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Mondo Disease Ontology (Rare Disease Subset)
MONDO_RARE
5181
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HRG
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http://identifiers.org/hgnc/5181
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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
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
