Phenotypes for disease #00524 (Apert (Apert syndrome), OMIM:101200)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000017616 - - - Unknown - - - - - Karen E. Heath 00019798
0000017617 - - - Unknown - - - - - Karen E. Heath 00019799
0000017662 - - - Unknown - - - - - Karen E. Heath 00019797
0000143352 Corpus callosum agenesis, small brain, mesocardia, syndactylies on hand and feet - Apert syndrome Isolated (sporadic) - - - - - Isabel Filges 00181106
0000252699 - - Apert Syndrome Familial, autosomal dominant - 00y11m - - - Malak Alghamdi 00334952
0000252701 - - Apert Syndrome Familial, autosomal dominant - 00y05m - - - Malak Alghamdi 00334954
0000252703 - - Apert Syndrome Familial, autosomal dominant - 00y06m - - - Malak Alghamdi 00334955
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