Meningitis

Symptom Information:

Symptom ID: HPO:0001287
Synonyms:
Meningitis (disorder) [Orphanet:43160]
Meningitis [Orphanet:43160]
Meningitis [OMIM:Meningitis]
Meningitis/meningeal syndrome [Orphanet:43160]
Meningitis [MedDRA:10027199]
Chronic meningitis [MedDRA:10027199]
Meningitis due to other nonbacterial organisms classified elsewhere [MedDRA:10027199]
Meningitis due to other organisms [MedDRA:10027199]
Meningitis NOS [MedDRA:10027199]
Meningitis of unspecified cause [MedDRA:10027199]
Meningitis, unspecified [MedDRA:10027199]
Infectious meningitis [MedDRA:10027199]
Meningism [MedDRA:10027197]
Meningism (finding) [Orphanet:43160]
Meningeal irritation (disorder) [Orphanet:43160]
Meningism [Orphanet:43160]
Quality:
Cross references:
Orphanet:43160 "Meningitis/meningeal syndrome" [Orphanet:43160]
OMIM: "Meningitis" [OMIM:Meningitis]
UMLS:C0025289 "Meningitis" [HPO:0001287]
UMLS:C0025289 "Meningitis" [Orphanet:43160]
UMLS:C0025287 "Meningism" [Orphanet:43160]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Meningitis 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)
                   Meningitis(HPO:0001287)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Central nervous system infections and inflammations(MedDRA:10007951)
       Meningitis NEC(MedDRA:10027187)
          Meningitis(HPO:0001287)
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE (OMIM:613500)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
Adult Still's disease (Orphanet:829)
Aplasia cutis - myopia (Orphanet:1117)
Arachnoiditis (Orphanet:137817)
Autosomal agammaglobulinemia (Orphanet:33110)
Beh├žet disease (Orphanet:117)
CANDIDIASIS, FAMILIAL, 2 (OMIM:212050)
CINCA syndrome (Orphanet:1451)
COMPLEMENT COMPONENT 4B DEFICIENCY (OMIM:614379)
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I (OMIM:613790)
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II (OMIM:613789)
Chronic granulomatous disease (Orphanet:379)
Cogan syndrome (Orphanet:1467)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
Familial Mediterranean fever (Orphanet:342)
Familial caudal dysgenesis (Orphanet:1768)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Follicular lymphoma (Orphanet:545)
Giant cell arteritis (Orphanet:397)
Granulomatosis with polyangiitis (Orphanet:900)
Griscelli disease type 2 (Orphanet:79477)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNOGLOBULIN M, LEVEL OF (OMIM:308250)
Isolated agammaglobulinemia (Orphanet:229717)
Kawasaki disease (Orphanet:2331)
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 (OMIM:308240)
Lyme disease (Orphanet:91546)
Mixed connective tissue disease (Orphanet:809)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary intestinal lymphangiectasia (Orphanet:90362)
Rift valley fever (Orphanet:319251)
Scrub typhus (Orphanet:83317)
Severe combined immunodeficiency due to complete RAG1/2 deficiency (Orphanet:331206)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
T-B+ severe combined immunodeficiency due to JAK3 deficiency (Orphanet:35078)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wiskott-Aldrich syndrome (Orphanet:906)
Wyburn-Mason syndrome (Orphanet:53719)
X-linked agammaglobulinemia (Orphanet:47)
Yellow fever (Orphanet:99829)