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| Additional findings_Paediatric v0.2 | FOXH1 |
Zornitza Stark gene: FOXH1 was added gene: FOXH1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: FOXH1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: FOXH1 were set to Congenital heart defects |
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