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Q33924011-F2033C03-AC5F-4FA3-A66E-7949DF5B9868
Q33924011-F2033C03-AC5F-4FA3-A66E-7949DF5B9868
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33924011-F2033C03-AC5F-4FA3-A66E-7949DF5B9868
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
P2860
Q33924011-F2033C03-AC5F-4FA3-A66E-7949DF5B9868
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33924011-F2033C03-AC5F-4FA3-A66E-7949DF5B9868
rank
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type
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wasDerivedFrom
c458ed6c0741195e3cd5e50d0db11a8613624021
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.