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| BabyScreen+ newborn screening v1.114 | EPHX1 | Tommy Li Added phenotypes Hypercholanemia, familial for gene: EPHX1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | EPHX1 |
Zornitza Stark gene: EPHX1 was added gene: EPHX1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene 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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