Phenotypes for disease #02626 (EDM5 (dysplasia, epiphyseal, multiple, type 5 (EDM-5)), OMIM:607078)

14 entries on 1 page. Showing entries 1 - 14.
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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     
0000173043 severely affected - - - - - - - - LOVD 00230568
0000173045 - - - Familial - - - - - LOVD 00230523
0000173046 - - - Familial - - - - - LOVD 00230527
0000173047 - - - Familial - - - - - LOVD 00230528
0000173048 - - - Familial - - - - - LOVD 00230529
0000173049 - - - Familial - - - - - LOVD 00230537
0000173050 - - - Familial - - - - - LOVD 00230546
0000173051 - - - Familial - - - - - LOVD 00230549
0000173052 - - - Familial - - - - - LOVD 00230554
0000173053 - - - Familial, autosomal dominant - - - - - LOVD 00230535
0000173054 - - - Familial, autosomal dominant - - - - - LOVD 00230548
0000173055 - - - Familial, autosomal dominant - - - - - LOVD 00230558
0000173056 - - - Familial, autosomal dominant - - - - - LOVD 00230561
0000173057 - - - Familial, autosomal dominant - - - - - LOVD 00230566
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