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| BabyScreen+ newborn screening v1.114 | SCO1 | Tommy Li Added phenotypes Hepatic failure, early onset, and neurologic disorder for gene: SCO1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | SCO1 |
Zornitza Stark gene: SCO1 was added gene: SCO1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SCO1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SCO1 were set to Hepatic failure, early onset, and neurologic disorder |
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