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Up to: Inborn disorder of purine or pyrimidine metabolism · Pyrimidine metabolism disease

Inborn disorder of pyrimidine metabolism

ANPM

0 trials tagged with this condition →

Mitochondrial DNA depletion syndrome, myopathic form 4 trials
Mitochondrial neurogastrointestinal encephalomyopathy 4 trials Sub-types →
Dihydropyrimidine dehydrogenase deficiency 3 trials
Beta-ureidopropionase deficiency 1 trial
Dihydropyrimidinuria 1 trial
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 1 trial
Orotic aciduria 1 trial Sub-types →
Developmental and epileptic encephalopathy, 50 0 trials
Hyper-beta-alaninemia 0 trials