Any autosomal recessive Emery-Dreifuss muscular dystrophy in which the cause of the disease is a mutation in the LMNA gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
scapuloperoneal myopathy
MONDO:0000727
Buschke-Ollendorff syndrome
MONDO:0008157
Pelger-Huet anomaly
MONDO:0008214
adult-onset autosomal dominant demyelinating leukodystrophy
MONDO:0008215
Hutchinson-Gilford progeria syndrome
MONDO:0008310
Greenberg dysplasia
MONDO:0008974