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| Additional findings_Paediatric v1.0 | ROR2 | Gene migrated from ENSG00000169071 to ENSG00000169071 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | ROR2 |
Zornitza Stark Mode of inheritance for gene ROR2 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Brachydactyly, type B1 for gene: ROR2 |
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| Additional findings_Paediatric v0.2 | ROR2 |
Zornitza Stark gene: ROR2 was added gene: ROR2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: ROR2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ROR2 were set to Robinow syndrome |
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