Phenotypes for disease #00573 (PRLMNS (Perlman syndrome (PRLMNS)), OMIM:267000)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000093283 Wilm tumor - - Familial, autosomal recessive 7m - - - - Gerard C.P. Schaafsma 00117902
0000093284 Wilm tumor - - Familial, autosomal recessive 14y - - - - Gerard C.P. Schaafsma 00117903
0000093285 - - - Familial, autosomal recessive 3y6m - - - - Gerard C.P. Schaafsma 00117904
0000093286 - - - Familial, autosomal recessive 1d - - - - Gerard C.P. Schaafsma 00117905
0000093287 Wilm tumor - - Familial, autosomal recessive 9m - - - - Gerard C.P. Schaafsma 00117906
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