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Mondo Disease Ontology (Rare Disease Subset)
MONDO_RARE
6493
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LAMC2
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http://identifiers.org/hgnc/6493
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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
epidermolysis bullosa, junctional 3A, intermediate
epidermolysis bullosa, junctional 3B, severe
