Gliosis

Symptom Information:

Symptom ID: HPO:0002171
Synonyms:
Cerebral gliosis [HPO:0002171]
Cerebral gliosis [OMIM:Cerebral gliosis]
Gliosis [OMIM:Gliosis]
Gliosis (27%) [OMIM:Gliosis (27%)]
Gliosis [MedDRA:10018341]
Quality:
Cross references:
OMIM: "Cerebral gliosis" [OMIM:Cerebral gliosis]
OMIM: "Gliosis" [OMIM:Gliosis]
OMIM: "Gliosis (27%)" [OMIM:Gliosis (27%)]
UMLS:C0017639 "Gliosis" [HPO:0002171]
Is a (Direct Parents):
HPO         Cerebellar gliosis
HPO         Abnormality of the glial cells
MedDRA Central nervous system inflammatory disorders NEC
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)
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)