Details of Disease

General Information of Disease (ID: DISJZIWH)

Disease Name Nystagmus 6, congenital, X-linked
Synonyms NYS6; NYSTAGMUS 6, congenital, X-linked; nystagmus 6, congenital, X-linked, X-linked recessive; nystagmus 6, congenital, X-linked
Disease Hierarchy
DIS4MF43: GPR143-related foveal hypoplasia
DISMYF5H: Acquired nystagmus
DISJZIWH: Nystagmus 6, congenital, X-linked
Disease Identifiers
MONDO ID
MONDO_0010435
UMLS CUI
C3151752
OMIM ID
300814
MedGen ID
463102

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
GPR143 OTWUA2AV Strong X-linked [1]
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References

1 Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus. Mol Vis. 2008 May 30;14:1015-9.