Details of Disease | DrugMAP

General Information of Disease (ID: DISRSWSN)

Disease Name	White-Kernohan syndrome
Disease Hierarchy	DISYKSRF: Genetic disease DISRSWSN: White-Kernohan syndrome
Disease Identifiers	MONDO ID MONDO_0859169 UMLS CUI C5543635 OMIM ID 619426 MedGen ID 1785087

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
DDB1	OTTR2L3Z	Strong	Autosomal dominant	[1]
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References

1	A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome. Am J Hum Genet. 2021 Apr 1;108(4):749-756. doi: 10.1016/j.ajhg.2021.03.007. Epub 2021 Mar 19.