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Up to: Congenital hematological disorder · Inclusion body myositis · Disorder of multiple glycosylation · Syndromic constitutional thrombocytopenia · Hereditary inclusion-body myopathy
GNE myopathy
Nonaka distal myopathy (described in Japan) and the quadriceps-sparing autosomal recessive inclusion body myopathy type 2 (IBM2; independently described in Iranian Jews and later in other Jewish and non-Jewish populations) constitute the same pathological entity, distinguished by the sparing of quadriceps.
This condition has no sub-types.