Carnitine palmitoyl transferase deficiency
MONDO:07002841 clinical trial for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Carnitine palmitoyl transferase 1A deficiency
(1)
Carnitine palmitoyltransferase II deficiency
(1)
Carnitine palmitoyl transferase II deficiency, myopathic form
(0)
Carnitine palmitoyl transferase II deficiency, neonatal form
(0)
Carnitine palmitoyl transferase II deficiency, severe infantile form
(0)
Broader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Disorder of fatty acid and ketone body metabolism
(3)
Disease of genetic or genomic mechanism
(2)
Inborn disorder of energy metabolism
(1)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)