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Mondo Disease Ontology (Rare Disease Subset)
MONDO_RARE
6490
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LAMB3
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http://identifiers.org/hgnc/6490
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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
junctional epidermolysis bullosa, non-Herlitz type
junctional epidermolysis bullosa Herlitz type
amelogenesis imperfecta type 1A
