Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be83d0afc89d8e8ca84beb8649f18a12b> ?p ?o ?g. }
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- Be83d0afc89d8e8ca84beb8649f18a12b hasDbXref "Orphanet:95716" @default.
- Be83d0afc89d8e8ca84beb8649f18a12b type Axiom @default.
- Be83d0afc89d8e8ca84beb8649f18a12b annotatedProperty IAO_0000115 @default.
- Be83d0afc89d8e8ca84beb8649f18a12b annotatedSource MONDO_0010132 @default.
- Be83d0afc89d8e8ca84beb8649f18a12b annotatedTarget "A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis." @default.