Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B777b590f4971ed2536f2100f629320b3> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B777b590f4971ed2536f2100f629320b3 NCIT_P378 "ACC/AHA" @default.
- B777b590f4971ed2536f2100f629320b3 type Axiom @default.
- B777b590f4971ed2536f2100f629320b3 annotatedProperty NCIT_P325 @default.
- B777b590f4971ed2536f2100f629320b3 annotatedSource NCIT_C34807 @default.
- B777b590f4971ed2536f2100f629320b3 annotatedTarget "A genetic syndrome inherited as an autosomal dominant trait. It is caused by mutations in the FBN1 gene. It is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens. Diagnosis is made based on the 2010 Revised Ghent Nosology for Marfan syndrome." @default.