Parent term(s)
peroxisomal disease
+
Term with siblings
peroxisomal biogenesis disorder +
acatalasia
alpha-methylacyl-CoA racemase deficiency
D-bifunctional protein deficiency
glutaric acidemia type 3
infantile Refsum disease
mevalonic aciduria
Mitchell syndrome
peroxisomal acyl-CoA oxidase deficiency
retinal dystrophy with leukodystrophy
Child term(s)
Heimler syndrome 1
Heimler syndrome 2
Peroxisome biogenesis disorder 10B
Peroxisome biogenesis disorder 11B
peroxisome biogenesis disorder 14B
peroxisome biogenesis disorder 1B
peroxisome biogenesis disorder 2B
peroxisome biogenesis disorder 3B
Peroxisome biogenesis disorder 4B
Peroxisome biogenesis disorder 5B
Peroxisome biogenesis disorder 6B
Peroxisome biogenesis disorder 7B
Peroxisome biogenesis disorder 8B
Peroxisome biogenesis disorder 9B
Zellweger syndrome
+
denotes an 'is-a' relationship