Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B00c9000f8413d2c4d64dde0fc542e70e> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B00c9000f8413d2c4d64dde0fc542e70e hasDbXref "Orphanet:91413" @default.
- B00c9000f8413d2c4d64dde0fc542e70e type Axiom @default.
- B00c9000f8413d2c4d64dde0fc542e70e annotatedProperty IAO_0000115 @default.
- B00c9000f8413d2c4d64dde0fc542e70e annotatedSource MONDO_0007735 @default.
- B00c9000f8413d2c4d64dde0fc542e70e annotatedTarget "Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported." @default.