Keratoconjunctivitis sicca

Symptom Information:

Symptom ID: HPO:0001097
Synonyms:
Dry eye syndrome [HPO:0001097]
Keratitis sicca [HPO:0001097]
Xerophthalmia [HPO:0001097]
Xerophthalmia [Orphanet:4620]
Conjunctival xerosis (disorder) [Orphanet:4620]
Xerophthalmia (disorder) [Orphanet:4620]
Dry eyes (finding) [Orphanet:4620]
Tear film insufficiency (disorder) [Orphanet:4620]
Keratoconjunctivitis sicca (disorder) [Orphanet:4620]
Dry eye (finding) [Orphanet:4620]
Dry Eye Syndromes [Orphanet:4620]
Dryness of eye [Orphanet:4620]
Keratoconjunctivitis Sicca [Orphanet:4620]
Keratoconjunctivitis sicca [OMIM:Keratoconjunctivitis sicca]
Xerophthalmia [OMIM:Xerophthalmia]
Xerophthalmia/dry eyes [Orphanet:4620]
Keratoconjunctivitis sicca [Orphanet:4620]
Tear film insufficiency, unspecified [Orphanet:4620]
Dry eye [Orphanet:4620]
Dry eye syndrome [Orphanet:4620]
Xerophthalmia [MedDRA:10048221]
Dry eye [MedDRA:10013774]
Conjunctival xerosis [MedDRA:10013774]
Dry eye NOS [MedDRA:10013774]
Dry eye syndrome [MedDRA:10013774]
Dry eyes [MedDRA:10013774]
Dryness of eyes [MedDRA:10013774]
Dryness under lids [MedDRA:10013774]
Eye dryness [MedDRA:10013774]
Eyes dry [MedDRA:10013774]
Keratoconjunctivitis sicca [MedDRA:10013774]
Keratoconjunctivitis sicca, not specified as Sjogren's [MedDRA:10013774]
Dry eyes aggravated [MedDRA:10013774]
Keratitis sicca [MedDRA:10013774]
Corneal xerosis [MedDRA:10013774]
Lacrimation decreased [MedDRA:10023642]
Lacrimation reduced [MedDRA:10023642]
Reduced lacrimal gland secretion [MedDRA:10023642]
Reduced tear production [MedDRA:10023642]
Tear film insufficiency, unspecified [MedDRA:10023642]
Tearing decreased [MedDRA:10023642]
Decreased tearing [OMIM:Decreased tearing]
Dry eyes [OMIM:Dry eyes]
Quality:
Cross references:
Orphanet:4620 "Xerophthalmia/dry eyes" [Orphanet:4620]
OMIM: "Keratoconjunctivitis sicca" [OMIM:Keratoconjunctivitis sicca]
OMIM: "Xerophthalmia" [OMIM:Xerophthalmia]
OMIM: "Decreased tearing" [OMIM:Decreased tearing]
OMIM: "Dry eyes" [OMIM:Dry eyes]
UMLS:C0043349 "Xerophthalmia" [Orphanet:4620]
UMLS:C0013238 "Dry Eye Syndromes" [Orphanet:4620]
UMLS:C0314719 "Dryness of eye" [Orphanet:4620]
UMLS:C0022575 "Keratoconjunctivitis Sicca" [Orphanet:4620]
Is a (Direct Parents):
HPO         Keratoconjunctivitis
MedDRA Fat soluble vitamin deficiencies and disorders
MedDRA Lacrimation disorders
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 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)
                               Keratoconjunctivitis sicca(HPO:0001097)
             Abnormality of the conjunctiva(HPO:0000502)
                Conjunctivitis(HPO:0000509)
                   Keratoconjunctivitis(HPO:0001096)
                      Keratoconjunctivitis sicca(HPO:0001097)
          Abnormal eye physiology(HPO:0012373)
             Inflammatory abnormality of the eye(HPO:0100533)
                Keratitis(HPO:0000491)
                   Keratoconjunctivitis(HPO:0001096)
                      Keratoconjunctivitis sicca(HPO:0001097)
                Conjunctivitis(HPO:0000509)
                   Keratoconjunctivitis(HPO:0001096)
                      Keratoconjunctivitis sicca(HPO:0001097)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Fat soluble vitamin deficiencies and disorders(MedDRA:10016250)
          Keratoconjunctivitis sicca(HPO:0001097)
Eye disorders(MedDRA:10015919)
    Eye disorders NEC(MedDRA:10015917)
       Lacrimation disorders(MedDRA:10072989)
          Keratoconjunctivitis sicca(HPO:0001097)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

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Beh├žet disease (Orphanet:117)
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Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia syndrome (Orphanet:79373)
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Familial esophageal achalasia (Orphanet:99723)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
Idiopathic achalasia (Orphanet:930)
Infant botulism (Orphanet:178478)
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT (OMIM:148210)
KID syndrome (Orphanet:477)
Limited systemic sclerosis (Orphanet:220407)
Mixed connective tissue disease (Orphanet:809)
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX (OMIM:260480)
Primary erythermalgia (Orphanet:90026)
Reynolds syndrome (Orphanet:779)
SJOGREN SYNDROME (OMIM:270150)
Sodium channelopathy-related small fiber neuropathy (Orphanet:306577)
TENORIO SYNDROME (OMIM:616260)
Thymoma (Orphanet:99867)