Phenotypes for disease #01045 (GBBB2 (syndrome, Opitz GBBB, type 2, autosomal dominant (GBBB2)), OMIM:145410)

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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     
0000025723 see paper; .. - - Familial, autosomal dominant - - - - - Johan den Dunnen 00029712
0000025724 see paper; .. - - Familial, autosomal dominant - - - - - Johan den Dunnen 00029713
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