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BabyScreen+ newborn screening v1.114 | NHP2 | Tommy Li Added phenotypes Dyskeratosis congenita for gene: NHP2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BabyScreen+ newborn screening v0.0 | NHP2 |
Zornitza Stark gene: NHP2 was added gene: NHP2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: NHP2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NHP2 were set to Dyskeratosis congenita |