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| Ataxia and cerebellar anomalies - narrow panel v0.5 | ELOVL5 |
Ellen McDonagh gene: ELOVL5 was added gene: ELOVL5 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Red Mode of inheritance for gene: ELOVL5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: ELOVL5 were set to Spinocerebellar ataxia 36 (#615957) Mode of pathogenicity for gene: ELOVL5 was set to Other - please provide details in the comments |
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