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| Genomic newborn screening: BabyScreen+ v2.0 | DECR1 | Gene migrated from ENSG00000104325 to ENSG00000104325 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | DECR1 |
Zornitza Stark gene: DECR1 was added gene: DECR1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: DECR1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DECR1 were set to 2,4-Dienoyl-CoA reductase deficiency |
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