Phenotypes for disease #02055 (Revesz (Revesz syndrome), OMIM:268130)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000078680 dyskeratosis congenita, Revesz syndrome - - Unknown - - - - - Johan den Dunnen 00100479
0000078682 autosomal-dominant dyskeratosis congenita, Revesz syndrome - - Familial, autosomal dominant - - - - - Johan den Dunnen 00100481
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