Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d> ?p ?o ?g. }
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- Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d hasDbXref "NCIT:C98905" @default.
- Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d type Axiom @default.
- Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d annotatedProperty IAO_0000115 @default.
- Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d annotatedSource MONDO_0009022 @default.
- Bf2f5fbd8d7f7c9cc43bdd6d87f92ce0d 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.