Details of RareLED ID 2017 |
| Primary information | |
|---|---|
| ID | 2017 |
| Disorder | Morquio B |
| Inheritance | Autosomal recessive |
| Organ Affected | Eye,Bones,Nervous System,Liver,Spleen,Muscle |
| Onset | Adult |
| Genotype-Phenotype Correlation | mutations such as the p.G438E, p.R201H, and p.S191N may be associated with late onset phenotypes |
| Refrences | 21497194 |