ORPHA:79257
GM1 gangliosidosis type 3
Also called Adult-onset GM1 gangliosidosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- All ages
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:79257 is classified under "Bone diseases" in the Orphanet nomenclature.