Congenital Isolated Acth Deficiency

Congenital Isolated Acth Deficiency is related to acth deficiency, isolated and cholestasis. An important gene associated with Congenital Isolated Acth Deficiency is TBX19 (T-Box Transcription Factor 19). Affiliated tissues include pituitary, and related phenotypes are neonatal hypoglycemia and adrenocorticotropin deficient adrenal insufficiency