Phenotypes for disease #03784 (SPG53 (paraplegia, spastic, type 53, autosomal recessive (SPG-53)), OMIM:614898)

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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     
0000041537 SPG, ataxia, hypomimia hereditary spastic paraplegia SPG53 Familial, autosomal recessive - - 04y - - Erik-Jan Kamsteeg 00054873
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