Phenotypes for disease #04369 (SCAX1 (ataxia, spinocerebellar?, X-linked type 1 (SCAX-1)), OMIM:302500)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000070608 mild IDD, autism, epilepsy, ataxia, improvement of neurologic symptoms on oral serine supplements; low CSF and plasma serine - - Familial, X-linked recessive - - - - - Johan den Dunnen 00092272
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