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MIRAGE
GM1 gangliosidosis type 1
Summary
- Definition
- A GM1 gangliosidosis that is characterized by rapid psychomotor deterioration beginning within 6 months of birth, generalized central nervous system involvement, hepatosplenomegaly, facial dysmorphism, macular cherry-red spots, skeletal dysplasia, and early death.
- Super Class
- GM1 gangliosidosis
External Links
- Disease Ontology
- DOID:0080502
- 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:0000158 | Macroglossia |
| HP:0000212 | Gingival overgrowth |
| HP:0000343 | Long philtrum |
| HP:0000365 | Hearing impairment |
| HP:0000369 | Low-set ears |
| HP:0000400 | Macrotia |
| HP:0000455 | Broad nasal tip |
| HP:0000618 | Blindness |
| HP:0000707 | Abnormality of the nervous system |
| HP:0000768 | Pectus carinatum |
