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Q52145439-D0EE1CBB-9C51-49E2-B7DF-2FE6EE84D42D
Q52145439-D0EE1CBB-9C51-49E2-B7DF-2FE6EE84D42D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52145439-D0EE1CBB-9C51-49E2-B7DF-2FE6EE84D42D
A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation.
P2860
Q52145439-D0EE1CBB-9C51-49E2-B7DF-2FE6EE84D42D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52145439-D0EE1CBB-9C51-49E2-B7DF-2FE6EE84D42D
rank
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type
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Statement
wasDerivedFrom
a6f127f5f5c315b5c804d1a15cb36c75d58176ea
P2860
Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein.