
102
CRN027 Corneal Neovascularization 51 0.049
103
EXP004 Exophthalmos 50 0.049
104
RTN003 Retinal Ischemia 50 0.049
105
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.049
106
CRB004 Cerebral Artery Occlusion 46 0.049
107
END072 Endotheliitis 46 0.049
108
PNN005 Panencephalitis, Subacute Sclerosing 44 0.049
109
MCL003 Macular Holes 44 0.049
110
CTS003 Coats Disease 42 0.049
111
LKD025 Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant 42 0.049
112
SPS057 Spasticity 41 0.049
113
SBP002 Subependymal Glioma 41 0.049
114
SPR066 Superficial Siderosis 40 0.049
115
CNG436 Congenital Disorder of Deglycosylation 40 0.049
116
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 40 0.049
117
WLL004 Wallerian Degeneration 40 0.049
118
SCR011 Scrapie 40 0.049
119
VTR003 Vitreous Detachment 40 0.049
120
DYS064 Dystonia 3, Torsion, X-Linked 39 0.049
121
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.049
122
P CMM008 Communicating Hydrocephalus 35 0.049
123
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.049
124
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 32 0.049
125
c SPN200 Spinocerebellar Ataxia, Autosomal Recessive 2 31 0.049
126
c PRK085 Parkinson Disease 1, Autosomal Dominant 31 0.049
127
NNT021 Neonatal Meningitis 26 0.049
128
c OTF003 Otofaciocervical Syndrome 2 24 0.049
129
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 24 0.049
130
ISC009 Ischemic Retinopathy 23 0.049
131
RDN004 Radin Blood Group Antigen 23 0.049
132
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 22 0.049
133
c FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 21 0.049
134
c CTS043 Cutis Laxa, Autosomal Recessive, Type Iid 20 0.049
135
c VTR009 Vitreoretinochoroidopathy Dominant 17 0.049
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