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| Additional findings_Paediatric v1.0 | TNNT2 | Gene migrated from ENSG00000118194 to ENSG00000118194 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | TNNT2 | Zornitza Stark Added phenotypes Familial hypertrophic cardiomyopathy for gene: TNNT2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | TNNT2 |
Zornitza Stark gene: TNNT2 was added gene: TNNT2 was added to Newborn Screening_BabySeq. Sources: BabySeq Category B gene,Expert Review Amber Mode of inheritance for gene: TNNT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: TNNT2 were set to Cardiomyopathy, dilated |
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