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Summary Literature (0)
MIM:612989 - OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7

Xenbase Genes: tmem126a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013069 - popliteal area
MONDO:0014753 - obsolete autosomal recessive optic atrophy

Disease Ontology (DO):
DOID:0111437 - optic atrophy 7