Pancreatic insufficiency-anemia-hyperostosis syndrome

MONDO:0012992

A rare syndromic mitochondrial disease in which the cause of the disease is a mutation in the COX4I2 gene. It is characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis.

Also known as: pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome, exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis

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