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| Genomic newborn screening: BabyScreen+ v2.0 | AXL | Gene migrated from ENSG00000167601 to ENSG00000167601 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | AXL |
Zornitza Stark gene: AXL was added gene: AXL was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: AXL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: AXL were set to Hypogonadotropic hypogonadism |
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