Conjunctivitis

Symptom Information:

Symptom ID: HPO:0000509
Synonyms:
CONJUNCTIVITIS, RECURRENT [HPO:0000509]
Conjunctivitis (disorder) [Orphanet:4580]
Conjunctivitis [Orphanet:4580]
Conjunctivitis [OMIM:Conjunctivitis]
Conjunctivitis, recurrent [OMIM:Conjunctivitis, recurrent]
Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis [Orphanet:4580]
Conjunctivitis [MedDRA:10010741]
Acute conjunctivitis [MedDRA:10010741]
Acute conjunctivitis, unspecified [MedDRA:10010741]
Acute follicular conjunctivitis [MedDRA:10010741]
Angular blepharoconjunctivitis [MedDRA:10010741]
Blepharo conjunctivitis [MedDRA:10010741]
Blepharoconjunctivitis [MedDRA:10010741]
Blepharoconjunctivitis, unspecified [MedDRA:10010741]
Chronic conjunctivitis [MedDRA:10010741]
Chronic conjunctivitis, unspecified [MedDRA:10010741]
Chronic follicular conjunctivitis [MedDRA:10010741]
Conjunctivitis aggravated [MedDRA:10010741]
Conjunctivitis chronic [MedDRA:10010741]
Conjunctivitis exacerbated [MedDRA:10010741]
Conjunctivitis in mucocutaneous disease [MedDRA:10010741]
Conjunctivitis NOS [MedDRA:10010741]
Conjunctivitis necrotic [MedDRA:10010741]
Conjunctivitis papillary [MedDRA:10010741]
Conjunctivitis, unspecified [MedDRA:10010741]
Discharge conjunctivitis [MedDRA:10010741]
Florid follicular conjunctivitis [MedDRA:10010741]
Other and unspecified conjunctivitis [MedDRA:10010741]
Other conjunctivitis [MedDRA:10010741]
Pseudomembranous conjunctivitis [MedDRA:10010741]
Rhinoconjunctivitis [MedDRA:10010741]
Serous conjunctivitis, except viral [MedDRA:10010741]
Simple chronic conjunctivitis [MedDRA:10010741]
Conjunctival discharge [MedDRA:10010741]
Follicular conjunctivitis [MedDRA:10010741]
Serous conjunctivitis, excl viral [MedDRA:10010741]
Toxic conjunctivitis [MedDRA:10010741]
Conjunctivitis (recurrent) [OMIM:Conjunctivitis (recurrent)]
Quality:
Cross references:
Orphanet:4580 "Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis" [Orphanet:4580]
OMIM: "Conjunctivitis" [OMIM:Conjunctivitis]
OMIM: "Conjunctivitis, recurrent" [OMIM:Conjunctivitis, recurrent]
OMIM: "Conjunctivitis (recurrent)" [OMIM:Conjunctivitis (recurrent)]
UMLS:C0009763 "Conjunctivitis" [HPO:0000509]
UMLS:C0009763 "Conjunctivitis" [Orphanet:4580]
Is a (Direct Parents):
MedDRA Conjunctival infections, irritations and inflammations
Orphanet Keratitis
Orphanet Abnormality of the eye
HPO         Abnormality of the conjunctiva
HPO         Inflammatory 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)
                Conjunctivitis(HPO:0000509)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the conjunctiva(HPO:0000502)
                Conjunctivitis(HPO:0000509)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular infections, irritations and inflammations(MedDRA:10021877)
       Conjunctival infections, irritations and inflammations(MedDRA:10010722)
          Conjunctivitis(HPO:0000509)
Database Frequency: 47 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE (OMIM:601495)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Autosomal agammaglobulinemia (Orphanet:33110)
Biotinidase deficiency (Orphanet:79241)
CANDLE syndrome (Orphanet:325004)
Congenital erythropoietic porphyria (Orphanet:79277)
Crouzon disease (Orphanet:207)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
DERMATITIS, ATOPIC (OMIM:603165)
Familial cold urticaria (Orphanet:47045)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hypoplasminogenemia (Orphanet:722)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
IMMUNODEFICIENCY, COMMON VARIABLE, 1 (OMIM:607594)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNODEFICIENCY, COMMON VARIABLE, 3 (OMIM:613493)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
JMP syndrome (Orphanet:324999)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
Kawasaki disease (Orphanet:2331)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
LACRIMAL DUCT DEFECT (OMIM:149700)
Lymphedema - distichiasis (Orphanet:33001)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Muckle-Wells syndrome (Orphanet:575)
Nakajo-Nishimura syndrome (Orphanet:2615)
Normocalcemic tumoral calcinosis (Orphanet:306658)
Poikiloderma with neutropenia (Orphanet:221046)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Proteasome disability syndrome (Orphanet:324977)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Severe combined immunodeficiency due to complete RAG1/2 deficiency (Orphanet:331206)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Transketolase deficiency (ORPHA:488618)
Tyrosinemia type 2 (Orphanet:28378)
Xeroderma pigmentosum complementation group A (Orphanet:276249)
Xeroderma pigmentosum complementation group C (Orphanet:276255)
Xeroderma pigmentosum complementation group D (Orphanet:276258)
Xeroderma pigmentosum complementation group E (Orphanet:276261)
Xeroderma pigmentosum variant (Orphanet:90342)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)