Keratitis

Symptom Information:

Symptom ID: HPO:0000491
Synonyms:
Keratitis (disorder) [Orphanet:4580]
Keratitis [Orphanet:4580]
Keratitis [OMIM:Keratitis]
Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis [Orphanet:4580]
Keratitis [MedDRA:10023332]
Certain types of keratoconjunctivitis [MedDRA:10023332]
Corneal inflammation [MedDRA:10023332]
Exposure keratoconjunctivitis [MedDRA:10023332]
Filamentary keratitis [MedDRA:10023332]
Inflammation corneal [MedDRA:10023332]
Keratitis NOS [MedDRA:10023332]
Keratitis or keratoconjunctivitis in exanthema [MedDRA:10023332]
Keratitis striate [MedDRA:10023332]
Keratitis superficial [MedDRA:10023332]
Keratitis vascular [MedDRA:10023332]
Keratitis vesicular [MedDRA:10023332]
Keratitis, unspecified [MedDRA:10023332]
Keratoconjunctivitis [MedDRA:10023332]
Keratoconjunctivitis, unspecified [MedDRA:10023332]
Limbar and corneal involvement in vernal conjunctivitis [MedDRA:10023332]
Macular keratitis [MedDRA:10023332]
Marginal keratitis [MedDRA:10023332]
Other and unspecified keratoconjunctivitis [MedDRA:10023332]
Other forms of keratitis [MedDRA:10023332]
Other keratoconjunctivitis [MedDRA:10023332]
Other superficial keratitis without conjunctivitis [MedDRA:10023332]
Phlyctenular keratoconjunctivitis [MedDRA:10023332]
Superficial keratitis without conjunctivitis [MedDRA:10023332]
Superficial keratitis, unspecified [MedDRA:10023332]
Unspecified keratitis [MedDRA:10023332]
Descemetitis [MedDRA:10023332]
Sclerokeratitis [MedDRA:10023332]
Quality:
Cross references:
Orphanet:4580 "Chronic uveitis/blepharitis/episcleritis/scleritis/conjonctivitis/keratitis" [Orphanet:4580]
OMIM: "Keratitis" [OMIM:Keratitis]
UMLS:C0022568 "Keratitis" [HPO:0000491]
UMLS:C0022568 "Keratitis" [Orphanet:4580]
Is a (Direct Parents):
HPO         Abnormality of corneal epithelium
MedDRA Corneal infections, oedemas and inflammations
Orphanet Abnormality of the eye
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 morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the cornea(HPO:0000481)
                      Abnormality of corneal epithelium(HPO:0011495)
                         Keratitis(HPO:0000491)
          Abnormal eye physiology(HPO:0012373)
             Inflammatory abnormality of the eye(HPO:0100533)
                Keratitis(HPO:0000491)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular infections, irritations and inflammations(MedDRA:10021877)
       Corneal infections, oedemas and inflammations(MedDRA:10011021)
          Keratitis(HPO:0000491)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant keratitis (Orphanet:2334)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Incontinentia pigmenti (Orphanet:464)
KERATITIS FUGAX HEREDITARIA (OMIM:148200)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Posterior polymorphous corneal dystrophy (Orphanet:98973)
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)