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| Genomic newborn screening: BabyScreen+ v2.0 | WNT7A | Gene migrated from ENSG00000154764 to ENSG00000154764 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | WNT7A |
Zornitza Stark gene: WNT7A was added gene: WNT7A was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: WNT7A was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: WNT7A were set to Ulna and fibula absence of with severe limb deficiency |
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