Catalog

Retinal dystrophy in GM2 gangliosidosis

No MMS code

Link to WHO Definition

Retinal dystrophy in GM2 gangliosidosis – http://id.who.int/icd/entity/827778106

This refers to persistent or acute damage to the retina of the eye, in a group of related genetic disorders that result from a deficiency of the enzyme beta-hexosaminidase.