GM1 gangliosidosis, type 2 (adult or chronic GM1-gangliosidosis)

Genetics

• autosomal recessive
• associated with defects in GLB1

Clinical manifestations

• mental_retardation
• spasticity
• ataxia
• rigidity
• seizure

More general terms

• GM1 gangliosidosis

Database

• OMIM: https://mirror.omim.org/entry/230600