Ullrich Congenital Muscular Dystrophy 2 (UCMD2)

Ullrich Congenital Muscular Dystrophy 2(来自ICD-11)

别称:

Ucmd2

Dystrophy, Muscular, Congenital, Ullrich, Type 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Ullrich Congenital Muscular Dystrophy 2, also known as ucmd2, is related to bethlem myopathy 1 and ullrich congenital muscular dystrophy 1. An important gene associated with Ullrich Congenital Muscular Dystrophy 2 is COL12A1 (Collagen Type XII Alpha 1 Chain). Affiliated tissues include bone, and related phenotypes are flexion contracture and motor delay

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