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Q52145439-5FCD2198-F8BA-41EF-AA2D-6FB82BB72CF2
Q52145439-5FCD2198-F8BA-41EF-AA2D-6FB82BB72CF2
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Statement
http://www.wikidata.org/entity/statement/Q52145439-5FCD2198-F8BA-41EF-AA2D-6FB82BB72CF2
A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation.
P2860
Q52145439-5FCD2198-F8BA-41EF-AA2D-6FB82BB72CF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52145439-5FCD2198-F8BA-41EF-AA2D-6FB82BB72CF2
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Statement
wasDerivedFrom
a6f127f5f5c315b5c804d1a15cb36c75d58176ea
P2860
Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome.