Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




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.

Page: 1