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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Autosomal genetic disease
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Autosomal dominant disease
Optic atrophy 5
rare
Identifiers
MONDO:0012543
OMIM:610708
Causal genes
DNM1L
Part of
Autosomal dominant disease
Hereditary optic atrophy
Also known as
OPA5
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