Oculopharyngodistal Myopathy 2 (OPDM2)

Oculopharyngodistal Myopathy 2(来自ICD-11)

别称:

Opdm2

Myopathy, Oculopharyngodistal, Type 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Oculopharyngodistal Myopathy 2, is also known as opdm2. An important gene associated with Oculopharyngodistal Myopathy 2 is GIPC1 (GIPC PDZ Domain Containing Family Member 1). Affiliated tissues include skeletal muscle, and related phenotypes are ptosis and emg: myopathic abnormalities

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