Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5ccc850b2303fc57d81a1bc0c4653eaa> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5ccc850b2303fc57d81a1bc0c4653eaa hasDbXref "Orphanet:50" @default.
- B5ccc850b2303fc57d81a1bc0c4653eaa type Axiom @default.
- B5ccc850b2303fc57d81a1bc0c4653eaa annotatedProperty IAO_0000115 @default.
- B5ccc850b2303fc57d81a1bc0c4653eaa annotatedSource MONDO_0010568 @default.
- B5ccc850b2303fc57d81a1bc0c4653eaa annotatedTarget "Aicardi syndrome is a rare neurodevelopmental disorder defined by the triad of agenesis of the corpus callosum (total or partial), typical chorioretinal lacunae and infantile spasms that affect almost exclusively females." @default.