Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B870faf8b8a37f655af00ba7633a93d0d> ?p ?o ?g. }
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- B870faf8b8a37f655af00ba7633a93d0d hasDbXref "Orphanet:95494" @default.
- B870faf8b8a37f655af00ba7633a93d0d type Axiom @default.
- B870faf8b8a37f655af00ba7633a93d0d annotatedProperty IAO_0000115 @default.
- B870faf8b8a37f655af00ba7633a93d0d annotatedSource MONDO_0013099 @default.
- B870faf8b8a37f655af00ba7633a93d0d annotatedTarget "Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy." @default.