All conditions under O
All 200+ conditions are caused by changes to specific genes. These genes are shown underneath each condition.
Skip to conditionsConditions
- OAS1 associated polymorphic autoinflammatory immunodeficiency
Associated gene: OAS1
- Ornithine transcarbamylase deficiency
Associated gene: OTC
- Orotic aciduria
Associated gene: UMPS
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Osteogenesis Imperfecta
12 associated genes- COL1A1
- COL1A2
- IFITM5
- BMP1
- FKBP10
- KDELR2
- MESD
- SERPINF1
- SERPINH1
- SPARC
- TMEM38B
- WNT1
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Osteopetrosis
5 associated genes- TCIRG1
- CLCN7
- TNFRSF11A
- SNX10
- CA2
- Osteoporosis-pseudoglioma syndrome
Associated gene: LRP5
- Otofaciocervical syndrome
Associated gene: PAX1
- OTOF related deafness
Associated gene: OTOF