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| Genomic newborn screening: BabyScreen+ v2.0 | CSF1R | Gene migrated from ENSG00000182578 to ENSG00000182578 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | CSF1R |
Zornitza Stark gene: CSF1R was added gene: CSF1R was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: CSF1R was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: CSF1R were set to Leukoencephalopathy, diffuse hereditary, with spheroids |
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