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| Genomic newborn screening: BabyScreen+ v2.0 | HMBS | Gene migrated from ENSG00000256269 to ENSG00000256269 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | HMBS |
Zornitza Stark gene: HMBS was added gene: HMBS was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: HMBS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: HMBS were set to Porphyria, acute intermittent |
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