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MIRAGE
GM1 gangliosidosis type 3
Summary
- Synonym
-
- adult-onset GM1 gangliosidosis
- Definition
- A GM1 gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and with age at onset ranges from 3 to 30 years.
- Super Class
- GM1 gangliosidosis
External Links
- Disease Ontology
- DOID:0080489
- Mondo Disease Ontology
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P16278 | Beta-galactosidase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001260 | Dysarthria |
| HP:0000926 | Platyspondyly |
| HP:0001350 | Slurred speech |
| HP:0000280 | Coarse facial features |
| HP:0001336 | Myoclonus |
| HP:0001761 | Pes cavus |
| HP:0001251 | Ataxia |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001332 | Dystonia |
| HP:0001744 | Splenomegaly |
