Phenotypes for disease #01291 (DSH (dyschromatosis symmetrica hereditaria (DSH)), OMIM:127400)

8 entries on 1 page. Showing entries 1 - 8.
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Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Individual ID     
0000173431 typical hyperpigmented and hypopigmented macules variable in shape and size on dorsal aspects hands and feet dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant 13y - 05y - - Johan den Dunnen 00230643
0000173432 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230644
0000173433 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230949
0000173434 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230950
0000173435 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230951
0000173436 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230952
0000173437 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230953
0000173438 see paper; ... dyschromatosis symmetrica hereditaria DSH Familial, autosomal dominant - - - - - Johan den Dunnen 00230954
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