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| Genomic newborn screening: BabyScreen+ v2.0 | TTN | Gene migrated from ENSG00000155657 to ENSG00000155657 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | TTN |
Zornitza Stark gene: TTN was added gene: TTN was added to gNBS. Sources: BabySeq Category B gene,Expert Review Amber,BabySeq Category A gene Mode of inheritance for gene: TTN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: TTN were set to Centronuclear myopathy; Cardiomyopathy, dilated |
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