Keratoconjunctivitis sicca
Symptom Information:
Symptom ID: | HPO:0001097 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Conjunctivitis(HPO:0000509) Keratoconjunctivitis(HPO:0001096) Keratoconjunctivitis sicca(HPO:0001097) Keratitis(HPO:0000491) Keratoconjunctivitis(HPO:0001096) Keratoconjunctivitis sicca(HPO:0001097) MedDRA: Eye disorders(MedDRA:10015919) Eye disorders NEC(MedDRA:10015917) Lacrimation disorders(MedDRA:10072989) Keratoconjunctivitis sicca(HPO:0001097) Metabolism and nutrition disorders(MedDRA:10027433) Vitamin related disorders(MedDRA:10047635) Fat soluble vitamin deficiencies and disorders(MedDRA:10016250) Keratoconjunctivitis sicca(HPO:0001097) |
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Database Frequency: | 25 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Adiposis dolorosa | (Orphanet:36397) |
Aniridia | (Orphanet:77) |
Antisynthetase syndrome | (Orphanet:81) |
Behçet disease | (Orphanet:117) |
Central bilateral macrogyria | (Orphanet:2431) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Ectodermal dysplasia - blindness | (Orphanet:1806) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
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) |