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Classic organic aciduria
MONDO:001921543 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Propionic acidemia
(8)
Barth syndrome
(4)
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
(4)
Biotinidase deficiency
(3)
Methylmalonic aciduria and homocystinuria type cblC
(3)
Isovaleric acidemia
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Methylmalonic aciduria, cblA type
(2)
3-hydroxy-3-methylglutaric aciduria
(1)
3-methylcrotonyl-CoA carboxylase 1 deficiency
(1)
3-methylcrotonyl-CoA carboxylase 2 deficiency
(1)
Beta-ketothiolase deficiency
(1)
Holocarboxylase synthetase deficiency
(1)
Methylmalonic acidemia with homocystinuria, type cblJ
(1)
Methylmalonic aciduria and homocystinuria
(1)
Methylmalonic aciduria and homocystinuria type cblF
(1)
Methylmalonic aciduria, cblB type
(1)
2-methylbutyryl-CoA dehydrogenase deficiency
(0)
3-hydroxyisobutyric aciduria
(0)
3-hydroxyisobutyryl-CoA hydrolase deficiency
(0)
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Inborn disorder of amino acid metabolism
(4)
Inborn organic aciduria
(4)
Disease of genetic or genomic mechanism
(2)
Amino acid metabolism disease
(0)
Disease by developmental or physiological process
(0)