Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5ae7f0f5d125f503f55bb2ef6e1d94a8> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5ae7f0f5d125f503f55bb2ef6e1d94a8 NCIT_P378 "NICHD" @default.
- B5ae7f0f5d125f503f55bb2ef6e1d94a8 type Axiom @default.
- B5ae7f0f5d125f503f55bb2ef6e1d94a8 annotatedProperty NCIT_P325 @default.
- B5ae7f0f5d125f503f55bb2ef6e1d94a8 annotatedSource NCIT_C131134 @default.
- B5ae7f0f5d125f503f55bb2ef6e1d94a8 annotatedTarget "A classic form of congenital adrenal hyperplasia characterized by complete absence of 21-hydroxylase activity, resulting in deficiency of glucocorticoids and mineralocorticoids accompanied by androgen excess, causing virilization in female infants. Mineralocorticoid deficiency results in renal salt-wasting, and, if untreated, hyponatremia, hyperkalemia, and shock." @default.