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| Genomic newborn screening: BabyScreen+ v2.0 | MESP2 | Gene migrated from ENSG00000188095 to ENSG00000188095 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | MESP2 |
Zornitza Stark gene: MESP2 was added gene: MESP2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MESP2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MESP2 were set to Spondylocostal dysostosis, autosomal recessive 2 |
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