Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B69668d0fee2f795639b68aaa48e9bb09> ?p ?o ?g. }
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- B69668d0fee2f795639b68aaa48e9bb09 hasDbXref "Orphanet:650" @default.
- B69668d0fee2f795639b68aaa48e9bb09 type Axiom @default.
- B69668d0fee2f795639b68aaa48e9bb09 annotatedProperty IAO_0000115 @default.
- B69668d0fee2f795639b68aaa48e9bb09 annotatedSource MONDO_0018999 @default.
- B69668d0fee2f795639b68aaa48e9bb09 annotatedTarget "LCAT (lecithin-cholesterol acyltransferase) deficiency is a rare lipoprotein metabolism disorder characterized clinically by corneal opacities, and sometimes renal failure and hemolytic anemia, and biochemically by severely reduced HDL cholesterol." @default.