(Q25377900)

English

familial congenital mirror movements

human disease

mirror movements

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default for all languages

No label defined

No description defined

Statements

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class of disease

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mirror movement disorder

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genetic association

1 reference

Mutations in DCC cause congenital mirror movements.

Identifiers

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GARD rare disease ID

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0 references

1 reference

Monarch Disease Ontology release 2018-06-29

27 July 2018

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