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PedAM

Pediatric Disease Annotations & Medicines




Disease rett syndrome
Phenotype C0041341|tuberous sclerosis complex
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PubMedID- 22946725 They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the pcdh 19 gene.

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