Phenotypes for disease #03504 (OI6 (osteogenesis imperfecta, type VI (OI6)), OMIM:613982)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000244875 clinically osteogenesis imperfecta, multiple fractures of long tubular bones 1y - Unknown - - - - - Andreas Laner 00326414
0000302284 no Dentinogenesis imperfecta (-HP:0000703), no Blue sclerae (-HP:0000592), Short stature (HP:0004322) - - Familial, autosomal recessive - - 00y14m Bone fracture (HP:0020110) - Thanakorn Theerapanon 00410180
0000325336 - - - Familial, autosomal recessive 01y - - - - Kim Worring 00435097
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