Encephalitis
Symptom Information:
Symptom ID: | HPO:0002383 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |