C120437Level 7
Congenital Isolated Adrenocorticotropic Hormone Deficiency
**Semantic type:** Finding
**Definition:** Adrenocorticotropic hormone (ACTH) deficiency due to mutation(s) in the TBX19 gene.
**Synonyms:** - Congenital Isolated ACTH Deficiency - Congenital Isolated ACTH Deficiency
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