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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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Meesmann corneal dystrophy
Corneal dystrophy, Meesmann, 1
rare
Identifiers
MONDO:0020791
OMIM:122100
Causal genes
KRT12
Part of
Meesmann corneal dystrophy
Also known as
MECD1
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