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| Genomic newborn screening: BabyScreen+ v2.0 | FREM1 | Gene migrated from ENSG00000164946 to ENSG00000164946 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | FREM1 |
Zornitza Stark gene: FREM1 was added gene: FREM1 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: FREM1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FREM1 were set to Manitoba oculotrichoanal syndrome |
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