Congenital Myopathy 19 (CMYP19)

Congenital Myopathy 19(来自ICD-11)

别称:

Myopathy, Congenital, Progressive, with Scoliosis

Cmyp19

Myosco

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Myopathy 19, is also known as myopathy, congenital, progressive, with scoliosis. An important gene associated with Congenital Myopathy 19 is PAX7 (Paired Box 7). Affiliated tissues include skeletal muscle, and related phenotypes are ptosis and gait disturbance

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