Oculopharyngeal Myopathy with Leukoencephalopathy 1 (OPML1)

Alias:

Myopathy, Oculopharyngeal, with Leukoencephalopathy, Type 1

Opml1

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Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Oculopharyngeal Myopathy with Leukoencephalopathy 1, is also known as myopathy, oculopharyngeal, with leukoencephalopathy, type 1. An important gene associated with Oculopharyngeal Myopathy with Leukoencephalopathy 1 is NUTM2B-AS1 (NUTM2B Antisense RNA 1). Affiliated tissues include skeletal muscle and brain, and related phenotypes are ptosis and dysarthria

Related ID：

MALACARDS：OCL077

OMIM：618637