Details of Disease | DrugMAP

General Information of Disease (ID: DIS7UKI2)

Disease Name	Hypotaurinemic retinal degeneration and cardiomyopathy
Synonyms	hypotaurinemic retinal degeneration and cardiomyopathy
Disease Hierarchy	DISYKSRF: Genetic disease DIS7UKI2: Hypotaurinemic retinal degeneration and cardiomyopathy
Disease Identifiers	MONDO ID MONDO_0007777 UMLS CUI C5542181 OMIM ID 145350 MedGen ID 1779589

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC6A6	DTHWCVA	Limited	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
SLC6A6	OT67U7G3	Limited	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.