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| Leukodystrophy v1.0 | STX11 | Gene migrated from ENSG00000135604 to ENSG00000135604 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Leukodystrophy v0.45 | STX11 |
Bryony Thompson gene: STX11 was added gene: STX11 was added to Leukodystrophy - paediatric_RMH. Sources: Expert list Mode of inheritance for gene: STX11 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: STX11 were set to Hemophagocytic lymphohistiocytosis, familial, 4 603552 Review for gene: STX11 was set to RED Added comment: It is unclear whether leukodystrophy is a feature of the condition. There are no reports of the gene associated with white matter changes. Sources: Expert list |
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