Blepharitis
Symptom Information:
Symptom ID: | HPO:0000498 | ||||||||||||||||
Synonyms: |
|
||||||||||||||||
Quality: | |||||||||||||||||
Cross references: |
|
||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||
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) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Blepharitis(HPO:0000498) Abnormality of the periorbital region(HPO:0000606) 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) |