Phenotypes for disease #00636 (OI3 (osteogenesis imperfecta, type III (OI3)), OMIM:259420)

17 entries on 1 page. Showing entries 1 - 17.
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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     
0000060490 Osteogenesis imperfecta, type III (OMIM:259420) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080921
0000104267 - - - Familial, autosomal dominant - - - - - Karina Silveira 00132062
0000104268 - - - Isolated (sporadic) - - - - - Karina Silveira 00132063
0000268047 - OI III - - - - - - - Raymond Dalgleish 00372770
0000318995 Bradydactyly, abnormal dentin, abnormal craniofacial features. - - Familial 05y - - - - Nassim Louail 00428048
0000321950 see paper; ..., recurrent bone fractures, short stature, blue sclerae, triangular face, missing teeth, dentinogenesis imperfecta , skeletal deformities, scoliosis - OI3 Familial, autosomal recessive 17y - - - - Kim Worring 00431357
0000322107 - - - Isolated (sporadic) 07y - - - - Kim Worring 00431537
0000322792 - - - Familial, autosomal dominant 29y - - - - Kim Worring 00432225
0000322793 - - - Familial, autosomal dominant 52y - - - - Kim Worring 00432226
0000322795 - - - Unknown 28y - - - - Kim Worring 00432228
0000322796 - - - Unknown 12y - - - - Kim Worring 00432229
0000322804 - - - Familial, autosomal dominant 23y - - - - Kim Worring 00432238
0000322806 - - - Familial, autosomal dominant 52y - - - - Kim Worring 00432239
0000322807 - - - Familial, autosomal dominant 06y - - - - Kim Worring 00432240
0000322808 - - - Familial, autosomal dominant 32y - - - - Kim Worring 00432241
0000325255 - - - Familial, autosomal recessive 00y00m - - - - Kim Worring 00435013
0000325256 - - - Familial, autosomal recessive 00y00m - - - - Kim Worring 00435015
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