Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba453591f9e07f4182721eb31e0fdacf4> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Ba453591f9e07f4182721eb31e0fdacf4 NCIT_P378 "NICHD" @default.
- Ba453591f9e07f4182721eb31e0fdacf4 type Axiom @default.
- Ba453591f9e07f4182721eb31e0fdacf4 annotatedProperty NCIT_P325 @default.
- Ba453591f9e07f4182721eb31e0fdacf4 annotatedSource NCIT_C126809 @default.
- Ba453591f9e07f4182721eb31e0fdacf4 annotatedTarget "An autosomal dominant condition due to mutation(s) in the NR3C1 gene, encoding the glucocorticoid receptor, resulting in decreased receptor affinity to glucocorticoids. Compensatory activation of the hypothalamic- pituitary-adrenal (HPA) axis, resulting in increased mineralocorticoid and androgen production; clinical manifestations of glucocorticoid deficiency are rare." @default.