ORPHA:79256
GM1 gangliosidosis type 2
Also called Juvenile GM1 gangliosidosis, Late-infantile GM1 gangliosidosis
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:79256 is classified under "Bone diseases" in the Orphanet nomenclature.