# GM1 gangliosidosis type 2

> GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis (see this term) characterized by normal early development and psychomotor regression between seven months and three years of age

**Wikidata**: [Q55998595](https://www.wikidata.org/wiki/Q55998595)  
**Source**: https://4ort.xyz/entity/gm1-gangliosidosis-type-2


## References

1. Monarch Disease Ontology release 2018-06-29
2. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000170266/MONDO_0009261)