OMIA:000666 : Mucopolysaccharidosis VI

Categories: Lysosomal storage disease

Possible human homologues (MIM numbers): 253200 (trait) , 611542 (gene)

Links to relevant human diseases in MONDO:

Cross-species summary: This disorder is a lysosomal storage disease, caused by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase.

Species in which this phene is found:
dog (Canis lupus familiaris)
domestic cat (Felis catus)

Edit History


  • Created by Frank Nicholas on 16 Sep 2005
  • Changed by Imke Tammen2 on 17 Apr 2021
  • Changed by Imke Tammen2 on 06 Jul 2021
  • Changed by Imke Tammen2 on 23 Jan 2023