General Information of Disease (ID: DISDWCBG)

Disease Name Cone-rod dystrophy 10
Synonyms cone-rod dystrophy type 10; CORD10; SEMA4A cone-rod dystrophy; cone-rod dystrophy caused by mutation in SEMA4A; cone-rod dystrophy 10
Definition Any cone-rod dystrophy in which the cause of the disease is a mutation in the SEMA4A gene.
Disease Hierarchy
DISY9RWN: Cone-rod dystrophy
DISDWCBG: Cone-rod dystrophy 10
Disease Identifiers
MONDO ID
MONDO_0012464
MESH ID
C564597
UMLS CUI
C1846529
OMIM ID
610283
MedGen ID
337598

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
SEMA4A OT8901H3 Limited Unknown [1]
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References

1 Severe retinal degeneration associated with disruption of semaphorin 4A. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2767-77. doi: 10.1167/iovs.04-0020.