Details of Disease

General Information of Disease (ID: DISILVN9)

Disease Name Oculomotor-abducens synkinesis
Synonyms OCABSN
Disease Hierarchy
DISYKSRF: Genetic disease
DISILVN9: Oculomotor-abducens synkinesis
Disease Identifiers
MONDO ID
MONDO_0030976
UMLS CUI
C5543116
OMIM ID
619215
MedGen ID
1789067

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
ACKR3 TTRQJTC Limited Unknown [1]
------------------------------------------------------------------------------------
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ACKR3 OTA6GA4F Limited Unknown [1]
------------------------------------------------------------------------------------

References

1 Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humans. Hum Mol Genet. 2019 Sep 15;28(18):3113-3125. doi: 10.1093/hmg/ddz137.