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Q43272843-42C3E69D-C40E-4A0B-A11E-2E2DC7B06C5F
Q43272843-42C3E69D-C40E-4A0B-A11E-2E2DC7B06C5F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43272843-42C3E69D-C40E-4A0B-A11E-2E2DC7B06C5F
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.
P921
Q43272843-42C3E69D-C40E-4A0B-A11E-2E2DC7B06C5F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43272843-42C3E69D-C40E-4A0B-A11E-2E2DC7B06C5F
rank
NormalRank
type
BestRank
Statement
P921
birth defect