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| Additional findings_Paediatric v1.0 | NPHS1 | Gene migrated from ENSG00000161270 to ENSG00000161270 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | NPHS1 |
Zornitza Stark gene: NPHS1 was added gene: NPHS1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: NPHS1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NPHS1 were set to Congenital nephrotic syndrome, Finnish type |
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