Dicarboxylic aminoaciduria

MONDO:0009110

Dicarboxylicaminoaciduria is characterized by infantile-onset hypoglycaemia and hyperprolinaemia associated, in certain cases, with intellectual deficit.

Also known as: dicarboxylic aminoaciduria, glutamate-aspartate transport defect, DCBXA, Dicarboxylicaminoaciduria, glutamate-aspartate Transport defect

0 clinical trials for this condition and its sub-types, 0 tagged with Dicarboxylic aminoaciduria itself.

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Part of

↑ Inborn disorder of amino acid transport (16)

Including sub-types (0) Tagged with Dicarboxylic aminoaciduria (0)

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