| 释义 |
mucolipidosis type III mucolipidosis type III Abbreviation: ML III
A rare autosomal recessive disease characterized by bone and joint anomalies, esp. of hip and spine development; eye diseases; and sometimes mild mental retardation. It typically becomes clinically recognizable in childhood or young adulthood. Synonym: pseudo-Hurler polydystrophySee also: mucolipidosis |