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Q28216575-9531CA72-1F02-4E3A-A5A7-517FF81FCADD
Q28216575-9531CA72-1F02-4E3A-A5A7-517FF81FCADD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28216575-9531CA72-1F02-4E3A-A5A7-517FF81FCADD
Smith-Lemli-Opitz (RHS) syndrome: holoprosencephaly and homozygous IVS8-1G-->C genotype
P921
Q28216575-9531CA72-1F02-4E3A-A5A7-517FF81FCADD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28216575-9531CA72-1F02-4E3A-A5A7-517FF81FCADD
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
82630af7e1151e88e8ae34ab9d05aea66cb2f3b3
P921
holoprosencephaly