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ENMyoclonus, Familial, 1 (MYOCL1)
Alias:
Myoclonus, Familial Cortical
Myocl1
Fcm
Familial Cortical Myoclonus
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Myoclonus, Familial, 1, also known as myoclonus, familial cortical, is related to intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies and follicular lymphoma. An important gene associated with Myoclonus, Familial, 1 is NOL3 (Nucleolar Protein 3). Related phenotypes are action myoclonus and insomnia
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MALACARDS
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