Gliosis
Symptom Information:
Symptom ID: | HPO:0002171 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Central nervous system infections and inflammations(MedDRA:10007951) Central nervous system inflammatory disorders NEC(MedDRA:10007952) Gliosis(HPO:0002171) |
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Database Frequency: | 48 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Alpers syndrome | (Orphanet:726) |
Bifunctional enzyme deficiency | (Orphanet:300) |
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 2 | (OMIM:615119) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
COFS syndrome | (Orphanet:1466) |
Central diabetes insipidus | (Orphanet:178029) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | (OMIM:614959) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105550) |
Familial acute necrotizing encephalopathy | (Orphanet:88619) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Frontotemporal dementia | (Orphanet:282) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
Huntington disease | (Orphanet:399) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
Juvenile Huntington disease | (Orphanet:248111) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
Leigh syndrome | (Orphanet:506) |
Microcephalic primordial dwarfism due to ZNF335 deficiency | (Orphanet:329228) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
Nasu-Hakola disease | (Orphanet:2770) |
Pontocerebellar hypoplasia type 2 | (Orphanet:2524) |
Pontocerebellar hypoplasia type 4 | (Orphanet:166063) |
Progressive non-fluent aphasia | (Orphanet:100070) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
Renal coloboma syndrome | (Orphanet:1475) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE | (OMIM:612936) |
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES | (OMIM:606688) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
[DEL] LEIGH SYNDROME, X-LINKED | (OMIM:308930) |