Phenotypes for disease #02998 (OI5 (osteogenesis imperfecta, type V (OI5)), OMIM:610967)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000257158 Recurrent fractures, microphthalmia Developmental delay - - Familial, autosomal recessive - - - - - Anju Shukla 00361765
0000321981 - - - Isolated (sporadic) 00y - - - - Kim Worring 00431388
0000322103 - - - Isolated (sporadic) 14y - - - - Kim Worring 00431427
0000323040 - - - Isolated (sporadic) 26y - - - - Kim Worring 00432478
0000323041 - - - Isolated (sporadic) 10y - - - - Kim Worring 00432479
0000324481 - - - Isolated (sporadic) 27y - - - - Kim Worring 00434127
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