Parent term(s)
peroxisomal disease
+
Term with siblings
D-bifunctional protein deficiency
acatalasia
alpha-methylacyl-CoA racemase deficiency
glutaric acidemia type 3
infantile Refsum disease
mevalonic aciduria
Mitchell syndrome
peroxisomal acyl-CoA oxidase deficiency
peroxisomal biogenesis disorder
+
retinal dystrophy with leukodystrophy
Child term(s)
denotes an 'is-a' relationship
denotes an 'is-a' relationship
denotes an 'is-a' relationship