Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B9570fffb36f2d0e4e9e5c339e1a24a30> ?p ?o ?g. }
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- B9570fffb36f2d0e4e9e5c339e1a24a30 hasDbXref "Orphanet:902" @default.
- B9570fffb36f2d0e4e9e5c339e1a24a30 type Axiom @default.
- B9570fffb36f2d0e4e9e5c339e1a24a30 annotatedProperty IAO_0000115 @default.
- B9570fffb36f2d0e4e9e5c339e1a24a30 annotatedSource MONDO_0010196 @default.
- B9570fffb36f2d0e4e9e5c339e1a24a30 annotatedTarget "A rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders." @default.