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1
Q51842731-19F368B7-74F9-46B6-8335-DB1999CE12ED
Q51842731-19F368B7-74F9-46B6-8335-DB1999CE12ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51842731-19F368B7-74F9-46B6-8335-DB1999CE12ED
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene.
P577
Q51842731-19F368B7-74F9-46B6-8335-DB1999CE12ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51842731-19F368B7-74F9-46B6-8335-DB1999CE12ED
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
29933acc505ea44009015f0d67e19007e135f3ee
P577
2008-11-01T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P577
4b0ea0428e9b6ba56ce11a7ed4e0c779