Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8d96482be1e35d10b007f9d7fbf422f1> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B8d96482be1e35d10b007f9d7fbf422f1 hasDbXref "Orphanet:633" @default.
- B8d96482be1e35d10b007f9d7fbf422f1 type Axiom @default.
- B8d96482be1e35d10b007f9d7fbf422f1 annotatedProperty IAO_0000115 @default.
- B8d96482be1e35d10b007f9d7fbf422f1 annotatedSource MONDO_0009877 @default.
- B8d96482be1e35d10b007f9d7fbf422f1 annotatedTarget "Laron syndrome is a congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration." @default.