Phenotypes for disease #06696 (SPG77 (Spastic paraplegia 77, autosomal recessive), OMIM:617046)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000312769 - - Hypotonia, Motor delay, Lower limb muscle weakness, Impaired pain sensation, Abnormal pyramidal sign, Delayed speech and language development, Joint hypermobility Familial, autosomal recessive 02y - - - Andreas Laner 00421533
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