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| Additional findings_Paediatric v0.2 | EPHX1 |
Zornitza Stark gene: EPHX1 was added gene: EPHX1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: EPHX1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: EPHX1 were set to Hypercholanemia, familial |
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