Phenotypes for disease #01857 (VBCH (disease, van Buchem (VBCH, hyperostosis corticalis generalisata)), OMIM:239100)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000085490 van Buchem disease (hyperostosis corticalis generalisata) - - Familial - - - - - Johan den Dunnen 00107725
0000085491 van Buchem disease (hyperostosis corticalis generalisata), see paper; ... - - Isolated (sporadic) 68y - - - - Johan den Dunnen 00107726
0000085492 van Buchem disease (hyperostosis corticalis generalisata) - - Isolated (sporadic) - - - - - Johan den Dunnen 00107727
0000085493 van Buchem disease (hyperostosis corticalis generalisata) - - Isolated (sporadic) - - - - - Johan den Dunnen 00107728
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