Diseases — O
11 diseases in this group. Each links to a full page: the emergence switch, the forced corrective direction, mapped agents, and the firewall. Direction only — no dose.
- Oculocutaneous albinism 1HOLD · ↓ DOWN · restore by supplyTYR
- Oculocutaneous albinism 2HOLD · ↓ DOWN · restore by supplyOCA2
- Oral-facial-digital syndrome type 1HOLD · ↓ DOWN · restore by supplyOFD1
- Omenn syndromeHOLD · ↓ DOWN · restore by supplyRAG2
- OpsismodysplasiaHOLD · ↓ DOWN · restore by supplyINPPL1
- Ornithine transcarbamylase deficiency OMIM 311250MATCH · ↑ UP · restore by clearOTC
- Hereditary orotic aciduriaMATCH · ↓ DOWN · restore by supplyUMPS
- Osteogenesis imperfecta IVMATCH · ↑ UP · restore by clearCOL1A2
- Osteogenesis imperfecta type IMATCH · ↓ DOWN · restore by clearCOL1A1
- Autosomal recessive osteopetrosis 4HOLD · ↓ DOWN · restore by supplyCLCN7
- Infantile malignant osteopetrosisMATCH · ↓ DOWN · restore by supplyTCIRG1