Details of Disease | DrugMAP

General Information of Disease (ID: DISJTA9T)

Disease Name	CNGA1-related retinopathy
Definition	An inherited retinopathy caused by bi-allelic variants in the CNGA1 gene.
Disease Hierarchy	DISGGL77: Inherited retinal dystrophy DISJTA9T: CNGA1-related retinopathy

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
CNGA1	TTHIQMC	Definitive	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CNGA1	OT0RXMJN	Definitive	Autosomal recessive	[1]
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References

1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.