Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4b39e5417dd1c6b511f323b587aa3882> ?p ?o ?g. }
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- B4b39e5417dd1c6b511f323b587aa3882 hasDbXref "Orphanet:519386" @default.
- B4b39e5417dd1c6b511f323b587aa3882 type Axiom @default.
- B4b39e5417dd1c6b511f323b587aa3882 annotatedProperty IAO_0000115 @default.
- B4b39e5417dd1c6b511f323b587aa3882 annotatedSource MONDO_0034971 @default.
- B4b39e5417dd1c6b511f323b587aa3882 annotatedTarget "A rare eyelid malposition disorder characterized by congenital abnormal inversion of the eyelid towards the globe, potentially causing mechanical irritation of the ocular surface by the eyelashes, which may lead to corneal abrasion and scarring with visual impairment. Typical initial symptoms are foreign body sensation, redness, tearing, and ocular discharge." @default.