Phenotypes for disease #00747 (XPD (xeroderma pigmentosum, complementation group D (XPD)), OMIM:278730)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000326357 see paper; ... - XPD Familial, autosomal recessive - - - - - Johan den Dunnen 00436177
0000326358 see paper; ... - XPD Familial, autosomal recessive - - - - - Johan den Dunnen 00436178
0000326359 see paper; ... - XPD Familial, autosomal recessive - - - - - Johan den Dunnen 00436179
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