Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb1df326fb593df6f8010fdfad518c325> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bb1df326fb593df6f8010fdfad518c325 hasDbXref "NCIT:C98905" @default.
- Bb1df326fb593df6f8010fdfad518c325 type Axiom @default.
- Bb1df326fb593df6f8010fdfad518c325 annotatedProperty IAO_0000115 @default.
- Bb1df326fb593df6f8010fdfad518c325 annotatedSource MONDO_0009022 @default.
- Bb1df326fb593df6f8010fdfad518c325 annotatedTarget "A congenital abnormality characterized by the complete absence of the corpus callosum. It may be an isolated abnormality or associated with other central nervous system abnormalities or syndromes. Clinical manifestations vary. In cases of isolated corpus callosum agenesis, symptoms may be absent or minimal. In cases that are associated with other central nervous system abnormalities or syndromes, symptoms include developmental delays, motor coordination difficulties, and vision impairment." @default.