Phenotypes for disease #00453 (Perry (Perry syndrome), OMIM:168605)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000016236 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017879
0000016237 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017880
0000016238 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017881
0000016239 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017882
0000016240 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017883
0000016241 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017884
0000016242 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017885
0000016243 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00017886
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