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| Ataxia v1.70 | Bryony Thompson Copied gene ABCD1 from panel Ataxia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.70 | ABCD1 |
Bryony Thompson gene: ABCD1 was added gene: ABCD1 was added to Ataxia - paediatric. Sources: Expert Review Green,Expert list,Royal Melbourne Hospital Mode of inheritance for gene: ABCD1 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Phenotypes for gene: ABCD1 were set to Adrenoleukodystrophy |
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