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| BabyScreen+ newborn screening v1.114 | PHOX2A | Tommy Li Added phenotypes Fibrosis of extraocular muscles, congenital for gene: PHOX2A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | PHOX2A |
Zornitza Stark gene: PHOX2A was added gene: PHOX2A was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: PHOX2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: PHOX2A were set to Fibrosis of extraocular muscles, congenital |
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