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| Additional findings_Paediatric v1.0 | LMX1B | Gene migrated from ENSG00000136944 to ENSG00000136944 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | LMX1B |
Zornitza Stark gene: LMX1B was added gene: LMX1B was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: LMX1B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: LMX1B were set to Nail patella syndrome |
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