Nemaline Myopathy 10 (NEM10)

Nemaline Myopathy 10(来自ICD-11)

别称:

Nem10

Myopathy, Nemaline, Type 10

Congenital Myopathy 10

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Nemaline Myopathy 10, also known as nem10, is related to nemaline myopathy and myopathy, and has symptoms including ophthalmoplegia, facial paresis and generalized muscle weakness. An important gene associated with Nemaline Myopathy 10 is LMOD3 (Leiomodin 3). Affiliated tissues include skeletal muscle, and related phenotypes are facial palsy and muscle weakness

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