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| BabyScreen+ newborn screening v1.114 | CEACAM16 | Tommy Li Added phenotypes Hearing loss, autosomal dominant for gene: CEACAM16 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | CEACAM16 |
Zornitza Stark gene: CEACAM16 was added gene: CEACAM16 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: CEACAM16 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: CEACAM16 were set to Hearing loss, autosomal dominant |
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