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1
Q38010028-8D74DFC2-0C80-4946-B816-CAA062CCCF01
Q38010028-8D74DFC2-0C80-4946-B816-CAA062CCCF01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38010028-8D74DFC2-0C80-4946-B816-CAA062CCCF01
RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family.
P2860
Q38010028-8D74DFC2-0C80-4946-B816-CAA062CCCF01
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38010028-8D74DFC2-0C80-4946-B816-CAA062CCCF01
rank
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type
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Statement
wasDerivedFrom
50a03aa8a7e6e49d04d46c238d49c5e31bd7ba15
P2860
Loss of function effect of RET mutations causing Hirschsprung disease.