Pancreatic agenesis 1

MONDO:0024547

Any pancreatic agenesis in which the cause of the disease is a mutation in the PDX1 gene.

Also known as: PDX1 pancreatic agenesis, pancreatic agenesis 1, pancreatic agenesis caused by mutation in PDX1, PAGEN1, Pagen, pancreatic hypoplasia, congenital

1 clinical trial for this condition and its sub-types, 1 tagged with Pancreatic agenesis 1 itself.

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Including sub-types (1) Tagged with Pancreatic agenesis 1 (1)

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Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Pancreatic agenesis 1

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth