Phenotypes for disease #03752 (OI13 (osteogenesis imperfecta, type XIII (OI13)), OMIM:614856)

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     
0000302272 Dentinogenesis imperfecta (HP:0000703), no Blue sclerae (-HP:0000592), no Hearing abnormality (-HP:0000364) - - Familial, autosomal recessive 06y - 03y Bone fracture (HP:0020110) - Thanakorn Theerapanon 00410168
0000323039 - - - Isolated (sporadic) 24y - - - - Kim Worring 00432477
0000325156 - - - Isolated (sporadic) 05y - - - - Kim Worring 00434910
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