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| Additional findings_Paediatric v1.0 | ASCL1 | Gene migrated from ENSG00000139352 to ENSG00000139352 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | ASCL1 |
Zornitza Stark gene: ASCL1 was added gene: ASCL1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: ASCL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: ASCL1 were set to Congenital central hypoventilation |
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