Epilepsy, familial adult myoclonic, 6

Synonyms: BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 6; CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 6

Available tests

1 test is in the database for this condition.

Clinical tests (1 available)

Molecular Genetics Tests

Sequence analysis of the entire coding region (1)

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TNRC6A
3 tests
Also known as: CAGH26, FAME6, GW1, GW182, TNRC6, TNRC6A
Summary: trinucleotide repeat containing adaptor 6A

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the nervous system
- Myoclonic tremor
  Myoclonic tremor
  - MedGen UID: 1739193
  - Concept ID: C5421572
  - Finding: Disease or Syndrome
  Abnormality of the nervous system
  See: Feature record | Search on this feature

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Clinical resources

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