Phenotypes for disease #05428 (atrophy, cerebellar (atrophy, cerebellar))

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000129342 - - see paper; ..., cerebellar atrophy, spinal motor neuronopathy Familial, autosomal recessive 02y04m - 00y08m - - Johan den Dunnen 00164232
0000129343 - - see paper; ..., cerebellar atrophy, spinal motor neuronopathy Familial, autosomal recessive - - - 1d - Johan den Dunnen 00164233
0000129344 - - see paper; ..., cerebellar atrophy, spinal motor neuronopathy Familial, autosomal recessive 04y06m - 00y00m01d - - Johan den Dunnen 00164234
0000129345 - - see paper; ..., cerebellar atrophy, spinal motor neuronopathy Familial, autosomal recessive 01y07m - 00y00m14d - - Johan den Dunnen 00164235
0000154695 progressive cerebellar atrophy, polyneuropathy MCSZ see paper; ... Familial, autosomal recessive - - - - - Johan den Dunnen 00206903
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