MeSH Browser

MeSH Supplementary: Epiblepharon of Upper Lid
Unique ID: C565051
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565051
Entry Term(s): Epiblepharon of Lower Lid
Registry Number: 0
Heading Mapped to: Eyelid Diseases / *congenital; Eyelids / *abnormalities
Frequency: 30
Note: A congenital, autosomal dominant eyelid abnormality that occurs mostly in Chinese populations. It is characterized by a horizontal fold of skin that stretches across the border of the eyelid, pressing the lashes against the eyeball. OMIM: 131450
Date of Entry: 2012/11/05
Revision Date: 2015/09/26

Epiblepharon of Upper Lid MeSH Supplementary Concept Data 2024