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- B40c6ff7da1a060238334a1f558e353f0 hasDbXref "Orphanet:1229" @default.
- B40c6ff7da1a060238334a1f558e353f0 type Axiom @default.
- B40c6ff7da1a060238334a1f558e353f0 annotatedProperty IAO_0000115 @default.
- B40c6ff7da1a060238334a1f558e353f0 annotatedSource MONDO_0009626 @default.
- B40c6ff7da1a060238334a1f558e353f0 annotatedTarget "A Mendelian disease characterized by the presence of microcephaly and intracranial calcifications at birth accompanied by neurological delay, seizures and a clinical course similar to that seen in patients after intrauterine infection with Toxoplasma gondii, Rubella, Cytomegalovirus, Herpes simplex (so-called TORCH syndrome), or other agents, despite repeated tests revealing the absence of any known infectious agent." @default.