Phenotypes for disease #03663 (SPAX5 (ataxia, spastic, type 5, autosomal recessive (SPAX-5)), OMIM:614487)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000353404 Ataxia, Global developmental delay, Hip dysplasia, Visual impairment, Failure to thrive, Positional foot deformity, Intellectual disability - - Familial, autosomal recessive 07y - - - - Andreas Laner 00468252
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