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| Genomic newborn screening: BabyScreen+ v2.0 | SYNE4 | Gene migrated from ENSG00000181392 to ENSG00000181392 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | SYNE4 |
Zornitza Stark gene: SYNE4 was added gene: SYNE4 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SYNE4 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SYNE4 were set to Hearing loss |
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