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| Genomic newborn screening: BabyScreen+ v2.0 | MYOZ2 | Gene migrated from ENSG00000172399 to ENSG00000172399 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | MYOZ2 |
Zornitza Stark gene: MYOZ2 was added gene: MYOZ2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MYOZ2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MYOZ2 were set to Cardiomyopathy, hypertrophic |
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