Keratoconjunctivitis

Symptom Information:

Symptom ID: HPO:0001096
Synonyms:
Keratoconjunctivitis [OMIM:Keratoconjunctivitis]
Quality:
Cross references:
OMIM: "Keratoconjunctivitis" [OMIM:Keratoconjunctivitis]
UMLS:C0022573 "Keratoconjunctivitis" [HPO:0001096]
Is a (Direct Parents):
HPO         Keratitis
HPO         Conjunctivitis
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)
                   Keratoconjunctivitis(HPO:0001096)
                Keratitis(HPO:0000491)
                   Keratoconjunctivitis(HPO:0001096)
          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)
                            Keratoconjunctivitis(HPO:0001096)
             Abnormality of the conjunctiva(HPO:0000502)
                Conjunctivitis(HPO:0000509)
                   Keratoconjunctivitis(HPO:0001096)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Hereditary mucoepithelial dysplasia (Orphanet:1839)