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| Genomic newborn screening: BabyScreen+ v2.0 | WNT5A | Gene migrated from ENSG00000114251 to ENSG00000114251 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | WNT5A |
Zornitza Stark gene: WNT5A was added gene: WNT5A was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: WNT5A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: WNT5A were set to Robinow syndrome |
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