Details of Disease

General Information of Disease (ID: DIS1492E)

Disease Name Mirror movements 4
Synonyms MRMV4; MIRROR MOVEMENTS 4
Disease Hierarchy
DISJLV92: Familial congenital mirror movements
DIS1492E: Mirror movements 4
Disease Identifiers
MONDO ID
MONDO_0032641
UMLS CUI
C4748869
OMIM ID
618264
MedGen ID
1648342

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
NTN1 TT0AH4L Strong Autosomal dominant [1]
NTN1 TT0AH4L Strong Genetic Variation [1]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
NTN1 OTUQH74P Strong Autosomal dominant [1]
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References

1 Mutations in the netrin-1 gene cause congenital mirror movements. J Clin Invest. 2017 Nov 1;127(11):3923-3936. doi: 10.1172/JCI95442. Epub 2017 Sep 25.