Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B808962342748ec7544b91705041dbce8> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B808962342748ec7544b91705041dbce8 hasDbXref "Orphanet:226307" @default.
- B808962342748ec7544b91705041dbce8 type Axiom @default.
- B808962342748ec7544b91705041dbce8 annotatedProperty IAO_0000115 @default.
- B808962342748ec7544b91705041dbce8 annotatedSource MONDO_0016411 @default.
- B808962342748ec7544b91705041dbce8 annotatedTarget "Hypothyroidism due to mutations in transcription factors involved in pituitary development or function is a type of central congenital hypothyroidism, a permanent thyroid deficiency that is present from birth, characterized by low levels of thyroid hormones caused by disorders in the development or function of the pituitary." @default.