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autosomal recessive limb-girdle muscular dystrophy type 2C
MONDO:0009677
Barth syndrome
MONDO:0010543
histiocytoid cardiomyopathy
MONDO:0010771
Kearns-Sayre syndrome
MONDO:0010787
Leber hereditary optic neuropathy
MONDO:0010788
autosomal recessive limb-girdle muscular dystrophy type 2F
MONDO:0011028