Phenotypes for disease #04672 (OI17 (osteogenesis imperfecta, type XVII (OI17)), OMIM:616507)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000325332 - - - Familial, autosomal recessive 19y - - - - Kim Worring 00435093
0000325333 - - - Familial, autosomal recessive 11y - - - - Kim Worring 00435094
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