Blepharitis

Symptom Information:

Symptom ID: HPO:0000498
Synonyms:
Blepharitis (disorder) [Orphanet:7500]
blepharitis [HPO:0000498]
Blepharitis [Orphanet:7500]
Blepharitis [OMIM:Blepharitis]
Blepharitis/eyelid inflammation [Orphanet:7500]
Blepharitis [MedDRA:10005148]
Blepharitis, unspecified [MedDRA:10005148]
Contact and allergic dermatitis of eyelid [MedDRA:10005148]
Dermatitis eyelid [MedDRA:10005148]
Inflammation of eyelids [MedDRA:10005148]
Noninfectious dermatoses of eyelid [MedDRA:10005148]
Other inflammations of eyelids [MedDRA:10005148]
Squamous blepharitis [MedDRA:10005148]
Ulcerative blepharitis [MedDRA:10005148]
Unspecified inflammation of eyelid [MedDRA:10005148]
Marginal blepharitis [MedDRA:10005148]
Quality:
Cross references:
Orphanet:7500 "Blepharitis/eyelid inflammation" [Orphanet:7500]
OMIM: "Blepharitis" [OMIM:Blepharitis]
UMLS:C2230188 "blepharitis" [HPO:0000498]
UMLS:C0005741 "Blepharitis" [Orphanet:7500]
Is a (Direct Parents):
MedDRA Lid, lash and lacrimal infections, irritations and inflammations
HPO         Inflammatory abnormality of the eye
HPO         Abnormality of the eyelid
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)
                Blepharitis(HPO:0000498)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Blepharitis(HPO:0000498)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Blepharitis(HPO:0000498)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular infections, irritations and inflammations(MedDRA:10021877)
       Lid, lash and lacrimal infections, irritations and inflammations(MedDRA:10024445)
          Blepharitis(HPO:0000498)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CANDIDIASIS, FAMILIAL, 8 (OMIM:615527)
Coffin-Lowry syndrome (Orphanet:192)
Cornelia de Lange syndrome (Orphanet:199)
Dystrophic epidermolysis bullosa (Orphanet:303)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hurler-Scheie syndrome (Orphanet:93476)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Leukonychia totalis (Orphanet:2387)
Moebius syndrome (Orphanet:570)
Neonatal inflammatory skin and bowel disease (Orphanet:294023)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Poikiloderma with neutropenia (Orphanet:221046)
Sea-blue histiocytosis (Orphanet:158029)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Xeroderma pigmentosum (Orphanet:910)