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| Genomic newborn screening: BabyScreen+ v2.0 | FTCD | Gene migrated from ENSG00000160282 to ENSG00000160282 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | FTCD |
Zornitza Stark gene: FTCD was added gene: FTCD was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: FTCD was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FTCD were set to Glutamate formiminotransferase deficiency |
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