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| Additional findings_Paediatric v1.0 | FOXN1 | Gene migrated from ENSG00000109101 to ENSG00000109101 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | FOXN1 |
Zornitza Stark gene: FOXN1 was added gene: FOXN1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: FOXN1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FOXN1 were set to Congenital alopecia with T-cell immunodeficiency |
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