Mirror movements 3

Summary

Any familial congenital mirror movements in which the cause of the disease is a mutation in the DNAL4 gene. [from MONDO]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Sequence analysis of the entire coding region (2)

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

DNAL4
7 tests
Also known as: MRMV3, PIG27, DNAL4
Summary: dynein axonemal light chain 4

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the cardiovascular system
- Situs inversus
  Situs inversus
  - MedGen UID: 1642262
  - Concept ID: C4551493
  - Finding: Congenital Abnormality
  Abnormality of the cardiovascular system
  See: Feature record | Search on this feature
Abnormality of the nervous system
- Bimanual synkinesia
  Bimanual synkinesia
  - MedGen UID: 473166
  - Concept ID: C0454455
  - Finding: Disease or Syndrome
  Abnormality of the nervous system
  See: Feature record | Search on this feature

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Clinical resources

Molecular resources

Consumer resources

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