NM_001369.3(DNAH5):c.13779G>C (p.Thr4593=) AND Primary ciliary dyskinesia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 27, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001424678.8
Allele description [Variation Report for NM_001369.3(DNAH5):c.13779G>C (p.Thr4593=)]
NM_001369.3(DNAH5):c.13779G>C (p.Thr4593=)
Condition(s)
- Name:
- Primary ciliary dyskinesia
- Synonyms:
- Ciliary dyskinesia
- Identifiers:
- MONDO: MONDO:0016575; MedGen: C0008780; OMIM: PS244400; Human Phenotype Ontology: HP:0012265
Assertion and evidence details
Last Updated: Sep 29, 2024