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| Genomic newborn screening: BabyScreen+ v2.0 | HYDIN | Gene migrated from ENSG00000157423 to ENSG00000157423 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | HYDIN |
Zornitza Stark gene: HYDIN was added gene: HYDIN was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: HYDIN was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: HYDIN were set to Primary ciliary dyskinesia |
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