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Mondo Disease Ontology (Rare Disease Subset)
MONDO_RARE
6423
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KRT16
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http://identifiers.org/hgnc/6423
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This is just here as a test because I lose it
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Subclass of:
Thing
Related from:
has material basis in germline mutation in
pachyonychia congenita 1
palmoplantar keratoderma, nonepidermolytic, focal 1
