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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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Nanophthalmia
Nanophthalmos 1
rare
Identifiers
MONDO:0010836
OMIM:600165
Causal genes
MYRF
Part of
Nanophthalmia
Also known as
nanophthalmos-1 · NNO1
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