Encephalitis

Symptom Information:

Symptom ID: HPO:0002383
Synonyms:
Encephalitis (disorder) [Orphanet:43150]
Encephalitis [Orphanet:43150]
Encephalitis [OMIM:Encephalitis]
Encephalitis [MedDRA:10014581]
Encephalitic reaction [MedDRA:10014581]
Encephalitis NOS [MedDRA:10014581]
Encephalitis-like symptom [MedDRA:10014581]
Meningoencephalitis [MedDRA:10014581]
Other causes of encephalitis [MedDRA:10014581]
Unspecified cause of encephalitis [MedDRA:10014581]
Cerebritis [MedDRA:10014581]
Cerebellitis [MedDRA:10014581]
Acute meningoencephalitis [MedDRA:10014581]
Meningoencephalitis [OMIM:Meningoencephalitis]
Quality:
Cross references:
Orphanet:43150 "Encephalitis" [Orphanet:43150]
OMIM: "Encephalitis" [OMIM:Encephalitis]
OMIM: "Meningoencephalitis" [OMIM:Meningoencephalitis]
UMLS:C0014038 "Encephalitis" [HPO:0002383]
UMLS:C0014038 "Encephalitis" [Orphanet:43150]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Encephalitis NEC
HPO         CNS infection
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                CNS infection(HPO:0011450)
                   Encephalitis(HPO:0002383)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Central nervous system infections and inflammations(MedDRA:10007951)
       Encephalitis NEC(MedDRA:10014599)
          Encephalitis(HPO:0002383)
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
Alexander disease (Orphanet:58)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Behçet disease (Orphanet:117)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Cataract - nephropathy - encephalopathy (Orphanet:1380)
Cogan syndrome (Orphanet:1467)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Crigler-Najjar syndrome (Orphanet:205)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
GM1 gangliosidosis (Orphanet:354)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
Hartnup syndrome (Orphanet:2116)
IMMUNODEFICIENCY 37 (OMIM:616098)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Immunoglobulin A vasculitis (Orphanet:761)
Incontinentia pigmenti (Orphanet:464)
L-2-hydroxyglutaric aciduria (Orphanet:79314)
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 (OMIM:308240)
Legionellosis (Orphanet:549)
Lyme disease (Orphanet:91546)
Marshall syndrome with periodic fever (Orphanet:42642)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Neurocutaneous melanocytosis (Orphanet:2481)
Nipah virus disease (Orphanet:99825)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Relapsing polychondritis (Orphanet:728)
Reynolds syndrome (Orphanet:779)
Rift valley fever (Orphanet:319251)
Scrub typhus (Orphanet:83317)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Subacute sclerosing leukoencephalitis (Orphanet:2806)
Typhoid (Orphanet:99745)
Viral hemorrhagic fever (Orphanet:341)
Whipple disease (Orphanet:3452)
Wiskott-Aldrich syndrome (Orphanet:906)
Yellow fever (Orphanet:99829)