OMIA:000666 : Mucopolysaccharidosis VI |
Categories: Lysosomal storage disease
Possible human homologues (MIM numbers): 253200 (trait) , 611542 (gene)
Links to MONDO diseases:
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