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Q48297715-3B3C89DF-F340-4B2F-B1BB-D4C16DF7832E
Q48297715-3B3C89DF-F340-4B2F-B1BB-D4C16DF7832E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48297715-3B3C89DF-F340-4B2F-B1BB-D4C16DF7832E
Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.
P2860
Q48297715-3B3C89DF-F340-4B2F-B1BB-D4C16DF7832E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48297715-3B3C89DF-F340-4B2F-B1BB-D4C16DF7832E
rank
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type
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Statement
wasDerivedFrom
01f9764c779a0ce0d31c13110d33fe455bbaf1e0
P2860
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.