Uveitis

Symptom Information:

Symptom ID: HPO:0000554
Synonyms:
Uveitis (disorder) [Orphanet:4580]
Uveitis [Orphanet:4580]
Uveitis [OMIM:Uveitis]
Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis [Orphanet:4580]
Uveitis [MedDRA:10046851]
Panuveitis [MedDRA:10046851]
Pars planitis [MedDRA:10046851]
Uveitis NOS [MedDRA:10046851]
Granulomatous uveitis [MedDRA:10046851]
Acute uveitis [MedDRA:10046851]
Panuveitis (rare) [OMIM:Panuveitis (rare)]
Quality:
Cross references:
Orphanet:4580 "Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis" [Orphanet:4580]
OMIM: "Uveitis" [OMIM:Uveitis]
OMIM: "Panuveitis (rare)" [OMIM:Panuveitis (rare)]
UMLS:C1963266 "Uveitis" [HPO:0000554]
UMLS:C0042164 "Uveitis" [Orphanet:4580]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Inflammatory abnormality of the eye
MedDRA Autoimmune disorders NEC
Orphanet Keratitis
HPO         Abnormality of the uvea
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Inflammatory abnormality of the eye(HPO:0100533)
                Uveitis(HPO:0000554)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the uvea(HPO:0000553)
                   Uveitis(HPO:0000554)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Autoimmune disorders NEC(MedDRA:10027657)
          Uveitis(HPO:0000554)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant neovascular inflammatory vitreoretinopathy (Orphanet:329211)
Behçet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Congenital blindness due to retinal non-attachment (Orphanet:300337)
Incontinentia pigmenti (Orphanet:464)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
Transketolase deficiency (ORPHA:488618)
Tubulointerstitial nephritis and uveitis syndrome (Orphanet:91500)
Tyrosinemia type 2 (Orphanet:28378)