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Q39141569-0A6D768A-7F66-4EDD-B083-75614F900214
Q39141569-0A6D768A-7F66-4EDD-B083-75614F900214
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http://www.wikidata.org/entity/statement/Q39141569-0A6D768A-7F66-4EDD-B083-75614F900214
Renal aplasia in humans is associated with RET mutations.
P2860
Q39141569-0A6D768A-7F66-4EDD-B083-75614F900214
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39141569-0A6D768A-7F66-4EDD-B083-75614F900214
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wasDerivedFrom
534d9ce0f7d92e6899f4528df7af5d001506a5e2
P2860
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.