Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb98c68b9ad19bbfb60d9ef3e7b4ce63d> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bb98c68b9ad19bbfb60d9ef3e7b4ce63d hasDbXref "Orphanet:226298" @default.
- Bb98c68b9ad19bbfb60d9ef3e7b4ce63d type Axiom @default.
- Bb98c68b9ad19bbfb60d9ef3e7b4ce63d annotatedProperty IAO_0000115 @default.
- Bb98c68b9ad19bbfb60d9ef3e7b4ce63d annotatedSource MONDO_0016410 @default.
- Bb98c68b9ad19bbfb60d9ef3e7b4ce63d annotatedTarget "Central or secondary congenital hypothyroidism is a type of permanent congenital hypothyroidism characterized by permanent thyroid hormone deficiency that is present from birth and secondary to a disorder in the thyroid-stimulating hormone (TSH) - thyrotropin-releasing hormone (TRH) system." @default.