NM_000257.4(MYH7):c.2585C>T (p.Ala862Val) AND Cardiomyopathy
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Sep 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001184308.14
Allele description [Variation Report for NM_000257.4(MYH7):c.2585C>T (p.Ala862Val)]
NM_000257.4(MYH7):c.2585C>T (p.Ala862Val)
Condition(s)
- Name:
- Cardiomyopathy (CMYO)
- Synonyms:
- Cardiomyopathies
- Identifiers:
- MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638
-
Enteropathy-Associated T-Cell Lymphoma
Enteropathy-Associated T-Cell LymphomaA primary peripheral T-cell lymphoma in the gastrointestinal tract, most often in the jejunum, associated with a history of CELIAC DISEASE or other gastrointestinal diseases....<br/>Year introduced: 2011MeSH
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Last Updated: Nov 3, 2024