Details of Disease | DrugMAP

General Information of Disease (ID: DISP865O)

Disease Name	DKC1-related disorder
Synonyms	DKC1-related disorder
Definition	Any dyskeratosis congenita in which the cause of the disease is a mutation in the DKC1 gene.
Disease Hierarchy	DISSXV0K: Dyskeratosis congenita DISP865O: DKC1-related disorder

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
DKC1	OTX7DJR6	Definitive	X-linked	[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.