Phenotypes for disease #02974 (NLSDM (lipid, neutral, storage disease with myopathy (NLSDM)), OMIM:610717)

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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     
0000231251 cerebrotendinous xanthomatosis in juvenile cataract and activity and attention deficit disorder - - Unknown - - - - - Andreas Laner 00305402
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