Details of Disease

General Information of Disease (ID: DISIODI8)

Disease Name Mirror movements 3
Synonyms MRMV3; mirror movements 3; DNAL4 familial congenital mirror movements; mirror movements type 3; familial congenital mirror movements caused by mutation in DNAL4
Definition Any familial congenital mirror movements in which the cause of the disease is a mutation in the DNAL4 gene.
Disease Hierarchy
DISJLV92: Familial congenital mirror movements
DISIODI8: Mirror movements 3
Disease Identifiers
MONDO ID
MONDO_0014478
UMLS CUI
C4015124
OMIM ID
616059
MedGen ID
863561

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
DNAL4 OTHGA93D Limited Unknown [1]
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References

1 The "primary" antiphospholipid syndrome: major clinical and serological features. Medicine (Baltimore). 1989 Nov;68(6):366-74.