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| Genomic newborn screening: BabyScreen+ v2.0 | TNXB | Gene migrated from ENSG00000168477 to ENSG00000168477 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | TNXB |
Zornitza Stark gene: TNXB was added gene: TNXB was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: TNXB was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TNXB were set to Ehlers-Danlos syndrome due to tenascin X deficiency |
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