Phenotypes for disease #02970 (OI7 (osteogenesis imperfecta, type VII (OI7)), OMIM:610682)

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     
0000060583 Osteogenesis imperfecta, type VII (OMIM:610682) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081014
0000302283 Dentinogenesis imperfecta (HP:0000703), Blue sclerae (HP:0000592), Brachycephaly (HP:0000248), Macrocephaly (HP:0000256) - - Familial, autosomal recessive 07y - 01y05m Bone fracture (HP:0020110) - Thanakorn Theerapanon 00410179
0000325331 - - - Familial, autosomal recessive 00y00m - - - - Kim Worring 00435092
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