Disease | cataract |
Phenotype | C0205711|pelizaeus-merzbacher disease |
Sentences | 1 |
PubMedID- 20881161 | In most cases of pelizaeus-merzbacher disease, hypomyelination with congenital cataract, hypomyelination with hypogonadotropic hypogonadism and hypodontia, pelizaeus-merzbacher-like disease, infantile gm1 and gm2 gangliosidosis and fucosidosis, the imaging pattern gives clues for the diagnosis. |
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