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Q55787818-C943B5FC-20C7-4CA2-A793-10A0A56FBA73
Q55787818-C943B5FC-20C7-4CA2-A793-10A0A56FBA73
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55787818-C943B5FC-20C7-4CA2-A793-10A0A56FBA73
homozygous 2p21 microdeletion syndrome
P31
Q55787818-C943B5FC-20C7-4CA2-A793-10A0A56FBA73
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55787818-C943B5FC-20C7-4CA2-A793-10A0A56FBA73
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a396a1d08b550aa98ec3a8625ace8988b29b9dd7
P31
developmental defect during embryogenesis