Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B9dd0bd2af629ad674183294f704f5cc1> ?p ?o ?g. }
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- B9dd0bd2af629ad674183294f704f5cc1 hasDbXref "Orphanet:649" @default.
- B9dd0bd2af629ad674183294f704f5cc1 type Axiom @default.
- B9dd0bd2af629ad674183294f704f5cc1 annotatedProperty IAO_0000115 @default.
- B9dd0bd2af629ad674183294f704f5cc1 annotatedSource MONDO_0010691 @default.
- B9dd0bd2af629ad674183294f704f5cc1 annotatedTarget "A rare X-linked genetic vitreoretinal condition characterized by abnormal retinal development with congenital blindness. Common associated manifestations include sensorineural hearing loss and developmental delay, intellectual disability and/or behavioral disorders." @default.