Search results for "gliosis"

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

125 hits were found for 'gliosis'

# Family MCID Name MIFTS Score
1
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 30 4.755
2
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 15 3.860
3
P LGH007 Leigh Syndrome 66 0.087
4
P HPT021 Hepatitis 63 0.087
5
PRS047 Prostatitis 53 0.087
6
END072 Endotheliitis 41 0.087
7
P PRS040 Prostate Cancer 87 0.071
8
CYS001 Cystic Fibrosis 84 0.071
9
HV1006 Hiv-1 78 0.071
10
P OVR042 Ovarian Cancer 69 0.071
11
TBR010 Tuberculosis 65 0.071
12
PCK002 Pick Disease 58 0.071
13
P SPR098 Supranuclear Palsy, Progressive 50 0.071
14
GLT021 Glutaricaciduria, Type I 37 0.071
15
NRN002 Neuronitis 36 0.071
16
c PNT013 Pontocerebellar Hypoplasia Type 4 30 0.071
17
c FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 25 0.071
18
c PNT017 Pontocerebellar Hypoplasia Type 1a 24 0.071
19
c HNT010 Huntington Disease-Like 1 21 0.071
20
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 16 0.071
21
P BRS047 Breast Cancer 100 0.050
22
P CLR023 Colorectal Cancer 91 0.050
23
P OBS005 Obesity 87 0.050
24
P RHM011 Rheumatoid Arthritis 87 0.050
25
P PNC035 Pancreatic Cancer 82 0.050
26
P AST005 Asthma 77 0.050
27
P OST012 Osteoarthritis 72 0.050
28
P NRB001 Neuroblastoma 69 0.050
29
P PRK057 Parkinson Disease, Late-Onset 69 0.050
30
P HMC003 Hemochromatosis 69 0.050
31
P HNT016 Huntington Disease 67 0.050
32
INS024 Insulin-Like Growth Factor I 67 0.050
33
P ART022 Arthritis 63 0.050
34
SRC014 Sarcoma 61 0.050
35
ART016 Aortic Aneurysm 60 0.050
36
P CRT072 Creutzfeldt-Jakob Disease 60 0.050
37
c ATM003 Autoimmune Thyroiditis 59 0.050
38
P CHR071 Charcot-Marie-Tooth Disease 58 0.050
39
P ASP006 Aspergillosis 58 0.050
40
P HYP117 Hypertriglyceridemia 58 0.050
41
P MCH002 Machado-Joseph Disease 58 0.050
42
P LYM118 Lymphoma 57 0.050
43
P HMN010 Hemangioma 57 0.050
44
c HPT016 Hepatitis B 57 0.050
45
LBR002 Leber Hereditary Optic Neuropathy 56 0.050
46
P GLB002 Glioblastoma 56 0.050
47
P RSP003 Respiratory Failure 55 0.050
48
P MYP004 Myopathy 54 0.050
49
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 54 0.050
50
P CNG018 Congenital Heart Block 53 0.050
51
SPT005 Spotted Fever 53 0.050
52
P PNC044 Pancreatitis 53 0.050
53
CRV038 Cervical Squamous Cell Carcinoma 52 0.050
54
P FBR017 Fibrosarcoma 51 0.050
55
P GLT023 Glutaric Acidemia Iic 51 0.050
56
HPT019 Hepatic Encephalopathy 51 0.050
57
ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.050
58
P LRY019 Laryngitis 50 0.050
59
P LRY016 Laryngeal Carcinoma 50 0.050
60
P THY032 Thyroiditis 49 0.050
61
DBT087 Diabetes Insipidus, Neurohypophyseal 49 0.050
62
P SYN001 Syndactyly 48 0.050
63
CNN005 Connective Tissue Disease 48 0.050
64
CHC001 Chickenpox 48 0.050
65
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 47 0.050
66
P NRP001 Neuropathy 47 0.050
67
NSH001 Nasu-Hakola Disease 47 0.050
68
DBF001 D-Bifunctional Protein Deficiency 47 0.050
69
c HPT007 Hepatitis E 46 0.050
70
c PRK024 Parkinson Disease, Juvenile, Type 2 46 0.050
71
GST045 Gastroenteritis 46 0.050
72
ANR040 Aneurysm 46 0.050
73
P GLM045 Glioma 46 0.050
74
HYP266 Hypoxia 46 0.050
75
MTC056 Mitochondrial Dna Depletion Syndrome 4a 45 0.050
76
WST005 West Nile Virus 45 0.050
77
CHL068 Cholestasis 45 0.050
78
CLF001 Cleft Lip 44 0.050
79
c CLR017 Clear Cell Sarcoma 44 0.050
80
P ENC018 Encephalopathy 43 0.050
81
c PRK059 Parkinson Disease 8 43 0.050
82
TTH006 Tooth Disease 43 0.050
83
c L2H001 L-2-Hydroxyglutaric Aciduria 43 0.050
84
RFT001 Rift Valley Fever 43 0.050
85
c SPN296 Spinocerebellar Ataxia 17 41 0.050
86
P CRV039 Cervicitis 41 0.050
87
LYM012 Lymphoplasmacytic Lymphoma 41 0.050
88
SDD007 Sudden Cardiac Death 39 0.050
89
c INF069 Infantile Neuroaxonal Dystrophy 1 39 0.050
90
c FRN043 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 3 39 0.050
91
PPL048 Papillorenal Syndrome 38 0.050
92
CSL001 Causalgia 38 0.050
93
P SYR001 Syringomyelia 38 0.050
94
c CRB101 Cerebrooculofacioskeletal Syndrome 1 36 0.050
95
INT013 Intramuscular Hemangioma 36 0.050
96
ANT039 Antisynthetase Syndrome 35 0.050
97
ABD004 Abdominal Tuberculosis 34 0.050
98
FBR019 Fibromatosis 33 0.050
99
EXT006 Extrahepatic Cholestasis 33 0.050
100
ACQ017 Acquired Von Willebrand Syndrome 32 0.050
101
P DCR004 Dacryocystitis 32 0.050
102
c PNT022 Pontocerebellar Hypoplasia Type 2a 31 0.050
103
c CNG023 Congenital Fibrosarcoma 31 0.050
104
ENC039 Encephalopathy, Familial, with Neuroserpin Inclusion Bodies 30 0.050
105
GRC002 Gracile Bone Dysplasia 28 0.050
106
SPR066 Superficial Siderosis 28 0.050
107
DYS171 Dystonia-Parkinsonism, X-Linked 28 0.050
108
MLY006 Molybdenum Cofactor Deficiency a 27 0.050
109
c LKD007 Leukodystrophy, Adult-Onset, Autosomal Dominant 26 0.050
110
c FRN045 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4 26 0.050
111
LGH016 Leigh Syndrome, French-Canadian Type 25 0.050
112
c SPS103 Spastic Paraplegia 50, Autosomal Recessive 24 0.050
113
NRS005 Neurosarcoidosis 23 0.050
114
P FRN040 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2 22 0.050
115
CMB044 Combined Oxidative Phosphorylation Deficiency 14 22 0.050
116
c MCR223 Microcephaly 10, Primary, Autosomal Recessive 21 0.050
117
c EPL097 Epileptic Encephalopathy, Early Infantile, 14 21 0.050
118
c LSS012 Lissencephaly, X-Linked 2 21 0.050
119
HRD162 Hereditary Motor and Sensory Neuropathy, Okinawa Type 20 0.050
120
MLY005 Molybdenum Cofactor Deficiency B 19 0.050
121
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 19 0.050
122
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 18 0.050
123
PRN028 Prion Disease with Protracted Course 15 0.050
124
c SPR049 Supranuclear Palsy, Progressive, 2 14 0.050
125
CLS006 Clasped Thumbs, Congenital 8 0.050