FHL1-related myopathy

MONDO:0800462

A group of myopathies that includes Emery-Dreifuss muscular dystrophy (EDMD), and two allelic disorders characterized by the presence of reducing body on histopathology, namely reducing body myopathy (RBM) and scapuloperoneal myopathy.

Also known as: FHL1-related myopathy

2 clinical trials for this condition and its sub-types, 0 tagged with FHL1-related myopathy itself.

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Part of

↑ Myopathy (990) ↑ Hereditary skeletal muscle disorder (406)

Sub-types of FHL1-related myopathy

Uruguay Faciocardiomusculoskeletal syndrome 0 trials
X-linked myopathy with postural muscle atrophy 0 trials
X-linked scapuloperoneal muscular dystrophy 0 trials
Myopathy, reducing body, X-linked, childhood-onset 0 trials
Myopathy, reducing body, X-linked, early-onset, severe 0 trials

Including sub-types (2) Tagged with FHL1-related myopathy (0)

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