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| Ataxia v2.0 | SDHA | Gene migrated from ENSG00000073578 to ENSG00000073578 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.109 | Bryony Thompson Copied gene SDHA from panel Ataxia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.109 | SDHA |
Bryony Thompson gene: SDHA was added gene: SDHA was added to Ataxia. Sources: Expert Review Amber,Expert list Mode of inheritance for gene: SDHA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SDHA were set to 10976639; 27683074 Phenotypes for gene: SDHA were set to Neurodegeneration with ataxia and late-onset optic atrophy, MIM# 619259 |
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