Details of Disease

General Information of Disease (ID: DISNP4QO)

Disease Name Cone-rod dystrophy 24
Disease Hierarchy
DISY9RWN: Cone-rod dystrophy
DISNP4QO: Cone-rod dystrophy 24
Disease Identifiers
MONDO ID
MONDO_0957240
UMLS CUI
C5830446
OMIM ID
620342
MedGen ID
1841082

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
UNC119 OTZN6BMJ Limited Unknown [1]
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References

1 HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model. Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3268-77.