Disease #00027 (OI (Osteogenesis imperfecta))

Official abbreviation OI
Name Osteogenesis imperfecta
OMIM ID -
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes COL1A1, COL1A2
Associated tissues -
Disease features -
Remarks -


Individuals

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Owner     
00000182 Nadiah Mohd Nawawi et al. (2018) - Malaysia - - - - OI - COL1A1 COL1A1 12 1 Nuur Athirah Binti Mohd Daud
00000183 Nadiah Mohd Nawawi et al. (2018) - Malaysia - - - - OI - COL1A2 COL1A2 4 1 Nuur Athirah Binti Mohd Daud
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