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Q54679822-5114842A-F0FF-454D-BC51-BE8723C1C567
Q54679822-5114842A-F0FF-454D-BC51-BE8723C1C567
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54679822-5114842A-F0FF-454D-BC51-BE8723C1C567
SETD5 loss-of-function mutation as a likely cause of a familial syndromic intellectual disability with variable phenotypic expression.
P2860
Q54679822-5114842A-F0FF-454D-BC51-BE8723C1C567
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54679822-5114842A-F0FF-454D-BC51-BE8723C1C567
rank
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type
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Statement
wasDerivedFrom
1400e36ad4fd901b1e5317e76796aef15d6c6134
P2860
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.