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| Additional findings_Paediatric v1.0 | PRDM16 | Gene migrated from ENSG00000142611 to ENSG00000142611 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | PRDM16 |
Zornitza Stark gene: PRDM16 was added gene: PRDM16 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: PRDM16 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: PRDM16 were set to Left ventricular noncompaction |
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