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| Genomic newborn screening: BabyScreen+ v2.0 | SEMA3A | Gene migrated from ENSG00000075213 to ENSG00000075213 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | SEMA3A |
Zornitza Stark gene: SEMA3A was added gene: SEMA3A was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SEMA3A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SEMA3A were set to Kallmann syndrome 1 |
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