Episcleritis

Symptom Information:

Symptom ID: HPO:0100534
Synonyms:
Episcleritis (disorder) [Orphanet:4580]
Episcleritis [Orphanet:4580]
Episcleritis [OMIM:Episcleritis]
Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis [Orphanet:4580]
Episcleritis [MedDRA:10015084]
Episcleritis NOS [MedDRA:10015084]
Episcleritis periodica fugax [MedDRA:10015084]
Nodular episcleritis [MedDRA:10015084]
Quality:
Cross references:
Orphanet:4580 "Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis" [Orphanet:4580]
OMIM: "Episcleritis" [OMIM:Episcleritis]
UMLS:C0014583 "Episcleritis" [Orphanet:4580]
Is a (Direct Parents):
MedDRA Scleral infections, irritations and inflammations
HPO         Abnormality of the sclera
HPO         Inflammatory abnormality of the eye
Orphanet Keratitis
Orphanet Abnormality of the eye
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)
                Episcleritis(HPO:0100534)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the sclera(HPO:0000591)
                   Episcleritis(HPO:0100534)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular infections, irritations and inflammations(MedDRA:10021877)
       Scleral infections, irritations and inflammations(MedDRA:10039700)
          Episcleritis(HPO:0100534)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

CANDLE syndrome (Orphanet:325004)
Faisalabad histiocytosis (Orphanet:254707)
H syndrome (Orphanet:168569)
JMP syndrome (Orphanet:324999)
Nakajo-Nishimura syndrome (Orphanet:2615)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Proteasome disability syndrome (Orphanet:324977)
Rosaï-Dorfman disease (Orphanet:158014)
Tyrosinemia type 2 (Orphanet:28378)