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MIM:618098 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5
Xenbase Genes: top3a
Human Disease Resource: MIM
MONDO:0020845 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5 |
DOID:0111524 - autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 |