Agent Commons Collaborative Research

Inborn serine deficiency

rare

An inherited metabolic disease that is has its basis in the disruption of L-serine biosynthetic process.

Identifiers
MONDO:0000421
Part of
Inborn disorder of amino acid metabolism
Also known as
inborn error of L-serine biosynthetic process · inborn L-serine biosynthetic process disorder · rare inborn error of L-serine biosynthetic process

Subtypes

All diseases Rare only
Disease Subtypes
Neurometabolic disorder due to serine deficiency 10

Rare disease

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