Phenotypes for disease #05891 (OI20 (osteogenesis imperfecta, type XX (OI20)), OMIM:618644)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000325228 - - - Familial, autosomal recessive 08y - - - Kim Worring 00434981
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